7 results on '"Anaya, J"'
Search Results
2. Rheumatoid arthritis association in Colombian population is restricted to HLA-DRB1*04 QRRAA alleles
- Author
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Anaya, J M, Correa, P A, Mantilla, R D, and Arcos-Burgos, M
- Published
- 2002
- Full Text
- View/download PDF
3. HLA-DR and DQB1 gene polymorphism in the North-western Colombian population.
- Author
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Correa, P.A., Whitworth, W.C., Kuffner, T., McNicholl, J., and Anaya, J-M.
- Subjects
GENETIC polymorphisms ,HLA histocompatibility antigens ,HUMAN population genetics - Abstract
HLA-DRB1, DRB3, DRB4, DRB5 and DQB1 polymorphisms were studied using molecular methods in a population of 100 unrelated healthy individuals from an area in north-west Colombia (Medellin) inhabited by the “Paisa”, a community with features of a genetically isolated group. The most frequently observed specificities at the DRB1 locus were *07 (16.4%) and *15 (12%), and at the DQB1 locus *02 (18.8%) and *03 (33.6%), of which *0302 was the most prevalent allele (14.3%). The most polymorphic specificities were DRB1*04, 13 and 11, and DQB1*06. Both the HLA-DRB1 and DQB1 loci were in linkage disequilibrium. Haplotypes were estimated using maximum likelihood methods. The most frequent two locus haplotype was DRB1*07-DQB1*02 (6.6%) and these specificities were in linkage disequilibrium. Several unusual possible haplotypes were observed. Both the HLA-DRB1 and DQB1 locus were in Hardy–Weinberg equilibrium. [ABSTRACT FROM AUTHOR]
- Published
- 2002
- Full Text
- View/download PDF
4. TNF microsatellites polymorphism is associated with rheumatoid arthritis. Confirming evidence in northwestern Colombians
- Author
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Gomez, L. M., Ruiz-Narváez, E. A., Pineda-Tamayo, R., Adriana Rojas-Villarraga, and Anaya, J. -M
- Subjects
Male ,Unclassified drug ,Protein function ,Tnf ,Hla antigen class 2 ,Gene sequence ,Gene locus ,Severity of Illness Index ,Linkage Disequilibrium ,Arthritis, Rheumatoid ,Risk Factors ,Haplotype ,Tumor necrosis factor-alpha ,Tumor necrosis factor d4 ,Middle aged ,Priority journal ,Allele ,Hla dqb1 antigen ,Sequence analysis ,Gene linkage disequilibrium ,Middle Aged ,Polymerase chain reaction ,Hla ,Regression Analysis ,Tumor necrosis factor c1 ,Female ,Regression analysis ,Age distribution ,Human ,Tumor necrosis factor b7 ,Adult ,Genotype ,rheumatoid ,Tumor necrosis factor ,Tumor necrosis factor b4 ,Genetic predisposition to disease ,Major clinical study ,Colombia ,Article ,Genetic ,Microsatellite repeats ,Genetic susceptibility ,Linkage disequilibrium ,Humans ,Genetic Predisposition to Disease ,Tumor necrosis factor 308g ,Rheumatoid arthritis ,Polymorphism ,Hla dr antigen ,Microsatellites ,Cytokine ,Disease severity ,Disease duration ,Tumor necrosis factor 238g ,Tumor necrosis factor a6 ,Genetic risk ,Tumor necrosis factor a7 ,Tumor necrosis factor a8 ,Genetic polymorphism ,Polymorphism, Genetic ,Logistic regression analysis ,Tumor necrosis factor alpha ,Tumor Necrosis Factor-alpha ,Arthritis ,Confidence interval ,Latin america ,Gene frequency ,Single nucleotide polymorphism ,Severity of illness index ,Clinical feature ,Risk factors ,Genetic association ,Tumor necrosis factor e3 ,Controlled study ,Microsatellite Repeats - Abstract
