Enalapril prevents clinical proteinuria in diabetic patients with low ejection fraction

Sarah E. Capes, Hertzel C. Gerstein, Abdissa Negassa, Salim Yusuf

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

OBJECTIVE - Clinical proteinuria is a risk factor for both end-stage renal disease and cardiovascular disease. The prevalence of clinical proteinuria, its correlates and predictive value, and the effect of ACE inhibitors in preventing clinical proteinuria in diabetic and nondiabetic patients with left ventricular (LV) dysfunction are unknown. RESEARCH DESIGN AND METHODS - The Studies of Left Ventricular Dysfunction (SOLVD) trials were analyzed to determine the baseline distribution of clinical proteinuria and related cardiovascular risk factors, the effect of baseline proteinuria on the risk of hospitalization for congestive heart failure (CHF) and mortality, and the effect of enalapril in preventing new clinical proteinuria. RESULTS - A total of 5,487 out of 6,797 SOLVD participants (81%) were assessed for proteinuria at baseline. A total of 177 patients (3.2%) had baseline proteinuria. These patients had significantly higher systolic (137 vs. 125 mmHg, P ≤ 0.001) and diastolic (83 vs. 77 mmHg, P ≤ 0.001) blood pressure levels, a higher prevalence of diabetes (41 vs. 18%, P ≤ 0.001), a lower ejection fraction (26.2 vs. 27.3%, P ≤ 0.05), and greater degree of CHF (New York Heart Association [NYHA] class III/IV in 22 vs. 10%, P ≤ 0.001) than patients without baseline proteinuria. Patients with baseline proteinuria also had higher rates of hospitalization for CHF (relative risk 1.81 [95% CI 1.37-2.41], P = 0.0001) and mortality (1.73 [1.34-2.24], P = 0.0001). Enalapril prevented clinical proteinuria in diabetic patients (0.38 [0.17-0.81], P = 0.0123) but not in nondiabetic patients (1.43 [0.77-2.63 ], P = 0.2622) without baseline proteinuria. CONCLUSIONS - Clinical proteinuria is an independent predictor of hospitalization for CHF and mortality in diabetic and nondiabetic patients with LV dysfunction. Enalapril significantly reduces the risk of clinical proteinuria in diabetic patients with LV dysfunction.

Original languageEnglish (US)
Pages (from-to)377-380
Number of pages4
JournalDiabetes Care
Volume23
Issue number3
StatePublished - Mar 2000
Externally publishedYes

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Enalapril
Proteinuria
Left Ventricular Dysfunction
Heart Failure
Hospitalization
Mortality
Hospital Distribution Systems
Angiotensin-Converting Enzyme Inhibitors
Chronic Kidney Failure

ASJC Scopus subject areas

  • Internal Medicine
  • Endocrinology, Diabetes and Metabolism

Cite this

Enalapril prevents clinical proteinuria in diabetic patients with low ejection fraction. / Capes, Sarah E.; Gerstein, Hertzel C.; Negassa, Abdissa; Yusuf, Salim.

In: Diabetes Care, Vol. 23, No. 3, 03.2000, p. 377-380.

Research output: Contribution to journalArticle

Capes, SE, Gerstein, HC, Negassa, A & Yusuf, S 2000, 'Enalapril prevents clinical proteinuria in diabetic patients with low ejection fraction', Diabetes Care, vol. 23, no. 3, pp. 377-380.
Capes, Sarah E. ; Gerstein, Hertzel C. ; Negassa, Abdissa ; Yusuf, Salim. / Enalapril prevents clinical proteinuria in diabetic patients with low ejection fraction. In: Diabetes Care. 2000 ; Vol. 23, No. 3. pp. 377-380.
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T1 - Enalapril prevents clinical proteinuria in diabetic patients with low ejection fraction

AU - Capes, Sarah E.

AU - Gerstein, Hertzel C.

