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Tight Control and Cardiovascular Disease (Part 2): ACCORD
June 30, 2008
This is my second report on the large studies of tight blood glucose control and cardiovascular disease risk in Type 2 diabetes that were presented at the ADA Scientific Sessions earlier this month. You can read about the results of the ADVANCE trial in "Tight Control and Cardiovascular Disease (Part 1): ADVANCE." This week, I’ll discuss the Action to Control Cardiovascular Risk in Diabetes, or ACCORD, trial.
The ACCORD trial made headlines earlier this year (see “The ACCORD Trial Findings: What You Should Know”) when its intensive blood-glucose-lowering arm was stopped early because a higher rate of death was found in that group. Now, the full results of the blood-glucose-lowering arm of the ACCORD trial have been published online in The New England Journal of Medicine (NEJM).
The ACCORD Trial
The main aim of the blood-glucose arm of the trial was to see whether a strategy of intensive blood glucose control—aiming for an HbA1c level of less than 6%—would reduce the risk of cardiovascular disease (defined as heart attack, stroke, or death from a cardiovascular cause) in people with Type 2 diabetes. Death from any cause was one of the other outcomes that was measured.
ACCORD participants had an average age of 62, body-mass index (BMI) of 32 (meaning that they were, on average, obese), and HbA1c of 8.3%, and had had diabetes for an average of 10 years at the beginning of the trial. Women accounted for 38% of participants. Participants were considered to be at high cardiovascular risk; 35% had had a prior “cardiovascular event” (heart attack or stroke), and the rest had either a major risk factor in addition to diabetes, such as left ventricular hypertrophy (enlargement of part of the heart) or microalbuminuria (a sign of kidney problems), or at least two of the following risk factors: high LDL (”bad”) cholesterol, low HDL (”good”) cholesterol, high blood pressure, obesity, or smoking.
The ACCORD participants were all randomly assigned to be in the intensive glucose control group or the standard group. Members of the intensive group saw a health-care professional every two months and monitored their blood glucose levels two to four times per day if their HbA1c levels were above target; the standard group was seen every four months and was only required to monitor once a day. Both groups were treated with a variety of drugs and insulin, but the intensive group tended to be prescribed more drugs. (For example, 52% of people in the intensive group took three oral diabetes drugs plus insulin, but only 16% of the standard group was prescribed this regimen.) By the time the study was stopped, the intensive group had a median HbA1c of 6.4% and the standard group had an Hba1c of 7.5%.
At this point, the researchers found the following:
So, unlike the ADVANCE trial, which simply found no cardiovascular benefit to intensively lowering blood glucose levels in people with diabetes and high cardiovascular risk, the ACCORD trial found evidence of harm. Why is this?
To see if they could explain the higher rates of death and cardiovascular death in the intensive-control group of ACCORD, the researchers performed further analyses considering people’s age, sex, ethnicity, other diseases, blood glucose control, current or severe hypoglycemia, diabetes drugs used, or combinations of these factors, but were not able to identify any group of people that was more likely to die in response to intensive treatment. Based on these analyses, Robert Byington, Ph.D., one of the lead ACCORD researchers, said that it was probably the “strategy of intensive glycemic lowering itself, compared to a standard approach, in a population of people with Type 2 diabetes at high risk for cardiovascular disease, [that] increases mortality over the course of three and a half years of treatment.”
In editorials published in NEJM analyzing the ACCORD and ADVANCE results, doctors not affiliated with the studies discussed a few other factors that may help explain the increased risk of death that was found in the ACCORD study. (You can read the full editorials here and here.)
You can view a chart comparing and contrasting the ACCORD and ADVANCE trials in more detail here.
The Take-Home Message
Also, as William T. Cefalu, M.D., pointed out in his NEJM editorial, participants in ACCORD who had not had a previous cardiovascular event or whose HbA1c at the start of the trial was under 8% “had significantly fewer fatal and nonfatal cardiovascular events than did patients at higher risk,” implying that intensive blood glucose control may be better at protecting people who have lower cardiovascular risk and/or start off with better diabetes control. Further clinical trials that are under way now will hopefully help shed more light on these questions in the next few years.
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