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ABSTRACT: Objective
To define glomerular filtration rate (GFR) decline, hypertension (HTN), and proteinuria in subjects with autosomal recessive polycystic kidney disease (ARPKD) and compare with 2 congenital kidney disease control groups in the Chronic Kidney Disease in Children cohort.Study design
GFR decline (iohexol clearance), rates of HTN (ambulatory/casual blood pressures), antihypertensive medication usage, left ventricular hypertrophy, and proteinuria were analyzed in subjects with ARPKD (n = 22) and 2 control groups: aplastic/hypoplastic/dysplastic disorders (n = 44) and obstructive uropathies (n = 44). Differences between study groups were examined with the Wilcoxon rank sum test.Results
Annualized GFR change in subjects with ARPKD was -1.4 mL/min/1.73 m(2) (-6%),
SUBMITTER: Dell KM
PROVIDER: S-EPMC5349855 | biostudies-literature | 2016 Apr
REPOSITORIES: biostudies-literature