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Para lograr una mayor supervivencia de los implantes dentales, es importante una sólida integración de los tejidos blandos en la región transmucosa con los pilares protésicos. El objetivo de este estudio fue evaluar si las superficies del pilar de titanio recubiertas con óxido de grafeno mejoraban la adhesión celular. Se ha demostrado que el óxido de grafeno favorece la integración y estabilidad de las células que componen los tejidos blandos periimplantarios, aumentando la biocompatibilidad, adhesión celular y propiedades antibacterianas del titanio. En este estudio se recubrieron las superficies de pilares de titanio anodizados de la empresa Nobel Biocare, mediante inmersión en una suspensión de óxido de grafeno con agua; posteriormente, se colocaron en una mufla a 180 °C durante 2 horas para fijar y secar el recubrimiento. Se caracterizó la película de óxido de grafeno mediante microscopía electrónica de barrido, espectroscopía por dispersión de rayos X (EDS) y mapeo elemental. Finalmente, se evaluaron los pilares protésicos de titanio anodizado con o sin recubrimiento de óxido de grafeno mediante ensayos de adhesión. La microscopía electrónica de barrido permitió observar las capas de óxido de grafeno depositadas sobre la superficie del pilar, el mapeo comprobó la presencia del carbono en toda la superficie y el EDS la presencia de carbono y titanio. Los ensayos biológicos demostraron un incremento significativo en la adhesión celular en los pilares de titanio recubierto con óxido de grafeno en comparación con sus contrapartes sin recubrir. Estos resultados permiten concluir que se lograron recubrir con éxito las superficies de los pilares de titanio anodizado con óxido de grafeno y que este recubrimiento tuvo una influencia favorable en la adhesión celular.

Abstract Invasive species significantly impact biodiversity and ecosystem services, yet understanding these effects at large spatial scales remains a challenge. Our study addresses this gap by assessing the current and potential future risks posed by 94 invasive species to seven key ecosystem services in Europe. We demonstrate widespread potential impacts, particularly on outdoor recreation, habitat maintenance, crop provisioning, and soil and nitrogen retention. Exposure to invasive species was higher in areas with lower provision of ecosystem services, particularly for regulating and cultural services. Exposure was also high in areas where ecosystem contributions to crop provision and nitrogen retention were at their highest. Notably, regions vital for ecosystem services currently have low invasion suitability, but face an average 77% increase in potential invasion area. Here we show that, while high-value ecosystem service areas at the highest risk represent a small fraction of Europe (0-13%), they are disproportionally important for service conservation. Our study underscores the importance of monitoring and protecting these hotspots to align management strategies with international biodiversity targets, considering both invasion vulnerability and ecosystem service sustainability.

Objective To assess organ damage, with emphasis on the cardiovascular system, over the different stages of the disease in a large SLE cohort.Methods Multicentre, longitudinal study of a cohort of 4219 patients with SLE enrolled in the Spanish Society of Rheumatology Lupus Registry. Organ damage was ascertained using the Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index (SDI). We longitudinally analysed SDI (globally and for each domain) over time only in the 1274 patients whose dates of damage events had been recorded.Results During the first year after diagnosis of SLE, 20% of the 1274 patients presented with new damage manifestations. At years 2 and 3, new damage was recorded in 11% and 9% of patients. The annual percentage of patients with new damage after year 5 decreased to 5%. In the first year with the disease, most damage was accumulated in the musculoskeletal, neuropsychiatric and renal systems; in later stages, most damage was in the musculoskeletal, ocular and cardiovascular systems. Considering ‘cerebrovascular accident’ and ‘claudication for 6 months’ as cardiovascular items, the cardiovascular system was the second most affected system during the early stages of SLE, with 19% of the patients who presented with damage affected at first year after diagnosis. During the late stages, 20–25% of the patients presenting with new damage did so in this modified cardiovascular domain of the SDI.Conclusions New damage occurs mainly during the first year following diagnosis of SLE. Cardiovascular damage is relevant in both the early and the late stages of the disease. Strategies to prevent cardiovascular damage should be implemented early after diagnosis of SLE.

Este estudio se centra en evaluar la diversidad de serpientes en los Distritos de Alanje, Bugaba, Boquerón y Renacimiento, en la provincia de Chiriquí, República de Panamá, considerando las influencias antropogénicas en los microhábitats. Además, abordamos la relación entre las fragmentaciones de los hábitats y la biodiversidad de serpientes, destacando la importancia de comprender el impacto humano en estas comunidades. El muestreo lo desarrollamos a lo largo de dos años en las estaciones seca, lluviosa y las transiciones entre ambas, evaluando de forma aleatoria las áreas. Los 82 ejemplares pertenecen a 6 familias, siendo Colubridae y Viperidae las más representadas. La proporción de especies no venenosas y venenosas fue de 7:4, resultando una prevalencia de las primeras. La curva de acumulación de especies sugiere que se alcanzó la saturación de especies al muestrear aproximadamente 50 ejemplares. Los resultados reflejan alta diversidad de serpientes en la región, con índices de biodiversidad que respaldan la variación en los hábitats prospectados. La abundancia de especies como Bothrops asper es la de mayor peligro para la salud humana, así como la identificación de especies vulnerables resaltan la importancia de su conservación. Los resultados proporcionan una visión adecuada de la diversidad de serpientes en los Distritos prospectados y demuestran la necesidad de continuar monitoreando y conservando estas poblaciones en el contexto de cambios ambientales y antropogénicos.

