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成人和老年队列中抑郁和焦虑的遗传风险特征。

Genetic risk profiles for depression and anxiety in adult and elderly cohorts.

机构信息

Genetic Epidemiology Unit of the Departments of Epidemiology and Clinical Genetics, Erasmus University Medical Centre, Rotterdam, The Netherlands.

出版信息

Mol Psychiatry. 2011 Jul;16(7):773-83. doi: 10.1038/mp.2010.65. Epub 2010 Jun 22.

Abstract

The first generation of genome-wide association studies (GWA studies) for psychiatric disorders has led to new insights regarding the genetic architecture of these disorders. We now start to realize that a larger number of genes, each with a small contribution, are likely to explain the heritability of psychiatric diseases. The contribution of a large number of genes to complex traits can be analyzed with genome-wide profiling. In a discovery sample, a genetic risk profile for depression was defined based on a GWA study of 1738 adult cases and 1802 controls. The genetic risk scores were tested in two population-based samples of elderly participants. The genetic risk profiles were evaluated for depression and anxiety in the Rotterdam Study cohort and the Erasmus Rucphen Family (ERF) study. The genetic risk scores were significantly associated with different measures of depression and explained up to ∼0.7% of the variance in depression in Rotterdam Study and up to ∼1% in ERF study. The genetic score for depression was also significantly associated with anxiety explaining up to 2.1% in Rotterdam study. These findings suggest the presence of many genetic loci of small effect that influence both depression and anxiety. Remarkably, the predictive value of these profiles was as large in the sample of elderly participants as in the middle-aged samples.

摘要

第一代全基因组关联研究(GWA 研究)为精神障碍提供了新的见解,这些研究揭示了这些障碍的遗传结构。我们现在开始意识到,许多基因,每个基因的贡献都很小,可能会解释精神疾病的遗传性。大量基因对复杂性状的贡献可以通过全基因组分析来分析。在一个发现样本中,根据对 1738 例成年病例和 1802 例对照的 GWA 研究,确定了抑郁症的遗传风险概况。在两个基于人群的老年参与者样本中测试了遗传风险评分。在鹿特丹研究队列和伊拉斯谟鲁芬家族(ERF)研究中评估了遗传风险概况与抑郁和焦虑的关系。遗传风险评分与不同的抑郁测量值显著相关,在鹿特丹研究中解释了高达 0.7%的抑郁方差,在 ERF 研究中解释了高达 1%的方差。抑郁的遗传评分也与焦虑显著相关,在鹿特丹研究中解释了高达 2.1%的焦虑。这些发现表明存在许多影响抑郁和焦虑的小效应遗传位点。值得注意的是,这些概况在老年参与者样本中的预测价值与中年样本一样大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d98/3142964/770e641c4837/mp201065f1.jpg

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