Postmenopause hormone treatment in women with NIDDM or impaired glucose tolerance: the MEDIA randomized clinical trial

Objective: To assess the biological safety of four hormone replacement trea tment (HRT) combinations in women with non insulin dependent diabetes melli tus (NIDDM) or impaired glucose tolerance (IGT). Subjects ann methods: Rand omized, double-blind, placebo-controlled trial to analyze the variation of fibrinogen, factor VII, PAI1, and TG blood levels in women (n = 99), with N IDDM or IGT, receiving a 3-month course of either oral oestradiol (1 or 2 m g) combined with Chlormadinone Acetate 5 mg, or transdermal oestradiol 50 m u /24 h in association with Norethisterone Acetate (11.2 or 22.4 mg), or pl acebo. Follow-up lasted 3 months. Results: Ninety nine patients, mean age 5 6 years (SD 5), mean diabetes duration 7 years (S.D. 7), mean glycated hemo globin (7.3%) were enrolled. There was no significant difference between th e groups for any of the primary hemostasis criteria (n = 77). Triglycerides (TG) variation significantly differed between groups, P = 0.01, from - 21% in the large patch group, to + 22% in the placebo group (n = 82). Treatmen t administration routes did not significantly differ for any of the criteri a. There was a significant difference in the total cholesterol variation be tween groups, from + 8.7% in the placebo group to - 10.8% in the oral 1 mg group (P = 0.001). Conclusion: The treatments had no highly deleterious eff ect in these patients with NIDDM or with IGT. Long-term trials can be perfo rmed with such patients, and an hormone treatment can be prescribed to reli eve symptoms. Since these patients had a well-controlled NIDDM, results mig ht be different in less well-controlled diabetes. The data do not support t he hypothesis of an impaired oestrogen effect in patients with NIDDM. (C) 2 37 Elsevier Science Ireland Ltd. All rights reserved.