荷兰终生抑郁症基因组研究:荷兰生物银行互联网合作(BIONIC)项目。

IF 1 4区 医学 Q4 GENETICS & HEREDITY Twin Research and Human Genetics Pub Date : 2024-02-01 Epub Date: 2024-03-18 DOI:10.1017/thg.2024.4
Floris Huider, Yuri Milaneschi, Jouke-Jan Hottenga, Mariska Bot, M Liset Rietman, Almar A L Kok, Tessel E Galesloot, Leen M 't Hart, Femke Rutters, Marieke T Blom, Didi Rhebergen, Marjolein Visser, Ingeborg Brouwer, Edith Feskens, Catharina A Hartman, Albertine J Oldehinkel, Eco J C de Geus, Lambertus A Kiemeney, Martijn Huisman, H Susan J Picavet, W M Monique Verschuren, Hanna M van Loo, Brenda W J H Penninx, Dorret I Boomsma
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引用次数: 0

摘要

在这篇队列概况文章中,我们介绍了作为 BIObanks Netherlands Internet Collaboration (BIONIC) 的一部分而建立的终生重度抑郁障碍 (MDD) 数据库。我们在荷兰各地收集了 132,850 名荷兰人的《精神疾病诊断与统计手册第五版》(DSM-5)终生重度抑郁障碍诊断数据。目前,其中 N = 66,684 人还拥有全基因组单核苷酸多态性 (SNP) 数据。我们之所以启动这个项目,是因为 MDD 复杂的遗传基础需要进行大规模的全人群研究和统一的深度表型分析。为了进行标准化的表型分析,我们开发了 LIDAS(终生抑郁评估调查),然后用它来测量 11 个荷兰队列中的 MDD。这些队列的数据与来自 5 个临床队列的诊断性访谈抑郁数据相结合,形成了 N = 29,650 个符合 DSM-5 标准的终生 MDD 病例(22%)和 94,300 个筛查对照的数据集。此外,来自队列的全基因组基因型数据被整合到一个全基因组关联研究(GWAS)数据集中,该数据集包含 N = 66,684 名荷兰人(25.3% 的病例)。表型数据包括基于 DSM-5 的 MDD 诊断、社会人口变量、生活方式和体重指数信息、抑郁症状和发作特征以及精神病诊断和治疗史。我们介绍了 BIONIC 表型和 GWAS 数据集的建立和协调情况,并概述了可用信息和样本特征。我们的下一步计划是在荷兰开展终生 MDD 的 GWAS,未来计划包括对抑郁症特征进行精细的遗传分析、国际合作和多组学研究。
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Genomics Research of Lifetime Depression in the Netherlands: The BIObanks Netherlands Internet Collaboration (BIONIC) Project.

In this cohort profile article we describe the lifetime major depressive disorder (MDD) database that has been established as part of the BIObanks Netherlands Internet Collaboration (BIONIC). Across the Netherlands we collected data on Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) lifetime MDD diagnosis in 132,850 Dutch individuals. Currently, N = 66,684 of these also have genomewide single nucleotide polymorphism (SNP) data. We initiated this project because the complex genetic basis of MDD requires large population-wide studies with uniform in-depth phenotyping. For standardized phenotyping we developed the LIDAS (LIfetime Depression Assessment Survey), which then was used to measure MDD in 11 Dutch cohorts. Data from these cohorts were combined with diagnostic interview depression data from 5 clinical cohorts to create a dataset of N = 29,650 lifetime MDD cases (22%) meeting DSM-5 criteria and 94,300 screened controls. In addition, genomewide genotype data from the cohorts were assembled into a genomewide association study (GWAS) dataset of N = 66,684 Dutch individuals (25.3% cases). Phenotype data include DSM-5-based MDD diagnoses, sociodemographic variables, information on lifestyle and BMI, characteristics of depressive symptoms and episodes, and psychiatric diagnosis and treatment history. We describe the establishment and harmonization of the BIONIC phenotype and GWAS datasets and provide an overview of the available information and sample characteristics. Our next step is the GWAS of lifetime MDD in the Netherlands, with future plans including fine-grained genetic analyses of depression characteristics, international collaborations and multi-omics studies.

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来源期刊
Twin Research and Human Genetics
Twin Research and Human Genetics 医学-妇产科学
CiteScore
1.50
自引率
11.10%
发文量
37
审稿时长
6-12 weeks
期刊介绍: Twin Research and Human Genetics is the official journal of the International Society for Twin Studies. Twin Research and Human Genetics covers all areas of human genetics with an emphasis on twin studies, genetic epidemiology, psychiatric and behavioral genetics, and research on multiple births in the fields of epidemiology, genetics, endocrinology, fetal pathology, obstetrics and pediatrics. Through Twin Research and Human Genetics the society aims to publish the latest research developments in twin studies throughout the world.
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