精神疾病的端粒长度:它不仅仅是一个衰老标志吗?

N. Monroy-Jaramillo, Elena Dyukova, C. Walss-Bass
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引用次数: 25

摘要

目的:精神疾病和药物使用障碍与过早的生物衰老有关。端粒长度(TL)被认为是衰老的标志,已经在精神疾病中进行了分析,并且在较小程度上在物质使用障碍中进行了分析,最近的研究结果表明,端粒长度可能与疾病病理有关。方法:我们对截至2016年6月发表在精神病学和药物使用障碍领域的TL研究进行了批判性和非系统的文献检索,重点关注描述机制的研究,包括将端粒生物学与遗传因素、压力和线粒体改变联系起来的研究(选择了104项研究)。结果:与对照组相比,重度抑郁症和焦虑症患者的白细胞端粒较短。其他精神疾病和药物使用障碍的结果尚无定论。这可能部分是由于药物治疗和反应的差异,因为研究表明一些精神药物可能调节TL。重要的是,一些研究在精神和物质使用障碍中建立了端粒机制、压力和线粒体功能之间的关系。结论:虽然需要进一步的纵向研究考虑端粒遗传学来澄清端粒和线粒体功能在精神疾病和物质使用障碍中的因果关系,但最近的研究结果表明,端粒可能不仅仅是衰老的标志。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Telomere length in psychiatric disorders: Is it more than an ageing marker?
Abstract Objectives: Psychiatric and substance-use disorders have been associated with premature biological ageing. Telomere length (TL), considered an ageing marker, has been analysed in psychiatric disorders, and to a lesser extent in substance-use disorders, with recent findings suggesting TL may be related to disease pathology. Methods: We conducted a critical and non-systematic literature search of TL studies published up to June 2016 in psychiatric and substance-use disorders, focussing on studies describing mechanisms, including studies linking telomere biology with genetic factors, stress and mitochondrial alterations (104 studies selected). Results: Patients with major depressive disorder and anxiety appear to have shorter leukocyte telomeres compared to controls. Inconclusive results are found for other psychiatric disorders and for substance-use disorders. This may be due in part to differences in medication treatment and response, as studies suggest that some psychotropic medications may modulate TL. Importantly, some studies establish a relationship between telomere machinery, stress and mitochondria function in psychiatric and substance-use disorders. Conclusions: While further longitudinal studies considering telomere genetics are needed to clarify the cause–effect link between telomeres and mitochondria function in psychiatric and substance-use disorders, the recent findings linking these biological processes suggest that telomeres may be more than ageing markers.
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