Background and objective: Hereditary kidney diseases (HKD) are a frequent cause of chronic kidney disease, and their diagnosis has increased since the introduction of next generation sequencing (NGS). In 2018, the Multidisciplinary Unit for Hereditary Kidney Diseases of the Region of Murcia (UMERH-RM) was founded based on the genetic study of HKD. The objective of this study is to analyze the results obtained in the first 3 years of operation, and to analyze the clinical factors associated to a final genetic diagnosis. Materials and methods: All the patients studied with the HKD gene panel were included. The characteristics between those who obtained a final genetic diagnosis and those who did not were compared. Results: A total of 360 patients were studied, detecting genetic variants in 164 not related patients (45.6%). 45 of these were variants of uncertain significance requiring a family co-segregation study, which was facilitated by the multidisciplinary unit. Overall, considering the results obtained with the NGS panel and the extended genomic studies, a final diagnostic yield of HRD of 33.3% (120/360) was achieved, and including incidental findings 35.6% (128/360).Two hundred and twenty-three patients with suspected Alport syndrome were studied. Diagnosis was confirmed in 28.5% (COL4A4 most frequent gene), more frequently women with an obvious compatible family history. They also had frequently microhematuria, although 5 patients without microhematuria confirmed the diagnosis. There were no differences in age, proteinuria, renal function, hearing loss, or ophthalmologic abnormalities. The most frequent finding in the renal biopsy was mesangial proliferation. We estimate that 39 patients avoided renal biopsy.A total of 101 patients with suspected PKD were also studied, 49.5% had a conclusive genetic result (most frequent gene PKD1), more frequently women, with larger kidney sizes (although 9 patients with normal kidney size confirmed diagnosis). Again, the most predictive characteristic of genetic outcome was family history. Conclusions: The implementation of an NGS panel for HKD, together with the multidisciplinary approach to cases, has improved the diagnostic performance of HKD. In our sample, autosomal dominant Alport syndrome is of highest incidence. Ophthalmological and auditory examinations did not contribute to the diagnosis. We have seen a significant decrease in the indication of renal biopsies thanks to molecular diagnosis. The multidisciplinary approach, with the active participation of nephrologists, paediatricians, clinical and molecular geneticists, with insistence on adequate patient phenotyping and review of their family history, offers a better interpretation of genetic variants, allowing reclassification of the diagnosis of some nephropathies, thus improving their management and genetic advice. Resumen: Antecedentes y objetivo: Las enfermedades renales hereditarias (ERH) son una causa frecuente de enfermedad renal crónica, habiéndose incrementado su diagnóstico desde la introducción de la secuenciación masiva (NGS). En 2018 se fundó la Unidad multidisciplinar de Enfermedades Renales Hereditarias de la Región de Murcia basándose en el estudio genético de las ERH mediante panel de genes. El objetivo de este estudio es analizar los resultados obtenidos en los primeros tres años de funcionamiento, así como analizar los factores clínicos que se asocian a la obtención de un diagnóstico genético final. Materiales y métodos: Se incluyeron los pacientes estudiados mediante panel de genes de ERH y se compararon las características entre los que obtuvieron un diagnóstico genético final y los que no. Resultados: Se estudiaron un total de 360 pacientes, detectándose variantes genéticas en 164 pacientes (45,6%) no relacionados familiarmente. Cuarenta y cinco de estas variantes eran de significado clínico incierto precisando estudio de cosegregación familiar, facilitado por la unidad multidisciplinar. Globalmente, considerando los resultados obtenidos con el panel de NGS realizado en el CBGC y los estudios genómicos ampliados, se consiguió un rendimiento diagnóstico final de ERH del 33,3% (120/360), contando hallazgos incidentales, del 35,6% (128/360).Se estudiaron 223 pacientes con sospecha de síndrome de Alport, confirmándose el diagnóstico en un 28,5% (gen más frecuente COL4A4), los cuales eran con más frecuencia mujeres, y con clara historia familiar compatible. También tenían con más frecuencia microhematuria, aunque 5 pacientes sin microhematuria confirmaron diagnóstico. No hubo diferencias en la edad, proteinuria, función renal, hipoacusia o alteraciones oftalmológicas. El hallazgo más frecuente en la biopsia renal fue la proliferación mesangial. Calculamos que 39 pacientes evitaron la realización de biopsia renal.Se estudiaron también 101 pacientes por sospecha de PQR, un 49,5% tuvieron un resultado genético concluyente (gen más frecuente PKD1), con mayor frecuencia mujeres, con tamaños renales mayores (aunque 9 pacientes con tamaño renal normal confirmaron diagnóstico). De nuevo la característica más predictiva de resultado genético fue la historia familiar. Conclusiones: La implementación de un panel de NGS para ERH, junto con el abordaje multidisciplinar de los casos, ha mejorado el rendimiento diagnóstico de las ERH. En nuestra muestra, hemos confirmado el síndrome de Alport autosómico dominante como el de mayor incidencia. Las exploraciones oftalmológicas y auditivas no contribuyeron al diagnóstico. Hemos visto un descenso importante en la indicación de biopsias renales gracias al diagnóstico molecular. El abordaje multidisciplinar, con la participación activa de nefrólogos, pediatras, genetistas clínicos y moleculares, con insistencia en el adecuado fenotipado del paciente y revisión de su historia familiar, ofrece una mejor interpretación de las variantes genéticas, permitiendo la reclasificación del diagnóstico de algunas nefropatías no filiadas como ERH, mejorando así su manejo y consejo genético.

Resumen: Antecedentes y objetivo: Las enfermedades renales hereditarias (ERH) son una causa frecuente de enfermedad renal crónica, habiéndose incrementado su diagnóstico desde la introducción de la secuenciación masiva (NGS). En 2018 se fundó la Unidad multidisciplinar de Enfermedades Renales Hereditarias de la Región de Murcia basándose en el estudio genético de las ERH mediante panel de genes. El objetivo de este estudio es analizar los resultados obtenidos en los primeros tres años de funcionamiento, así como analizar los factores clínicos que se asocian a la obtención de un diagnóstico genético final. Materiales y métodos: Se incluyeron los pacientes estudiados mediante panel de genes de ERH y se compararon las características entre los que obtuvieron un diagnóstico genético final y los que no. Resultados: Se estudiaron un total de 360 pacientes, detectándose variantes genéticas en 164 pacientes (45,6%) no relacionados familiarmente. Cuarenta y cinco de estas variantes eran de significado clínico incierto precisando estudio de cosegregación familiar, facilitado por la unidad multidisciplinar. Globalmente, considerando los resultados obtenidos con el panel de NGS realizado en el CBGC y los estudios genómicos ampliados, se consiguió un rendimiento diagnóstico final de ERH del 33,3% (120/360), contando hallazgos incidentales, del 35,6% (128/360).Se estudiaron 223 pacientes con sospecha de síndrome de Alport, confirmándose el diagnóstico en un 28,5% (gen más frecuente COL4A4), los cuales eran con más frecuencia mujeres, y con clara historia familiar compatible. También tenían con más frecuencia microhematuria, aunque 5 pacientes sin microhematuria confirmaron diagnóstico. No hubo diferencias en la edad, proteinuria, función renal, hipoacusia o alteraciones oftalmológicas. El hallazgo más frecuente en la biopsia renal fue la proliferación mesangial. Calculamos que 39 pacientes evitaron la realización de biopsia renal.Se estudiaron también 101 pacientes por sospecha de PQR, un 49,5% tuvieron un resultado genético concluyente (gen más frecuente PKD1), con mayor frecuencia mujeres, con tamaños renales mayores (aunque 9 pacientes con tamaño renal normal confirmaron diagnóstico). De nuevo la característica más predictiva de resultado genético fue la historia familiar. Conclusiones: La implementación de un panel de NGS para ERH, junto con el abordaje multidisciplinar de los casos, ha mejorado el rendimiento diagnóstico de las ERH. En nuestra muestra, hemos confirmado el síndrome de Alport autosómico dominante como el de mayor incidencia. Las exploraciones oftalmológicas y auditivas no contribuyeron al diagnóstico. Hemos visto un descenso importante en la indicación de biopsias renales gracias al diagnóstico molecular. El abordaje multidisciplinar, con la participación activa de nefrólogos, pediatras, genetistas clínicos y moleculares, con insistencia en el adecuado fenotipado del paciente y revisión de su historia familiar, ofrece una mejor interpretación de las variantes genéticas, permitiendo la reclasificación del diagnóstico de algunas nefropatías no filiadas como ERH, mejorando así su manejo y consejo genético. Abstract: Background and objective: Hereditary kidney diseases (HKD) are a frequent cause of chronic kidney disease, and their diagnosis has increased since the introduction of next generation sequencing (NGS). In 2018, the Multidisciplinary Unit for Hereditary Kidney Diseases of the Region of Murcia (UMERH-RM) was founded based on the genetic study of HKD. The objective of this study is to analyze the results obtained in the first 3 years of operation, and to analyze the clinical factors associated to a final genetic diagnosis. Materials and methods: All the patients studied with the HKD gene panel were included. The characteristics between those who obtained a final genetic diagnosis and those who did not were compared. Results: A total of 360 patients were studied, detecting genetic variants in 164 not related patients (45.6%). 45 of these were variants of uncertain significance requiring a family co-segregation study, which was facilitated by the multidisciplinary unit. Overall, considering the results obtained with the NGS panel and the extended genomic studies, a final diagnostic yield of HRD of 33.3% (120/360) was achieved, and including incidental findings 35.6% (128/360).Two hundred and twenty-three patients with suspected Alport syndrome were studied. Diagnosis was confirmed in 28.5% (COL4A4 most frequent gene), more frequently women with an obvious compatible family history. They also had frequently microhematuria, although 5 patients without microhematuria confirmed the diagnosis. There were no differences in age, proteinuria, renal function, hearing loss, or ophthalmologic abnormalities. The most frequent finding in the renal biopsy was mesangial proliferation. We estimate that 39 patients avoided renal biopsy.A total of 101 patients with suspected PKD were also studied, 49.5% had a conclusive genetic result (most frequent gene PKD1), more frequently women, with larger kidney sizes (although 9 patients with normal kidney size confirmed diagnosis). Again, the most predictive characteristic of genetic outcome was family history. Conclusions: The implementation of an NGS panel for HKD, together with the multidisciplinary approach to cases, has improved the diagnostic performance of HKD. In our sample, autosomal dominant Alport syndrome is of highest incidence. Ophthalmological and auditory examinations did not contribute to the diagnosis. We have seen a significant decrease in the indication of renal biopsies thanks to molecular diagnosis. The multidisciplinary approach, with the active participation of nephrologists, paediatricians, clinical and molecular geneticists, with insistence on adequate patient phenotyping and review of their family history, offers a better interpretation of genetic variants, allowing reclassification of the diagnosis of some nephropathies, thus improving their management and genetic advice.

