Hum. Reprod. Advance Access originally published online on January 29, 2007
Human Reproduction 2007 22(5):1200-1209; doi:10.1093/humrep/dem005
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Metformin versus oral contraceptive pill in polycystic ovary syndrome: a Cochrane review
1 Division of Obstetrics and Gynaecology, School of Women's and Children's Health, University of New South Wales, Royal Hospital for Women, Sydney, NSW, 2031, Australia 2 Department of Reproductive Medicine, Royal Hospital for Women, Sydney, NSW, Australia 3 IVFAustralia, Sydney, NSW, Australia 4 National Women's Department of Obstetrics and Gynaecology, University of Auckland, Auckland, New Zealand 5 Fertility Centre Scandinavia, Stockholm Storangsvagen 10, Stockholm, Sweden
6 To whom correspondence should be addressed at: Division of Obstetrics and Gynaecology, School of Women's and Children's Health, Level 1 Women's Health Institute, Royal Hospital for Women, Locked Bag 2000, Randwick, Sydney, NSW 2031, Australia. Fax: 61 2 9382 6444; E-mail: mfcostello{at}unsw.edu.au
BACKGROUND: The object of this review was to compare metformin versus oral contraceptive pill (OCP) treatment in polycystic ovary syndrome.
METHODS: A systematic review and meta-analysis employing the principles of the Cochrane Menstrual Disorders and Subfertility Group was undertaken.
RESULTS: Four randomized controlled trials (RCTs) (104 subjects) were included. Limited data demonstrated no evidence of a difference in effect between metformin and the OCP on hirsutism, acne or development of type 2 diabetes mellitus. There were no trials assessing diagnosis of cardiovascular disease or endometrial cancer. Metformin, in comparison with the OCP, was less effective in improving menstrual pattern [Peto odds ratio (OR) 0.08, 95% confidence interval (CI) 0.010.45) and in reducing the serum total testosterone level weighted mean difference (WMD) 0.54, 95% CI 0.220.86] but more effective in reducing fasting insulin (WMD 3.46, 95% CI 5.39 to 1.52) and not increasing fasting triglyceride (WMD 0.48, 95% CI 0.86 to 0.09) levels. Limited data demonstrated no evidence of a difference in effect between the two therapies on reducing fasting glucose or total cholesterol levels and severe adverse events.
CONCLUSIONS: The limited RCT evidence to date does not show adverse metabolic risk with the use of the OCP compared with metformin. Further long-term RCTs are required.
Key words: meta-analysis/metformin/oral contraceptive pill/polycystic ovary syndrome
Submitted on November 29, 2006; accepted on January 3, 2007.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
M. Jensterle, A. Janez, B. Mlinar, J. Marc, J. Prezelj, and M. Pfeifer Impact of metformin and rosiglitazone treatment on glucose transporter 4 mRNA expression in women with polycystic ovary syndrome. Eur. J. Endocrinol., June 1, 2008; 158(6): 793 - 801. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Cosma, B. A. Swiglo, D. N. Flynn, D. M. Kurtz, M. L. LaBella, R. J. Mullan, M. B. Elamin, P. J. Erwin, and V. M. Montori Insulin Sensitizers for the Treatment of Hirsutism: A Systematic Review and Metaanalyses of Randomized Controlled Trials J. Clin. Endocrinol. Metab., April 1, 2008; 93(4): 1135 - 1142. [Abstract] [Full Text] [PDF] |
||||

