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0902CZR01NL537SS0901 RENAAL Altering the Course of Renal Disease in Hypertensive Patients with Type 2 Diabetes and Nephropathy with the A II Antagonist.

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Presentation on theme: "0902CZR01NL537SS0901 RENAAL Altering the Course of Renal Disease in Hypertensive Patients with Type 2 Diabetes and Nephropathy with the A II Antagonist."— Presentation transcript:

1 0902CZR01NL537SS0901 RENAAL Altering the Course of Renal Disease in Hypertensive Patients with Type 2 Diabetes and Nephropathy with the A II Antagonist Losartan

2 0902CZR01NL537SS0901 An investigator initiated, multicenter, double-blind, randomized, placebo-controlled study to evaluate the renal protective effects of losartan in hypertensive patients with Type 2 diabetes and nephropathy 1513 Patients; 250 Centers; 28 Countries RENAAL Reduction of Endpoints in NIDDM with the A II Antagonist Losartan Steering CommitteeChairB. M. Brenner, MD Data and Safety Monitoring CommitteeChairC.E. Mogensen, MD Clinical Endpoint Adjudication Committee ChairS. Haffner, MD Coordinating Center: Merck Research LabsStudy DirectorS. Shahinfar, MD Brenner BM et al New Engl J Med 2001;345(12):861-869.

3 0902CZR01NL537SS0901 RENAAL Primary Hypothesis Long-term treatment with losartan versus placebo (alone or in combination with conventional anti hypertensive therapy*) in Type 2 diabetic patients with hypertension and nephropathy will increase the time to first event and decrease the incidence of doubling of sCr, ESRD or death. Brenner BM et al New Engl J Med 2001;345(12):861-869. * Excluding ACEIs and other AIIAs

4 0902CZR01NL537SS0901 Losartan compared to placebo (alone or in combination with conventional antihypertensive therapy*) in hypertensive patients with Type 2 diabetes and nephropathy will: increase the time to first event and decrease the incidence of cardiovascular morbidity/mortality reduce proteinuria decrease the rate of progression of renal disease RENAAL Secondary Hypothesis Brenner BM et al New Engl J Med 2001;345(12):861-869. * Excluding ACEIs and other AIIAs

5 0902CZR01NL537SS0901 RENAAL Study Design *CT=conventional therapy: Open-label calcium-channel blocker, diuretic, beta blocker, alpha blocker, or centrally acting agents. 4 Wks Losartan 100 mg qd (+CT) Maintain conventional antihypertensive therapy (CT)* (excluding ACEI, AIIA) Losartan 100 mg qd (+CT) Placebo (+CT) Goal trough BP: < 140/<90 mmHg n=1513 Placebo (+CT) Losartan 50 mg qd (+CT) Placebo (+CT) 8 Wks 6 Wks Mean follow-up 3.4 years Brenner BM et al J Renin-Angio-Aldo System 2000;1(4):328-335.

6 0902CZR01NL537SS0901 RENAAL Inclusion/Exclusion Criteria Inclusion criteria Type 2 diabetes Age 31-70 years Proteinuria: urine alb:cr >300 mg/g, >25 mg/mmol Serum Creatinine: 1.3-3.0 mg/dl, 115-265 µmol/L* Exclusion criteria Type 1 diabetes Known non-diabetic renal disease or renal artery stenosis Recent history of MI, CABG, PTCA, CVA, TIA History of heart failure HbA 1c >12% *Lower limit 1.5 mg/dl (133 µmol/L) in male patients >60 kg Brenner BM et al J Renin-Angio-Aldo System 2000;1(4):328-335. Brenner BM et al New Engl J Med 2001;345(12):861-869.

7 0902CZR01NL537SS0901 RENAAL Enrollment by Region n=1513 Europe 19% Latin America 18% North America 46% Asia 17% Brenner BM et al New Engl J Med 2001;345(12):861-869.

8 0902CZR01NL537SS0901 RENAAL Baseline Characteristics (I) Age, years Male, % Female, % Race, % Asian Black Caucasian Hispanic Other Systolic (mmHg) Diastolic (mmHg) BMI (kg/m 2 ) % Losartan (+CT) (n=751) 60 62 38 16 17 48 19 2 152 82 30 Placebo (+CT) (n=762) 60 65 35 18 14 50 18 1 153 82 29 Brenner BM et al New Engl J Med 2001;345(12):861-869.

9 0902CZR01NL537SS0901 RENAAL Primary Composite Endpoint and Components DsCr, ESRD, Death Doubling of sCr ESRD Death ESRD or Death Losartan (+CT) (n=751) n (%) 327 (43.5) 162 (21.6) 147 (19.6) 158 (21.0) 255 (34.0) 359 (47.1) 198 (26.0) 194 (25.5) 155 (20.3) 300 (39.4) P-Value 0.02 0.006 0.002 0.88 0.01 % Risk Reduction 16 25 28 -2 20 95% CI (2, 28) (8, 39) (11, 42) (-27, 19) (5, 32) Composite and Components Placebo (+CT) (n=762) n (%) Brenner BM et al New Engl J Med 2001;345(12):861-869.