Objective: To examine the contribution of tumor necrosis factor alpha (TNF) microsatellite (a to e) polymorphism to the genetic risk of developing rheumatoid arthritis (RA) in a northwestern Colombian population. Methods: This was an association study in which 108 RA patients and 222 matched individuals were enrolled. HLA-DRB1 and DQB1 polymorphisms were evaluated to examine for linkage disequilibrium between these loci and TNF microsatellites. Genotyping was performed using denaturing polyacrylamide gels and polymerase chain reaction-sequence techniques. Results: By unconditional logistic regression analysis, the TNFa6 allele (OR= 2.37, 95%CI 1.07-5.24) and the TNFb4 allele (OR= 3.01, 95%CI 1.07-9.00) were observed to be associated with disease. These associations were independent of HLA-DR and HLA-DQ since linkage disequilibrium between HLA class II and TNF microsatellites was not observed. In addition, patients with the TNFa8 allele had a five times greater risk of developing extra-articular manifestations as compared to patients without this allele (OR = 5.07, 95%CI 1.14-22.52), regardless of age and the duration of disease. Haplotype analysis disclosed a protective effect for TNFa7/b7/c1/d4/e3/-308G/-238G. Conclusion: These results confirm that the TNF locus exerts a primary influence on both susceptibility to and the severity of RA. © Copyright Clinical and Experimental Rheumatology 2007.
5. Risk factors associated with pulmonary arterial hypertension in Colombian patients with systemic sclerosis: Review of the literature
- Author
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Coral-Alvarado, P., Rojas-Villarraga, A., Latorre, M. C., Mantilla, R. D., Restrepo, J. F., Pardo, A. L., Chalem, P., Rondón, F., Jáuregui, E., Juan C. Rueda, Cañas, C., Hincapie, M. E., Pineda-Tamayo, R., Alvarez, F., Iglesias-Gamarra, A., Diaz, F. J., and Anaya, J. -M
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Adult ,Male ,Data base ,pulmonary ,Major clinical study ,Colombia ,Pulmonary arterial hypertension ,Article ,Pulmonary hypertension ,Pulmonary fibrosis ,Scleroderma ,Hyperpigmentation ,Microstomia ,Humans ,Middle aged ,Priority journal ,Aged ,Hypopigmentation ,Logistic regression analysis ,Questionnaire ,Confidence interval ,Anemia ,Dysphagia ,Odds ratio ,systemic ,Gastroesophageal reflux ,Risk factors ,Hypertension ,Systemic sclerosis ,Female ,Lung fibrosis ,Risk factor ,Human - Abstract
Objective. Considering the significant morbidity and mortality of pulmonary arterial hypertension (PAH) in patients with systemic sclerosis (SSc) and the lack of precise information on disease in Latin America, we investigated the clinical and laboratory characteristics associated with PAH in Colombian patients with SSc and review the literature. Methods. This multicenter study included patients followed at 5 rheumatology units that were systematically assessed using a pretested questionnaire on clinical and immunological variables, focusing on PAH. Conditional logistic regression was employed to assess association between PAH and specific clinical characteristics. A systematic review of the literature was performed through electronic databases. Results. Of a total of 349 patients with SSc, 61 (17%) met the criteria for PAH. Pulmonary fibrosis [adjusted odds ratio (AOR) 7.37, 95% CI 3.67-14.81, p less than 0.0001], microstomia (AOR 3.3, 95% CI 1.70-6.28, p less than 0.0001), gastroesophageal reflux (AOR 2.41, 95% CI 1.31-4.43, p = 0.005), dysphagia (AOR 2.7, 95% CI 1.49-4.77, p = 0.001), hyperpigmentation (AOR 2.15, 95% CI 1.11-4.16, p = 0.02), and hypopigmentation (AOR 2.4, 95% CI 1.26-4.64, p = 0.008) were the most prevalent clinical characteristics associated with PAH, while anemia (AOR 5.4, 95% CI 1.98-14.93, p = 0.001) was observed as the unique laboratory risk factor. Association between subtypes of SSc and PAH was not observed. Significant differences in both clinical and laboratory data were observed among different series. Conclusion. PAH may be a frequent complication of SSc in the Colombian population regardless of disease subtype. The identified clinical and laboratory risk factors might assist earlier diagnosis and guide decisions on therapeutic interventions on this critical complication of SSc. The reasons underlying the reported divergences among patients from different ethnicities are not fully understood, but it is most likely that both genetic and environmental factors are responsible for them.