Introduction. Cirrhosis is one of the ten leading causes of death in the Western hemisphere and entails a significant cost of health care. Objective. To describe the sociodemographic, clinical, and laboratory characteristics of patients older than 18 years who received care for acute decompensation of cirrhosis in the emergency services of three highly complex centers in Medellín, Colombia. Materials and methods. This was an observational retrospective cohort study from clinical records. The results were analyzed by frequency measures and represented in tables and graphics. Results. In total, 576 clinical records met the inclusion criteria; 287 were included for analysis, and 58.9% were men, with an average age of 64 (± 13.5) years. The most frequent causes of cirrhosis were alcohol intake (47.7%), cryptogenic or unspecified etiology (29.6%), and non-alcoholic fatty liver disease (9.1%). The main reasons for visiting the emergency department were the presence of edema and/or ascites (34.1%), suspicion of gastrointestinal bleeding (26.5%), abdominal pain (14.3%) and altered mental status (13.9%). The most frequent clinical manifestations of an acute decompensation of cirrhosis were ascites (45.6%), variceal hemorrhage (25.4%), hepatic encephalopathy (23.0%), and spontaneous bacterial peritonitis (5.2%). During their treatment, 56.1% of the patients received intravenous antibiotics; 24.0%, human albumin; 24.0%, vasoactive support, and 27.5%, blood products; 21.3% required management in an intensive or intermediate care unit, registering 53 deceased patients for a mortality of 18.5%. Conclusion. Patients who consult the emergency services due to acute decompensation of cirrhosis demand a high amount of health resources, frequently present associated complications, and a high percentage requires management in critical care units and shows a high in-hospital mortality rate.

Currently, in some marble quarries, the amount of waste amounts to 80%. The ReValoMur research project aimed to generate the necessary knowledge for the production of a new cementitious material, based on plastic waste from agriculture and waste derived from the extraction and/or transformation of natural stone, as a means of valorization of these industrial sectors in the Region of Murcia, in order to develop an optimal material of a more ecological scale within the productive range, focused on additive manufacturing as a potential technology for the rationalization and reuse of waste, that is, underused resources.

The concentration effect of Tradescantia spathacea (T. spathacea) as corrosion inhibitor of API 5L X52 steel in 0.5 M of H2SO4 was studied here through electrochemical and gravimetric techniques. To achieve it, samples of the material were prepared to be submitted to each of the tests. Results from electrochemical impedance spectroscopy (EIS) showed that there was an optimum concentration of the inhibitor in which is reached the maximum inhibition efficiency, displaying the best inhibition characteristics for this system with a maximum inhibition of 89% by using 400 ppm. However, the efficiency decreased until 40% when the temperature was increased to 60°C. Potentiodynamic polarization curves (PDP) revealed that some of the present compounds of T. spathacea may affect anodic and cathodic process, so it can be classified as a mix-type corrosion inhibitor for API 5L X52 in sulfuric acid. Also, this compound followed an adsorption mechanism; this can be described through a Frumkin isotherm with an adsorption standard free energy difference (ΔG°) of −56.59 kJmol−1. Metal surface was studied through scanning electron microscope, results revealed that by adding inhibitor, the metal surface is protected; also, they evidenced low damages compared with the surface with no inhibitor. Finally, Tradescantia spathacea inhibited the corrosion process with 82% efficiency.

With the objective to characterize the gingival index (GI) and its progression, 218 domestic cats in a subtropical region of Mexico were studied. All teeth of each cat were examined with a periodontal probe to determine the GI; in addition, the absence of teeth was recorded. Six months later, the teeth of the 38 cats were again examined to assess any progression of the GI and loss of teeth. From the 218 cats, 33.0% of them develop some degree of gingival inflammation; from those, 61.5% were classified as GI 1. Age, sex, and neutered status were associated with tooth affections. Missed teeth were observed in 35% of the cats, particularly for molars 109 and 209 in both sexes. After six months, the number of teeth with GI 1 decreased to 20%. The gingival problems in cats have not been well studied, particularly at the speed they progress and how this can affect the loss of teeth; under the conditions of this study, a high frequency of gingival inflammation even at early age was demonstrated, with a rapid tooth loss. Although young males were more prone to develop gingivitis, females tend to loss more teeth. Non-neutered cats tended to develop more dental affections.

Metronidazole (MTZ) is the most common drug used against Trichomonas vaginalis (T. vaginalis) infections; however, treatment failures and high rates of recurrence of trichomoniasis have been reported, suggesting the presence of resistance in T. vaginalis to MTZ. Therefore, research into new therapeutic options against T. vaginalis infections has become increasingly urgent. This study investigated the trichomonacidal activity of a series of five imidazole carbamate compounds (AGR-1, AGR-2, AGR-3, AGR-4, and AGR-5) through in vitro susceptibility assays to determine the IC50 value of each compound. All five compounds demonstrated potent trichomonacidal activity, with IC50 values in the nanomolar range and AGR-2 being the most potent (IC50 400 nM). To gain insight into molecular events related to AGR-induced cell death in T. vaginalis, we analyzed the expression profiles of some metabolic genes in the trophozoites exposed to AGR compounds and MTZ. It was found that both AGR and MTZ compounds reduced the expression of the glycolytic genes (CK, PFK, TPI, and ENOL) and genes involved in metabolism (G6PD, TKT, TALDO, NADHOX, ACT, and TUB), suggesting that disturbing these key metabolic genes alters the survival of the T. vaginalis parasite and that they probably share a similar mechanism of action. Additionally, the compounds showed low cytotoxicity in the Caco-2 and HT29 cell lines, and the results of the ADMET analysis indicated that these compounds have pharmacokinetic properties similar to those of MTZ. The findings offer significant insights that can serve as a basis for future in vivo studies of the compounds as a potential new treatment against T. vaginalis.

The parasite Trichomonas vaginalis is the etiologic agent of trichomoniasis, the most common non-viral sexually transmitted disease worldwide. This infection often remains asymptomatic and is related to several health complications. The traditional treatment for trichomoniasis is the use of drugs of the 5-nitroimidazole family, such as metronidazole; however, scientific reports indicate an increasing number of drug-resistant strains. Benzimidazole derivatives could offer an alternative in the search for new anti-trichomonas drugs. In this sense, two attractive candidates are the compounds O2N-BZM7 and O2N-BZM9 (1H-benzimidazole derivatives), since, through in vitro tests, they have shown a higher trichomonacide activity. In this study, we determined the effect on the expression level of metabolic genes in T. vaginalis. The results show that genes involved in redox balance (NADHOX, G6PD::6PGL) are overexpressed, as well as the gene that participates in the first reaction of glycolysis (CK); on the other hand, structural genes such as ACT and TUB are decreased in expression in trophozoites treated with the compound O2N-BZM9, which would probably affect its morphology, motility and virulence. These results align with the trichomonacidal activity of the compounds, with benzimidazole O2N-BZM9 being the most potent, with an IC50 value of 4.8 μM. These results are promising for potential future therapeutic applications.

