Polycystic Ovary Syndrome Clinical Trial
Polycystic ovary syndrome (PCOS) is a common endocrinopathy affecting 6.5%-6.7% of women in
reproductive age, and is commonly associated with obesity, menstrual irregularity, insulin
resistance (IR), infertility, and clinical hyperandrogenism and/or hyperandrogenemia (1,2).
PCOS is also associated with increased risk of abnormal lipoproteins and hypertension, as
well as cardiovascular or cerebrovascular morbidity (3). The lipid and lipoprotein profile
in androgenized women with poly cystic ovaries is similar to the made pattern with higher
levels of cholesterol, low-density lipoprotein (LDL), and lower levels of high-density
lipoprotein (HDL), and this abnormal pattern is independent of body weight (4). Insulin
resistance is associated with reproductive abnormalities in women with PCOS. Improving
insulin sensitivity through both lifestyle and pharmacological intervention can ameliorate
these abnormalities. Insulin resistance in women with PCOS is common (up to 50%), both in
obese and nonobese women (5), and disordered insulin action precedes the increase in
androgen.
Treatment for PCOS subjects typically includes, implementation of lifestyle changes
especially weight loss and adjuvant pharmaceutical intervention including oral
contraceptives, anti-androgen therapy and insulin-lowering drugs (such as, metformin) (6).
Metformin is a biguanide used extensively in type 2 diabetes. It inhibits hepatic glucose
production and increases peripheral insulin sensitivity, but dose not cause hypoglycemia.
Several studies have shown an increase in insulin sensitivity and pregnancy rate accompanied
by decreased insulin and androgen levels in PCOS patients taking metformin (7).
The 3-hydroxy-3-methylglutaryl coenzyme A (HMG-COA) reductase inhibitors (statins) are the
rate-limiting step in cholesterol biosynthesis, and inhibition of this enzyme decreases
cholesterol synthesis and a compensatory increase in the expression of LDL receptors in the
liver. Statins reduce plasma triglycerides in dose-dependent fashion and also have a modest
HDL-raising effect which is not dose-dependent (8,9). Furthermore, statins pose other
cardio-protective properties, including antioxidant and anti-inflammatory actions (10,11).
Some studies have reported that simvastatin decreases serum androgen levels in women with
PCOS (12,13) by inhibiting proliferation and steroidogenesis of ovarian theca-interstitial
cells (14). According to these previous findings, we hypothesized that combination therapy
with simvastatin and metformin will result in lower androgen levels and cardiovascular risk
factors in women with PCOS.
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Outcomes Assessor), Primary Purpose: Treatment
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
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