THE ACTION TO CONTROL CARDIOVASCULAR RISK IN DIABETES STUDY (ACCORD) Dr. Anita Chekuri CVA Ltd Background Epidemiologic analyses suggest that the risk for CVD in patients with diabetes increases in a graded fashion with increases HbA1c, BP, LDL, and TG and with a decrease in HDL. Diabetics without Hx of MI have same risk of a coronary event as do non-diabetics with previous MI To determine whether CVD event rates can be reduced in patients with T2DM who are at high risk for CVD events by intensively targeting 3 important CVD risk factors: hyperglycemia, dyslipidemia, and elevated blood pressure. Buse J. Action to Control Cardiovascular Risk in Diabetes (ACCORD) Trial: Design and Methods The American Journal of Cardiology 2007;99:21-33. Haffner SM, Lehto S, Ronnemaa T, Pyöräla K, Laakso M. Mortality from coronary heart disease in subjects with type 2 diabetes and in nondiabetic subjects with and without prior myocardial infarction. N Engl J Med 1998;339:229-234 2 X 2 Factorial Design BP trial Lipid trial Glycaemic trial SBP<110 mmHg SBP<140 mmHg Group A Group B Total HbAIC < 6% 1178 1193 1383 1374 5128 HbAIC 7.07.9% 1184 1178 1370 1391 5123 2362 2371 2753 2765 Total 4733 5518 Buse J. Action to Control Cardiovascular Risk in Diabetes (ACCORD) Trial: Design and Methods The American Journal of Cardiology 2007;99:21-33. 10251 Eligibility Stable Type 2 Diabetes for 3+ months A1C >7.5% AND <9% (more meds) OR <11% (fewer meds) Age 40-79 + previous CVD events OR Age 55-79 with: anatomical ASCVD, albuminuria, LVH OR > 2 CVD risk factors (dyslipidemia, hypertension, smoking, obesity) BMI < 45; Cr < 1.5 (133 uM) No frequent/recent serious hypoglycemia Able/willing to take insulin, do glucose monitoring Eligible for BP or Lipid Trial LDL 60-180 mg/dl HDL < 55 mg/dl (women, blacks), < 50 (all others) TG <750 (not on lipid therapy) or <400 (on lipid therapy) The ACCORD study group. Effects of intensive glucose lowering in type 2 diabetes. N Engl J Med 2008;358:2545-2559. The ACCORD Study Group. Effects of combination lipid therapy in type 2 diabetes mellitus. N Engl J Med 2010. DOI: 10.1056/NEJMoa1001282 ACCORD Glycaemic Control Arm Dr. Anita Chekuri CVA Ltd Background An increase of 1% in the HbAIC is associated with an increase of 18% in the risk of cardiovascular events1 Determine whether therapeutically targeting normal HbAIC levels (< 6.0%) would reduce the rate of cardiovascular events, as compared to targeting HbAIC from 7.0 to 7.9%2 The finding of higher mortality in the intensivetherapy group led to termination of the intensive regimen 17 months before the scheduled end of the study2 1Selvin E, Marinopoulos S, Berkenblit G, et al. Meta-analysis: glycosylated hemoglobin and cardiovascular disease in diabetes mellitus. Ann Intern Med 2004;141:421-431 2The ACCORD study group. Effects of intensive glucose lowering in type 2 diabetes. N Engl J Med 2008;358:25452559. Randomization BP trial Lipid trial Glycaemic trial SBP<110 mmHg SBP<140 mmHg Group A Group B Total HbAIC < 6% 1178 1193 1383 1374 5128 HbAIC 7.07.9% 1184 1178 1370 1391 5123 2362 2371 2753 2765 Total 4733 5518 10251 The ACCORD study group. Effects of intensive glucose lowering in type 2 diabetes. N Engl J Med 2008;358:2545-2559. Outcomes Primary First occurrence of nonfatal MI, nonfatal Stroke, or death from CV disease. Secondary Death from any cause. Also measured the effect of the intervention on microvascular