Code-modulated visual evoked potentials (c-VEPs) are an innovative control signal utilized in brain-computer interfaces (BCIs) with promising performance. Prior studies on steady-state visual evoked potentials (SSVEPs) have indicated that the spatial frequency of checkerboard-like stimuli influences both performance and user experience. Spatial frequency refers to the dimensions of the individual squares comprising the visual stimulus, quantified in cycles (i.e., number of black-white squares pairs) per degree of visual angle. However, the specific effects of this parameter on c-VEP-based BCIs remain unexplored. Therefore, the objective of this study is to investigate the role of spatial frequency of checkerboard-like visual stimuli in a c-VEP-based BCI. Sixteen participants evaluated selection matrices with eight spatial frequencies: C001 (0 c/°, 1×1 squares), C002 (0.15 c/°, 2×2 squares), C004 (0.3 c/°, 4×4 squares), C008 (0.6 c/°, 8×8 squares), C016 (1.2 c/°, 16×16 squares), C032 (2.4 c/°, 32×32 squares), C064 (4.79 c/°, 64×64 squares), and C128 (9.58 c/°, 128×128 squares). These conditions were tested in an online spelling task, which consisted of 18 trials each conducted on a 3×3 command interface. In addition to accuracy and information transfer rate (ITR), subjective measures regarding comfort, ocular irritation, and satisfaction were collected. Significant differences in performance and comfort were observed based on different stimulus spatial frequencies. Although all conditions achieved mean accuracy over 95% after 2.1 s of trial duration, C016 stood out in terms user experience. The proposed condition not only achieved a mean accuracy of 96.53% and 164.54 bits/min with a trial duration of 1.05s, but also was reported to be significantly more comfortable than the traditional C001 stimulus. Since both features are key for BCI development, higher spatial frequencies than the classical black-to-white stimulus might be more adequate for c-VEP systems. Hence, we assert that the spatial frequency should be carefully considered in the development of future applications for c-VEP-based BCIs.

Introduction: Despite the benefits of physical exercise (PE) for patients with chronic kidney disease (CKD), the number of Nephrology services that have PE programs is limited. Objectives: To describe the degree of knowledge of PE benefits in patients with CKD among professionals, as well as the level of implementation and characteristics of PE programs in Nephrology services in Spain. Methods: A questionnaire on the degree of knowledge and prescription of PE in patients with CKD was designed and sent to members of the Spanish Nephrology and Nephrology Nursing Societies, as well as to physiotherapists and professionals in the Sciences of Physical Activity and Sport (PASS). Results: 264 professionals participated. 98.8% agreed on the importance of prescribing PE, but only 20.5% carry out an assessment of functional capacity and 19.3% have a PE program for patients with CKD in their centre. The most frequent programs are performed for haemodialysis patients and strength and aerobic resistance exercises are combined. A physiotherapist or a PASS usually participates in its prescription. The main barriers were the absence of human and/or physical resources and the lack of training. Conclusions: Healthcare workers know the benefits of PE in patients with CKD. However, the implementation of these programs in Spain is low, motivated by the lack of resources and training of professionals. We must establish strategies to guarantee an adequate functional capacity within the care of our patients. Resumen: Introducción: A pesar de los beneficios del ejercicio físico (EF) para pacientes con enfermedad renal crónica (ERC), el número de servicios de Nefrología que han implementado programas de EF es limitado. Objetivos: Describir el grado de conocimiento del EF en pacientes con ERC entre los profesionales, así como el nivel de implementación y las características de los programas de EF en los servicios de Nefrología en España. Métodos: Se diseñó un cuestionario sobre el grado de conocimiento y de prescripción del EF en pacientes con ERC que se envió a los socios de la Sociedad Española de Nefrología y de la Sociedad Española de Enfermería Nefrológica, así como a fisioterapeutas y profesionales de las Ciencias de la Actividad Física y del Deporte (CAFyD). Resultados: Participaron 264 profesionales. El 98,8% coincidían en la importancia de prescribir EF, pero solo el 20,5% realizan una valoración de la capacidad funcional y solo el 19,3% disponen de un programa de EF para pacientes con ERC en su centro. Los programas más frecuentes están dirigidos a pacientes en hemodiálisis y combinan ejercicios de fuerza y de resistencia aeróbica. En la prescripción habitualmente interviene un fisioterapeuta o un PASS. Las principales barreras fueron la ausencia de recursos humanos y/o físicos y la falta de formación. Conclusiones: Los profesionales sanitarios conocen los beneficios del EF en el paciente renal. Sin embargo, la implementación de estos programas en España es baja, debido a la falta de recursos y a la falta de formación de los profesionales. Debemos establecer estrategias para garantizar una adecuada capacidad funcional dentro de los cuidados de nuestros pacientes.

Plaque Psoriasis (PP) and periodontitis are inflammatory disorders with a bidirectional association. They both have a qualitatively similar immune-modulatory cascade, cytokine profile, and a recently described dysbiosis. Different oral bacterial species compositions in the periodontal pocket might play a role in the development of PP. To describe the subgingival microbiota of the Mexican population with PP and the periodontal conditions. Subjects were divided into two groups: periodontal health (PH) (PH-non-PP, PH-PP) and periodontitis (PD) (P-non-PP, PD-PP). Following clinical examination, the patients were classified into three groups according to the degree of psoriasis as measured by the Psoriasis Area Severity Index (PASI) and the periodontal status according to the parameters of the American Academy of Periodontology (AAP). Subgingival microbiota samples of each patient were used to determine 40 species of periodontal bacteria by checkerboard DNA-DNA hybridization. IL-2 and IL-6 were measured by ELISA. Of the forty-eight patients with PP, 21 patients had PH and 27 patients had PD. PD-PP group has a significant increase in the percentage of plaque, gingival redness, pocket probing depth, and clinical attachment loss (P 5 related to periodontitis with the predominance of Actinomyces periodontal, irrespective of their periodontal condition. Finally, the severity of psoriasis could be unbalanced in subgingival microbiota and increase the risk to develop periodontitis.

Resumen: Introducción: A pesar de los beneficios del ejercicio físico (EF) para pacientes con enfermedad renal crónica (ERC), el número de servicios de Nefrología que han implementado programas de EF es limitado. Objetivos: Describir el grado de conocimiento del EF en pacientes con ERC entre los profesionales, así como el nivel de implementación y las características de los programas de EF en los servicios de Nefrología en España. Métodos: Se diseñó un cuestionario sobre el grado de conocimiento y de prescripción del EF en pacientes con ERC que se envió a los socios de la Sociedad Española de Nefrología y de la Sociedad Española de Enfermería Nefrológica, así como a fisioterapeutas y profesionales de las Ciencias de la Actividad Física y del Deporte (CAFyD). Resultados: Participaron 264 profesionales. El 98,8% coincidían en la importancia de prescribir EF, pero solo el 20,5% realizan una valoración de la capacidad funcional y solo el 19,3% disponen de un programa de EF para pacientes con ERC en su centro. Los programas más frecuentes están dirigidos a pacientes en hemodiálisis y combinan ejercicios de fuerza y de resistencia aeróbica. En la prescripción habitualmente interviene un fisioterapeuta o un CAFyD. Las principales barreras fueron la ausencia de recursos humanos y/o físicos y la falta de formación. Conclusiones: Los profesionales sanitarios conocen los beneficios del EF en el paciente renal. Sin embargo, la implementación de estos programas en España es baja, debido a la falta de recursos y a la falta de formación de los profesionales. Debemos establecer estrategias para garantizar una adecuada capacidad funcional dentro de los cuidados de nuestros pacientes. Abstract: Introduction: Despite the benefits of physical exercise (PE) for patients with chronic kidney disease (CKD), the number of Nephrology services that have PE programs is limited. Objectives: To describe the degree of knowledge of PE benefits in patients with CKD among professionals, as well as the level of implementation and characteristics of PE programs in Nephrology services in Spain. Methods: A questionnaire on the degree of knowledge and prescription of PE in patients with CKD was designed and sent to members of the Spanish Nephrology and Nephrology Nursing Societies, as well as to physiotherapists and professionals in the Sciences of Physical Activity and Sport (CAFyD). Results: 264 professionals participated. 98.8% agreed on the importance of prescribing PE, but only 20.5% carry out an assessment of functional capacity and 19.3% have a PE program for patients with CKD in their center. The most frequent programs are performed for hemodialysis patients and strength and aerobic resistance exercises are combined. A physiotherapist or a CAFyD usually participates in its prescription. The main barriers were the absence of human and/or physical resources and the lack of training. Conclusions: Healthcare workers know the benefits of PE in patients with CKD. However, the implementation of these programs in Spain is low, motivated by the lack of resources and training of professionals. We must establish strategies to guarantee an adequate functional capacity within the care of our patients.

