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对日本精神分裂症患者血液样本的表观遗传时钟分析。

Epigenetic clock analysis of blood samples from Japanese schizophrenia patients.

作者信息

Okazaki Satoshi, Otsuka Ikuo, Numata Shusuke, Horai Tadasu, Mouri Kentaro, Boku Shuken, Ohmori Tetsuro, Sora Ichiro, Hishimoto Akitoyo

机构信息

Department of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Japan.

Department of Psychiatry, Graduate School of Biomedical Sciences, Tokushima University, Tokushima, Japan.

出版信息

NPJ Schizophr. 2019 Feb 27;5(1):4. doi: 10.1038/s41537-019-0072-1.

DOI:10.1038/s41537-019-0072-1
PMID:30814520
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6393510/
Abstract

The accelerated aging hypothesis of schizophrenia (SCZ) has been proposed. DNA methylation profiles were developed for determining "epigenetic age." Here, we assessed intrinsic and extrinsic epigenetic age acceleration (IEAA and EEAA, respectively) in SCZ. We examined two independent cohorts of Japanese ancestry. The first cohort consisted of 80 patients with SCZ under long-term or repeated hospitalization and 40 controls, with the economical DNA pooling technique. The second cohort consisted of 24 medication-free patients with SCZ and 23 controls. Blood of SCZ subjects exhibited decreased EEAA in the first cohort (p = 0.0162), but not in the second cohort. IEAA did not differ in either cohort. We performed replication analyses using publicly available datasets from European ancestry (three blood and one brain datasets). One blood dataset showed increased EEAA in SCZ (p = 0.0228). Overall, our results provide evidence for decreased EEAA in SCZ associated with hospitalization in the Japanese population.

摘要

精神分裂症(SCZ)的加速衰老假说已被提出。通过DNA甲基化谱来确定“表观遗传年龄”。在此,我们评估了SCZ患者的内在和外在表观遗传年龄加速(分别为IEAA和EEAA)。我们研究了两个独立的日本血统队列。第一个队列由80名长期或反复住院的SCZ患者和40名对照组成,采用经济的DNA池技术。第二个队列由24名未服药的SCZ患者和23名对照组成。在第一个队列中,SCZ受试者的血液EEAA降低(p = 0.0162),但在第二个队列中未降低。两个队列中的IEAA均无差异。我们使用来自欧洲血统的公开可用数据集(三个血液数据集和一个大脑数据集)进行了重复分析。一个血液数据集显示SCZ患者的EEAA增加(p = 0.0228)。总体而言,我们的结果为日本人群中SCZ患者与住院相关的EEAA降低提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28a3/6393510/74db3feb2d70/41537_2019_72_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28a3/6393510/2ca7513ad449/41537_2019_72_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28a3/6393510/37f3e3a6ee80/41537_2019_72_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28a3/6393510/74db3feb2d70/41537_2019_72_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28a3/6393510/2ca7513ad449/41537_2019_72_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28a3/6393510/37f3e3a6ee80/41537_2019_72_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28a3/6393510/74db3feb2d70/41537_2019_72_Fig3_HTML.jpg

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Traumatic stress and accelerated DNA methylation age: A meta-analysis.创伤后应激与加速的 DNA 甲基化年龄:一项荟萃分析。
Psychoneuroendocrinology. 2018 Jun;92:123-134. doi: 10.1016/j.psyneuen.2017.12.007. Epub 2017 Dec 27.
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Increased serum levels and promoter polymorphisms of macrophage migration inhibitory factor in schizophrenia.
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Meta-analysis of epigenetic aging in schizophrenia reveals multifaceted relationships with age, sex, illness duration, and polygenic risk.精神分裂症表观遗传衰老的荟萃分析揭示了与年龄、性别、疾病持续时间和多基因风险的多方面关系。
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Accelerated epigenetic aging and decreased natural killer cells based on DNA methylation in patients with untreated major depressive disorder.基于DNA甲基化的未治疗的重度抑郁症患者表观遗传加速衰老及自然杀伤细胞减少
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