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Association of Urinary Oxalate Excretion With the Risk of Chronic Kidney Disease Progression

Authors :
Kumar Sharma
Jing Chen
Tariq Shafi
Xiaoming Zhang
James P. Lash
Dawei Xie
Chi-yuan Hsu
Ragnar Palsson
Anand Srivastava
Harold I. Feldman
Sushrut S. Waikar
Jiang He
Gary C. Curhan
John C. Lieske
Source :
JAMA Internal Medicine. 179:542
Publication Year :
2019
Publisher :
American Medical Association (AMA), 2019.

Abstract

Oxalate is a potentially toxic terminal metabolite that is eliminated primarily by the kidneys. Oxalate nephropathy is a well-known complication of rare genetic disorders and enteric hyperoxaluria, but oxalate has not been investigated as a potential contributor to more common forms of chronic kidney disease (CKD).To assess whether urinary oxalate excretion is a risk factor for more rapid progression of CKD toward kidney failure.This prospective cohort study assessed 3123 participants with stages 2 to 4 CKD who enrolled in the Chronic Renal Insufficiency Cohort study from June 1, 2003, to September 30, 2008. Data analysis was performed from October 24, 2017, to June 17, 2018.Twenty-four-hour urinary oxalate excretion.A 50% decline in estimated glomerular filtration rate (eGFR) and end-stage renal disease (ESRD).This study included 3123 participants (mean [SD] age, 59.1 [10.6] years; 1414 [45.3%] female; 1423 [45.6%] white). Mean (SD) eGFR at the time of 24-hour urine collection was 42.9 (16.8) mL/min/1.73 m2. Median urinary excretion of oxalate was 18.6 mg/24 hours (interquartile range [IQR], 12.9-25.7 mg/24 hours) and was correlated inversely with eGFR (r = -0.13, P .001) and positively with 24-hour proteinuria (r = 0.22, P .001). During 22 318 person-years of follow-up, 752 individuals reached ESRD, and 940 individuals reached the composite end point of ESRD or 50% decline in eGFR (CKD progression). Higher oxalate excretion was independently associated with greater risks of both CKD progression and ESRD: compared with quintile 1 (oxalate excretion,11.5 mg/24 hours) those in quintile 5 (oxalate excretion, ≥27.8 mg/24 hours) had a 33% higher risk of CKD progression (hazard ratio [HR], 1.33; 95% CI, 1.04-1.70) and a 45% higher risk of ESRD (HR, 1.45; 95% CI, 1.09-1.93). The association between oxalate excretion and CKD progression and ESRD was nonlinear and exhibited a threshold effect at quintiles 3 to 5 vs quintiles 1 and 2. Higher vs lower oxalate excretion (at the 40th percentile) was associated with a 32% higher risk of CKD progression (HR, 1.32; 95% CI, 1.13-1.53) and 37% higher risk of ESRD (HR, 1.37; 95% CI, 1.15-1.63). Results were similar when treating death as a competing event.Higher 24-hour urinary oxalate excretion may be a risk factor for CKD progression and ESRD in individuals with CKD stages 2 to 4.

Details

ISSN :
21686106
Volume :
179
Database :
OpenAIRE
Journal :
JAMA Internal Medicine
Accession number :
edsair.doi.dedup.....aa20c09016e659a783d1bfa228390967