Hypergonadotropic hypogonadic amenorrhea (World Health Organization III) and osteoporosis
To assess the bone mineral density in World Health Organization (WHO) III women after hormone replacement therapy. We studied the bone mineral density of 41 women with premature ovarian failure (hypergonadotropic hypogonadic amenorrhea—WHO III) before and during hormone replacement therapy. All WHO...
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Published in | Fertility and sterility Vol. 57; no. 1; pp. 37 - 41 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
New York, NY
Elsevier Inc
01.01.1992
Elsevier Science |
Subjects | |
Online Access | Get full text |
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Summary: | To assess the bone mineral density in World Health Organization (WHO) III women after hormone replacement therapy.
We studied the bone mineral density of 41 women with premature ovarian failure (hypergonadotropic hypogonadic amenorrhea—WHO III) before and during hormone replacement therapy.
All WHO III women were recruited from the Outpatient Department of the First Department of Gynecology and Obstetrics, University of Vienna Medical School, Austria, a public University Hospital.
Forty-one patients, 30 healthy women.
Twenty-eight of 41 WHO III women received cyclic hormone replacement therapy consisting of 0.625 mg conjugated estrogen (days 1 to 30) and 5 mg medrogeston (days 20 to 30) in addition, with a 7-day interval.
The bone mineral density was evaluated by single photon absorptiometry and dual energy x ray absorptiometry every 6 months (single photon absorptiometry six times, dual energy x ray absorptiometry four times).
The bone mineral density in young women with hypergonadotropic hypogonadic amenorrhea (WHO III) was lower than in age-matched controls. Hormone replacement therapy produced an increase in bone mineral density in 28 WHO III women, whereas bone mineral density remained quite constant in the women without therapy.
Hormone replacement therapy increases the bone mineral density of women with hypergonadotropic hypogonadic amenorrhea. Hormones should be substituted early and consistently in affected patients. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0015-0282 1556-5653 |
DOI: | 10.1016/S0015-0282(16)54773-6 |