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Acomplia Cuts Diabetes Patients Risks

来源:www.webmd.com
摘要:June12,2006--Acomplia,anexperimentalweightlossweightlossdrug,helpsobesepeoplewithtype2diabetesdiabetesloseweight,reducewaistsize,andevencontrolbloodsugarandbloodfats。Surprisingly,Acomplia‘sbeneficialeffectonbloodsugarsandfatswent57%beyondthebenefit......

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June 12, 2006 -- Acomplia, an experimental weight lossweight loss drug, helps obese people with type 2 diabetesdiabetes lose weight, reduce waist size, and even control blood sugar and blood fats.

Surprisingly, Acomplia's beneficial effect on blood sugars and fats went 57% beyond the benefit that would have been expected from weight loss alone. The drug, which affects the body's cannabinoid system, appears to reduce interrelated risks for heart and metabolic diseases.

The benefits seen were in addition to the benefits of standard, ongoing treatment with Glucophage or the family of diabetes drugs called sulfonylureas. Researcher Andr?cheen, MD, PhD, head of diabetes at the University of Li? in Belgium, reported the findings at this week's annual meeting of the American Diabetes Association, held June 9-13 in Washington.

"These findings support the use of for reducing cardiometabolic risk in patients with type 2 diabetes, and show that the benefits achieved are additional to those of background oral antidiabetic therapy," Scheen and colleagues wrote in their presentation abstract.

The findings come from an international clinical trial of more than 1,000 men and women with diabetes. The average study patient was 56 years old and obese, with a 43.3-inch waistline. At study entry, patients' average hemoglobin A1c (HbA1c) level was 7.5%. HbA1c measures average blood sugar levels over the past three months. Normal HbA1c levels range from 4% to 6%.

Acomplia lowered HbA1c levels by 0.6%. That may not sound like much, but recent studies indicate every 1% increase in HbA1c raises the risk of death -- from all causes -- by 24% for men and 28% for women.


SOURCES: Scheen, A. X. Presentation to the Annual Scientific Sessions of the American Diabetes Association, Washington, June 9-13, 2006; Abstract 560-P. Khaw, K.-T. Annals of Internal Medicine, Sept. 21, 2004; vol 141: pp 413-420.

作者: DanielDeNoon 2006-7-4
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