Urinary Sodium and Potassium Excretion and CKD Progression

被引:7
|
作者
He, Jiang [1 ,2 ]
Mills, Katherine T. [1 ]
Appel, Lawrence J. [3 ]
Yang, Wei [4 ]
Chen, Jing [1 ,2 ]
Lee, Belinda T. [2 ]
Rosas, Sylvia E. [4 ]
Porter, Anna [5 ]
Makos, Gail [6 ]
Weir, Matthew R. [7 ]
Hamm, L. Lee [1 ,2 ]
Kusektt, John W. [8 ]
机构
[1] Tulane Univ, Dept Epidemiol, New Orleans, LA 70112 USA
[2] Tulane Univ, Dept Med, New Orleans, LA 70112 USA
[3] Johns Hopkins Sch Med, Welch Ctr Prevent Epidemiol & Clin Res, Baltimore, MD USA
[4] Univ Penn, Sch Med, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USA
[5] Univ Illinois, Coll Med, Dept Med, Chicago, IL USA
[6] St John Hosp & Med Ctr, Div Nephrol, Detroit, MI USA
[7] Univ Maryland, Sch Med, Dept Med, Baltimore, MD 21201 USA
[8] NIDDK, Div Kidney Urol & Hematol Dis, NIH, Bethesda, MD 20892 USA
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2016年 / 27卷 / 04期
基金
美国国家卫生研究院;
关键词
CHRONIC RENAL-INSUFFICIENCY; CHRONIC KIDNEY-DISEASE; MODEST SALT REDUCTION; BLOOD-PRESSURE; DIETARY-SODIUM; RISK; OUTCOMES; METAANALYSIS; ASSOCIATION;
D O I
10.1681/ASN.2015010022
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:1202 / 1212
页数:11
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