早衰的临床和生物学变异对认知功能的影响

E. Malyutina, E. Fesenko, E. A. Sanches, Viktoriya D. Ismanova, O. Kuzminov, Federal Medical Medical Technologies
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引用次数: 0

摘要

背景:目前,老年学作为一门相关的医学和生物学学科的发展遵循概念的路径;在经典老年学中有三种:脆弱、内在能力和恢复力;在预防医学中有一种——早衰。本研究的目的:研究早衰患者的各种临床和生物学变异的认知功能特征。同时,对认知和心理功能的重视不够,而认知和心理功能在很大程度上是弹性形成的基础。材料与方法:共纳入1214人。他们全部被分成两组。根据早衰的特定临床和生物学变异的存在,在每组中确定亚组。所有参与研究的患者都进行了认知心理测试。结果:最危险的早衰选择是心脏、大脑、线粒体、绝经期(女性)、雄性停经期(男性)和混合变异早衰。此外,随着年龄的增长,性别差异也在增加。在55 ~ 64岁存在线粒体、雄性停经和早衰混合变异的年龄组中,男性的认知脆弱性高于女性。因此,55 ~ 64岁女性线粒体变异组的MMSE测试得分为28.2±0.08分,男性为- 24.4±0.07分(p<0.05)。绝经期变异体MMSE测试得分为27.1±0.04分,男性男性为24.2±0.03分(p<0.05)。在混合变异中,女性的MMSE测试得分为25.1±0.16分,而男性为23.2±0.16分(p<0.05)。结论:55-64岁的男性和女性在线粒体、绝经期(女性)、雄性停经期(男性)和早衰混合变异中最容易出现认知和心理脆弱性,而男性身份进一步增加了这种脆弱性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of clinical and biological variants of premature aging on cognitive functionality
Background: Currently, the development of gerontology as a related medical and biological discipline follows the path of concepts; there are three of them in classical gerontology: frailty, intrinsic capacity and resilience, and in preventive medicine – one – premature aging. The aim of the study: To study the features of cognitive functioning of people with various clinical and biological variants of premature aging. At the same time, insufficient attention is paid to cognitive and psychological functionality, which is largely the basis for the formation of resilience. Materials and methods: The study included 1214 people. All of them were divided into two groups. Subgroups were identified in each group, depending on the presence of a particular clinical and biological variant of premature aging. All patients included in the study underwent cognitive psychological testing. Results: The most risky options of premature aging are cardiac, cerebral, mitochondrial, menopausal (in women), andropausal (in men) and mixed variants of premature aging. Moreover, with increasing age, gender differences increase. In the 55-64-year-old age group with mitochondrial, andropausal, and mixed variants of premature aging, the cognitive vulnerability of men was higher than that of women. So, if in women in the 55-64-year-old age group with the mitochondrial variant in women, the MMSE test score was 28.2±0.08 points, then in men – 24.4±0.07 (p<0.05). In the menopausal variant, the MMSE test score was 27.1±0.04 points, in the andropausal variant in men – 24.2±0.03 (p<0.05). In the mixed variant, the MMSE test score for women was 25.1±0.16 points, while for men it was 23.2±0.16 (p<0.05). Conclusion: 55-64-year-old men and women are most susceptible to cognitive and psychological vulnerability in mitochondrial, menopausal (in women), andropausal (in men) and mixed variants of premature aging, and being a male further increases this vulnerability.
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