Low dose combination therapy for the prevention of type 2 diabetes
In a pioneering study, researchers including Lunenfeld Senior Investigator Dr. Bernie Zinman have shown that use of low-dose combination therapy reduces the risk of progression to type 2 diabetes by two thirds, in people at risk of developing the disease.
Toronto – June 14, 2010
In a pioneering study, researchers including Lunenfeld Senior
Investigator Dr. Bernie Zinman have shown that use of low-dose
combination therapy reduces the risk of progression to type 2 diabetes
by two thirds, in people at risk of developing the disease. The study
was published online on June 3 in the prestigious scientific journal
The Lancet.
“The idea behind the trial was that by combining lower doses of
two drugs, we might see the benefits of both, without the side effects
typically associated with these medications,” said Dr.
Zinman.
The CAnadian Normoglycemia Outcomes
Evaluation (CANOE) trial was a double-blind, randomized
controlled study of 207 patients who exhibited elevated levels of blood
sugar and impaired glucose tolerance (IGT), known pre-conditions of
diabetes. Patients received either a combination of two diabetes
medications, rosiglitazone and metformin, at low doses twice daily, or
placebo, for median periods of three to nine years. The primary outcome
of the study was time to the development of
diabetes.
Both rosiglitazone and metformin are drugs that, in the past, were
typically prescribed individually in patients with diabetes, depending
on the severity and progression of their illness. Rosiglitazone helps
the body better use insulin, while metformin helps the liver reduce its
production of glucose. While each medication has been shown to reduce
the development of diabetes in at-risk patients, this therapeutic
benefit has also been associated with significant adverse
effects.
In the study, 103 patients received low-dose combination therapy,
and 104 received placebo. After analysis, it was shown that type 2
diabetes occurred in significantly fewer individuals in the active
treatment group (14/13.6%) than in the placebo group (41/39.4%).
Combination therapy reduced the relative risk of diabetes by 66%
compared with placebo. The absolute risk reduction was 26%, meaning
only four people at risk required combination therapy to prevent one
case of diabetes.
Furthermore, 70 (80%) of the patients in the treatment group
regressed to normal glucose tolerance, compared with 52 (53%) in the
placebo group. Sensitivity to insulin (a measure of the responsiveness
of the body to control glucose in response to insulin) further
decreased in the placebo group by the end of the study, but was
stabilized in the combination treatment group. Both groups experienced
a decline in pancreatic beta-cell function (another diabetes
indicator), but there was no difference in the rate of decline between
the two groups.
“This is the first time that low-dose combination therapy was
proven to have such a beneficial effect in diabetes, in the context of
disease prevention,” said Dr. Zinman. “Our study shows positive
complementary effects, with minimal adverse effects.”
Some of the recent media attention on the study has focused on the
controversy surrounding the use of rosiglitazone (Avandia®),
due to its apparent links to cardiovascular disease and increased
fracture risk. The CANOE study did not show any cardiac-related side
effects or fluid retention (a potential marker of future heart effects)
from combination therapy after four years.
“Our study was a relatively small one, and was not designed to
assess cardiac outcomes,” said Dr. Zinman. “Trials of that nature
typically include thousands of patients.” Dr. Zinman noted that larger
long-term studies assessing low-dose combination therapy with these
agents will be needed to establish cardiovascular benefit and risk, and
overall long-term safety, including fracture
risk.
Diabetes has reached epidemic proportions worldwide and is a
leading cause of heart disease, stroke, blindness, kidney failure and
limb amputation. Several studies have shown that lifestyle changes and
appropriate pharmacologic therapy can significantly reduce the
development of type 2 diabetes in people at risk of the disease.
“We need to do whatever we can to curb this epidemic,” said Dr.
Zinman. “The most effective way to prevent the complications of
diabetes is to prevent diabetes in the first place.”










