This study is being done to evaluate whether the medication, febuxostat, can improve the degree of insulin resistance and other features of the metabolic syndrome (high blood pressure, elevated insulin levels, excess body fat around the waist, and/or high cholesterol) by lowering uric acid levels in the blood.
The metabolic syndrome (MS) is characterized by a constellation of metabolic features including dyslipidemia, hyperglycemia, hypertension, obesity, and insulin resistance. This cluster of features is strongly associated with type 2 diabetes, atherosclerotic cardiovascular disease, and increased cardiovascular and all-cause mortality. Hyperuricemia (elevated serum uric acid) is associated with insulin resistance and features of the MS in cross-sectional epidemiological studies. However, it remains unclear whether this association is causal or simply coincidental. If hyperuricemia CAUSES insulin resistance, then lowering serum uric acid by pharmacological means may result in improved insulin sensitivity and reversal of features of the metabolic syndrome. In some recent small studies, lowering serum uric acid with allopurinol was associated with improvement in some of the features and/or complications of the MS: Allopurinol use resulted in reduction in blood pressure in adolescents and improvement in exercise capacity in patients with chronic stable angina. A low urine pH is strongly associated with insulin resistance, and individual features of the metabolic syndrome. Similarly, a low fractional excretion of uric acid is also associated with metabolic syndrome feature. We therefore would like to examine the effect on febuxostat on these two parameters which have been linked with the metabolic syndrome. The goal of this study is to evaluate whether pharmacological lowering of serum uric acid with the medication febuxostat is associated with improvement in the degree of insulin resistance and various features of the metabolic syndrome.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
24
One 40 mg tablet once a day for 6 months
UT Southwestern Medical Center
Dallas, Texas, United States
BMI
Time frame: 6 months
Serum Uric Acid
Time frame: 6 months
Serum Creatinine
Time frame: 6 months
Ambulatory Systolic Blood Pressure
Systolic BP by ambulatory blood pressure monitor.
Time frame: 6 months
Ambulatory Diastolic Blood Pressure
Diastolic BP by ambulatory blood pressure monitor.
Time frame: 6 months
Serum Glucose
Time frame: 6 months
Serum Insulin
Time frame: 6 months
Insulin Sensitivity Measured by HOMA (HOmeostasis Model Assessment)
Time frame: 6 months
Seum Total Cholesterol
Time frame: 6 months
Serum HDL-cholesterol
Time frame: 6 months
Serum Triglycerides
Time frame: 6 months
Urine Uric Acid
Time frame: 6 months
Urine Creatinine
Time frame: 6 months
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Fractional Excretion UA
Time frame: 6 months
Urine pH
Time frame: 6 months