TY - JOUR
T1 - Cyst number but not the rate of cystic growth is associated with the mutated gene in autosomal dominant polycystic kidney disease
AU - Harris, Peter C.
AU - Bae, Kyongtae T.
AU - Rossetti, Sandro
AU - Torres, Vicente E.
AU - Grantham, Jared J.
AU - Chapman, Arlene B.
AU - Guay-Woodford, Lisa M.
AU - King, Bernard F.
AU - Wetzel, Louis H.
AU - Baumgarten, Deborah A.
AU - Kenney, Philip J.
AU - Consugar, Mark
AU - Klahr, Saulo
AU - Bennett, William M.
AU - Meyers, Catherine M.
AU - Zhang, Qin
AU - Thompson, Paul A.
AU - Zhu, Fang
AU - Miller, J. Philip
PY - 2006/11
Y1 - 2006/11
N2 - Data from serial renal magnetic resonance imaging of the Consortium of Radiologic Imaging Study of PICD (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.
AB - Data from serial renal magnetic resonance imaging of the Consortium of Radiologic Imaging Study of PICD (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.
UR - http://www.scopus.com/inward/record.url?scp=33750689517&partnerID=8YFLogxK
U2 - 10.1681/ASN.2006080835
DO - 10.1681/ASN.2006080835
M3 - Article
C2 - 17035604
AN - SCOPUS:33750689517
SN - 1046-6673
VL - 17
SP - 3013
EP - 3019
JO - Journal of the American Society of Nephrology
JF - Journal of the American Society of Nephrology
IS - 11
ER -