AI Article Synopsis

  • The study investigated the effects of a 3-month treatment combining oral hormonal contraceptives with either metformin or rosiglitazone on hormone levels and fat-related hormones in women with polycystic ovary syndrome (PCOS).
  • A significant reduction in hormones like leptin, resistin, and neuropeptide Y was observed in both treatment groups, along with a notable decrease in body weight specifically for the metformin group.
  • Overall, the results indicate that this treatment may lower cardiovascular risks associated with insulin resistance in women suffering from PCOS.

Article Abstract

Aim: The study was aimed at elucidating the influence of a 3-month treatment with routine therapeutic regimens--oral hormonal contraceptives (OHC) with antiandrogenic activity (a standard combination of ethynil estradiol 35 microg plus cyproterone acetate 2 mg) in combination with insulin sensitizing agents--metformin (Group I) and rosiglitazone (Group II) on adipose tissue hormones and hypothalamic neuropeptide Y (NPY) in women with polycystic ovary syndrome.

Patients And Methods: The study included 66 overweight insulin resistant women with PCOS according to the recent ESHRE-ASRM criteria randomized into 2 age-matched therapeutic groups.

Results: Significant decrease of leptin (P < 0.01; P = 0.001, resp.), resistin (P < 0.01; P < 0.01, resp.), tumour necrosis factor alpha (TNF alpha) (P = 0.001; P < 0.001, resp.), and NPY (P < 0.05; P < 0.001, resp.) was observed in both groups after treatment. These findings were in parallel with a significant decrease in the anthropometric parameters of body weight in the metformin group only. No significant changes in hormonal characteristics of the groups were found except for a significant decrease in androstenedione and DHEA-S (P < 0.05) in the metformin group and in 17-OH-progesterone (P < 0.05) in the rosiglitazone group. HDL-cholesterol rose and diastolic blood pressure fell significantly (P < 0.05) in the metformin group.

Conclusion: Our data suggest beneficial effects of the treatment on potential cardiovascular risk in insulin resistant PCOS women.

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Source
http://dx.doi.org/10.2478/v10153-011-0052-3DOI Listing

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