10 RENAAL Primary Components ESRD Months % with event 012243648 0 10 20 30 p=0.002 Risk Reduction: 28% P L ESRD or Death P (+ CT) L (+ CT) Months % with event 0122436 48 0 10 20 30 40 50 751714625 37569 762715610 34742 P L p=0.01 Risk Reduction: 20% Doubling of Serum Creatinine Months % with event p=0.006 Risk Reduction: 25% 751692583329 52 762689554 295 36 P (+ CT) L (+ CT) 012243648 0 10 20 30 P L P (+ CT) L (+ CT) 751714 625 37569 762715 610 34742 Brenner BM et al New Engl J Med 2001;345(12):861-869. 0902CZR01NL537SS0901

11 RENAAL Blood Pressures (mmHg) BaselineYear 1Year 2Study End L (+CT) S/D152/82146/78143/77140/74 P (+CT) S/D153/82150/80144/77142/74 L (+CT) MAP105.5100.999.195.9 P (+CT) MAP106.0103.199.796.8 L (+CT) PP 69.4 67.866.266.7 P (+CT) PP 70.8 69.867.167.4 S/D: Systolic/Diastolic MAP: Mean arterial pressure PP: Pulse pressure Brenner BM et al New Engl J Med 2001;345(12):861-869. L = losartan P = placebo CT = conventional therapy

12 0902CZR01NL537SS0901 RENAAL Dose of Losartan 100 mg QD Losartan* n=751 % 71 * Patients who took the dose more than 50% of the time. Brenner BM et al New Engl J Med 2001;345(12):861-869.  The daily dose of losartan ranged from 50-100 mg

13 0902CZR01NL537SS0901 RENAAL Concurrent Antihypertensive Medications Therapeutic Class Calcium-Channel Blocker (%) - Dihydropyridine (%) Diuretic (%) Alpha blocker (%) Beta blocker (%) Centrally acting agents (%) Losartan n=751 77.9 60.7 83.8 40.2 34.1 18.0 Placebo n=762 81.1 63.9 84.0 45.7 36.7 21.7 Brenner BM et al New Engl J Med 2001;345(12):861-869..

14 0902CZR01NL537SS0901 CV Morbidity/Mortality Heart Failure MI RENAAL Secondary Composite Endpoint and Components Losartan (+CT) (N=751) n (%) 247 (32.9) 89 (11.9) 50 (6.7) Placebo (+CT) (N=762) n (%) 268 (35.2) 127 (16.7) 68 (8.9) P-Value 0.26 0.005 0.08 % Risk Reduction 10 32 28 Composite and Components Brenner BM et al New Engl J Med 2001;345(12):861-869.

15 0902CZR01NL537SS0901 RENAAL First Hospitalization for Heart Failure 012243648 Months 0 5 10 15 20 % with event Risk Reduction: 32% p=0.005 P (+CT) L (+CT) 76268561637553 75170163738874 P L Brenner BM et al New Engl J Med 2001;345(12):861-869. L = losartan P = placebo CT = conventional therapy

16 0902CZR01NL537SS0901 RENAAL Change from Baseline in Proteinuria Proteinuria measured as the urine albumin:creatinine ratio from a first morning void. 012243648 Months Median Percent Change -60 -40 -20 0 20 40 751661558438167 p<0.001 P (+CT) L (+CT) 762632529390130 P L 35% Overall Reduction Brenner BM et al New Engl J Med 2001;345(12):861-869. L = losartan P = placebo CT = conventional therapy

17 0902CZR01NL537SS0901 RENAAL Rate of Progression of Renal Disease (median 1/sCr Slope) LosartanPlacebo 0 -.02 -.04 -.06 -.08 dl/mg/yr -0.056 -0.069 p=0.01 18% reduction (+CT) Brenner BM et al New Engl J Med 2001;345(12):861-869. sCr=serum creatinine

18 0902CZR01NL537SS0901 RENAAL Summary ( I )  In hypertensive patients with Type 2 diabetes and nephropathy: –losartan delayed the onset of the primary composite endpoint (DsCr/ESRD/Death) and delayed the progression to ESRD. –losartan reduced proteinuria and the rate of decline in renal function (1/sCr slope). –losartan reduced the incidence of hospitalization for heart failure. –these benefits were largely independent of achieved blood pressure. Brenner BM et al New Engl J Med 2001;345(12):861-869.

19 0902CZR01NL537SS0901 RENAAL Summary ( II )  In hypertensive patients with Type 2 diabetes and nephropathy: –losartan and placebo, on a background of conventional therapy, showed no significant difference on all-cause mortality, MI, stroke, revascularization, hospitalizations for unstable angina, and death due to CV disease. –losartan was generally well tolerated in this patient population. Brenner BM et al New Engl J Med 2001;345(12):861-869.

20 0902CZR01NL537SS0901 RENAAL Conclusions  Losartan confers significant benefits on renal outcomes in Type 2 diabetic patients with hypertension and nephropathy.  Losartan therapy results in a significant reduction in hospitalizations for heart failure.  Losartan is generally well tolerated.  Benefits of losartan seen in RENAAL complement many previous losartan studies which demonstrate a reduction in microalbuminuria and macroalbuminuria. Brenner BM et al New Engl J Med 2001;345(12):861-869.


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