Cited by 67Bone health and osteoporosis researchMenopause: Health Impacts and TreatmentsEstrogen and related hormone effects

Endogenous Levels of Serum Estradiol and Sex Hormone Binding Globulin Determine Bone Mineral Density, Bone Remodeling, the Rate of Bone Loss, and Response to Treatment with Estrogen in Elderly Women

Rapuri, Prema B., Gallagher, J. Christopher, Haynatzki, Gleb·2004·The Journal of Clinical Endocrinology & Metabolism

Abstract

A total of 489 elderly women aged 65-75 yr who participated in a 3-yr, randomized, blinded osteoporosis trial underwent measurements of serum estradiol, bioavailable estradiol, and SHBG. At baseline, bone mineral density (BMD) was lower at the femoral sites (7-19%, P 165 nmol/liter), compared with women in the highest tertiles of total estradiol [>13.3 pg/ml (49 pmol/liter)] and bioavailable estradiol [>4 pg/ml (14 pmol/liter)] or lowest tertile for SHBG (<113 nmol/liter). Bone markers were increased in women in the lowest tertile for serum total estradiol (not significant) and bioavailable estradiol (P < 0.05) and highest tertile for SHBG (P < 0.05). In the longitudinal study, the rate of bone loss in the placebo group was significantly higher in total body (P < 0.05) and spine (P < 0.05) in women in the lowest tertile, compared with the highest tertile of serum bioavailable estradiol. After treatment with conjugated equine estrogens 0.625 mg/d, the increase in BMD was 4-6% higher at the femoral sites (P < 0.05), total body (P < 0.05), and spine (not significant), in the lowest tertile, compared with the highest tertile of serum bioavailable estradiol or highest tertile, compared with the lowest tertile of serum SHBG. In summary, small variations in endogenous serum estradiol and high serum SHBG determine differences in BMD and rate of bone loss in elderly women and also affect the response to treatment with estrogen. Women with a serum estradiol level of less than 9 pg/ml (…

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Crossref · 10.1210/jc.2004-0434

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Authors
Rapuri, P. B., Gallagher, J. C., & Haynatzki, G.
Affiliations
Creighton University (US)
Corresponding author
Rapuri, Prema B.
Venue
The Journal of Clinical Endocrinology & Metabolism
Published
2004-10
Volume
89
Issue
10
Pages
4954-4962
ISSN
  • 0021-972X (ISSN-L)
  • 1945-7197
OpenAlex
W2035163399
Cited by
67
References
1
Citations by year
2026: 1 · 2024: 2 · 2023: 3 · 2022: 2 · 2021: 4 · 2020: 1 · 2019: 3 · 2018: 1 · 2017: 1 · 2016: 1 · 2015: 4 · 2014: 2 · 2013: 2 · 2012: 2
FWCI
7.13
Type
journal article
Language
en
Open access
closed
Locations
  • The Journal of Clinical Endocrinology & Metabolism (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (5r01ag010358-05, 5u01ag010373-08)
  • National Institute on Aging (R01AG10358, UO1-AG10373)
Topics
  • Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Menopause: Health Impacts and Treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Estrogen and related hormone effects
Keywords
serum estradiol, sex hormone-binding globulin, bioavailable estradiol, bone mineral density, bone loss, bone remodeling, bone turnover markers, osteoporosis, conjugated equine estrogens, older women, menopause, postmenopausal osteoporosis, femoral bone density, spine bone density
MeSH terms
Aged, Estradiol, Female, Humans, Longitudinal Studies, Osteoporosis, Sex Hormone-Binding Globulin, Bone Density, Estrogen Replacement Therapy, Bone Remodeling

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