| Literature DB >> 17035604 |
Peter C Harris1, Kyongtae T Bae, Sandro Rossetti, Vicente E Torres, Jared J Grantham, Arlene B Chapman, Lisa M Guay-Woodford, Bernard F King, Louis H Wetzel, Deborah A Baumgarten, Philip J Kenney, Mark Consugar, Saulo Klahr, William M Bennett, Catherine M Meyers, Qin Jean Zhang, Paul A Thompson, Fang Zhu, J Philip Miller.
Abstract
Data from serial renal magnetic resonance imaging of the Consortium of Radiologic Imaging Study of PKD (CRISP) autosomal dominant polycystic kidney disease (PKD) population showed that cystic expansion occurs at a consistent rate per individual, although it is heterogeneous in the population, and that larger kidneys are associated with more rapid disease progression. The significance of gene type to disease progression is analyzed in this study of the CRISP cohort. Gene type was determined in 183 families (219 cases); 156 (85.2%) had PKD1, and 27 (14.8%) had PKD2. PKD1 kidneys were significantly larger, but the rate of cystic growth (PKD1 5.68%/yr; PKD2 4.82%/yr) was not different (P = 0.24). Cyst number increased with age, and more cysts were detected in PKD1 kidneys (P < 0.0001). PKD1 is more severe because more cysts develop earlier, not because they grow faster, implicating the disease gene in cyst initiation but not expansion. These insights will inform the development of targeted therapies in autosomal dominant PKD.Entities:
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Year: 2006 PMID: 17035604 DOI: 10.1681/ASN.2006080835
Source DB: PubMed Journal: J Am Soc Nephrol ISSN: 1046-6673 Impact factor: 10.121