Influence of methyltestosterone postmenopausal therapy on plasma lipids, inflammatory factors, glucose metabolism and visceral fat: a randomized study

Eur J Endocrinol. 2006 Jan;154(1):131-9. doi: 10.1530/eje.1.02065.

Abstract

Background: There has been a growing interest in treating postmenopausal women with androgens. However, hyperandrogenemia in females has been associated with increased risk of cardiovascular disease.

Objective: We aimed to assess the effects of androgen replacement on cardiovascular risk factors.

Design: Thirty-seven postmenopausal women aged 42-62 years that had undergone hysterectomy were prospectively enrolled in a double-blind protocol to receive, for 12 months, percutaneous estradiol (E2) (1 mg/day) combined with either methyltestosterone (MT) (1.25 mg/day) or placebo.

Methods: Along with treatment, we evaluated serum E2, testosterone, sex hormone-binding globulin (SHBG), free androgen index, lipids, fibrinogen, and C-reactive protein; glucose tolerance; insulin resistance; blood pressure; body-mass index; and visceral and subcutaneous abdominal fat mass as assessed by computed tomography.

Results: A significant reduction in SHBG (P < 0.001) and increase in free testosterone index (P < 0.05; Repeated measures analysis of variance) were seen in the MT group. Total cholesterol, triglycerides, fibrinogen, and systolic and diastolic blood pressure were significantly lowered to a similar extent by both regimens, but high-density lipoprotein cholesterol decreased only in the androgen group. MT-treated women showed a modest rise in body weight and gained visceral fat mass relative to the other group (P < 0.05), but there were no significant detrimental effects on fasting insulin levels and insulin resistance.

Conclusion: This study suggests that the combination of low-dose oral MT and percutaneous E2, for 1 year, does not result in expressive increase of cardiovascular risk factors. This regimen can be recommended for symptomatic postmenopausal women, although it seems prudent to perform baseline and follow-up lipid profile and assessment of body composition, especially in those at high risk of cardiovascular disease.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Abdominal Fat / anatomy & histology
  • Abdominal Fat / drug effects*
  • Acute-Phase Proteins / metabolism*
  • Administration, Oral
  • Adult
  • Blood Glucose / metabolism*
  • Blood Pressure / drug effects
  • C-Reactive Protein / metabolism
  • Estrogen Replacement Therapy*
  • Female
  • Fibrinogen / metabolism
  • Humans
  • Hysterectomy
  • Lipids / blood*
  • Methyltestosterone / administration & dosage
  • Methyltestosterone / therapeutic use*
  • Middle Aged
  • Ovariectomy
  • Postmenopause*
  • Sex Hormone-Binding Globulin / metabolism

Substances

  • Acute-Phase Proteins
  • Blood Glucose
  • Lipids
  • Sex Hormone-Binding Globulin
  • Fibrinogen
  • C-Reactive Protein
  • Methyltestosterone