神经精神障碍的精神分裂症特异性和高度多效性遗传风险评分的神经生物学相关性。

IF 5.8 1区 医学 Q1 PSYCHIATRY
Lydia M Federmann, Lisa Sindermann, Sabrina Primus, Federico Raimondo, Konrad Oexle, Janik Goltermann, Juliane Winkelmann, Markus M Nöthen, Katrin Amunts, Thomas W Mühleisen, Sven Cichon, Simon B Eickhoff, Felix Hoffstaedter, Udo Dannlowski, Kaustubh R Patil, Andreas J Forstner
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引用次数: 0

摘要

神经精神疾病表现出共同的和独特的神经生物学相关性。一项跨疾病全基因组关联研究(GWAS)发现23个高度多效单核苷酸多态性(snp)与至少4种神经精神疾病相关,22个snp主要与精神分裂症相关。探索它们与大脑相关特征的联系可能会促进对它们独特的神经生物学过程的理解。利用英国生物银行的数据(n = 28,952),本研究检测了高度多效性snp的遗传风险评分(GRS) (PleioPsych-GRS)和主要与精神分裂症相关snp的遗传风险评分(SCZ-GRS)与154项皮质下体积、皮质厚度和表面积测量以及12项与心理健康相关的结果之间的关系。为了在个体SNP水平上产生进一步的见解,使用GWAS汇总统计检查了SNP与大脑结构之间的关联。PleioPsych-GRS与多次校正后的脑结构无显著相关性。SCZ-GRS与外侧眶额区表面积增加、壳核体积增加等显著相关。PleioPsych-GRS和SCZ-GRS分别与心理健康相关的8项和4项结果相关。两个高度多效性和10个与scz相关的snp与几种脑结构表型相关。综上所述,这些发现表明,高度多效性snp和主要与精神分裂症相关的snp的GRSs与大脑结构和与心理健康相关的结果有部分不同的关联。因此,研究精神分裂症特异性和多效性变异可以提高我们对神经精神疾病的神经生物学的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neurobiological correlates of schizophrenia-specific and highly pleiotropic genetic risk scores for neuropsychiatric disorders.

Neuropsychiatric disorders show shared and distinct neurobiological correlates. A cross-disorder genome-wide association study (GWAS) identified 23 highly pleiotropic single-nucleotide polymorphisms (SNPs) that were associated with at least four neuropsychiatric disorders, and 22 SNPs that were associated predominantly with schizophrenia. Exploring their link to brain-related traits might advance understanding their distinct neurobiological processes. Using the UK Biobank data (n = 28,952), this study examined the association of both a genetic risk score (GRS) for highly pleiotropic SNPs (PleioPsych-GRS), and a GRS for predominantly schizophrenia-associated SNPs (SCZ-GRS) with 154 measures of subcortical volume, cortical thickness, and surface area as well as 12 outcomes related to mental health. To generate further insights at the individual SNP level, the association between SNPs and brain structure was examined using GWAS summary statistics. The PleioPsych-GRS showed no significant association with brain structure after correction for multiple testing. The SCZ-GRS showed a significant association with an increased surface area of the lateral orbitofrontal region, and an increased volume of the putamen, among others. The PleioPsych-GRS and the SCZ-GRS were associated with eight and four outcomes related to mental health, respectively. Two highly pleiotropic and 10 SCZ-associated SNPs were associated with several structural brain phenotypes. Taken together, these findings indicated that GRSs of highly pleiotropic SNPs and predominantly schizophrenia-associated SNPs have partly distinct associations with brain structure and outcomes related to mental health. Thus, investigating schizophrenia-specific and pleiotropic variants may improve our understanding of the neurobiology of neuropsychiatric disorders.

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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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