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共济失调毛细血管扩张症的遗传学与流行病学

Genetics and epidemiology of ataxia-telangiectasia.

作者信息

Swift M

出版信息

Kroc Found Ser. 1985;19:133-46.

PMID:3864935
Abstract

According to the Hardy-Weinberg principle, the frequency in the general population of heterozygous carriers of a gene causing an autosomal recessive syndrome in homozygotes is likely to be between 0.1% and 5%. It is thus important to know whether carriers of the AT gene have a risk of cancer or diabetes greater than comparable noncarriers. A retrospective study of blood relatives in 26 AT families, and follow-up of the obligatory heterozygotes in those families, demonstrated an excess of diabetes, deaths from cancer, and deaths from ischemic heart disease among obligatory or probable AT heterozygotes. Hypotheses about the disease-predisposing effects of the AT gene in the heterozygote are now being reexamined, retrospectively and prospectively, in almost 150 newly identified AT families. Specific tests for the AT gene will permit even more rigorous tests of these hypotheses.

摘要

根据哈迪-温伯格原理,在一般人群中,导致纯合子患常染色体隐性综合征的基因杂合携带者的频率可能在0.1%至5%之间。因此,了解共济失调毛细血管扩张症(AT)基因携带者患癌症或糖尿病的风险是否高于非携带者具有重要意义。一项对26个共济失调毛细血管扩张症家庭中的血亲进行的回顾性研究,以及对这些家庭中必然的杂合子进行的随访,结果显示,必然或可能的共济失调毛细血管扩张症杂合子中糖尿病、癌症死亡和缺血性心脏病死亡的人数过多。目前,正在对近150个新发现的共济失调毛细血管扩张症家庭进行回顾性和前瞻性研究,以重新审视关于共济失调毛细血管扩张症基因在杂合子中引发疾病的假设。针对共济失调毛细血管扩张症基因的特定检测将使这些假设得到更严格的验证。

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