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Prioritizing Schizophrenia Endophenotypes for Future Genetic Studies: An Example Using Data from the COGS-1 Family Study

机译:优先考虑精神分裂症的内表型以用于未来的遗传研究:以来自COGS-1家族研究的数据为例

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摘要

Past studies describe numerous endophenotypes associated with schizophrenia (SZ), but many endophenotypes may overlap in information they provide, and few studies have investigated the utility of a multivariate index to improve discrimination between SZ and healthy community comparison subjects (CCS). We investigated 16 endophenotypes from the first phase of the Consortium on the Genetics of Schizophrenia, a large, multi-site family study, to determine whether a subset could distinguish SZ probands and CCS just as well as using all 16.Participants included 345 SZ probands and 517 CCS with a valid measure for at least one endophenotype. We used both logistic regression and random forest models to choose a subset of endophenotypes, adjusting for age, gender, smoking status, site, parent education, and the reading subtest of the Wide Range Achievement Test. As a sensitivity analysis, we re-fit models using multiple imputations to determine the effect of missing values.We identified four important endophenotypes: antisaccade, Continuous Performance Test-Identical Pairs 3-digit version, California Verbal Learning Test, and emotion identification. The logistic regression model that used just these four endophenotypes produced essentially the same results as the model that used all 16 (84% vs. 85% accuracy).While a subset of endophenotypes cannot replace clinical diagnosis nor encompass the complexity of the disease, it can aid in the design of future endophenotypic and genetic studies by reducing study cost and subject burden, simplifying sample enrichment, and improving statistical power of locating genetic regions associated with schizophrenia that may be the easiest to identify initially.
机译:过去的研究描述了许多与精神分裂症(SZ)相关的内表型,但许多内表型可能会在其提供的信息中重叠,并且很少有研究研究多变量指数在改善SZ和健康社区比较对象(CCS)之间的区别上的作用。我们调查了精神分裂症遗传学联盟第一阶段的16种内表型,这是一个大型的多站点家庭研究,以确定亚群是否可以区分SZ先证者和CCS以及是否使用全部16名参与者包括345个SZ先证者517 CCS,至少可对一种内表型进行有效测量。我们使用逻辑回归和随机森林模型来选择一个内表型子集,并根据年龄,性别,吸烟状况,场所,父母的教育程度和广泛成就测试的阅读子测试进行调整。为了进行敏感性分析,我们使用多个插值重新拟合模型以确定缺失值的影响。我们确定了四种重要的内表型:反扫视,连续性行为测验-三对相同数字对,加利福尼亚语言学习测验和情绪识别。仅使用这四种内表型的逻辑回归模型产生的结果与使用全部16种内表型的模型基本相同(准确率分别为84%和85%),尽管内表型的一部分无法代替临床诊断或涵盖疾病的复杂性,通过降低研究成本和受试者负担,简化样品富集并提高定位与精神分裂症相关的遗传区域的统计能力(可能最容易识别),可以帮助设计未来的表型和遗传研究。

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