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队列特征描述:瑞典强迫症和慢性抽动障碍的流行病学和遗传学研究(EGOS)。

Cohort profile: Epidemiology and Genetics of Obsessive-compulsive disorder and chronic tic disorders in Sweden (EGOS).

机构信息

Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Division of Tics, OCD and Related Disorders, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

出版信息

Soc Psychiatry Psychiatr Epidemiol. 2020 Oct;55(10):1383-1393. doi: 10.1007/s00127-019-01822-7. Epub 2020 Jan 6.

Abstract

PURPOSE

The EGOS study (Epidemiology and Genetics of Obsessive-compulsive disorder and chronic tic disorders in Sweden) is a large-scale, epidemiological, prospective cohort that is used to identify genetic and environmental risk factors in the etiology of obsessive-compulsive disorder (OCD) and chronic tic disorders (CTD).

METHODS

Individuals born between January 1954 and December 1998 with at least two diagnoses of OCD or CTD at different timepoints in the National Patient Register (NPR), and followed between January 1997 and December 2012, represent the EGOS source population (n = 20,374). The Swedish Multi-Generation Registry (MGR) are then used to define family relatedness for all cases and additional phenotypic and demographic data added to the resultant database. To create an epidemiologically valid subset of the source cohort that also includes biospecimens and additional phenotyping, we contact cases from within the source population. To date, 6832 invitations have been sent out and 1853 (27%) have elected to participate in the EGOS biospecimen collection.

RESULTS

To date, 1608 biological samples have been collected, of which 1249 are genotyped and 832 supplementary Obsessive-Compulsive Inventory-Revised (OCI-R) and/or Florida Obsessive-Compulsive Inventory (FOCI) have been completed by individuals with OCD and/or CTD, age 16-64 years. DNA samples are genotyped using Infinium Global Screening Array and will undergo whole-exome sequencing in the future. Detailed information is available for each individual through linkage to the Swedish national registers, e.g., identification of additional psychiatric diagnoses, medical diagnoses, birth-related variables, and relevant demographic and social data.

CONCLUSION

EGOS benefits from a genetically homogeneous sample with epidemiological ascertainment, minimizing the risk of confounding due to population stratification on ascertainment bias. In addition, this study is built upon clinical diagnoses of OCD and CTD in specialized psychiatric care, which reduces further biases and case misclassification.

摘要

目的

EGOS 研究(瑞典强迫症和慢性抽动障碍的流行病学和遗传学)是一项大规模的、前瞻性的队列研究,旨在确定强迫症(OCD)和慢性抽动障碍(CTD)发病机制中的遗传和环境风险因素。

方法

在国家患者登记处(NPR)中至少有两次 OCD 或 CTD 诊断的个体,出生于 1954 年 1 月至 1998 年 12 月之间,随访时间为 1997 年 1 月至 2012 年 12 月,构成 EGOS 源人群(n=20374)。然后,使用瑞典多代登记处(MGR)来定义所有病例的家族相关性,并将额外的表型和人口统计学数据添加到最终数据库中。为了创建一个具有生物样本和额外表型的源队列的流行病学有效子集,我们联系源人群中的病例。迄今为止,已发出 6832 份邀请,有 1853 人(27%)选择参加 EGOS 生物样本采集。

结果

迄今为止,已采集了 1608 个生物样本,其中 1249 个进行了基因分型,832 个 OCD 和/或 CTD 患者完成了补充的强迫症清单修订版(OCI-R)和/或佛罗里达强迫症清单(FOCI)。年龄在 16-64 岁之间。DNA 样本使用 Infinium Global Screening Array 进行基因分型,并将在未来进行全外显子测序。通过与瑞典国家登记处的链接,可以获得每个个体的详细信息,例如,确定其他精神科诊断、医学诊断、出生相关变量以及相关人口统计学和社会数据。

结论

EGOS 受益于具有遗传同质性的样本,具有流行病学确定,最大限度地减少了由于在确定偏差方面的人群分层而导致的混杂风险。此外,这项研究建立在专门的精神科护理中对 OCD 和 CTD 的临床诊断之上,从而减少了进一步的偏差和病例分类错误。

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