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基于互联网的 MGS2 对照样本:精神疾病的自我报告。

The Internet-based MGS2 control sample: self report of mental illness.

机构信息

Center for Psychiatric Genetics, Department of Psychiatry and Behavioral Sciences, NorthShore University HealthSystem, Evanston, Ill 60201-3137, USA.

出版信息

Am J Psychiatry. 2010 Jul;167(7):854-65. doi: 10.1176/appi.ajp.2010.09071050. Epub 2010 Jun 1.

Abstract

OBJECTIVE

The Molecular Genetics of Schizophrenia (MGS2) project recruited an adult control sample of non-Hispanic European-ancestry (N=3,364) and African American (N=1,301) subjects.

METHOD

Subjects gave consent to deposit phenotypic data and blood samples into a repository for general research use, with full anonymization of the sample. The authors compared the control sample with population census data for demographic data and with previous population surveys for anthropometrics and prevalences of psychiatric disorders as estimated by an Internet-administered questionnaire.

RESULTS

The full MGS2 control sample includes 4,665 subjects (European-ancestry: N=3,364; African American: N=1,301), of whom 3,626 were included in the MGS2 genome-wide association study (GWAS). The sample is generally demographically representative of the U.S. population, except for being older and more female, educated, and affluent, although all strata are represented. Self-reported ancestry was consistent with genotypic and census data. Lifetime prevalences for depressive, anxiety, and substance use diagnoses were higher than in previous population-based surveys, probably due to use of an abbreviated self-report instrument. However, patterns such as sex ratios, comorbidity, and demographic associations were consistent with previous reports. DNA quality for the Internet collected/evaluated control sample was comparable to that of the face-to-face case sample.

CONCLUSIONS

The Internet-based methods facilitated the rapid collection of large and anonymized non-Hispanic European-ancestry and African American control samples that have been validated as being generally representative for many aspects of demography, ancestry, and morbidity. Utilization of clinical screening data shared with the scientific community may permit investigators to select appropriate controls for some studies.

摘要

目的

精神分裂症的分子遗传学(MGS2)项目招募了一个非西班牙裔欧洲血统的成年对照组(N=3364)和非裔美国人(N=1301)。

方法

受试者同意将表型数据和血液样本存入一个存储库,用于一般研究用途,并对样本进行完全匿名化。作者将对照样本与人口普查数据进行了比较,以获取人口统计学数据,并与之前的人口调查进行了比较,以获取通过互联网管理的问卷估计的人体测量学和精神障碍患病率。

结果

完整的 MGS2 对照组包括 4665 名受试者(欧洲血统:N=3364;非裔美国人:N=1301),其中 3626 名受试者纳入了 MGS2 全基因组关联研究(GWAS)。该样本在人口统计学上通常代表美国人口,除了年龄较大、女性比例较高、受教育程度较高和富裕程度较高外,尽管所有阶层都有代表。自我报告的祖先与基因型和人口普查数据一致。终身抑郁、焦虑和物质使用诊断的患病率高于以前的基于人群的调查,这可能是由于使用了简短的自我报告工具。然而,性别比例、共病和人口统计学关联等模式与以前的报告一致。通过互联网收集/评估的对照组的 DNA 质量与面对面病例样本相当。

结论

基于互联网的方法促进了快速收集大量匿名的非西班牙裔欧洲血统和非裔美国对照组样本,这些样本在人口统计学、祖先和发病率的许多方面都被证明具有代表性。利用与科学界共享的临床筛查数据,可能允许研究人员为某些研究选择适当的对照。

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The Internet-based MGS2 control sample: self report of mental illness.基于互联网的 MGS2 对照样本:精神疾病的自我报告。
Am J Psychiatry. 2010 Jul;167(7):854-65. doi: 10.1176/appi.ajp.2010.09071050. Epub 2010 Jun 1.

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