Initial 17β-Estradiol dose for treating vasomotor symptoms

Morris Notelovitz, John P. Lenihan, Michele McDermott, Irwin J. Kerber, Nayan Nanavati, Joan Carles Arce

Research output: Contribution to journalArticle

149 Scopus citations

Abstract

Objective: To compare the efficacy of different doses of 17β-estradiol (E2) for relief of vasomotor symptoms in menopausal women. Methods: This was a randomized, double-masked, placebo-controlled, 12-week study in which 333 menopausal women with moderate or severe hot flushes were assigned to treatment with 0.25 mg, 0.5 mg, 1 mg, or 2 mg oral micronized 17β-E2, or placebo. The number and severity of hot flushes were recorded daily. Results: There was a significant linear correlation between increased dosage of 17β-E2 and decreased moderate to severe hot flushes per week (P < .001). Rapid reduction in moderate to severe hot flushes was only achieved with 1 and 2 mg, showing a significant difference from placebo at week 4 (P < .05). At week 4, half the women on placebo had reduced moderate to severe hot flushes of at least 52%; the corresponding figures were 56%, 69%, 86%, and 91% for 0.25, 0.5, 1, and 2 mg, respectively. At week 12, all doses except 0.25 mg were significantly better than placebo for reducing moderate to severe hot flushes (P < .001). Although there were no significant differences, twice as many women in the 2-mg group discontinued treatment due to adverse events, compared with the placebo group. Conclusion: Oral micronized 17β-E2 showed a dose-response effect for reducing moderate and severe hot flushes in menopausal women. 17β-E2 1 mg appeared to be the most useful initial dose. Copyright (C) 2000 The American College of Obstetricians and Gynecologists.

Original languageEnglish (US)
Pages (from-to)726-731
Number of pages6
JournalObstetrics and gynecology
Volume95
Issue number5
DOIs
StatePublished - May 1 2000

ASJC Scopus subject areas

  • Obstetrics and Gynecology

Fingerprint Dive into the research topics of 'Initial 17β-Estradiol dose for treating vasomotor symptoms'. Together they form a unique fingerprint.

Cite this