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Assessment and Characterization of Phenotypic Heterogeneity of Anxiety Disorders across Five Large Cohorts

机译:五个大型队列焦虑症表型异质性的评估和表征

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摘要

To achieve sample sizes necessary for effectively conducting genome-wide association studies (GWAS), researchers often combine data from samples possessing multiple potential sources of heterogeneity. This is particularly relevant for psychiatric disorders, where symptom self-report, differing assessment instruments, and diagnostic comorbidity complicates the phenotypes and contribute to difficulties with detecting and replicating genetic association signals. We investigated sources of heterogeneity of anxiety disorders (ADs) across five large cohorts used in a GWAS meta-analysis project using a dimensional structural modeling approach including confirmatory factor analyses (CFA) and measurement invariance (MI) testing. CFA indicated a single-factor model provided the best fit in each sample with the same pattern of factor loadings. MI testing indicated degrees of failure of metric and scalar invariance which depended on the inclusion of the effects of sex and age in the model. This is the first study to examine the phenotypic structure of psychiatric disorder phenotypes simultaneously across multiple, large cohorts used for GWAS. The analyses provide evidence for higher order invariance but possible break-down at more detailed levels that can be subtly influenced by included covariates, suggesting caution when combining such data. These methods have significance for large-scale collaborative studies that draw on multiple, potentially heterogeneous datasets.
机译:为了获得有效开展全基因组关联研究(GWAS)所需的样本量,研究人员通常将来自具有多种潜在异质性来源的样本中的数据进行组合。这与精神疾病特别相关,在精神疾病中,症状的自我报告,不同的评估工具和诊断合并症会使表型复杂化,并导致检测和复制遗传关联信号困难。我们使用尺寸结构建模方法(包括验证性因素分析(CFA)和测量不变性(MI)测试)调查了GWAS荟萃分析项目中使用的五个大型队列的焦虑症(AD)异质性来源。 CFA指出,单因素模型可以在每个样本中以相同的因素加载模式提供最佳拟合。 MI测试表明度量和标量不变性的失败程度取决于模型中性别和年龄的影响。这是第一项同时检查用于GWAS的多个大型队列中精神病性表型的表型结构的研究。分析为高阶不变性提供了证据,但在更详细的水平上可能发生的分解可能会受到所包含的协变量的微妙影响,建议在组合此类数据时要谨慎。这些方法对于利用多个可能具有异构数据集的大规模协作研究具有重要意义。

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