6. Tuberculosis in patientes treated with tumor necrosis factoralpha antagonists living in an endemic area. Is the risk worthwhile?
- Author
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Adriana Rojas-Villarraga, Agudelo, C. A., Pineda-Tamayo, R., Porras, A., Matute, G., and Anaya, J. M.
- Subjects
Monoclonal antibody ,Adult ,Male ,Endemic diseases ,Immunology ,Anti-Inflammatory Agents ,Colombia ,Risk Assessment ,Article ,Antibodies ,Drug antagonism ,Autoimmune Diseases ,Antiinflammatory agent ,Risk Factors ,Autoimmune disease ,Case report ,Monoclonal ,Tuberculosis ,Humans ,Middle aged ,Bacteria (microorganisms) ,Aged ,Tumor necrosis factor alpha ,Tumor Necrosis Factor-alpha ,Tumor necrosis factor-alpha/immunology ,Female ,Risk factor ,Human - Abstract
Tumor necrosis factor alpha antagonists (TNFA) are biological agents to treat chronic inflammatory and autoimmune diseases. However, their use is associated with an increased rate of tuberculosis, endemic mycoses, and intracellular bacterial infections. Since tuberculosis is moderately to highly endemic in Colombia, the risk of these infections in patients treated with TNFAs may be higher than previously reported in Colombia. Recently, four patients have developed tuberculosis during TNFA therapy. Tuberculosis appeared between 3 to 24 months after initiation of TFNA therapy and was independent of previous tuberculin skin test status. A review of the relevant literature and recommendations are presented as guides for surveillance and prophylaxis on a country-wide basis.
7. Clinical and immunological characteristics of type 1 diabetes mellitus in a northwestern Colombian population
- Author
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Tobon, G.J., Arango, A., Abad, V., García, J., Cuervo, H., Velásquez, A., Angel, I.D., Vega, P., Abad, A., and Anaya, J.-M.
- Subjects
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ENDOCRINE diseases , *DIABETES , *INSULIN resistance , *TYROSINE - Abstract
Abstract: We underwent a project aimed to define the clinical and immunological characteristics of type 1 diabetes (T1D) in a Colombian population. This was a multicenter and cross-sectional study. Patients were systematically interviewed and their medical records reviewed, using a questionnaire that sought information about demographic, clinical and immunological characteristics. Glutamic acid decarboxylase antibodies (GADA), tyrosine phosphatase antibodies (IA-2A) and insulin antibodies (IAA) were examined by radioimmunoassay. There were 107 patients with T1D. Male:female ratio was 1:1. Half of the patients developed diabetes ketoacidosis at onset. GADA, IA-2A, and IAA were detected in 45%, 40%, and 69% of the cases, respectively. GADA positive patients were older and had a less duration of disease than patients without these autoantibodies (p <0.01). Association between breast feeding with the presence of antibodies or clinical characteristics was not observed. The results highlight some differences of T1D expression according to geographic location and ethnicity. Differences in age at onset and clinical variables may point to an environmental factor or deficient access to health care system. Genetic studies underway will provide important information in this population. These results might help to define public health policies in our population to improve T1D diagnosis, patients’ quality of life and their outcome. [Copyright &y& Elsevier]
- Published
- 2006
- Full Text
- View/download PDF
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