Serum uric acid is a GFR-independent long-term predictor of acute and chronic renal insufficiency: the Jerusalem Lipid Research Clinic cohort study

被引:63
作者
Ben-Dov, Iddo Z. [1 ]
Kark, Jeremy D. [2 ]
机构
[1] Rockefeller Univ, Lab RNA Mol Biol, New York, NY 10065 USA
[2] Hebrew Univ Jerusalem, Epidemiol Unit, Hadassah Sch Publ Hlth & Community Med, IL-91120 Jerusalem, Israel
基金
美国国家卫生研究院; 以色列科学基金会;
关键词
acute kidney injury; chronic kidney disease; cohort study; mortality; uric acid; CHRONIC-KIDNEY-DISEASE; BLOOD-PRESSURE; METABOLIC SYNDROME; OXIDATIVE STRESS; HYPERURICEMIA; PROGRESSION; RISK; ALLOPURINOL; MARKER; HYPOURICEMIA;
D O I
10.1093/ndt/gfq740
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background. Kidney disease is commonly accompanied by hyperuricemia. However, the contribution of serum uric acid (SUA) to kidney injury is debated. Our objective was to assess the long-term prediction of renal failure by SUA. Methods. Visit 2 participants in the Jerusalem Lipid Research Clinic cohort with normal baseline kidney function were followed for 24-28 years. SUA levels were assessed for associations with acute renal failure (ARF) and chronic renal failure (CRF) as defined by hospital discharge records, and mortality, ascertained through linkage with the national population registry. Results. Among 2449 eligible participants (1470 men, 979 women aged 35-78 years in 1976-79), SUA was positively linked with male sex, serum creatinine and components of the metabolic syndrome but was lower in smokers and in diabetic subjects. The 22- to 25-year incidence of hospital-diagnosed kidney failure (145 first events, 67% CRF) and the 24- to 28-year mortality (587 events) were higher in subject with hyperuricemia (>6.5 mg/dL in men and >5.3 mg/dL in women, reflecting the upper quintiles), independent of baseline kidney function and covariates. Hyperuricemia conferred adjusted hazard ratios of 1.36 (P = 0.003), 2.14 (P < 0.001) and 2.87 (P = 0.003) for mortality, CRF and ARF, respectively. Conclusions. SUA predicts renal failure incidence and all-cause mortality independently of demographic and clinical covariates. These results lend support to the undertaking of clinical trials to examine the effect of uric acid-lowering strategies on kidney outcomes.
引用
收藏
页码:2558 / 2566
页数:9
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