Introduction and objectiveVideo games are crucial to the entertainment industry, nonetheless they can be challenging to access for those with severe motor disabilities. Brain-computer interfaces (BCI) systems have the potential to help these individuals by allowing them to control video games using their brain signals. Furthermore, multiplayer BCI-based video games may provide valuable insights into how competitiveness or motivation affects the control of these interfaces. Despite the recent advancement in the development of code-modulated visual evoked potentials (c-VEPs) as control signals for high-performance BCIs, to the best of our knowledge, no studies have been conducted to develop a BCI-driven video game utilizing c-VEPs. However, c-VEPs could enhance user experience as an alternative method. Thus, the main goal of this work was to design, develop, and evaluate a version of the well-known ‘Connect 4' video game using a c-VEP-based BCI, allowing 2 users to compete by aligning 4 same-colored coins vertically, horizontally or diagonally.MethodsThe proposed application consists of a multiplayer video game controlled by a real-time BCI system processing 2 electroencephalograms (EEGs) sequentially. To detect user intention, columns in which the coin can be placed was encoded with shifted versions of a pseudorandom binary code, following a traditional circular shifting c-VEP paradigm. To analyze the usability of our application, the experimental protocol comprised an evaluation session by 22 healthy users. Firstly, each user had to perform individual tasks. Afterward, users were matched and the application was used in competitive mode. This was done to assess the accuracy and speed of selection. On the other hand, qualitative data on satisfaction and usability were collected through questionnaires.ResultsThe average accuracy achieved was 93.74% ± 1.71%, using 5.25 seconds per selection. The questionnaires showed that users felt a minimal workload. Likewise, high satisfaction values were obtained, highlighting that the application was intuitive and responds quickly and smoothly.ConclusionsThis c-VEP based multiplayer video game has reached suitable performance on 22 users, supported by high motivation and minimal workload. Consequently, compared to other versions of “Connect 4” that utilized different control signals, this version has exhibited superior performance.

The compound parabolic concentrator (CPC) is a core technology in the field of solar concentration. Nevertheless, it only has one degree of freedom in the choice of its half-acceptance angle. In this study, extending the idea of the three-dimensional CPC, a design method for new kinds of concentrators having a CPC shape at each profile with various acceptance angles in all directions is proposed. The feature of this method is that the receiver can take any shape. Here, elliptical and rectangular receivers are assumed, and the shape and concentration performance of the concentrators with multiple CPC profiles and an elliptical receiver (MultiPro-ECPCs) and the concentrators with multiple CPC profiles and a rectangular receiver (MultiPro-RCPCs) are derived. The new designs are compared to the conventional CPC and a mirrorless flat receiver through ray-tracing simulations in terms of energy distribution on the receiver, optical efficiency, and optical concentration ratio based on axial and solar angles. The results show that in terms of optical efficiency, the MultiPro-RCPCs cover a wider range of incident angles after the 3DCPC. In terms of the optical concentration ratio, the MultiPro-ECPC with a longitudinal half-acceptance angle of 15° has the highest peak value of 19.5, followed by the MultiPro-RCPC. This study enlightens that with the concentration system settings adapted to the acceptance range of the proposed concentrators, a higher concentration can be achieved with the MultiPro-ECPC and MultiPro-RCPC compared to the conventional CPC.

Several microaerophilic parasites such as Giardia lamblia, Trichomonas vaginalis, and Plasmodium falciparum are major disease-causing organisms and are responsible for spreading infections worldwide. Despite significant progress made in understanding the metabolism and molecular biology of microaerophilic parasites, chemotherapeutic treatment to control it has seen limited progress. A current proposed strategy for drug discovery against parasitic diseases is the identification of essential key enzymes of metabolic pathways associated with the parasite’s survival. In these organisms, glucose-6-phosphate dehydrogenase::6-phosphogluconolactonase (G6PD:: 6PGL), the first enzyme of the pentose phosphate pathway (PPP), is essential for its metabolism. Since G6PD:: 6PGL provides substrates for nucleotides synthesis and NADPH as a source of reducing equivalents, it could be considered an anti-parasite drug target. This review analyzes the anaerobic energy metabolism of G. lamblia, T. vaginalis, and P. falciparum, with a focus on glucose metabolism through the pentose phosphate pathway and the significance of the fused G6PD:: 6PGL enzyme as a therapeutic target in the search for new drugs.

The sheet-metal-forming process is crucial in manufacturing various products, including pipes, cans, and containers. Despite its significance, controlling this complex process is challenging and may lead to defects and inefficiencies. This study introduces a novel approach to monitor the sheet-metal-forming process, specifically focusing on the rolling of cans in the oil-and-gas sector. The methodology employed in this work involves the application of temporal-signal-processing and artificial-intelligence (AI) techniques for monitoring and optimizing the manufacturing process. Temporal-signal-processing techniques, such as Markov transition fields (MTFs), are utilized to transform time series data into images, enabling the identification of patterns and anomalies. synamic time warping (DTW) aligns time series data, accommodating variations in speed or timing across different rolling processes. K-medoids clustering identifies representative points, characterizing distinct phases of the rolling process. The results not only demonstrate the effectiveness of this framework in monitoring the rolling process but also lay the foundation for the practical application of these methodologies. This allows operators to work with a simpler characterization source, facilitating a more straightforward interpretation of the manufacturing process.

Abstract Background The diagnosis of migraine is mainly clinical and self-reported, which makes additional examinations unnecessary in most cases. Migraine can be subtyped into chronic (CM) and episodic (EM). Despite the very high prevalence of migraine, there are no evidence-based guidelines for differentiating between these subtypes other than the number of days of migraine headache per month. Thus, we consider it timely to perform a systematic review to search for physiological evidence from functional activity (as opposed to anatomical structure) for the differentiation between CM and EM, as well as potential functional biomarkers. For this purpose, Web of Science (WoS), Scopus, and PubMed databases were screened. Findings Among the 24 studies included in this review, most of them (22) reported statistically significant differences between the groups of CM and EM. This finding is consistent regardless of brain activity acquisition modality, ictal stage, and recording condition for a wide variety of analyses. That speaks for a supramodal and domain-general differences between CM and EM that goes beyond a differentiation based on the days of migraine per month. Together, the reviewed studies demonstrates that electro- and magneto-physiological brain activity (M/EEG), as well as neurovascular and metabolic recordings from functional magnetic resonance imaging (fMRI) and positron emission tomography (PET), show characteristic patterns that allow to differentiate between CM and EM groups. Conclusions Although a clear brain activity-based biomarker has not yet been identified to distinguish these subtypes of migraine, research is approaching headache specialists to a migraine diagnosis based not only on symptoms and signs reported by patients. Future studies based on M/EEG should pay special attention to the brain activity in medium and fast frequency bands, mainly the beta band. On the other hand, fMRI and PET studies should focus on neural circuits and regions related to pain and emotional processing.

