Barua Moumita, Cil Onur, Paterson Andrew D, Wang Kairon, He Ning, Dicks Elizabeth, Parfrey Patrick, Pei York
Division of Nephrology and Genomic Medicine, Department of Medicine, University of Toronto and University Health Network, Toronto, Ontario, Canada.
J Am Soc Nephrol. 2009 Aug;20(8):1833-8. doi: 10.1681/ASN.2009020162. Epub 2009 May 14.
Mutations of PKD1 and PKD2 account for 85 and 15% of cases of autosomal dominant polycystic kidney disease (ADPKD), respectively. Clinically, PKD1 is more severe than PKD2, with a median age at ESRD of 53.4 versus 72.7 yr. In this study, we explored whether a family history of renal disease severity predicts the mutated gene in ADPKD. We examined the renal function (estimated GFR and age at ESRD) of 484 affected members from 90 families who had ADPKD and whose underlying genotype was known. We found that the presence of at least one affected family member who developed ESRD at age < or =55 was highly predictive of a PKD1 mutation (positive predictive value 100%; sensitivity 72%). In contrast, the presence of at least one affected family member who continued to have sufficient renal function or developed ESRD at age >70 was highly predictive of a PKD2 mutation (positive predictive value 100%; sensitivity 74%). These data suggest that close attention to the family history of renal disease severity in ADPKD may provide a simple means of predicting the mutated gene, which has prognostic implications.
PKD1和PKD2的突变分别占常染色体显性多囊肾病(ADPKD)病例的85%和15%。临床上,PKD1比PKD2更严重,ESRD的中位年龄分别为53.4岁和72.7岁。在本研究中,我们探讨了肾脏疾病严重程度的家族史是否能预测ADPKD中的突变基因。我们检查了来自90个已知潜在基因型的ADPKD家族的484名受影响成员的肾功能(估计肾小球滤过率和ESRD年龄)。我们发现,至少有一名在55岁及以下发生ESRD的受影响家庭成员的存在高度预测PKD1突变(阳性预测值100%;敏感性72%)。相反,至少有一名肾功能持续充足或在70岁以上发生ESRD的受影响家庭成员的存在高度预测PKD2突变(阳性预测值100%;敏感性74%)。这些数据表明,密切关注ADPKD中肾脏疾病严重程度的家族史可能提供一种预测突变基因的简单方法,这具有预后意义。