Outcomes of Combined Cardiovascular Risk Factor Management Strategies in Type 2 Diabetes: The ACCORD Randomized Trial

Author:

Margolis Karen L.1,O’Connor Patrick J.1,Morgan Timothy M.2,Buse John B.3,Cohen Robert M.4,Cushman William C.5,Cutler Jeffrey A.6,Evans Gregory W.2,Gerstein Hertzel C.7,Grimm Richard H.8,Lipkin Edward W.9,Narayan K.M.Venkat10,Riddle Matthew C.11,Sood Ajay12,Goff David C.13

Affiliation:

1. HealthPartners Institute for Education and Research, Minneapolis, MN

2. Wake Forest University School of Medicine, Winston-Salem, NC

3. University of North Carolina School of Medicine, Chapel Hill, NC

4. Cincinnati Veterans Affairs Medical Center and University of Cincinnati, Cincinnati, OH

5. Memphis Veterans Affairs Medical Center, Memphis, TN

6. National Heart, Lung, and Blood Institute, Bethesda, MD

7. McMaster University, Hamilton, Ontario, Canada

8. Berman Center for Outcomes and Clinical Research, Minneapolis, MN

9. University of Washington, Seattle, WA

10. Emory University, Atlanta, GA

11. Oregon Health and Science University, Portland, OR

12. Louis Stokes Veterans Affairs Medical Center and Case Western Reserve University, Cleveland, OH

13. Colorado School of Public Health, Aurora, CO

Abstract

OBJECTIVE To compare effects of combinations of standard and intensive treatment of glycemia and either blood pressure (BP) or lipids in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial. RESEARCH DESIGN AND METHODS ACCORD enrolled 10,251 type 2 diabetes patients aged 40–79 years at high risk for cardiovascular disease (CVD) events. Participants were randomly assigned to hemoglobin A1c goals of <6.0% (<42 mmol/mol; intensive glycemia) or 7.0–7.9% (53–63 mmol/mol; standard glycemia) and then randomized a second time to either 1) systolic BP goals of <120 mmHg (intensive BP) or <140 mmHg (standard BP) or 2) simvastatin plus fenofibrate (intensive lipid) or simvastatin plus placebo (standard lipid). Proportional hazards models were used to assess combinations of treatment assignments on the composite primary (deaths due to CVD, nonfatal myocardial infarction [MI], and nonfatal stroke) and secondary outcomes. RESULTS In the BP trial, risk of the primary outcome was lower in the groups intensively treated for glycemia (hazard ratio [HR] 0.67; 95% CI 0.50–0.91), BP (HR 0.74; 95% CI 0.55–1.00), or both (HR 0.71; 95% CI 0.52–0.96) compared with combined standard BP and glycemia treatment. For secondary outcomes, MI was significantly reduced by intensive glycemia treatment and stroke by intensive BP treatment; most other HRs were neutral or favored intensive treatment groups. In the lipid trial, the general pattern of results showed no evidence of benefit of intensive regimens (whether single or combined) compared with combined standard lipid and glycemia treatment. The mortality HR was 1.33 (95% CI 1.02–1.74) in the standard lipid/intensive glycemia group compared with the standard lipid/standard glycemia group. CONCLUSIONS In the ACCORD BP trial, compared with combined standard treatment, intensive BP or intensive glycemia treatment alone improved major CVD outcomes, without additional benefit from combining the two. In the ACCORD lipid trial, neither intensive lipid nor glycemia treatment produced an overall benefit, but intensive glycemia treatment increased mortality.

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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