The Anorexia Nervosa Genetics Initiative (ANGI): Overview and methods.

The Anorexia Nervosa Genetics Initiative (ANGI): Overview and methods.
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神经性厌食症遗传学倡议 (ANGI):概述和方法。

DOI:
10.1016/j.cct.2018.09.015
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发表时间:
2018
影响因子:
2.2
通讯作者:
--
中科院分区:
医学4区
文献类型:
--
作者:
Thornton,LauraM;Munn-Chernoff,MelissaA;Baker,JessicaH;Juréus,Anders;Parker,Richard;Henders,AnjaliK;Larsen,JanneT;Petersen,Liselotte;Watson,HunnaJ;Yilmaz,Zeynep;Kirk,KatherineM;Gordon,Scott;Leppä,VirpiM;Martin,FelicityC;

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背景遗传因素导致神经性厌食症(anorexia nervosa,AN),并且第一个全基因组显著位点已经被发现。我们描述了神经性厌食症遗传学倡议(ANGI)的方法和程序,该倡议是一项国际合作,旨在迅速招募13,000名AN患者和祖先匹配的对照。我们目前的样本特点和实用程序的在线饮食失调诊断问卷适合大规模的遗传和人口research.MethodsANGI招募来自美国(US),澳大利亚/新西兰(ANZ),瑞典(SE),和丹麦(DK)。招募是通过国家登记册(SE,DK);治疗中心(US,ANZ,SE,DK);和社会和传统媒体(US,ANZ,SE)。所有病例均根据DSM-IV或ICD-10标准(不包括闭经)进行终生AN诊断。招募的对照组没有饮食失调行为的终身史。为了评估在线进食障碍问卷(ED 100 K-V1)的阳性和阴性预测有效性,109名女性还完成了DSM-IV(SCID)的结构化临床访谈,模块H.ResultsBlood样本和临床信息收集自13,363名终生AN患者和对照组。在线诊断表型是有效和高效的,问卷的有效性是acceptable.ConclusionsOur多管齐下的招聘方法是非常有效的快速招聘,并可以作为一个模型,由其他团体的努力。在一些国家,患有AN的人在网上的人数很多,使得互联网/社交媒体成为非常有效的招聘工具。ANGI大大增加了精神病基因组学联盟的样本收集。ANGI是一项注册的临床试验:clinicaltrials.govNCT01916538; https://clinicaltrials.gov/ct2/show/NCT01916538? cond=厌食症+神经症&draw= 1 & rank =3。
BackgroundGenetic factors contribute to anorexia nervosa (AN); and the first genome-wide significant locus has been identified. We describe methods and procedures for the Anorexia Nervosa Genetics Initiative (ANGI), an international collaboration designed to rapidly recruit 13,000 individuals with AN and ancestrally matched controls. We present sample characteristics and the utility of an online eating disorder diagnostic questionnaire suitable for large-scale genetic and population research.MethodsANGI recruited from the United States (US), Australia/New Zealand (ANZ), Sweden (SE), and Denmark (DK). Recruitment was via national registers (SE, DK); treatment centers (US, ANZ, SE, DK); and social and traditional media (US, ANZ, SE). All cases had a lifetime AN diagnosis based on DSM-IV or ICD-10 criteria (excluding amenorrhea). Recruited controls had no lifetime history of disordered eating behaviors. To assess the positive and negative predictive validity of the online eating disorder questionnaire (ED100K-v1), 109 women also completed the Structured Clinical Interview for DSM-IV (SCID), Module H.ResultsBlood samples and clinical information were collected from 13,363 individuals with lifetime AN and from controls. Online diagnostic phenotyping was effective and efficient; the validity of the questionnaire was acceptable.ConclusionsOur multi-pronged recruitment approach was highly effective for rapid recruitment and can be used as a model for efforts by other groups. High online presence of individuals with AN rendered the Internet/social media a remarkably effective recruitment tool in some countries. ANGI has substantially augmented Psychiatric Genomics Consortium AN sample collection. ANGI is a registered clinical trial: clinicaltrials.govNCT01916538; https://clinicaltrials.gov/ct2/show/NCT01916538?cond=Anorexia+Nervosa&draw=1&rank=3.
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影响因子: --
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