7 results on '"Terekhov MV"'
Search Results
2. Heparin-polynitroxide derivatives: first application as site specific MRT imaging contrast media for vascular wall
- Author
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Terekhov, MV, primary, Sen, V, additional, Golubev, V, additional, Weber, S, additional, Scholz, AW, additional, Muenzel, T, additional, Kleschyov, AL, additional, and Schreiber, LM, additional
- Published
- 2010
- Full Text
- View/download PDF
3. [A clinical case of reverse left ventricular remodeling in patient with pathogenic TTN mutation. Case report].
- Author
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Nasonova SN, Meshkov AN, Zhirov IV, Osmolovskaya YF, Shoshina AA, Gagloev AV, Dzhumaniiazova IH, Zelenova EA, Erema VV, Gusakova MS, Ivanov MV, Terekhov MV, Kashtanova DA, Nekrasova AI, Mitrofanov SI, Shingaliev AS, Yudin VS, Keskinov AA, Gomyranova NV, Chubykina UV, Ezhov MV, Tereshchenko SN, Yudin SM, and Boytsov SA
- Subjects
- Humans, Mutation, Male, Adult, Echocardiography methods, Connectin genetics, Cardiomyopathy, Dilated genetics, Cardiomyopathy, Dilated physiopathology, Cardiomyopathy, Dilated diagnosis, Ventricular Remodeling genetics, Ventricular Remodeling physiology
- Abstract
Dilated cardiomyopathy (DCM) is a leading cause of heart failure, sudden cardiac death, and heart transplantation in young patients. The causes of DCM are varied and include genetic factors and metabolic, infectious, toxic and others factors. Today it is known that germline mutations in more than 98 genes can be associated with the occurrence of DCM. However, the penetrance of these genes often depends on a combination of factors, including modifiable ones, i.e. those that change under the influence of the environment. About 20-25% of genetically determined forms of DCM are due to mutations in the titin gene ( TTN ). Titin is the largest protein in the body, which is an important component of the sarcomer. Although titin is the largest protein in the human body, its role in the physiology of heart and disease is not yet fully understood. However, a mutation in the TTN gene may later represent a potential therapeutic target for genetic and acquired cardiomyopathy. Thus, the analysis of clinical cases of cardiomyopathy in patients with identified mutations in the TTN gene is of great scientific interest. The article presents a clinical case of manifestation of DCM in patient with a revealed pathogenic variant of mutation in the gene TTN and reverse left ventricular remodeling of the against the background of optimal therapy of heart failure in a subsequent outpatient observation.
- Published
- 2024
- Full Text
- View/download PDF
4. Genetics of psycho-emotional well-being: genome-wide association study and polygenic risk score analysis.
- Author
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Yakovchik AY, Tolynyova DV, Kashtanova DA, Sutulova ER, Ivanov MV, Mamchur AA, Erema VV, Matkava LR, Terekhov MV, Rumyantseva AM, Blinova OI, Akinshina AI, Mitrofanov SI, Yudin VS, Makarov VV, Keskinov AА, Kraevoy SA, and Yudin SM
- Abstract
Background: Psycho-emotional well-being is essential for living a life of satisfaction and fulfillment. However, depression and anxiety have become the leading mental health issues worldwide, according to the World Health Organization. Both disorders have been linked to stress and other psychological factors. Their genetic basis remains understudied., Methods: In 2020-2021, the psycho-emotional well-being of 30,063 Russians with no known psychiatric history was assessed using the Hospital Anxiety and Depression Scale (HADS) for general mental health and the HADS subscale A (anxiety) for anxiety. Following the original instructions, an anxiety score of ≥11 points was used as the anxiety threshold. A genome-wide association study was performed to find associations between anxiety and HADS/HADS-A scores using linear and logistic regressions based on HADS/HADS-A scores as binary and continuous variables, respectively. In addition, the links between anxiety, sociodemographic factors (such as age, sex, and employment), lifestyle (such as physical activity, sleep duration, and smoking), and markers of caffeine and alcohol metabolism were analyzed. To assess the risk of anxiety, polygenic risk score modeling was carried out using open-access software and principal component analysis (PCA) to simplify the calculations (ROC AUC = 89.4 ± 2.2% on the test set)., Results: There was a strong positive association between HADS/HADS-A scores and sociodemographic factors and lifestyle. New single-nucleotide polymorphisms (SNPs) with genome-wide significance were discovered, which had not been associated with anxiety or other stress-related conditions but were located in genes previously associated with bipolar disorder, schizophrenia, or emotional instability. The CACNA1C variant rs1205787230 was associated with clinical anxiety (a HADS-A score of ≥11 points). There was an association between anxiety levels (HADS-A scores) and genes involved in the activity of excitatory neurotransmitters: PTPRN2 (rs3857647) , DLGAP4 (rs8114927) , and STK24 (rs9517326) ., Conclusion: Our results suggest that calcium channels and monoamine neurotransmitters, as well as SNPs in genes directly or indirectly affecting neurogenesis and synaptic functions, may be involved in the development of increased anxiety. The role of some non-genetic factors and the clinical significance of physiological markers such as lifestyle were also demonstrated., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2024 Yakovchik, Tolynyova, Kashtanova, Sutulova, Ivanov, Mamchur, Erema, Matkava, Terekhov, Rumyantseva, Blinova, Akinshina, Mitrofanov, Yudin, Makarov, Keskinov, Kraevoy and Yudin.)
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- 2024
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- View/download PDF
5. Cognitive impairment in long-living adults: a genome-wide association study, polygenic risk score model and molecular modeling of the APOE protein.
