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瑞典前列腺癌的分离分析:支持显性遗传

Segregation analysis of prostate cancer in Sweden: support for dominant inheritance.

作者信息

Grönberg H, Damber L, Damber J E, Iselius L

机构信息

Department of Oncology, Umeå University, Sweden.

出版信息

Am J Epidemiol. 1997 Oct 1;146(7):552-7. doi: 10.1093/oxfordjournals.aje.a009313.

Abstract

Several epidemiologic studies have shown familial aggregation of prostate cancer. To assess the nature of familial clustering of prostate cancer, a complex segregation analysis was performed on a population-based sample of 2,857 nuclear families ascertained through an affected father diagnosed with prostate cancer in Sweden during 1959-1963. The segregation analysis, using a large, unselected population of prostate cancer families, revealed that the observed clustering of prostate cancer was best explained by a high risk allele inherited in a dominant mode, with a high population frequency (1.67%) and a moderate lifetime penetrance (63%). This study confirms the result from one earlier published segregation analysis and provides the context for interpreting the recently published linkage of hereditary prostate cancer families to chromosome 1q 24-25 (HPC1).

摘要

多项流行病学研究表明前列腺癌存在家族聚集性。为评估前列腺癌家族聚集的性质,对1959年至1963年期间在瑞典通过确诊患有前列腺癌的患病父亲确定的2857个核心家庭的人群样本进行了复杂分离分析。使用大量未经选择的前列腺癌家族人群进行的分离分析表明,观察到的前列腺癌聚集现象最好由以显性模式遗传的高风险等位基因来解释,该等位基因在人群中的频率较高(1.67%)且终生外显率中等(63%)。本研究证实了先前发表的一项分离分析的结果,并为解释最近发表的遗传性前列腺癌家族与1号染色体24 - 25区域(HPC1)的连锁关系提供了背景。

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