The purpose of this study is to determine whether cardiovascular disease (CVD) risk markers, β-cell function, and insulin sensitivity can be improved by targeting mechanisms of both diabetes and CVD – using an antioxidant, an ARB, or an anti-inflammatory agent - in patients with impaired glucose tolerance (IGT)in a randomized, controlled trial.

Condition	Intervention
Impaired Glucose Tolerance (IGT)	Drug: Aspirin  Drug: Alpha lipoic acid  Drug: Olmesartan  Drug: Placebo

Further Study Details: 

Primary Outcomes: Brachial artery flow mediated dilation (endothelial function)
Secondary Outcomes: Insulin sensitivity and beta cell function; Inflammatory markers; Markers of oxidative stress
Expected Total Enrollment:  120

Diabetes is a common, major health problem in the United States, and it significantly increases the risk of developing heart disease, which is the leading cause of death. Research studies have shown that the risk of heart disease is increased, even in the “pre-diabetes” or impaired glucose tolerance (IGT) stage, before the onset of true diabetes. While many studies have shown that aggressive management of diabetes lowers the risk of heart disease, at the present time, it is not known how best to treat patients with impaired glucose tolerance (pre-diabetes) to prevent the development of heart disease. It is also not known where in the range of blood sugar levels risk begins to increase. The purpose of this study is to determine: (1) whether medications, which target pathways involved in the development of heart disease, can decrease the risk of heart disease in individuals with impaired glucose tolerance, and (2) whether a “high” blood sugar level measured one hour after drinking a standard high-sugar drink is associated with an increased risk of heart disease even in individuals who have no evidence of diabetes or pre-diabetes. The purpose of Aim 1 of this study is to determine whether medications, which target pathways involved in the development of heart disease, can decrease the risk of heart disease in individuals with impaired glucose tolerance. One hundred-twenty volunteers with impaired glucose tolerance and 30 volunteers with normal glucose tolerance (normal blood sugars after ingesting a standard high-sugar drink) will be recruited from the “Screening for Impaired Glucose Tolerance” (SIGT) study. The 30 volunteers with normal glucose tolerance will not take any study medication, but will undergo medical testing to determine their risk of heart disease at the beginning of the study, after which their participation in the study will be complete. The 120 volunteers with impaired glucose tolerance will be randomly assigned to one of four medications to be taken over a one-year period: (1) alpha lipoic acid (an antioxidant, dietary supplement), (2) olmesartan (a drug used to treat high blood pressure), (3) aspirin (an anti-inflammatory drug), and (4) placebo (an inactive, “dummy” pill). Subjects with impaired glucose tolerance will undergo medical testing to determine their risk of heart disease at the beginning of the study (before beginning study medications), after 3 months of intervention, and again at the end of the study (12 months after enrollment). Test results will be compared between the subjects taking each of the active medications and those taking placebo, to determine if the medications leads to a significant reduction in the risk for the development of heart disease. The medical tests used in this study are currently used in medical practice, and include blood and urine specimens, ultrasound testing of the artery at the arm, and an insulin sensitivity test (test of how effectively the body uses sugar). All visits and tests will be conducted in the General Clinical Research Centers of Emory University Hospital and Grady Memorial Hospital. The purpose of Aim 2 of this study is to determine whether a “high” blood sugar level measured one hour after drinking a standard high-sugar drink (1-hour blood sugar level) is associated with an increased risk of heart disease even in individuals who have no evidence of diabetes or pre-diabetes. Seventy-five volunteers with normal glucose tolerance (normal blood sugars after ingesting a standard high-sugar drink) will be recruited from the SIGT study, as well as 15 subjects with impaired glucose tolerance and 15 with diabetes. The subjects with normal glucose tolerance will be grouped into those with “low”, “middle”, and “high” 1-hour blood sugar levels. All subjects will undergo medical testing (as in Aim 1 above) to determine their risk of heart disease. Test results of subjects with “low”, “middle”, and “high” 1-hour blood sugar levels will be compared against one another, as well as against those of subjects with IGT and diabetes. If subjects with normal glucose tolerance but “high” 1-hour blood sugar levels are found to have increased risk for heart disease compared to those with “low” 1-hour blood sugar levels, then the 1-hour blood sugar levels may provide important information regarding an increased risk of heart disease even in individuals with normal glucose tolerance but “high” 1-hour blood sugar levels – a population which otherwise would not be identified with the current standard tests used for the diagnosis of diabetes and pre-diabetes. Over 40 million Americans have pre-diabetes (impaired glucose tolerance), which is associated with an increased risk of the development both diabetes and heart disease. Findings from these studies will provide important insights into the pathways that lead to the development of heart disease related to pre-diabetes, prevention of heart disease in the pre-diabetic population, and identification of individuals at high risk for heart disease earlier in their natural history – even before the onset of pre-diabetes.

Ages Eligible for Study:  18 Years   -   75 Years,  Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

Inclusion Criteria:

• Impaired glucose intolerance

Exclusion Criteria:

• Diagnosis of diabetes; taking an ACE-I, ARB, or aspirin; have systolic blood pressure >140 mm Hg; have a chronic inflammatory disorder (i.e. rheumatoid arthritis, inflammatory bowel disease, sinusitis); vascular disease (cardiac, peripheral, cerebral); renal insufficiency or hepatic abnormalities; gastrointestinal bleeding (defined as gastric or duodenal ulcer, hematemesis, and/or blood in the stool) or significant other upper gastrointestinal problems (i.e. gastritis) within the previous 6 months; anemia or a history of bleeding disorder; have a history of ARB or aspirin allergy; have the syndrome of asthma, rhinitis, and nasal polyps; have other medical problems which would preclude their taking potential study medications for 12 months; are pregnant or have a positive pregnancy test; are breast feeding; are unable or unwilling to tolerate having one catheter in each arm for 4 hours (see below); have health status such that the envisioned blood sampling would confer a physiologic risk; have other physical, social, or behavioral problems which would decrease the likelihood that they would remain in the study for 12 months; or who do not appear capable of giving informed consent.

Please refer to this study by ClinicalTrials.gov identifier  NCT00122447

Edith Woodward, RN      404-778-1688    edith_woodward@emoryhealthcare.org

Georgia
      Emory University Hospital, Atlanta,  Georgia,  30322,  United States; Recruiting
      Grady Health System, Atlanta,  Georgia,  30303,  United States; Recruiting

Study chairs or principal investigators

Mary K Rhee, MD, MS,  Principal Investigator,  Emory University   

Study ID Numbers:  RR-017643-MKR; Sankyo-CS-866
Record last reviewed:  July 2005
Last Updated:  July 25, 2005
Record first received:  July 21, 2005
ClinicalTrials.gov Identifier:  NCT00122447
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-07-26