Autosomal dominant polycystic kidney disease (ADPKD) is the most frequent cause of genetic renal disease and accounts for 6–10% of patients on kidney replacement therapy (KRT).Very few prospective, randomized trials or clinical studies address the diagnosis and management of this relatively frequent disorder. No clinical guidelines are available to date. This is a revised consensus statement from the previous 2014 version, presenting the recommendations of the Spanish Working Group on Inherited Kidney Diseases, which were agreed to following a literature search and discussions. Levels of evidence mostly are C and D according to the Centre for Evidence-Based Medicine (University of Oxford). The recommendations relate to, among other topics, the use of imaging and genetic diagnosis, management of hypertension, pain, cyst infections and bleeding, extra-renal involvement including polycystic liver disease and cranial aneurysms, management of chronic kidney disease (CKD) and KRT and management of children with ADPKD. Recommendations on specific ADPKD therapies are provided as well as the recommendation to assess rapid progression. Resumen: La poliquístosis renal autosómica dominante (PQRAD) es la causa más frecuente de nefropatía genética y representa entre 6 a 10% de los pacientes en terapia de reemplazo renal (TRR).Muy pocos ensayos prospectivos, aleatorizados o estudios clínicos abordan el diagnóstico y el tratamiento de este trastorno relativamente frecuente. No hay guías clínicas disponibles hasta la fecha. Esta es un docuemento de consenso revisada de la versión anterior de 2014, que presenta las recomendaciones del Grupo de Trabajo Español de Enfermedades Renales Hereditarias, acordadas tras la búsqueda bibliográfica y discusiones. Los niveles de evidencia en su mayoría son C y D según el Centro de Medicina Basada en Evidencia (Universidad de Oxford). Las recomendaciones se relacionan, entre otros temas, con el uso de diagnóstico por imágenes y genético, el manejo de la hipertensión, el dolor, las infecciones y el sangrado quístico, la afectación extrarrenal, incluida la enfermedad poliquística hepática y los aneurismas craneales, el manejo de la enfermedad renal crónica (ERC) y el TRR asi como el seguimiento de niños con PQRAD. Se proporcionan recomendaciones sobre terapias específicas para la PQRAD, así como la recomendación para evaluar la rápida progresión.

Resumen: La poliquistosis renal autosómica dominante (PQRAD) es la causa más frecuente de nefropatía genética y representa entre el 6 y el 10% de los pacientes en terapia de reemplazo renal (TRR).Muy pocos ensayos prospectivos, aleatorizados o estudios clínicos abordan el diagnóstico y el tratamiento de este trastorno relativamente frecuente. No hay guías clínicas disponibles hasta la fecha. Este es un documento de consenso revisada de la versión anterior del 2014, que presenta las recomendaciones del Grupo de Trabajo Español de Enfermedades Renales Hereditarias, acordadas tras la búsqueda bibliográfica y discusiones. Los niveles de evidencia en su mayoría son C y D según el Centro de Medicina Basada en Evidencia (Universidad de Oxford). Las recomendaciones se relacionan, entre otros temas, con el uso de diagnóstico por imágenes y genético, el manejo de la hipertensión, el dolor, las infecciones y el sangrado quístico, la afectación extrarrenal, incluida la enfermedad poliquística hepática y los aneurismas craneales, el manejo de la enfermedad renal crónica y el TRR, así como el seguimiento de niños con PQRAD. Se proporcionan recomendaciones sobre terapias específicas para la PQRAD, así como la recomendación para evaluar la rápida progresión. Abstract: Autosomal dominant polycystic kidney disease (ADPKD) is the most frequent cause of genetic renal disease and accounts for 6–10% of patients on kidney replacement therapy (KRT).Very few prospective, randomized trials or clinical studies address the diagnosis and management of this relatively frequent disorder. No clinical guidelines are available to date. This is a revised consensus statement from the previous 2014 version, presenting the recommendations of the Spanish Working Group on Inherited Kidney Diseases, which were agreed to following a literature search and discussions. Levels of evidence mostly are C and D according to the Centre for Evidence-Based Medicine (University of Oxford). The recommendations relate to, among other topics, the use of imaging and genetic diagnosis, management of hypertension, pain, cyst infections and bleeding, extra-renal involvement including polycystic liver disease and cranial aneurysms, management of chronic kidney disease and KRT and management of children with ADPKD. Recommendations on specific ADPKD therapies are provided as well as the recommendation to assess rapid progression.

El derecho canónico vigente desde el CIC 83 ha rechazado la posibilidad de atribuir responsabilidad penal a las personas jurídicas. Sin embargo, el derecho canónico siempre reconoció a las corporaciones como sujetos de responsabilidad penal, y así constaba por ejemplo en el CIC 17. Por ello, en el presente artículo pretendemos analizar los fundamentos en virtud de los cuales el derecho canónico siempre reconoció la responsabilidad penal corporativa. A tal efecto estudiamos en primer lugar las fuentes bíblicas en que se destruyen unas ciudades que se conciben como corporaciones, y en segundo lugar a los principales autores de los siglos XII y XIII en que se da forma a la doctrina canónica que pervivirá inmutada hasta el reciente año de 1983.

En el presente trabajo se presenta una síntesis y discusión sobre la presencia de patologías congénitas y defectos del desarrollo en individuos de diferentes periodos arqueológicos de la costa de la región de Antofagasta, en el norte de Chile, las que se concentran en el esqueleto axial. A pesar de ser un número bajo (n: 6), se realiza una comparación con aquellas reportadas para la zona costera de Arica y Tarapacá, obteniéndose que las diferencia entre ambas zonas no es estadísticamente significativa. Considerando antecedentes ambientales y etnohistóricos de la zona, se propone que una combinación a la exposición de diferentes contaminantes naturales, junto a un sistema de parentesco endogámico serían las causas más probables de la aparición de estas patologías.

El propósito de este estudio fue explorar el proceso de apropiación de medios digitales en escuelas interculturales rurales aplicando un enfoque naturalista que se orienta a comprender e interpretar las experiencias desde sus propios protagonistas. Participaron profesores, directoras y estudiantes de ocho escuelas de la región de la Araucanía. Complementariamente se aplicó un cuestionario a 49 profesores de escuelas rurales interculturales de la región. Los principales resultados establecen que las circunstancias generadas por la pandemia impulsaron una digitalización creciente y acelerada del mundo de la vida y el trabajo de las comunidades educativas, configurando para las y los profesores un contexto complejo que condiciona la apropiación que ellos y ellas hacen de los medios digitales, tanto en su quehacer institucional como en su vida cotidiana. Este proceso de apropiación es principalmente orientado por estas comunidades a la potenciación del Ser Mapuche.

