Bear J C, McManamon P, Morgan J, Payne R H, Lewis H, Gault M H, Churchill D N
Am J Med Genet. 1984 May;18(1):45-53. doi: 10.1002/ajmg.1320180108.
Few reports are available on the age-related risk of relatives of affected persons to manifest adult polycystic kidney disease (APKD). For 371 persons in 17 kindreds, at risk for APKD by virtue of having an affected first degree relative, we calculated the estimated probability of clinical diagnosis of APKD to be 0.011 by age 20, 0.041 by age 30, 0.115 by age 40, 0.299 by age 50, and 0.404 by age 60 years (expected = 0.50). Ultrasonographic examination of 172 asymptomatic persons at risk showed definite APKD in 60. The probability of ultrasonographic detection of asymptomatic APKD is estimated as 0.222, 0.657, and 0.855 at age 5, 15, and 25 years, respectively. The probability of having APKD following normal ultrasonogram results (conservatively assuming 90% specificity) is estimated as 0.46, 0.28, and 0.14 for persons at 50% risk in their first, second, or third decade. The marginal benefit of ultrasound as a diagnostic test for APKD for persons in the second or third decade is estimated as 0.37 and 0.41, respectively for a "positive" test and 0.22 and 0.37 for a "negative" test.
关于成人多囊肾病(APKD)患者亲属出现与年龄相关的发病风险的报道较少。对于17个家族中的371人,由于有一位患病的一级亲属而有患APKD的风险,我们计算出20岁时临床诊断为APKD的估计概率为0.011,30岁时为0.041,40岁时为0.115,50岁时为0.299,60岁时为0.404(预期概率为0.50)。对172名有患病风险的无症状者进行超声检查,发现其中60人确诊为APKD。5岁、15岁和25岁时超声检测无症状APKD的概率分别估计为0.222、0.657和0.855。对于在第一个、第二个或第三个十年中有50%患病风险的人,超声检查结果正常(保守地假设特异性为90%)后患APKD的概率估计分别为0.46、0.28和0.14。对于处于第二个或第三个十年的人,超声作为APKD诊断测试的边际效益,“阳性”测试分别估计为0.37和0.41,“阴性”测试分别估计为0.22和0.37。