Cyst Number but Not the Rate of Cystic Growth Is Associated with the Mutated Gene in Autosomal Dominant Polycystic Kidney Disease
Open Access
- 1 November 2006
- journal article
- Published by Wolters Kluwer Health in Journal of the American Society of Nephrology
- Vol. 17 (11) , 3013-3019
- https://doi.org/10.1681/asn.2006080835
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.Keywords
This publication has 37 references indexed in Scilit:
- Volume Progression in Polycystic Kidney DiseaseNew England Journal of Medicine, 2006
- Loss of Polycystin-1 in Human Cyst-Lining Epithelia Leads to Ciliary DysfunctionJournal of the American Society of Nephrology, 2006
- Defining a Link with Autosomal-Dominant Polycystic Kidney Disease in Mice with Congenitally Low Expression of Pkd1The American Journal of Pathology, 2006
- Sonographic Assessment of the Severity and Progression of Autosomal Dominant Polycystic Kidney Disease: The Consortium of Renal Imaging Studies in Polycystic Kidney Disease (CRISP)American Journal of Kidney Diseases, 2005
- Lowering of Pkd1 expression is sufficient to cause polycystic kidney diseaseHuman Molecular Genetics, 2004
- A Functional Floxed Allele of Pkd1 that Can Be Conditionally Inactivated In VivoJournal of the American Society of Nephrology, 2004
- Magnetic resonance measurements of renal blood flow as a marker of disease severity in autosomal-dominant polycystic kidney disease11Thomas Andreoli, M.D., served as Guest Editor for this paper.Kidney International, 2003
- Comparison of phenotypes of polycystic kidney disease types 1 and 2The Lancet, 1999
- Somatic Inactivation of Pkd2 Results in Polycystic Kidney DiseaseCell, 1998
- Factors affecting the progression of renal disease in autosomal-dominant polycystic kidney diseaseKidney International, 1992