» Articles » PMID: 12234312

Mild Renal Insufficiency is Associated with Increased Cardiovascular Mortality: The Hoorn Study

Overview
Journal Kidney Int
Publisher Elsevier
Specialty Nephrology
Date 2002 Sep 18
PMID 12234312
Citations 117
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Cardiovascular mortality is extremely high in end-stage renal disease. Cardiovascular mortality risk also is increased in selected (high-risk) individuals with mild to moderate impairment of renal function. It is not clear whether a similar association exists in the general population and, if so, through what mechanisms. We investigated the association of renal function with all-cause and cardiovascular mortality in a population-based cohort and explored potential mechanisms underlying any such relationship.

Methods: An age-, sex-, and glucose-tolerance-stratified sample (N = 631) of a population-based cohort aged 50 to 75 years was followed prospectively. After up to 10.2 years of follow-up, 117 subjects had died (50 of cardiovascular causes). At baseline, renal function was estimated by the serum creatinine level, the Cockcroft-Gault formula and Levey's equation.

Results: At baseline, the mean age was 64 +/- 7 years, 48% were men, 55% had hypertension, and 27% (by design) had type 2 diabetes. Serum creatinine was 91.7 +/- 19.0 micromol/L; creatinine clearance as estimated by the Cockroft-Gault formula was 72.5 +/- 13.7 mL/min/1.73 m(2), and the glomerular filtration rate (GFR) estimated by Levey's equation was 67.8 +/- 12.1 mL/min/1.73 m(2). Renal function was inversely associated with all-cause and with cardiovascular mortality. Relative risks (95% confidence intervals) were 1.08 (1.04 to 1.13) and 1.11 (1.07 to 1.16) per 5 micromol/L increase of serum creatinine; 1.07 (0.98 to 1.17) and 1.15 (1.01 to 1.31) for each decrease of 5 mL/min/1.73 m(2) creatinine clearance; and 1.15 (1.05 to 1.26) and 1.26 (1.12 to 1.42) for each decrease of 5 mL/min/1.73 m(2) of GFR. These associations remained after adjusting for age, sex, glucose tolerance status, hypertension, prior cardiovascular disease, low-density lipoprotein cholesterol, homocysteine, (micro)albuminuria, von Willebrand factor, soluble vascular adhesion molecule-1 and C-reactive protein. Analyses in diabetic and hypertensive subjects gave similar results.

Conclusion: Mild to moderate loss of renal function is strongly associated with an increased risk of cardiovascular mortality. The mechanism behind this association is unclear but does not appear to involve common risk factors such as hypertension, diabetes or hyperhomocysteinemia. Estimation of renal function by relatively simple methods therefore may be a valuable tool for cardiovascular risk assessment over and above that provided by conventional risk factors. Our results were obtained in a general middle-aged to elderly population, and thus have broad applicability.

Citing Articles

Urinary Dickkopf-3 as a Potential Marker for Estimated Glomerular Filtration Rate Decline in Patients With Heart Failure.

Pieper D, Sandek A, Schafer A, Dihazi H, Dihazi G, Leha A J Am Heart Assoc. 2024; 13(23):e036637.

PMID: 39604022 PMC: 11681579. DOI: 10.1161/JAHA.124.036637.


Association of Dialysate Bicarbonate with Arrhythmia in the Monitoring in Dialysis Study.

Ravi K, Tumlin J, Roy-Chaudhury P, Koplan B, Costea A, Kher V Kidney360. 2024; 5(10):1490-1499.

PMID: 39480910 PMC: 11556930. DOI: 10.34067/KID.0000000000000537.


Consequences of low estimated glomerular filtration rate either before or early after kidney donation.

Evans M, Helgeson E, Rule A, Vock D, Matas A Am J Transplant. 2024; 24(10):1816-1827.

PMID: 38878866 PMC: 11439579. DOI: 10.1016/j.ajt.2024.04.023.


Novel Perspectives in Chronic Kidney Disease-Specific Cardiovascular Disease.

Xu C, Tsihlis G, Chau K, Trinh K, Rogers N, Julovi S Int J Mol Sci. 2024; 25(5).

PMID: 38473905 PMC: 10931927. DOI: 10.3390/ijms25052658.


HMG CoA reductase inhibitors (statins) for people with chronic kidney disease not requiring dialysis.

Tunnicliffe D, Palmer S, Cashmore B, Saglimbene V, Krishnasamy R, Lambert K Cochrane Database Syst Rev. 2023; 11:CD007784.

PMID: 38018702 PMC: 10685396. DOI: 10.1002/14651858.CD007784.pub3.