Diabetes Care
29:2046-2052,
2006
DOI: 10.2337/dc06-0248
© 2006 by the American Diabetes Association
Pathophysiology/Complications Original Article |
Glomerular Filtration Rate, Cardiorenal End Points, and All-Cause Mortality in Type 2 Diabetic Patients
Wing Yee So, MBCHB, FRCP1,
Alice P.S. Kong, MBCHB, FRCP1,2,
Ronald C.W. Ma, MBBCHIR, MA, MRCP1,
Risa Ozaki, MBCHB, MRCP1,
Cheuk Chun Szeto, MBCHB, FRCP1,
Norman N. Chan3,
Vanessa Ng, MBCHB, MRCP1,
Chung Shun Ho, PHD4,
Christopher W.K. Lam, PHD4,
Chun Chung Chow, MBCHB, FRCP1,
Clive S. Cockram, MD, FRCP1,
Juliana C.N. Chan, MD, FRCP1 and
Peter C.Y. Tong, MBCHB, FRCP1
1 Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Shantin, N.T., Hong Kong
2 Li Ka Shing Institute of Health Sciences, Hong Kong, Hong Kong
3 Qualigenics Diabetes Centre, Hong Kong, Hong Kong
4 Department of Chemical Pathology, The Chinese University of Hong Kong, Prince of Wales Hospital, Shantin, N.T., Hong Kong
Address correspondence and reprint requests to Dr. Juliana C.N. Chan, Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, N.T., Hong Kong SAR. E-mail: jchan{at}cuhk.edu.hk
OBJECTIVEChronic kidney disease (CKD) predicts cardiovascular disease (CVD) in the general population. We investigated the effects of stages of renal function using the estimated glomerular filtration rate (eGFR) on all-cause mortality and cardiovascular end points in a prospective cohort of Chinese type 2 diabetic patients.
RESEARCH DESIGN AND METHODSBetween 1995 and 2000, 4,421 patients without macrovascular disease or end-stage renal disease were recruited. Renal function was assessed by eGFR, as calculated by the abbreviated Modification of Diet in Renal Disease Study Group formula. Clinical end points included all-cause mortality, cardiovascular end point (cardiovascular death, new admissions due to angina, myocardial infarction, stroke, revascularization, or heart failure), and renal end point (reduction in eGFR by >50%, progression of eGFR to stage 5, or dialysis or renal death).
RESULTSAfter a median follow-up period of 39.4 months (interquartile range 20.355), all-cause mortality rate increased from 1.2% (95% CI 0.81.7) to 18.3% (9.127.5) (P for trend <0.001) as renal function deteriorated from stage 1 (eGFR 90 ml/min per 1.73 m2) to stage 4 (1529 ml/min per 1.73 m2). The respective rate of new cardiovascular end points also increased from 2.6% (2.03.3) to 25.3% (15.035.7) (P for trend <0.001). After adjustment for covariates (age, sex, albuminuria, use of renin-angiotensin-aldosterone system [RAAS] inhibitors, lipids, blood pressure, and glycemic control), hazard ratios across different stages of eGFR ( 90, 6089, 3059, and 1529 ml/min per 1.73 m2) for all-cause mortality were 1.00, 1.27, 2.34, and 9.82 (P for trend <0.001), for cardiovascular end points were 1.00, 1.04, 1.05, and 3.23 (P for trend <0.001), and for renal end points were 1.00, 1.36, 3.34, and 27.3 (P for trend <0.001), respectively.
CONCLUSIONSChinese type 2 diabetic patients with reduced eGFR were at high risk of developing cardiovascular end points and all-cause mortality, independent of albuminuria and metabolic control.
Abbreviations: ACR, albumin-to-creatinine ratio CKD, chronic kidney disease CVD, cardiovascular disease eGFR, estimated glomerular filtration rate RAAS, renin-angiotensin-aldosterone system

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Copyright © 2006 by the American Diabetes Association.
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