disease, hypoglycemia, cognition, and quality of life. Intensive glycaemic control arm terminated in 3.5 years (instead of 5.6 years as planned for) The ACCORD study group. Effects of intensive glucose lowering in type 2 diabetes. N Engl J Med 2008;358:2545-2559. Baseline Characteristics Age Women Median DM Duration Previous CVD Event White/Black Current Smoker Mean BMI Mean SBP/DBP Mean/Median A1C Mean FG Mean LDL / HDL Intensive (N = 5128) Standard (N = 5123) 62.2 38.7 62.2 38.4 10 10 35.6 34.8 64.4/19.7 14.3 32.2 136.2/74.8 8.3 / 8.1 175 105 / 47 64.5/18.9 13.7 32.2 136.5/75.0 8.3 / 8.1 176 105 / 47 The ACCORD study group. Effects of intensive glucose lowering in type 2 diabetes. N Engl J Med 2008;358:2545-2559. Median Glycated Hemoglobin Levels at Each Study Visit The Action to Control Cardiovascular Risk in Diabetes Study Group. N Engl J Med 2008;358:2545-2559 Adverse Events, Clinical Measures, Tobacco Use, and Use of Nonglycemic Medication after Randomization The Action to Control Cardiovascular Risk in Diabetes Study Group. N Engl J Med 2008;358:2545-2559 Primary and Secondary Outcomes The Action to Control Cardiovascular Risk in Diabetes Study Group. N Engl J Med 2008;358:2545-2559 Kaplan-Meier Curves for the Primary Outcome and Death from Any Cause The Action to Control Cardiovascular Risk in Diabetes Study Group. N Engl J Med 2008;358:2545-2559 Hazard Ratios for the Primary Outcome and Death from Any Cause in Prespecified Subgroups The Action to Control Cardiovascular Risk in Diabetes Study Group. N Engl J Med 2008;358:2545-2559 Observations Targeting HbAIC levels below 6.0% increased the rate of death from any cause after a mean of 3.5 years Magnitude of reduction Speed of reduction Adverse drug interactions at high doses Rate of hypoglycaemia The ACCORD study group. Effects of intensive glucose lowering in type 2 diabetes. N Engl J Med 2008;358:2545-2559. Number of Participants With One or More Severe Hypoglycemia Events Requiring Medical Assistance (n and %) Intensive Group Standard Group # Events ** n % n % 1 400 7.8 130 2.5 2 82 1.6 34 0.7 3 to 5 43 0.8 10 0.2 >5 6 0.1 0 0 **Cumulative number of events The ACCORD study group. Effects of intensive glucose lowering in type 2 diabetes. N Engl J Med 2008;358:2545-2559. Mortality By Treatment Group and Severe Hypoglycemia Overall Intensive Glycemia 1.4% / year Standard Glycemia 1.1% / year Hazard Ratio (257 Deaths) (203 Deaths) 1.22 (1.01, 1.46) Never Experienced a Hypoglycemic Event Experienced Hypoglycemic Event 1.3% / year 2.8% / year (223 Deaths) 1.1% / year (186 Deaths) (34 Deaths) 4.9% / year (17 Deaths) 1.24 (1.02, 1.50) 0.54 (030, 0.96) Mortality Higher in Intensive Group Mortality Higher in Standard Group (95% CI) Interaction P < 0.01 The ACCORD study group. Effects of intensive glucose lowering in type 2 diabetes. N Engl J Med 2008;358:2545-2559. Can we blame it all on hypoglycaemia? Intensive Strategy Intensive Strategy Higher Rates of Hypoglycemia Higher Mortality Higher Rates of Hypoglycemia And can ACCORD distinguish these? Higher Mortality No! The ACCORD study group. Effects of intensive glucose lowering in type 2 diabetes. N Engl J Med 2008;358:2545-2559. Observations Targeting HbAIC levels below 6.0% increased the rate of death from any cause after a mean of 3.5 years Magnitude of reduction Speed of reduction Rate of hypoglycaemia Adverse drug interactions at high doses Longer time duration increases