AU - Negassa, Abdissa

AU - Yusuf, Salim

PY - 2000/3

Y1 - 2000/3

N2 - OBJECTIVE - Clinical proteinuria is a risk factor for both end-stage renal disease and cardiovascular disease. The prevalence of clinical proteinuria, its correlates and predictive value, and the effect of ACE inhibitors in preventing clinical proteinuria in diabetic and nondiabetic patients with left ventricular (LV) dysfunction are unknown. RESEARCH DESIGN AND METHODS - The Studies of Left Ventricular Dysfunction (SOLVD) trials were analyzed to determine the baseline distribution of clinical proteinuria and related cardiovascular risk factors, the effect of baseline proteinuria on the risk of hospitalization for congestive heart failure (CHF) and mortality, and the effect of enalapril in preventing new clinical proteinuria. RESULTS - A total of 5,487 out of 6,797 SOLVD participants (81%) were assessed for proteinuria at baseline. A total of 177 patients (3.2%) had baseline proteinuria. These patients had significantly higher systolic (137 vs. 125 mmHg, P ≤ 0.001) and diastolic (83 vs. 77 mmHg, P ≤ 0.001) blood pressure levels, a higher prevalence of diabetes (41 vs. 18%, P ≤ 0.001), a lower ejection fraction (26.2 vs. 27.3%, P ≤ 0.05), and greater degree of CHF (New York Heart Association [NYHA] class III/IV in 22 vs. 10%, P ≤ 0.001) than patients without baseline proteinuria. Patients with baseline proteinuria also had higher rates of hospitalization for CHF (relative risk 1.81 [95% CI 1.37-2.41], P = 0.0001) and mortality (1.73 [1.34-2.24], P = 0.0001). Enalapril prevented clinical proteinuria in diabetic patients (0.38 [0.17-0.81], P = 0.0123) but not in nondiabetic patients (1.43 [0.77-2.63 ], P = 0.2622) without baseline proteinuria. CONCLUSIONS - Clinical proteinuria is an independent predictor of hospitalization for CHF and mortality in diabetic and nondiabetic patients with LV dysfunction. Enalapril significantly reduces the risk of clinical proteinuria in diabetic patients with LV dysfunction.

AB - OBJECTIVE - Clinical proteinuria is a risk factor for both end-stage renal disease and cardiovascular disease. The prevalence of clinical proteinuria, its correlates and predictive value, and the effect of ACE inhibitors in preventing clinical proteinuria in diabetic and nondiabetic patients with left ventricular (LV) dysfunction are unknown. RESEARCH DESIGN AND METHODS - The Studies of Left Ventricular Dysfunction (SOLVD) trials were analyzed to determine the baseline distribution of clinical proteinuria and related cardiovascular risk factors, the effect of baseline proteinuria on the risk of hospitalization for congestive heart failure (CHF) and mortality, and the effect of enalapril in preventing new clinical proteinuria. RESULTS - A total of 5,487 out of 6,797 SOLVD participants (81%) were assessed for proteinuria at baseline. A total of 177 patients (3.2%) had baseline proteinuria. These patients had significantly higher systolic (137 vs. 125 mmHg, P ≤ 0.001) and diastolic (83 vs. 77 mmHg, P ≤ 0.001) blood pressure levels, a higher prevalence of diabetes (41 vs. 18%, P ≤ 0.001), a lower ejection fraction (26.2 vs. 27.3%, P ≤ 0.05), and greater degree of CHF (New York Heart Association [NYHA] class III/IV in 22 vs. 10%, P ≤ 0.001) than patients without baseline proteinuria. Patients with baseline proteinuria also had higher rates of hospitalization for CHF (relative risk 1.81 [95% CI 1.37-2.41], P = 0.0001) and mortality (1.73 [1.34-2.24], P = 0.0001). Enalapril prevented clinical proteinuria in diabetic patients (0.38 [0.17-0.81], P = 0.0123) but not in nondiabetic patients (1.43 [0.77-2.63 ], P = 0.2622) without baseline proteinuria. CONCLUSIONS - Clinical proteinuria is an independent predictor of hospitalization for CHF and mortality in diabetic and nondiabetic patients with LV dysfunction. Enalapril significantly reduces the risk of clinical proteinuria in diabetic patients with LV dysfunction.

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