4.7 Article

Urinary Sodium and Potassium Excretion and CKD Progression

Journal

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
Volume 27, Issue 4, Pages 1202-1212

Publisher

AMER SOC NEPHROLOGY
DOI: 10.1681/ASN.2015010022

Keywords

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Funding

  1. National Institute of Diabetes and Digestive and Kidney Diseases [R01-DK074615, U01-DK060990, U01-DK060984, U01-DK061022, U01-DK061021, U01-DK061028, U01-DK060980, U01-DK060963, U01-DK060902]
  2. University of Pennsylvania Clinical and Translational Science Award National Institutes of Health (NIH)/National Center for Advancing Translational Sciences [UL1-TR000003]
  3. Johns Hopkins University [UL1-TR000424]
  4. University of Maryland [GCRC M01-RR16500]
  5. Clinical and Translational Science Collaborative of Cleveland [UL1-TR000439]
  6. Michigan Institute for Clinical and Health Research [UL1-TR000433]
  7. University of Illinois at Chicago Grant CTSA [UL1-RR029879]
  8. Tulane University Translational Research in Hypertension and Renal Biology [P30-GM103337]
  9. Kaiser NIH/National Center for Research Resources Grant UCSF-CTSI [UL1-RR024131]

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CKD is a major risk factor for ESRD, cardiovascular disease, and premature death. Whether dietary sodium and potassium intake affect CKD progression remains unclear. We prospectively studied the association of urinary sodium and potassium excretion with CKD progression and all-cause mortality among 3939 patients with CKD in the Chronic Renal Insufficiency Cohort Study. Urinary sodium and potassium excretion were measured using three 24-hour urine specimens, and CKD progression was defined as incident ESRD or halving of eGFR. During follow-up, 939 CKD progression events and 540 deaths occurred. Compared with the lowest quartile of urinary sodium excretion (<116.8 mmol/24 h), hazard ratios (95% confidence intervals) for the highest quartile of urinary sodium excretion (>= 194.6 mmol/24 h) were 1.54 (1.23 to 1.92) for CKD progression, 1.45 (1.08 to 1.95) for all-cause mortality, and 1.43 (1.18 to 1.73) for the composite outcome of CKD progression and all-cause mortality after adjusting for multiple covariates, including baseline eGFR. Additionally, compared with the lowest quartile of urinary potassium excretion (<39.4 mmol/24 h), hazard ratios for the highest quartile of urinary potassium excretion (>= 67.1 mmol/24 h) were 1.59 (1.25 to 2.03) for CKD progression, 0.98 (0.71 to 1.35) for all-cause mortality, and 1.42 (1.15 to 1.74) for the composite outcome. These data indicate that high urinary sodium and potassium excretion are associated with increased risk of CKD progression. Clinical trials are warranted to test the effect of sodium and potassium reduction on CKD progression.

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