Study of Sildenafil Citrate on Insulin Resistance in African American



Status:Completed
Conditions:Obesity Weight Loss, Endocrine
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:18 - 60
Updated:4/21/2016
Start Date:April 2011
End Date:August 2013

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Effect of Sildenafil Citrate on Insulin Resistance and Endothelial Function in Obese African American Women

Obesity has a greater detrimental impact on the health of African American women than on any
other racial or gender group. Nearly 80% of African American women are overweight or obese
in the United States. Hypertension and insulin resistance are more prevalent among African
American women as compared to men and Caucasians. These conditions put them at increased
risk for the development of diabetes mellitus and cardiovascular disease.

Recent studies have reported that a substance named Nitric Oxide (NO)may have some
beneficial effect on how the body handles blood sugar and blood pressure. Of interest,some
studies have shown that African Americans have decreased function of NO in their blood
vessels.

In this study proposal the investigators will test if increasing NO function with a PDE-5
inhibitor (sildenafil citrate) will improve pre-diabetes and the health of the inner layer
of the blood vessels in obese African American women.


Inclusion Criteria:

- Race will be self-defined, but only subjects who report both parents of the same race
will be included.

- Age 18-60 years old.

- The investigators will recruit subjects with wide range of BMI 30-45 kg/m2.

- Subjects who have metabolic syndrome or who have a fasting insulin >13. The diagnosis
include 3 of the following:

Fasting blood glucose of greater than 100 Triglyceride levels of greater than 150 HDL
cholesterol of less than 50 in women Blood pressure of at least 130/85, or on blood
pressure medicine Waist girth of more than 35 inches in women. Subjects of childbearing
potential will be required to have a negative serum/urine pregnancy test. In addition,
they will be asked to use a reliable contraceptive method prior to enrollment as
determined by the PI (Dr. Cyndya Shibao).

Exclusion Criteria:

- Previous allergic reactions to any of the study medication (sildenafil) or inability
to take study medications as prescribed during the course of the study.

- Type 1 or 2 diabetes mellitus as defined by a fasting glucose of 126 mg/dl or
greater.

- Use of antidiabetic medication (insulin, metformin, sulfonylurea, troglitazone)

- Cardiovascular disease such as myocardial infarction within 6 months prior to
enrollment, presence of angina pectoris, significant arrhythmia, congestive heart
failure (LV hypertrophy acceptable), deep vein thrombosis, pulmonary embolism, second
or third degree heart block, mitral valve stenosis, aortic stenosis or hypertrophic
cardiomyopathy.

- Current smokers.

- Significant weight change >5% from baseline in the past three months.

- Pregnancy or breast-feeding.

- History of serious neurological disease such as cerebral hemorrhage stroke, transient
ischemic attack.

- History or presence of immunological or hematological disorders.

- Clinical significant gastrointestinal impairment that could interfere with drug
absorption.

- Impaired hepatic function (aspartate amino transaminase [AST] and/or alanine amino
transaminase [ALT] >1.5X upper limit of normal range).

- Impaired renal function (estimated glomerular filtration rate (eGFR) of <60mL/min).

- Any underlying or acute disease requiring regular medication which could possibly
pose a threat to the subject or make implementation of the protocol or interpretation
of the study results difficult.

- History of alcohol or drug abuse.

- Mental conditions rendering the subject unable to understand the nature, scope and
possible consequences of the study.

- Inability to comply with the protocol, e.g. uncooperative attitude, inability to
return for follow-up visits, and unlikelihood of completing the study.

- Patients must not be taking nitratest in any form (e.g., nitroglycerin, isosorbide
dinitrate, nitroprusside, and others) during this study

- Patients on alpha-blocking drugs (doxazosin, terazosin , or prazosin) will be
excluded

- Patients on protease inhibitors (ritonavir and others) will be excluded
We found this trial at
1
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2201 West End Ave
Nashville, Tennessee 37232
(615) 322-7311
Vanderbilt University Vanderbilt offers undergraduate programs in the liberal arts and sciences, engineering, music, education...
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