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iPSYCH2012 病例-队列样本:深入研究严重精神障碍的遗传和环境结构的新方向。

The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders.

机构信息

iPSYCH, The Lundbeck Foundation Initiative for Integrative Psychiatric Research, Aarhus, Denmark.

National Centre for Register-Based Research, Business and Social Sciences, Aarhus University, Aarhus V, Denmark.

出版信息

Mol Psychiatry. 2018 Jan;23(1):6-14. doi: 10.1038/mp.2017.196. Epub 2017 Sep 19.


DOI:10.1038/mp.2017.196
PMID:28924187
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5754466/
Abstract

The Integrative Psychiatric Research (iPSYCH) consortium has established a large Danish population-based Case-Cohort sample (iPSYCH2012) aimed at unravelling the genetic and environmental architecture of severe mental disorders. The iPSYCH2012 sample is nested within the entire Danish population born between 1981 and 2005, including 1 472 762 persons. This paper introduces the iPSYCH2012 sample and outlines key future research directions. Cases were identified as persons with schizophrenia (N=3540), autism (N=16 146), attention-deficit/hyperactivity disorder (N=18 726) and affective disorder (N=26 380), of which 1928 had bipolar affective disorder. Controls were randomly sampled individuals (N=30 000). Within the sample of 86 189 individuals, a total of 57 377 individuals had at least one major mental disorder. DNA was extracted from the neonatal dried blood spot samples obtained from the Danish Neonatal Screening Biobank and genotyped using the Illumina PsychChip. Genotyping was successful for 90% of the sample. The assessments of exome sequencing, methylation profiling, metabolome profiling, vitamin-D, inflammatory and neurotrophic factors are in progress. For each individual, the iPSYCH2012 sample also includes longitudinal information on health, prescribed medicine, social and socioeconomic information, and analogous information among relatives. To the best of our knowledge, the iPSYCH2012 sample is the largest and most comprehensive data source for the combined study of genetic and environmental aetiologies of severe mental disorders.

摘要

综合精神病学研究(iPSYCH)联盟建立了一个大型丹麦基于人群的病例队列样本(iPSYCH2012),旨在揭示严重精神障碍的遗传和环境结构。iPSYCH2012 样本嵌套在 1981 年至 2005 年之间出生的整个丹麦人群中,包括 1472762 人。本文介绍了 iPSYCH2012 样本,并概述了未来的关键研究方向。病例被确定为精神分裂症患者(N=3540)、自闭症患者(N=16146)、注意力缺陷/多动障碍患者(N=18726)和情感障碍患者(N=26380),其中 1928 人患有双相情感障碍。对照组是随机抽样的个体(N=30000)。在 86189 人的样本中,共有 57377 人至少患有一种主要精神障碍。从丹麦新生儿筛查生物库获得的新生儿干血斑样本中提取 DNA,并使用 Illumina PsychChip 进行基因分型。90%的样本进行了基因分型。外显子测序、甲基化谱分析、代谢组学谱分析、维生素 D、炎症和神经营养因子的评估正在进行中。对于每个个体,iPSYCH2012 样本还包括健康、处方药物、社会和社会经济信息以及亲属中的类似信息的纵向信息。据我们所知,iPSYCH2012 样本是研究严重精神障碍遗传和环境病因的最大和最全面的数据源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d18/5754466/c354f824fe70/mp2017196f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d18/5754466/ef2698892a8d/mp2017196f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d18/5754466/c354f824fe70/mp2017196f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d18/5754466/ef2698892a8d/mp2017196f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d18/5754466/c354f824fe70/mp2017196f2.jpg

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本文引用的文献

[1]
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.

Nat Genet. 2018-11-26

[2]
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[3]
Evaluation of whole genome amplified DNA to decrease material expenditure and increase quality.

Mol Genet Metab Rep. 2017-4-25

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Polygenic Risk Score for Schizophrenia and Treatment-Resistant Schizophrenia.

Schizophr Bull. 2017-9-1

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RNA sequencing of archived neonatal dried blood spots.

Mol Genet Metab Rep. 2016-12-24

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An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype.

Biol Psychiatry. 2016-12-8

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Schizophr Res. 2017-6

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The implications of the shared genetics of psychiatric disorders.

Nat Med. 2016-10-26

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Influence of Polygenic Risk Scores on the Association Between Infections and Schizophrenia.

Biol Psychiatry. 2016-4-19

[10]
Predicting ADHD by Assessment of Rutter's Indicators of Adversity in Infancy.

PLoS One. 2016-6-29

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