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Large U.K. database shows sulfonylurea mortality link


By MITCHEL L. ZOLER, Internal Medicine News Digital Network


    BARCELONA – Treatment of type 2 diabetes with a sulfonylurea drug
    was tied to a significantly increased risk of death in two large U.K.
    epidemiology studies with a total of more than 100,000 patients.
    These and other recent findings that raised questions about the safety
    and efficacy of sulfonylurea drugs for type 2 diabetes
    highlight the need for regulatory reassessment of the sulfonylurea drug
    class, Craig J. Currie, Ph.D., said at the annual meeting of
    the European Association for the Study of Diabetes.
    "The safety of sulfonylureas needs urgent evaluation," said
    Dr. Currie, professor of applied pharmacoepidemiology
    at Cardiff (Wales) University.
    "Regulatory agencies have to take this seriously.
    " He noted that current U.K. recommendations from the U.K.
    National Institute for Health and Care Excellence (NICE)
    cite sulfonylurea drugs as the top second-line drug treatment
    for patients with type 2 diabetes if monotherapy with metformin fails.
    Last year, management guidelines from the American Diabetes
    Association and the EASD listed sulfonylurea drugs
    as candidate second-line agents after metformin along with
    several other drug classes (Diabetes Care 2012;35:1364-79).
    Mitchel L. Zoler/IMNG Medical Media Dr. Craig J. Currie

    But others cautioned of the risk for unrecognized confounding
    when using observational data to gauge drug safety.
    "I’m not sure they can get rid of all the confounders;
    the patients [treated with a sulfonylurea] may just be fundamentally
    different.
    In most clinical trials we did not see harm" from sulfonylureas,
    commented Dean T. Eurich, Ph.D.,
    a pharmacoepidemiologist at the University of Alberta in Edmonton.
    Both studies reported by Dr. Currie and his associates used data collected by the Clinical Practice Research Datalink ,
    an observational database of the U.K. National Health Service
    that routinely collects data from a representative sample of
    British patients.
    In one study, they focused on patients who began initial therapy
    for type 2 diabetes during 2000-2012 with metformin monotherapy,
    76,811 patients,
    or sulfonylurea monotherapy, 15.687 patients.
    During an average 3-year follow-up,
    the all-cause mortality rate was roughly 14 deaths/1,000 patient-years
    for those on metformin, and about 45/1,000 patient-years for those
    on a sulfonylurea.
    After adjustment for many potential confounders, including
    age, sex, body mass index, duration of diabetes, serum creatinine,
    and hemoglobin A1c level, the analysis found a relative 58%
    increased risk for death in the sulfonylurea patients compared with
    those taking metformin, a statistically significant difference,
    reported Christopher L. Morgan, a researcher at Cardiff University.
     
    The second study compared patients who began a two-drug combination
    regimen during 2007-2013, comprising 33,983 patients who began
    metformin plus a sulfonylurea and
    7,864 who began metformin plus a dipeptidyl peptidase-4 inhibitor.
    The adjusted rate of all-cause mortality was a relative 36% higher among patients treated with a sulfonylurea, compared with those treated
    with a DPP-4 inhibitor, Dr. Currie reported.
    Metformin plus a sulfonylurea is the most commonly used drug
    combination for treating type 2 diabetes worldwide, Dr. Currie noted.
    He speculated that sulfonylureas may boost mortality by increasing
    insulin levels and thereby causing more episodes of severe hypoglycemia
    than other oral diabetes drugs.
     
    View on the News Potential confounding
    clouds observational analyses Results from clinical trials that
    included patients treated with sulfonylurea drugs have not shown
    evidence of harm from these drugs.
    Major trials such as ACCORD, ADVANCE, and UKPDS ran
    subgroup analyses to try to look at whether certain drugs seemed to drive poor outcomes, and nothing has been reported for sulfonylureas.
     
    In contrast, observational studies like the ones reported by Dr. Currie and Mr. Morgan have shown links between sulfonylurea treatment and
    worse outcomes, but these analyses face the problem that
    physicians prescribe various diabetes drugs to very different groups
    of patients.
    We can use fancy statistical models to try to adjust for this,
    but it’s not clear that they adjust for all possible confounding factors.
    For example, one of the big differences between sulfonylureas and
    other possible second-line drugs that patients might get is cost.
    So socioeconomic differences might exist between the patients who
    received a sulfonylurea and those who received a DPP-4 inhibitor that
    were not included in the adjustments.
    Many factors enter into the decision for a physician to prescribe one drug
    or another.
    A major limitation of the sulfonylurea drugs is that they have never been
    the subject of a large, well-designed study to test
    their cardiovascular safety, such as the studies begun a few years ago
    for several newer drugs following suggestions of a problem
    with rosiglitazone.
    One problem we know for certain about sulfonylureas is that
    they pose more of a risk for causing hypoglycemic events
    than do other oral drugs, and there is increasing evidence that
    severe hypoglycemic events can affect the rates of
    cardiovascular outcomes.
    There is also good evidence that the glycemic control exerted by
    sulfonylureas is not as durable as that of other drugs, and
    they also cause weight gain, so for several reasons,
    the sulfonylurea class is gradually being bypassed in favor of
    other options.
    However, many of the alternative agents have their own limitations,
    especially higher cost.
    Clinicians need to weigh the suggestions of harm caused by sulfonylurea
    drugs against their better affordability.
    If patients can’t afford their diabetes medications, they won’t take them,
    and undertreated diabetes may pose an even greater risk.
    Much more definitive data on the efficacy and safety of sulfonylurea drugs should come from the Cardiovascular Outcome Study of Linagliptin versus Glimeprimide in Patients With Type 2 Diabetes (CAROLINA).
    These results should be the make or break for sulfonylureas,
    but data from this study are not expected until 2018.
    Dean T. Eurich, Ph.D., is a pharmacoepidemiologist at the University
    of Alberta in Edmonton.
    He made these comments in an interview.
    He said he had no relevant financial disclosures.
    10/30/13 Major finding: Type 2 diabetes monotherapy with sulfonylurea
    was linked with 58% higher mortality, compared with metformin
    monotherapy, during a mean 3-year follow-up.
    Data source: A review of 92,498 U.K. patients who started treatment
    for type 2 diabetes with either metformin or sulfonylurea monotherapy
    during 2000-2012.
    Disclosures: The study was funded by Astra Zeneca and Bristol-Myers
    Squibb. Dr. Currie said he owns a drug-consultant company that has done work for several drug companies. Mr. Morgan and Dr. Eurich said
    they had no relevant financial disclosures.
    VIEW ON THE NEWS
    Potential confounding clouds observational analyses
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