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与海马体体积相关的新遗传位点。

Novel genetic loci associated with hippocampal volume.

机构信息

Imaging Genetics Center, USC Mark and Mary Stevens Neuroimaging & Informatics Institute, Keck School of Medicine of University of Southern California, Los Angeles, California 90292, USA.

Department of Epidemiology, Erasmus University Medical Center, 3015 CE Rotterdam, The Netherlands.

出版信息

Nat Commun. 2017 Jan 18;8:13624. doi: 10.1038/ncomms13624.

Abstract

The hippocampal formation is a brain structure integrally involved in episodic memory, spatial navigation, cognition and stress responsiveness. Structural abnormalities in hippocampal volume and shape are found in several common neuropsychiatric disorders. To identify the genetic underpinnings of hippocampal structure here we perform a genome-wide association study (GWAS) of 33,536 individuals and discover six independent loci significantly associated with hippocampal volume, four of them novel. Of the novel loci, three lie within genes (ASTN2, DPP4 and MAST4) and one is found 200 kb upstream of SHH. A hippocampal subfield analysis shows that a locus within the MSRB3 gene shows evidence of a localized effect along the dentate gyrus, subiculum, CA1 and fissure. Further, we show that genetic variants associated with decreased hippocampal volume are also associated with increased risk for Alzheimer's disease (r=-0.155). Our findings suggest novel biological pathways through which human genetic variation influences hippocampal volume and risk for neuropsychiatric illness.

摘要

海马体结构是一个整体上参与情景记忆、空间导航、认知和应激反应的脑结构。在几种常见的神经精神疾病中,都发现了海马体积和形状的结构异常。为了确定海马结构的遗传基础,我们对 33536 个人进行了全基因组关联研究(GWAS),发现了六个与海马体积显著相关的独立位点,其中四个是新的。在新的位点中,三个位于基因内(ASTN2、DPP4 和 MAST4),一个位于 SHH 上游 200kb 处。海马亚区分析表明,MSRB3 基因内的一个位点在齿状回、下托、CA1 和裂脑区显示出局部效应的证据。此外,我们还表明,与海马体积减小相关的遗传变异也与阿尔茨海默病风险增加相关(r=-0.155)。我们的研究结果表明,人类遗传变异通过新的生物学途径影响海马体积和神经精神疾病的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef6c/5253632/2fd41633a897/ncomms13624-f1.jpg

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