BackgroundDecrements in performance and the propensity for increased mind-wandering (i.e., task-unrelated thoughts) across time-on-task are two pervasive phenomena observed when people perform vigilance tasks. In the present study, we asked whether processes that lead to vigilance decrement and processes that foster the propensity for mind-wandering (MW) can be dissociated or whether they share a common mechanism. In one experiment, we introduced two critical manipulations: increasing task demands and applying anodal high-definition transcranial direct current stimulation (HD-tDCS) to the left dorsolateral prefrontal cortex.MethodSeventy-eight participants were randomly assigned to one of four groups resulting from the factorial combination of task demand (low, high) and stimulation (anodal, sham). Participants completed the sustained attention to response task (SART), which included thought probes on intentional and unintentional MW. In addition, we investigated the crucial role of alpha oscillations in a novel approach. By assessing pre-post resting EEG, we explored whether participants’ variability in baseline alpha power predicted performance in MW and vigilance decrement related to tDCS or task demands, respectively, and whether such variability was a stable characteristic of participants.ResultsOur results showed a double dissociation, such that task demands exclusively affected vigilance decrement, while anodal tDCS exclusively affected the rate of MW. Furthermore, the slope of the vigilance decrement function and MW rate (overall, intentional and unintentional) did not correlate. Critically, resting state alpha-band activity predicted tDCS-related gains in unintentional MW alone, but not in vigilance decrement, and remained stable after participants completed the task.ConclusionThese results show that when a sustained attention task involving executive vigilance, such as the SART, is designed to elicit both vigilance decrement effects and MW, the processes leading to vigilance decrement should be differentiated from those responsible for MW, a claim that is supported by the double dissociation observed here and the lack of correlation between the measures chosen to assess both phenomena. Furthermore, the results provide the first evidence of how individual differences in alpha power at baseline may be of crucial importance in predicting the effects of tDCS on MW propensity.

Proton therapy allows the treatment of specific areas and avoids the surrounding tissues. However, this technique has uncertainties in terms of the distal dose fall-off. A promising approach to studying the proton range is the use of nanoparticles as proton-activatable agents that produce detectable signals. For this, we developed an iron oxide nanoparticle doped with Zn (IONP@Zn-cit) with a hydrodynamic size of 10 nm and stability in serum. Cytotoxicity, defined as half of the surveillance, was 100 μg Zn/mL in the U251 cell line. The effect on clonogenic cell death was tested after X-ray irradiation, which suggested a radioprotective effect of these nanoparticles at low concentrations (1–10 μg Zn/mL). To evaluate the production of positron emitters and prompt-gamma signals, IONP@Zn-cit was irradiated with protons, obtaining prompt-gamma signals at the lowest measured concentration (10 mg Zn/mL). Finally, 67Ga-IONP@Zn-cit showed accumulation in the liver and spleen and an accumulation in the tumor tissue of 0.95% ID/g in a mouse model of U251 cells. These results suggest the possibility of using Zn nanoparticles as proton-activatable agents to verify the range by prompt gamma detection and face the challenges of prompt gamma detection in a specific biological situation, opening different avenues to go forward in this field.

Abstract Current theoretical accounts on the oscillatory nature of sustained attention predict that entrainment via transcranial alternating current stimulation (tACS) at alpha and theta frequencies on specific areas of the prefrontal cortex could prevent the drops in vigilance across time-on-task. Nonetheless, most previous studies have neglected both the fact that vigilance comprises two dissociable components (i.e., arousal and executive vigilance) and the potential role of differences in arousal levels. We examined the effects of theta- and alpha-tACS over the right dorsolateral prefrontal cortex in both components of vigilance and in participants who differed in arousal level according to their chronotype and time of testing. Intermediate-types performed the vigilance tasks when their arousal level was optimal, whereas evening-types performed the vigilance tasks when their arousal levels were non-optimal. Both theta- and alpha-tACS improved arousal vigilance in the psychomotor vigilance task (PVT), whereas alpha-tACS, but not theta-tACS, improved executive vigilance in the sustained attention to response task (SART), and counteracted the typical vigilance decrement usually observed in this task. Importantly, these stimulation effects were only found when arousal was low (i.e., with evening-types performing the tasks at their non-optimal time of day). The results support the multicomponent view of vigilance, the relevance of heeding individual differences in arousal, and the role of alpha oscillations as a long-range cortical scale synchronization mechanism that compensates the decrements in performance as a function of time-on-task by exerting and maintaining cognitive control attributed to activation of the right dorsolateral prefrontal cortex.

Glucose-6-phosphate dehydrogenase (G6PD) deficiency, affecting an estimated 500 million people worldwide, is a genetic disorder that causes human enzymopathies. Biochemical and genetic studies have identified several variants that produce different ranges of phenotypes; thus, depending on its severity, this enzymopathy is classified from the mildest (Class IV) to the most severe (Class I). Therefore, understanding the correlation between the mutation sites of G6PD and the resulting phenotype greatly enhances the current knowledge of enzymopathies’ phenotypic and genotypic heterogeneity, which will assist both clinical diagnoses and personalized treatments for patients with G6PD deficiency. In this review, we analyzed and compared the structural and functional data from 21 characterized G6PD variants found in the Mexican population that we previously characterized. In order to contribute to the knowledge regarding the function and structure of the variants associated with G6PD deficiency, this review aimed to determine the molecular basis of G6PD and identify how these mutations could impact the structure, stability, and function of the enzyme and its relation with the clinical manifestations of this disease.

This research explores a novel Mexican Sign Language (MSL) lexicon video dataset containing the dynamic gestures most frequently used in MSL. Each gesture consists of a set of different versions of videos under uncontrolled conditions. The MX-ITESO-100 dataset is composed of a lexicon of 100 gestures and 5000 videos from three participants with different grammatical elements. Additionally, the dataset is evaluated in a two-step neural network model as having an accuracy greater than 99% and thus serves as a benchmark for future training of machine learning models in computer vision systems. Finally, this research provides an inclusive environment within society and organizations, in particular for people with hearing impairments.

This research leads with the analysis of a structural joint. Different arrays of steel sheets were joined using bolts. The structures were built in a metallic box filled with Granitic 0/3 sand. This box was used as a rigid body to transmit impacts and the sand as a medium to interact between the body and the structure. Then, an optical set-up was placed to measure the interaction of the impact along the different arrays. Measurements were made 5 cm before and 5 cm after the bolt. Results were analyzed by performing signal filtering and approaching a mathematical solution revealing that impact interaction can be harmonic or damped oscillations with more than 98% accuracy.

Scientific evidence demonstrates the positive impact that physical exercise has on the quality of life (QOL) of patients with chronic kidney disease (CKD). However, no study has proposed a model investigating the effect physical exercise has on the QOL of end-stage renal disease (ESRD) patients, considering the most frequent associated diseases (diabetes/hypertension). The objectives were (1) to explore the relationship between physical exercise and the QOL of adults with ESRD, and (2) to examine the moderating and/or mediating role of relevant patient variables. This non-interventional study utilized an ex post facto retrospective data analysis design with a sample of 310 patients with ESRD through two validated questionnaires. The dependent variables were the QOL scale (KDQOL-SF), and the physical function dimension (EFFISICA). The independent variables were the regular practice of intense physical activity (DEPINTE) and the daily time (in hours) the patient is in a sedentary attitude (TiParado). The moderating variables were the clinical situation and associated diseases. The mediator variable used was the body mass index. Bivariate and multiple regression analyses were conducted. Findings suggest implementing intense physical activity in transplant recipients and programmes to avoid sedentary lifestyles in dialysis patients have a positive effect in the QOL of ESRD patients.

Giardiasis, which is caused by Giardia lamblia infection, is a relevant cause of morbidity and mortality worldwide. Because no vaccines are currently available to treat giardiasis, chemotherapeutic drugs are the main options for controlling infection. Evidence has shown that the nitro drug nitazoxanide (NTZ) is a commonly prescribed treatment for giardiasis; however, the mechanisms underlying NTZ’s antigiardial activity are not well-understood. Herein, we identified the glucose-6-phosphate::6-phosphogluconate dehydrogenase (GlG6PD::6PGL) fused enzyme as a nitazoxanide target, as NTZ behaves as a GlG6PD::6PGL catalytic inhibitor. Furthermore, fluorescence assays suggest alterations in the stability of GlG6PD::6PGL protein, whereas the results indicate a loss of catalytic activity due to conformational and folding changes. Molecular docking and dynamic simulation studies suggest a model of NTZ binding on the active site of the G6PD domain and near the structural NADP+ binding site. The findings of this study provide a novel mechanistic basis and strategy for the antigiardial activity of the NTZ drug.

