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Erschienen in: Osteoporosis International 11/2005

01.11.2005 | Original Article

Bone mass and mineral metabolism in HIV+ postmenopausal women

verfasst von: Michael Yin, Jay Dobkin, Karen Brudney, Carolyn Becker, Janis L. Zadel, Monica Manandhar, Vicki Addesso, Elizabeth Shane

Erschienen in: Osteoporosis International | Ausgabe 11/2005

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Abstract

The objective of this cross-sectional study was to estimate the prevalence of and risk factors for osteoporosis in HIV+ postmenopausal women. Bone mineral density (BMD) by dual energy X-ray absorptiometry (DXA) and biochemical indices of mineral metabolism were measured in 31 Hispanic and African American HIV+ postmenopausal women. BMD was compared with 186 historical controls, matched for age, ethnicity and postmenopausal status. Mean BMD was significantly lower at the lumbar spine and total hip in the HIV+ group, as compared with controls. Prevalence of osteoporosis was higher in the HIV+ group than controls at the lumbar spine (42% vs 23%, p =0.03) and total hip (10% vs 1%, p =0.003). Among HIV+ women, time since menopause and weight were significant predictors of BMD, while duration or class of antiretroviral therapy (ART), AIDS diagnosis, nadir CD4, steroid use, and vitamin D deficiency were not. Prevalence of osteoporosis is substantially higher in HIV+ Hispanic and African-American postmenopausal women than in controls. Established osteoporosis risk factors were more important in predicting BMD than factors associated with HIV infection and ART. Long-term management of the growing female HIV population should include the evaluation for and management of osteoporosis.
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Metadaten
Titel
Bone mass and mineral metabolism in HIV+ postmenopausal women
verfasst von
Michael Yin
Jay Dobkin
Karen Brudney
Carolyn Becker
Janis L. Zadel
Monica Manandhar
Vicki Addesso
Elizabeth Shane
Publikationsdatum
01.11.2005
Verlag
Springer-Verlag
Erschienen in
Osteoporosis International / Ausgabe 11/2005
Print ISSN: 0937-941X
Elektronische ISSN: 1433-2965
DOI
https://doi.org/10.1007/s00198-005-1845-0

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