- Author
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Kashtanova DA, Mamchur AA, Dzhumaniyazova IH, Ivanov MV, Erema VV, Zelenova EA, Yakovchik AY, Gusakova MS, Rumyantseva AM, Terekhov MV, Matkava LR, Akopyan AA, Strazhesko ID, Yudin VS, Makarov VV, Kraevoy SA, Tkacheva ON, and Yudin SM
- Abstract
Background: Cognitive impairment is an irreversible, aging-associated condition that robs people of their independence. The purpose of this study was to investigate possible causes of this condition and propose preventive options., Methods: We assessed cognitive status in long-living adults aged 90+ ( n = 2,559) and performed a genome wide association study using two sets of variables: Mini-Mental State Examination scores as a continuous variable (linear regression) and cognitive status as a binary variable (> 24, no cognitive impairment; <10, impairment) (logistic regression)., Results: Both variations yielded the same polymorphisms, including a well-known marker of dementia, rs429358in the APOE gene. Molecular dynamics simulations showed that this polymorphism leads to changes in the structure of alpha helices and the mobility of the lipid-binding domain in the APOE protein., Conclusion: These changes, along with higher LDL and total cholesterol levels, could be the mechanism underlying the development of cognitive impairment in older adults. However, this polymorphism is not the only determining factor in cognitive impairment. The polygenic risk score model included 45 polymorphisms (ROC AUC 69%), further confirming the multifactorial nature of this condition. Our findings, particularly the results of PRS modeling, could contribute to the development of early detection strategies for predisposition to cognitive impairment in older adults., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2023 Kashtanova, Mamchur, Dzhumaniyazova, Ivanov, Erema, Zelenova, Yakovchik, Gusakova, Rumyantseva, Terekhov, Matkava, Akopyan, Strazhesko, Yudin, Makarov, Kraevoy, Tkacheva and Yudin.)
- Published
- 2023
- Full Text
- View/download PDF
6. Mortality and survival in nonagenarians during the COVID-19 pandemic: Unstable equilibrium of aging.
- Author
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Kashtanova DA, Erema VV, Gusakova MS, Sutulova ER, Yakovchik AY, Ivanov MV, Taraskina AN, Terekhov MV, Matkava LR, Rumyantseva AM, Yudin VS, Akopyan AA, Strazhesko ID, Kordiukova IS, Akinshina AI, Makarov VV, Tkacheva ON, Kraevoy SA, and Yudin SM
- Abstract
Introduction: Aging puts the human body under an immense stress and makes it extremely susceptible to many diseases, often leading to poor outcomes and even death. Long-living individuals represent a unique group of people who withstood the stress of time and offer an abundance of information on the body's ability to endure the pressure of aging. In this study, we sought to identify predictors of overall one-year mortality in 1641 long-living individuals. Additionally, we analyzed risk factors for COVID-19-related morality, since statistics demonstrated an extreme vulnerability of older adults., Methods: We conducted a two-stage evaluation, including a comprehensive geriatric assessment for major aging-associated: frailty, cognitive impairment, frontal lobe dysfunction, chronic pain, anxiety, risk of falls, sensory deficit, depression, sarcopenia, risk of malnutrition, fecal and urinary incontinence, dependence in Activities of Daily Living, dependence in Instrumental Activities of Daily Living, polypragmasia, and orthostatic hypotension; extensive blood testing, a survey, and a one-year follow-up interview., Results: The most reliable predictors of overall mortality were cognitive impairment, malnutrition, frailty, aging-associated diseases and blood markers indicating malnutrition-induced metabolic dysfunctions (decreased levels of protein fractions, iron, 25-hydroxyvitamin D, and HDL), and aging biomarkers, such as IGF-1 and N-terminal pro b-type natriuretic peptide. In post-COVID 19 participants, the most significant mortality predictors among geriatric syndromes were depression, frontal lobe dysfunction and frailty, and similar to overall mortality blood biomarkers - 25-hydroxyvitamin D, IGF-1, HDL as well as high white blood cell, neutrophils counts and proinflammatory markers. Based on the results, we built a predictive model of overall mortality in the long-living individuals with f-score=0.76., Conclusion: The most sensitive and reliable predictors of mortality were modifiable. This is another evidence of the critical importance of proper geriatric care and support for individuals in their "golden years". These results could facilitate geriatric institutions in their pursuit for providing improved care and could aid physicians in detecting early signs of potentially deadly outcomes. Additionally, our findings could be used in developing day-to-day care guidelines, which would greatly improve prevention statistics., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2023 Kashtanova, Erema, Gusakova, Sutulova, Yakovchik, Ivanov, Taraskina, Terekhov, Matkava, Rumyantseva, Yudin, Akopyan, Strazhesko, Kordiukova, Akinshina, Makarov, Tkacheva, Kraevoy and Yudin.)
- Published
- 2023
- Full Text
- View/download PDF
7. [Cardiac angiosarcoma].
- Author
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Kir'ianov NA, Terekhov MV, Sukhanov SA, Lozhkin EA, and Nikolaeva NB
- Subjects
- Adult, Fatal Outcome, Female, Heart Neoplasms diagnostic imaging, Hemangiosarcoma diagnostic imaging, Humans, Pregnancy, Radiography, Ultrasonography, Heart Neoplasms pathology, Hemangiosarcoma pathology
- Abstract
The paper outlines the authors'case of cardiac angiosarcoma. It provides the gross and microscopic characteristics of this tumor and procedures for its clinical and immunomorphological diagnosis.
- Published
- 2011
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