Renal function and risk for cardiovascular events in type 2 diabetic patients with hypertension:: the RENAAL and LIFE studies

被引:22
作者
Eijkelkamp, Wouter B. A.
Zhang, Zhongxin
Brenner, Barry M.
Cooper, Mark E.
Devereux, Richard B.
Dahlof, Bjoern
Ibsen, Hans
Keane, William F.
Lindholm, Lars H.
Olsen, Michael H.
Parving, Hans-Henrik
Remuzzi, Giuseppe
Shahinfar, Shahnaz
Snapinn, Steven M.
Wachtell, Kristian
de Zeeuw, Dick
机构
[1] Univ Groningen, Med Ctr, Dept Clin Pharmacol, NL-9713 AV Groningen, Netherlands
[2] Merck & Co Inc, Merck Res Labs, Whitehouse Stn, NJ USA
[3] Brigham & Womens Hosp, Dept Med, Div Renal, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA 02115 USA
[5] Baker Med Res Inst, Melbourne, Vic, Australia
[6] Cornell Univ, Weill Med Coll, New York, NY USA
[7] Sahlgrenska Hosp Ostra, Dept Med, Gothenburg, Sweden
[8] Glostrup Univ Hosp, Dept Internal Med, Glostrup, Denmark
[9] Umea Univ Hosp, S-90185 Umea, Sweden
[10] Steno Diabet Ctr, DK-2820 Gentofte, Denmark
[11] Aarhus Univ, Fac Hlth Sci, Aarhus, Denmark
[12] Mario Negri Inst Pharmacol Res, I-24100 Bergamo, Italy
[13] Rigshosp, Dept Cardiol, Copenhagen, Denmark
关键词
angiotensin II receptor blocker; cardiovascular outcome; hypertension; intervention; renal function; serum creatinine; type; 2; diabetes;
D O I
10.1097/HJH.0b013e328014953c
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Objective To investigate whether a threshold exists for cardiovascular risk in type 2 diabetic patients with hypertension, the association between renal fun Design and methods The RENAAL and LIFE studies enrolled 1513 and 1195 patients with type 2 diabetes and hypertension, respectively. The relationship between baseline serum creatinine and the risk for a composite outcome of myocardial infarction, stroke or cardiovascular death was examined using Cox regression models. To adjust for heterogeneity between studies and treatment groups, these factors were included as strata when applicable. The analyses were conducted with adjustment for age, gender, smoking, alcohol use, blood pressure, heart rate, total and high-density lipoprotein (HDL) cholesterol, hemoglobin, albuminuria and prior cardiovascular disease. Results The hazard ratios across the baseline serum creatinine categories < 0.9 mg/dl, 0.9-1.2 mg/dl, 1.2-1.6 mg/dl, 1.6-2.8 mg/dl and >= 2.8 mg/dl were 0.51 ( 95% confidence interval 0.34, 0.74), 0.74 ( 0.55, 1.00), 1.00 ( reference), 1.24 ( 0.96, 1.59) and 1.67 ( 1.17, 2.91), respectively. Baseline serum creatinine ( per mg/dl) strongly predicted the composite cardiovascular endpoint in LIFE [2.82(1.74,4.56), P < 0.001], RENAAL [ 1.41(1.12,1.79), P < 0.001], as well as the combined studies [1.51(1.21,1.87), P < 0.001]. Conclusion A progressively higher risk for the composite cardiovascular endpoint was observed with incremental baseline serum creatinine in type 2 diabetic patients with hypertension, even within the normal range. Thus, there appears to be no serum creatinine threshold level for an increased cardiovascular risk. Baseline serum creatinine was a major independent risk factor for cardiovascular disease (www.ClinicalTrials.gov number NCT00308347).
引用
收藏
页码:871 / 876
页数:6
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