In this research, an impact reaction which was provoked far from its origins was studied. A metal box filled with sand was used to emulate a rigid body in which a steel bar was embedded; these conditions simulated the fuselage and wing, respectively, and the impact was applied to the rigid body and the measurement to the bar. For this, an optical technique was used to measure the relative displacement of the steel bar, and the measurements are obtained by applying digital image correlation; 2D images were obtained from the speckles generated as a reflection of the beam on the material. The results were studied through the modified Gauss–Newton analytical approach obtaining a maximum standard error deviation of 0.144 from the experimental results.

Estudios de animales silvestres en cautiverio muestran que estos pueden albergar diversos grupos parasitarios que pueden afectar su salud. En la presente investigación se examinó el material fecal de 26 serpientes de la familia Viperidae, mantenidas en cautiverio en el CEREO, Universidad de Panamá, aplicando las siguientes técnicas: Concentración Parasitaria (Ritchie y Willis Moloy), Recuento y Confirmación de helmintos (Kato Kats), y tinciones de Ziehl Neelsen, y Giemsa, para confirmación de especies de coccidios y hematozoarios respectivamente; con la finalidad de determinar los parásitos de los sistemas digestivos y sanguíneos que estos especímenes albergaban. Los resultados revelan que 92% (24/26) de la población presenta alguna forma (estadio) parasitario. La composición de la diversidad parasítica que exhiben los ejemplares positivos está conformada por Entamoeba hartmanni 46.2% (12/26); Enteromonas, y Balantidium, ambos con 26.9% (7/26); Strongyloides, Chilomastix, Cyclospora, y Oxyurus 23.1% (6/26); Uncinaria e Hymenolepis nana 19.2% (5/26); Hymenolepis diminuta, y Entamoeba invadens 15.4% (4/26); Trichostrongylus 11.5% (3/26); Retortamonas 7.7% (2/26); Porocephalus, Eimeria, Giardia, Isospora, y Cryptosporidium 3.8% (1/26).

Landslide susceptibility maps are widely used in land management and urban planning to delimit potentially problematic areas. In this article we improve their reliability by acting on the frequency ratio method and map classification systems. For the frequency ratio method, we have worked with continuous variables and established intervals grouped by probability according to the landslide inventory and based on the characteristics of the data rather than on standard divisions. For map classification systems, we have compared the efficacy of conventional classifications and those based on the concepts of sensitivity and specificity, with the specificity classifications being supported by the information offered by available comparative data. Both strategies make it possible to avoid subjective and repetitive procedures that are alien to the nature of the data being assessed. We present a case study in the 23,000 km2 Region of Valencia where a total of 48 different susceptibility maps were generated. We demonstrate that the methods applied in this study to calculate the frequency ratio provide an improvement in specificity in areas of high susceptibility while maintaining good sensitivity. In particular, the Area Under Curve (AUC) values increase from 0.67 for the conventional methods to 0.76 with the methods proposed in this work. This improvement is transferred to susceptibility mapping much more clearly when classifications that incorporate sensitivity, and especially specificity parameters, are used.

Jaw malformations imply an important problem during the commercial production of Seriola lalandi larvae and juvenile fish in Chile and New Zealand. Since the rate of malformations in other fish species has been associated with the content of long-chain PUFA (LC-PUFA) in neutral lipids of the diet, the relationship between body LC-PUFA and the rate of malformations, together with a transcriptomic analysis of genes related to the metabolism and transport of lipids in commercially produced S. lalandi larvae have been investigated in the present work. A total of 10 batches of S. lalandi larvae were obtained and cultured at about 22 °C following the protocols of a Chilean commercial hatchery during the spawning season. There were three larval batches that were collected in August (austral winter), three batches that were obtained in October (spring), and finally four spawning events that were obtained in December-January (spring-summer). The rate and type of jaw malformations, the profile of long-chain PUFA (LC-PUFA) of total lipids during larval culture, and the distribution of LC-PUFA were analyzed. Additionally, a transcriptome analysis related to lipid metabolism in 40-day-old larvae was performed. As a result, a decrease in the rate of malformations was recorded from August to December. DHA showed a steep decrease between days 1 and 10 of culture, probably due to the consumption of yolk sac lipids, but a higher proportional change was noted in larvae that hatched during August. The DHA content in polar lipids (PL) and neutral lipids (NL) of 40-day-old larvae increased from August to December, so that the abundance of DHA was higher in PL in larvae that hatched in December, but it was higher in NL in those larvae that hatched in October. In conclusion, the rate of jaw malformations was associated with the rapid decline in DHA during early larval life and the highest abundance of DHA in neutral lipids at the end of the larval life.

Background: Brucella canis is the etiological agent of canine brucellosis, a worldwide neglected zoonosis that constitutes one of the major infectious causes of infertility and reproductive failure in dogs. Although genomic information available for this pathogen has increased in recent years, here we report the first genome sequencing of a B. canis strain in Chile, and the differences in virulence genes with other B. canis strains. Results: Genome assembly produced a total length of 3,289,216 bp, N50 of 95,163 and GC% of 57.27, organized in 54 contigs in chromosome I, and 21 contigs in chromosome II. The genome annotation identified a total of 1981 CDS, 3 rRNA and 36 tRNA in chromosome I, and 1113 CDS and 10 tRNA in chromosome II. There is little variation between the different strains and the SCL isolate. Phylogenetic analysis showed that the Chilean SCL strain is closely related to B. canis and B. suis strains. Small differences were found when compared to the Serbian isolate, but all strains shared the same recent common ancestor. Finally, changes in the sequence of some virulence factors showed that the SCL strain is similar to other South American B. canis strains. Conclusions: This work sequenced and characterized the complete genome of B. canis strain SCL, evidencing the complete presence of all the genes of the virB operon, and minor changes in outer membrane proteins and in the urease operon. Our data suggest that B. canis was introduced from North America and then spread throughout the South American continent.How to cite: Borie C, Bravo C, Dettleff P, et al. First genome sequence of Chilean Brucella canis SCL strain provides insights on the epidemiology and virulence factors, explaining differences between geographical origins Electron J Biotechnol 2020;49. https://dx.doi.org/10.1016/j.ejbt.2020.10.002.

RESUMEN Introducción: Los comportamientos sexuales compulsivos (CSC) son definidos como las dificultades para controlar impulsos o conductas sexuales inapropiadas o excesivas. Estos generan malestar subjetivo o deterioro en el funcionamiento diario de la persona en forma de fantasías, excitación recurrente, impulsos o actividad no parafílica (Kraus el al., 2016). Pueden ejercer como mecanismo de regulación, tanto de emociones como de impulsos. El presente estudio analiza la relación entre estos factores de riesgo, el consumo de sustancias y los CSC en población joven-adulta (18 a 30 años). Método: La muestra recogida fue de 351 personas (66,1% mujeres, 33, 9% hombres). Para el análisis de los datos se utilizaron estadísticos descriptivos de comparación de medias (t de Student) y de correlación de variables (correlación de Pearson). Resultados: El grupo de hombres y personas homosexuales/bisexuales presentaron un mayor nivel de CSC. Además, se encontraron correlaciones significativas entre lo CSC, la falta de regulación emocional y la impulsividad y el consumo de alcohol/cannabis. Conclusiones: Este estudio sugiere la necesidad de seguir investigando acerca de los CSC y su etiología.