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用于家族性腺瘤性息肉病症状前诊断的连锁DNA标记

Linked DNA markers for presymptomatic diagnosis of familial adenomatous polyposis.

作者信息

Dunlop M G, Wyllie A H, Steel C M, Piris J, Evans H J

机构信息

University of Edinburgh Department of Clinical Surgery, UK.

出版信息

Lancet. 1991 Feb 9;337(8737):313-6. doi: 10.1016/0140-6736(91)90940-q.

Abstract

41 symptom-free individuals aged 0-39 years who were at risk of familial adenomatous polyposis (FAP) were genotyped with six linked DNA probes. 28 individuals were informative for probes flanking the gene and 14 people assigned a probe-derived risk of over 0.93 were subsequently shown to be affected by clinical screening. 4 individuals who had been discharged from follow-up were designated high risk by this method. In those screened negative, risk was calculated from genotypic, colonic, and CHRPE findings and 89% of subjects had a risk below 0.003. An integrated risk analysis may have an important place in screening programmes for FAP.

摘要

对41名年龄在0至39岁、有家族性腺瘤性息肉病(FAP)风险的无症状个体,使用六种连锁DNA探针进行基因分型。28名个体对该基因两侧的探针有信息价值,14名被判定探针衍生风险超过0.93的个体随后经临床筛查显示患病。4名已终止随访的个体通过此方法被判定为高风险。在筛查为阴性的个体中,根据基因型、结肠和先天性视网膜色素上皮肥大(CHRPE)结果计算风险,89%的受试者风险低于0.003。综合风险分析在FAP筛查项目中可能具有重要地位。

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