ethylmethylhydroxypyridine-succinate has been researched along with Diabetes-Mellitus--Type-2* in 2 studies
1 trial(s) available for ethylmethylhydroxypyridine-succinate and Diabetes-Mellitus--Type-2
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[Additional advantages of mexicor used in combined therapy of coronary heat disease and diabetes mellitus of 2nd type].
This open prospective randomized 16-week study of combined therapy of coronary heat disease (CHD) and and diabetes mellitus of 2nd type (DM2) with secondary non-alcoholic fatty liver disease (NAFLD) including mexicor was designed to estimate structural and functional liver characteristics. Mexicor was shown to act as a hepatoprotector reducing the frequency of cytolithic syndrome when used together with statins in combined therapy of atherogenic dyslipidemia. It also significantly decreased the number of patients with elevated levels of gamma-glutamyltranspeptidase. These changes suggest favourable prognosis for patients with CHD and DM2 because enhanced activity of this enzyme is believed to be a predictor of high cardiovascular risk. Mexicor promoted combined hypolipidemic effect, reduced the degree of insulin resistance, improved hepatic metabolism, and lowered cardiovascular risks in patients with CHD and DM2. Topics: Aged; Coronary Disease; Diabetes Mellitus, Type 2; Drug Therapy, Combination; Fatty Liver; Female; gamma-Glutamyltransferase; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Male; Middle Aged; Non-alcoholic Fatty Liver Disease; Prospective Studies; Pyridines; Treatment Outcome | 2013 |
1 other study(ies) available for ethylmethylhydroxypyridine-succinate and Diabetes-Mellitus--Type-2
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[The efficacy of ethylmethylhydroxypyridine succinate in patients with cerebrovascular pathology complicated with diabetes mellitus and metabolic syndrome].
Arterial hypertension, diabetes mellitus, obesity and dyslipidemia continue to be the main risk factors for diseases of the circulatory system and the leading causes of mortality in the world, the combination of these diseases significantly increases the likelihood of the development and more rapid progression of cardiovascular and cerebrovascular pathology. Improving approaches to the diagnosis and treatment of these diseases is a priority problem in modern medicine. Currently, there is no universal drug that can influence all stages of pathological process in both cerebrovascular diseases and diabetes mellitus, and the problem of rational use of drugs in patients with comorbid pathology has not been completely resolved. A difficult clinical task includes not only the timely detection of the disease and the correct diagnosis, but also the choice of the safest and most effective medicine. A number of clinical studies have demonstrated the efficacy of mexidol in the treatment of this category of patients, which is determined by its complex, pleiotropic and multimodal mechanisms of action.. Основными факторами риска болезней системы кровообращения и ведущими причинами смертности в мире продолжают оставаться артериальная гипертония, сахарный диабет, ожирение и дислипидемия, причем сочетание этих заболеваний существенно повышает вероятность развития и более быстрого прогрессирования кардио- и цереброваскулярной патологии. Совершенствование подходов к диагностике и терапии этих заболеваний является приоритетной проблемой современной медицины. В настоящее время не существует универсального препарата, позволяющего повлиять на все звенья патологического процесса как при цереброваскулярных заболеваниях, так и при сахарном диабете, и проблема рационального использования лекарственных средств у пациентов с коморбидной патологией окончательно не решена. Непростая клиническая задача заключается не только в своевременном выявлении заболевания и постановке правильного диагноза, но и в выборе наиболее безопасного и эффективного препарата. В ряде клинических исследований продемонстрирована эффективность Мексидола при лечении этой категории пациентов, что определяется его комплексным, плейотропным и мультимодальным механизмом действия. Topics: Cardiovascular Diseases; Cerebrovascular Disorders; Diabetes Mellitus; Diabetes Mellitus, Type 2; Humans; Metabolic Syndrome; Pyridines | 2020 |