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共济失调毛细血管扩张症杂合子的癌症风险。

Cancer risks in A-T heterozygotes.

作者信息

Easton D F

机构信息

Section of Epidemiology, Institute of Cancer Research, Belmont, UK.

出版信息

Int J Radiat Biol. 1994 Dec;66(6 Suppl):S177-82. doi: 10.1080/09553009414552011.

Abstract

It is well established that ataxia-telangiectasia (A-T) patients suffer a grossly elevated risk of cancer, particularly lymphoma and leukaemia, but the possibility of an excess cancer risk of cancer in heterozygotes carriers of A-T mutations is more controversial. A number of studies indicate that female relatives of A-T patients suffer excess risk of breast cancer; based on an overview of all currently available data the estimated relative risk of breast cancer to A-T heterozygotes is 3.9-fold (95% CI 2.1-7.2). There is some suggestion that relative risk declines with age. In contrast, there is no consistent evidence of a risk from any other cancer; the estimated risk from all studies is 1.9 (95% CI 1.5-2.5) but some studies show a larger effect whilst others show no excess risk. On the basis of these results and the likely frequency of the A-T gene, A-T heterozygotes would account for between 1 and 13% of breast cancer cases, with 3.8% being the best estimate. However, unless the breast cancer risk has been seriously underestimated, the A-T gene will make little contribution to familial breast cancer.

摘要

共济失调毛细血管扩张症(A-T)患者患癌症的风险显著升高,尤其是淋巴瘤和白血病,这一点已得到充分证实,但A-T突变杂合携带者患癌风险增加的可能性更具争议性。多项研究表明,A-T患者的女性亲属患乳腺癌的风险增加;根据目前所有可用数据的概述,A-T杂合子患乳腺癌的估计相对风险为3.9倍(95%置信区间2.1-7.2)。有迹象表明相对风险会随着年龄下降。相比之下,没有一致的证据表明存在来自其他任何癌症的风险;所有研究的估计风险为1.9(95%置信区间1.5-2.5),但一些研究显示影响更大,而另一些研究则未显示出额外风险。基于这些结果以及A-T基因的可能频率,A-T杂合子将占乳腺癌病例的1%至13%,最佳估计为3.8%。然而,除非乳腺癌风险被严重低估,否则A-T基因对家族性乳腺癌的影响不大。

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