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Cited by 143Ovarian function and disordersLipoproteins and Cardiovascular HealthAcne and Rosacea Treatments and Effects

The DOI matches its Crossref record; 51 of the 51 references it cites were found in a registry or an index.

Effects of Simvastatin and Oral Contraceptive Agent on Polycystic Ovary Syndrome: Prospective, Randomized, Crossover Trial

Banaszewska, Beata, Pawelczyk, Leszek, Spaczynski, Robert Z., Dziura, James, Duleba, Antoni J.·2007·The Journal of Clinical Endocrinology & Metabolism
DOI 10.1210/jc.2006-1988
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Abstract

CONTEXT: Polycystic ovary syndrome (PCOS) is associated with hyperandrogenism and cardiovascular risks including dyslipidemia and systemic inflammation. In vitro, statins decrease proliferation and steroidogenesis of ovarian theca-interstitial cells. OBJECTIVE: The study objective was to compare effects of two treatments of PCOS: simvastatin plus oral contraceptive pill (OCP) vs. OCP alone. DESIGN: In a prospective, crossover trial, 48 women with PCOS were randomized to either simvastatin plus OCP for 12 wk followed by OCP alone for an additional 12 wk, or to OCP alone for 12 wk and, subsequently, simvastatin plus OCP for an additional 12 wk. Evaluations were performed at baseline, after 12 wk (crossover), and after 24 wk. Data were analyzed using a random effects model. SETTING: The study was conducted in an academic medical center. PRIMARY OUTCOME: Serum total testosterone was the primary outcome measure. RESULTS: Total testosterone decreased by 38% after Statin + OCP, whereas OCP alone led to a 26% decrease; the statin-attributable effect was significant (P < 0.004). Free testosterone declined by 58% after Statin + OCP, significantly more than the 35% decline after OCP alone (P = 0.006). Hirsutism decreased by 8.1% after Statin + OCP, a greater effect than the 4.7% decrease after OCP alone (P = 0.02). Statin decreased LH, but not FSH or prolactin. Statin + OCP decreased total and low-density lipoprotein cholesterol by 7.5% and 20%, respectively. OCP alone led to a 5% increase of total cholesterol without effect on low-density lipoprotein cholesterol. Statin prevented OCP induced increase of triglycerides. C-reactive protein decreased by 45% after Statin + OCP, a significantly different effect (P = 0.006) than a 6% increase after OCP alone. Soluble vascular cell adhesion molecule 1 decreased by 18% after Statin + OCP, a greater decline than the 10% decrease after OCP alone (P = 0.01). CONCLUSIONS: Simvastatin improved endocrine/clinical aspects of PCOS and had beneficial effects on lipid profile and markers of systemic inflammation.

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Metadata

Authors
Banaszewska, B., Pawelczyk, L., Spaczynski, R. Z., Dziura, J., & Duleba, A. J.
Affiliations
  • Poznan University of Medical Sciences (PL)
  • Department of Gynecology/Obstetrics (B.B., L.P., R.Z.S.), Poznan University of Medical Sciences, 60-535 Poznan, Poland
  • Yale University (US)
  • Department of Obstetrics and Gynecology (A.J.D.), Yale University School of Medicine, New Haven, Connecticut 06520
ORCID
Venue
The Journal of Clinical Endocrinology & Metabolism
Publisher
The Endocrine Society
Published
2006-11-14
Volume
92
Issue
2
Pages
456-461
ISSN
  • 0021-972X (ISSN-L)
  • 1945-7197
DOI
10.1210/jc.2006-1988
OpenAlex
W1995813378
Cited by
143
References
51
Citations by year
2026: 2 · 2025: 5 · 2024: 2 · 2023: 5 · 2022: 3 · 2021: 3 · 2020: 3 · 2019: 6 · 2018: 7 · 2017: 5 · 2016: 7 · 2015: 7 · 2014: 7 · 2013: 12 · 2012: 8
FWCI
11.99
Type
journal article
Language
en
Open access
closed
Locations
  • The Journal of Clinical Endocrinology & Metabolism (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (5r01hd040207-04)
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01 HD40207)
Topics
  • Health Sciences › Medicine › Reproductive Medicine › Ovarian function and disorders
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipoproteins and Cardiovascular Health
  • Health Sciences › Medicine › Dermatology › Acne and Rosacea Treatments and Effects
Keywords
polycystic ovary syndrome, simvastatin, oral contraceptives, hyperandrogenism, testosterone, free testosterone, hirsutism, luteinizing hormone, cholesterol, triglycerides, C-reactive protein, soluble vascular cell adhesion molecule-1, inflammation, cardiovascular risk, statins, theca-interstitial cells, ovarian steroidogenesis, dyslipidemia
MeSH terms
Adult, Hypolipidemic Agents, Contraceptives, Oral, Combined, Drug Therapy, Combination, Estrogens, Ethinyl Estradiol, Female, Humans, Pituitary Hormones, Polycystic Ovary Syndrome, Prospective Studies, Testosterone, Treatment Outcome, Desogestrel, Cross-Over Studies, Simvastatin

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