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解析精神分裂症遗传模型的传递方式。

Resolving genetic models for the transmission of schizophrenia.

作者信息

McGue M, Gottesman I I, Rao D C

出版信息

Genet Epidemiol. 1985;2(1):99-110. doi: 10.1002/gepi.1370020110.

Abstract

Although family studies have consistently reported elevated rates of schizophrenia among the relatives of schizophrenics, the exact nature of the transmission of the disorder remains uncertain. Genetic models hypothesized to explain the transmission of schizophrenia include the generalized single locus and multifactorial threshold models. Here we briefly describe these models and test their goodness-of-fit to a single data set on the pooled morbid risks of schizophrenia among the relatives of schizophrenic probands in nine different classes of relatives with five different degrees of genetic relatedness. The generalized single locus model is rejected, while a pure polygenic threshold model does fit the observed risks. Allowance for environmental sources of familial resemblance under the multifactorial threshold model significantly improved the fit of the model to the data. An application of the multifactorial model to family data on tuberculosis is also reported. For tuberculosis, a strong familial environmental but not genetic effect was found, consistent with the known infectious etiology of this condition, showing that the finding of a strong genetic effect upon schizophrenia is not a necessary bias of these methods of analysis. The implications of these results for the search for major gene effects in schizophrenia are discussed.

摘要

尽管家族研究一直报告称精神分裂症患者的亲属中精神分裂症发病率较高,但该疾病的确切遗传方式仍不确定。为解释精神分裂症遗传方式而提出的遗传模型包括广义单基因座模型和多因素阈值模型。在此,我们简要描述这些模型,并检验它们对一个数据集的拟合优度,该数据集涉及九种不同亲属类别、具有五种不同遗传相关程度的精神分裂症先证者亲属中精神分裂症的合并发病风险。广义单基因座模型被否定,而纯多基因阈值模型确实符合观察到的风险。在多因素阈值模型下考虑家族相似性的环境因素来源,显著改善了模型对数据的拟合。本文还报告了多因素模型在结核病家族数据中的应用。对于结核病,发现了强烈的家族环境效应而非遗传效应,这与该疾病已知的感染病因一致,表明在精神分裂症中发现强烈的遗传效应并非这些分析方法必然存在的偏差。本文讨论了这些结果对寻找精神分裂症主要基因效应的意义。

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