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基因标记与情感障碍之间可能存在联系的证据。

Evidence for possible linkage between genetic markers and affective disorders.

作者信息

Hill E M, Wilson A F, Elston R C, Winokur G

机构信息

Department of Biometry and Genetics, Louisiana State University Medical Center, New Orleans.

出版信息

Biol Psychiatry. 1988 Dec;24(8):903-17. doi: 10.1016/0006-3223(88)90225-9.

Abstract

Studies of the underlying components of affective disorders are particularly difficult because of the confounding effects of both genetic and environmental factors. Linkage analysis is a useful tool in delineating the etiology of affective disorders, as it is unlikely that linkage between behavioral traits and blood group polymorphisms could result from environmental effects. The present study used the robust Haseman and Elston sibpair method to analyze linkage between 24 genetic markers and affective disorder in 34 nuclear families from 25 pedigrees (195 people). The probands were ascertained as part of the ongoing NIMH Collaborative Depression Study. Indications of linkage between familial pure depressive disease and MNS and depression spectrum disease and ORM were found, as had been previously suggested. There was also suggestive evidence for linkage between the latter and GC. Results are discussed in terms of methodological differences with previous studies.

摘要

由于遗传和环境因素的混杂效应,对情感障碍潜在成分的研究格外困难。连锁分析是描绘情感障碍病因的一种有用工具,因为行为特征与血型多态性之间的连锁不太可能由环境效应导致。本研究采用强大的哈斯曼和埃尔斯顿同胞对法,对来自25个家系(195人)的34个核心家庭中的24个遗传标记与情感障碍之间的连锁进行分析。先证者是正在进行的美国国立精神卫生研究所协作抑郁症研究的一部分。正如之前所提示的,发现家族性单纯抑郁症与MNS以及抑郁谱系疾病与ORM之间存在连锁迹象。对于后者与GC之间的连锁也有提示性证据。根据与先前研究在方法学上的差异对结果进行了讨论。

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