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Some diabetes drugs provide advantages in weight, cholesterol control.


Most oral medications prescribed for Type 2 diabetes type 2 diabetes
n.
See diabetes mellitus.
 are similarly effective for reducing blood glucose blood glucose Diabetology The principal sugar produced by the body from food–especially carbohydrates, but also from proteins and fats; glucose is the body's major source of energy, is transported to cells via the circulation and used by cells in the presence , but the drug metformin metformin /met·for·min/ (met-for´min) an antihyperglycemic agent that potentiates the action of insulin, used in the treatment of type 2 diabetes mellitus.

met·for·min
n.
 is less likely to cause weight gain and may be more likely than other treatments to decrease so-called bad cholesterol bad cholesterol LDL-cholesterol Cardiovascular disease Cholesterol transported in the circulation by low-density lipoprotein, the elevation of which is directly related to the risk of CAD and cholesterol-related morbidity See LDL-cholesterol. Cf Good cholesterol. , according to a report funded by AHRQ AHRQ,
n.pr See Agency for Healthcare Research and Quality.
. A version of the analysis was posted in the online version of "Annals of Internal Medicine Annals of Internal Medicine (Ann Intern Med) is an academic medical journal published by the American College of Physicians (ACP). It publishes research articles and reviews in the area of internal medicine. Its current editor is Harold C. Sox. ."

The federally funded analysis is based on scientific evidence found in 216 published studies. The report summarizes the effectiveness, risks and estimated costs for 10 drugs: Precose (acarbose acarbose /acar·bose/ (a´kahr-bos) an a inhibitor used in treatment of type 2 diabetes mellitus.
acarbose,
n brand name: Precose, Prandase;
drug class:
), Amaryl (glimepiride), Glucotrol (glipizide), Micronase, DiaBeta, Glynase PresTab (glyburide), Glucophage, Riomet, Fortamet (metformin), Glyset (miglitol), Starlix (nateglinide), Actos (pioglitazone), Prandin (repaglinide repaglinide /re·pag·li·nide/ (re-pag´li-nid) an oral hypoglycemic agent used in the treatment of type 2 diabetes mellitus.
repaglinide Warning - High-alert drug! 
) and Avandia (rosiglitazone).

"As more people are diagnosed with Type 2 diabetes and with the growing array of treatment choices, this is a landmark review," said AHRQ Director Carolyn Clancy, M.D. "This summary of scientific evidence is not only an important tool for clinicians and patients seeking the most appropriate therapy, but it also points out in what areas we need more research to confront this disease."

As new classes of oral diabetes medications have become available, patients and clinicians have faced a growing list of treatment options. Earlier scientific reviews have highlighted some differences between medications, but AHRQ's new analysis is the first to summarize evidence on the effectiveness and adverse events for all approved oral medications commonly used in the United States for Type 2 diabetes.

Diabetes patients typically are monitored with tests that check the percentage of hemoglobin A1c hemoglobin A1c Glycosylated hemoglobin, see there  (HbA1c) in their blood. Checking for HbA1c is a more reliable indicator of chronic high blood sugar than checking blood glucose itself. According to the AHRQ review, most diabetes drugs offer about a one point absolute reduction in HbA1c. In those cases, for example, a diabetes patient's HbA1c might drop from 8 to 7 (with 5 being normal in patients who don't have diabetes). Nateglinide, acarbose and miglitol lower HbA1c by about half that much. Combining diabetes medications, evidence shows, often works better at reducing HbA1c.

AHRQ's analysis of published studies, completed by the agency's Johns Hopkins University Johns Hopkins University, mainly at Baltimore, Md. Johns Hopkins in 1867 had a group of his associates incorporated as the trustees of a university and a hospital, endowing each with $3.5 million. Daniel C.  Evidence-based Practice Center in Baltimore, also concluded:

* Metformin and acarbose do not increase weight among diabetes patients. Other diabetes drugs (glimepiride, glipizide, glyburide, pioglitazone, repaglinide, and rosiglitazone) have been shown to increase weight by an average of two pounds to 11 pounds.

* Blood levels of low-density lipoprotein, which may amplify risks of heart attack and stroke, consistently decrease (by about 10 milligrams per deciliter deciliter /dec·i·li·ter/ (dL) (des´i-le?ter) one tenth (10minus;1) of a liter; 100 milliliters.
Deciliter (dL)
100 cubic centimeters (cc).

Mentioned in: Hypercholesterolemia
) in patients taking metformin and increase (by similar amounts) in patients taking rosiglitazone and pioglitazone.

* Pioglitazone and rosiglitazone cause a small but significant increase in high-density lipoprotein, which promotes the breakdown and removal of cholesterol from the body.

* Glimepiride, glipizide, glyburide and repaglinide are associated with hypoglycemia hypoglycemia: see diabetes.
hypoglycemia

Below-normal levels of blood glucose, quickly reversed by administration of oral or intravenous glucose. Even brief episodes can produce severe brain dysfunction.
 more than other diabetes drugs.

* Metformin and acarbose are generally more likely than other diabetes medications to cause gastrointestinal problems such as diarrhea. Patients who used metformin alone were more likely to experience problems than those using the drug at a lower dose in combination with glimepiride, glipizide, glyburide, pioglitazone or rosiglitazone.

* Patients who take pioglitazone and rosiglitazone have a greater risk of congestive heart failure congestive heart failure, inability of the heart to expel sufficient blood to keep pace with the metabolic demands of the body. In the healthy individual the heart can tolerate large increases of workload for a considerable length of time.  compared with those who take metformin, glimepiride, glipizide or glyburide. While one recent analysis raised the possibility that rosiglitazone may also increase heart attack risks, authors of the AHRQ analysis concluded that current evidence is not sufficient to make a meaningful assessment.

* More, longer studies are needed to understand the impact of oral diabetes drugs on patients' quality of life and whether long-term use causes adverse side effects or reduces important complications of diabetes such as heart disease and kidney disease. Additional research is needed to study interactions between the drugs and to compare therapeutic combinations of the drugs, according to the report.

The report, "Comparative Effectiveness and Safety of Oral Diabetes Medications for Adults with Type 2 Diabetes", is the newest analysis from AHRQ's Effective Health Care program, authorized by the Medicare Prescription Drug, Improvement and Modernization Act. That program represents an important federal effort to compare alternative treatments for health conditions and make the findings public. The program is intended to help patients, doctors, nurses and others choose the most effective treatments. Information can be found at http://www.effectivehealthcare.ahrq.gov
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Title Annotation:Drug Safety
Publication:Adverse Event Reporting News
Article Type:Report
Geographic Code:1USA
Date:Jul 16, 2007
Words:713
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