Insulin resistance in clomiphene responders and non-responders with polycystic ovarian disease and therapeutic effects of metformin
Objectives: To evaluate the clinical features, endocrine and metabolic profiles in clomiphene (CC) responders and non-responders with polycystic ovarian disease (PCOD), and to examine the effects of metformin (MTF) on the above parameters of CC resistance. Methods: A prospective clinical trial was u...
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Published in: | International journal of gynecology and obstetrics Vol. 75; no. 1; pp. 43 - 50 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Shannon
Elsevier Ireland Ltd
01-10-2001
Elsevier Science |
Subjects: | |
Online Access: | Get full text |
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Summary: | Objectives: To evaluate the clinical features, endocrine and metabolic profiles in clomiphene (CC) responders and non-responders with polycystic ovarian disease (PCOD), and to examine the effects of metformin (MTF) on the above parameters of CC resistance.
Methods: A prospective clinical trial was undertaken at the infertility division of a university teaching hospital. Forty-one CC responders were selected and their hormonal and clinical features were determined. Forty-one CC-resistant PCOD women were also selected and clinical features; metabolic and hormonal profiles before and after treatment with MTF 1500 mg/day for 6–8 weeks were evaluated. Women who failed to conceive were treated by CC while continuing to take MTF.
Results: CC responders had higher insulin levels while non-responders were hyperinsulinemic. Menstrual irregularities improved in 30%. Mean±S.D. area under curve of insulin decreased from 297.58±191.33 to 206±0.1 mIU/ml per min (
P=0.005). Only 39.39% ovulated and 24.24% conceived.
Conclusion: PCOD is associated with insulin resistance (IR) particularly in CC-resistant women. Insulin resistance and androgen levels are significantly higher in obese patients. MTF therapy improved hyperandrogenemia, IR, and pregnancy rate. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0020-7292 1879-3479 |
DOI: | 10.1016/S0020-7292(01)00470-2 |