benefits of mortality from non-fatal MI, but also increases risk of death The ACCORD study group. Effects of intensive glucose lowering in type 2 diabetes. N Engl J Med 2008;358:2545-2559. Kaplan-Meier Curves for the Primary Outcome and Death from Any Cause The Action to Control Cardiovascular Risk in Diabetes Study Group. N Engl J Med 2008;358:2545-2559 Observations Targeting HbAIC levels below 6.0% increased the rate of death from any cause after a mean of 3.5 years Magnitude of reduction Speed of reduction Rate of hypoglycaemia Adverse drug interactions at high doses Longer time duration increases benefits of mortality from non-fatal MI, but also increases risk of death The ACCORD study group. Effects of intensive glucose lowering in type 2 diabetes. N Engl J Med 2008;358:2545-2559. ACCORD Lipid Control Arm Dr. Anita Chekuri CVA Ltd Background To investigate whether combination therapy of statin (lower LDL) + fibrate (raise HDL, lower TG), as compared to statin monotherapy was superior in reducing rate of CV events in high risk Type 2 diabetics The ACCORD Study Group. Effects of combination lipid therapy in type 2 diabetes mellitus. N Engl J Med 2010. DOI: 10.1056/NEJMoa1001282 Method 5518 high risk for CV events on Simvastatin started at randomization Treatment group – add fenofibrate at 1 month- 2765 Placebo group- 2753 Follow-up- 4.7 years The ACCORD Study Group. Effects of combination lipid therapy in type 2 diabetes mellitus. N Engl J Med 2010. DOI: 10.1056/NEJMoa1001282 Randomization BP trial Lipid trial Glycaemic trial SBP<110 mmHg SBP<140 mmHg Group A Group B Total HbAIC < 6% 1178 1193 1383 1374 5128 HbAIC 7.07.9% 1184 1178 1370 1391 5123 2362 2371 2753 2765 Total 4733 5518 10251 The ACCORD Study Group. Effects of combination lipid therapy in type 2 diabetes mellitus. N Engl J Med 2010. DOI: 10.1056/NEJMoa1001282 Outcomes Primary: First occurrence of nonfatal MI, nonfatal Stroke, or death from CV disease Secondary: Primary plus revascularization or hospitalization for CCF (expanded macrovascular outcome) Combination of fatal coronary event, nonfatal MI, or unstable angina (major coronary disease events) Death from any cause Hospitalization due to HF The ACCORD Study Group. Effects of combination lipid therapy in type 2 diabetes mellitus. N Engl J Med 2010. DOI: 10.1056/NEJMoa1001282 Results Mean LDL decrease of 100.0 to 81.1 in Fenofibrate group 101.1 to 80.0 in placebo group The ACCORD Study Group. Effects of combination lipid therapy in type 2 diabetes mellitus. N Engl J Med 2010. DOI: 10.1056/NEJMoa1001282 Lipid Values The ACCORD Study Group. N Engl J Med 2010;10.1056/NEJMoa1001282 Prespecified Primary and Secondary Outcomes The ACCORD Study Group. N Engl J Med 2010;10.1056/NEJMoa1001282 Kaplan-Meier Analyses of the Primary Outcome, Expanded Macrovascular Outcome, and Death The ACCORD Study Group. N Engl J Med 2010;10.1056/NEJMoa1001282 Hazard Ratios for the Primary Outcome in Prespecified Subgroups The ACCORD Study Group. N Engl J Med 2010;10.1056/NEJMoa1001282 Observations No significant difference in primary outcome between groups In subgroup analysis, sex difference was significant. Men seemed to benefit from Fenofibrate. Suggestion of heterogenisity with baseline TG and HDL levels. The ACCORD Study Group. Effects of combination lipid therapy in type 2 diabetes mellitus. N Engl J Med 2010. DOI: 10.1056/NEJMoa1001282 Thank You Any Questions?.........