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锂反应性情感障碍患者家族中的遗传模式。

Mode of inheritance in families of patients with lithium-responsive affective disorders.

作者信息

Alda M, Grof P, Grof E, Zvolsky P, Walsh M

机构信息

Department of Psychiatry, University of Ottawa, Royal Ottawa Hospital, Canada.

出版信息

Acta Psychiatr Scand. 1994 Oct;90(4):304-10. doi: 10.1111/j.1600-0447.1994.tb01598.x.

Abstract

A better understanding of the role of genetic factors in affective disorders is likely to result from investigating more homogeneous populations. To achieve this goal, we have systematically studied patients who are excellent responders to long-term lithium treatment and their relatives. In the families of 71 such probands, we have analyzed the mode of inheritance by comparing the observed morbidity risks with the risks expected under different genetic models. The results demonstrate major-gene effects in the transmission of primary affective disorders; the polygenic model with sex-specific thresholds could be rejected. Discrimination between the autosomal and X-chromosome models was not possible, but the autosomal recessive model predicts more realistic, gender-specific frequencies of affective disorders in the general population. These results suggest that autosomal recessive inheritance deserves serious consideration in molecular genetic investigations.

摘要

通过对更同质化的人群进行研究,有望更好地理解遗传因素在情感障碍中的作用。为实现这一目标,我们系统地研究了对长期锂盐治疗反应良好的患者及其亲属。在71名此类先证者的家族中,我们通过比较观察到的发病风险与不同遗传模型下预期的风险,分析了遗传模式。结果表明,在原发性情感障碍的传递中存在主基因效应;具有性别特异性阈值的多基因模型可被排除。无法区分常染色体和X染色体模型,但常染色体隐性模型预测一般人群中情感障碍的性别特异性频率更为现实。这些结果表明,常染色体隐性遗传在分子遗传学研究中值得认真考虑。

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