GWAS of biological aging to find longevity genes in schizophrenia.

IF 3.5 3区 医学 Q1 CLINICAL NEUROLOGY
Jessica Qian, Corinne Fischer, Amer Burhan, Michael Mak, Philip Gerretsen, Nathan Kolla, Nzaar Al-Chalabi, Zanib Chaudhary, Aisha Qureshey, Ali Bani-Fatemi, Ariel Graff, Gary Remington, Vincenzo De Luca
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引用次数: 0

Abstract

Schizophrenia (SCZ) is a severe psychotic disorder associated with premature mortality and aging. Moreover, the symptoms and progression of psychiatric disorders in general are associated with decreased lifespan, biological aging, and poorer medical outcomes. In this study, we investigated the relationship between several epigenetic clocks and scanned the entire genome for association in a cohort of SCZ individuals (n = 107). Biological age was computed from blood DNA methylation (DNAm) and tested for association against  common  variants across the genome using general linear models. Genes affecting epigenetic age acceleration in our cohort were found mainly when using the telomeric length clock rather than the other biological clocks. These findings pair with existing evidence that there are some genes associated with longevity and suggest further investigations of  putative biological mechanisms for morbidity and premature mortality, not only in patients with SCZ but also in the general population.

生物衰老的全球基因组研究,寻找精神分裂症的长寿基因。
精神分裂症(SCZ)是一种严重的精神障碍,与过早死亡和衰老有关。此外,精神疾病的症状和进展一般与寿命缩短、生物衰老和较差的医疗结果有关。在这项研究中,我们调查了几种表观遗传时钟之间的关系,并对 SCZ 患者队列(107 人)的全基因组进行了关联扫描。根据血液DNA甲基化(DNAm)计算出生物年龄,并使用一般线性模型测试了与整个基因组常见变异的关联。在我们的队列中,影响表观遗传年龄加速的基因主要是在使用端粒长度时钟而不是其他生物钟时发现的。这些发现与现有的证据相吻合,即有一些基因与长寿有关,并建议进一步调查发病率和过早死亡率的假定生物机制,不仅在严重自闭症患者中,而且在普通人群中也是如此。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.80
自引率
4.30%
发文量
154
审稿时长
6-12 weeks
期刊介绍: The original papers published in the European Archives of Psychiatry and Clinical Neuroscience deal with all aspects of psychiatry and related clinical neuroscience. Clinical psychiatry, psychopathology, epidemiology as well as brain imaging, neuropathological, neurophysiological, neurochemical and moleculargenetic studies of psychiatric disorders are among the topics covered. Thus both the clinician and the neuroscientist are provided with a handy source of information on important scientific developments.
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