期刊
OSTEOPOROSIS INTERNATIONAL
卷 18, 期 10, 页码 1345-1353出版社
SPRINGER LONDON LTD
DOI: 10.1007/s00198-007-0428-7
关键词
bone mineral density; case-population-control; fragility fractures; HIV positive; premenopausal; women
This Canadian study of bone health showed that HIV+ women were more likely to have had fragility fractures (OR 1.7) but had BMD values that were not different than women from a national population-based cohort. Introduction Given that 17.5 million women globally are HIV-infected and living longer on anti-retroviral therapy (ART+), it is essential to determine whether they are at risk for osteoporosis as is currently assumed. Methods Assessment of osteoporosis risk factors and lifetime low-trauma (fragility) fracture history used a common interviewer-administered questionnaire and phantom-adjusted bone mineral density (BMD). This study compared HIV+ Canadian women with age- and region-matched control women (1:3) from a national population-based study of osteoporosis. Results One hundred and thirty-eight HIV+ women ( 100 ART+,38 ART-) were compared with 402 controls. There were no differences in age (37.7 vs. 38.0 years), BMI ( 25.0 vs. 26.2), family history of osteoporosis, exercise history, alcohol or calcium intakes, age at menarche, oral contraceptive use or parity. HIV+ cases included more Aboriginal and Black women ( 12.5% and 16.2 vs. 2% and 1%, respectively), smoked and used injection drugs (53%) more, were more often treated with glucocorticoids, had oligomenorrhea, and reported 10-kg weight cycling. Significantly more HIV+ women reported lifetime fragility fractures (26.1% vs. 17.3; OR 1.7, 95% CI 1.1, 2.6). HIV+ and control women did not differ in BMD: spine 1.0 +/- 0.12 vs. 1.0 +/- 0.14 g/ cm(2) ( diff. 0.0, 95% CI - 0.27, 0.27) or total femur 0.91 +/- 0.15 vs. 0.93 +/- 0.12 g/ cm2 ( diff 0.02, 95% CI + 0.005, - 0.045). Conclusion HIV+ women reported significantly more past osteoporotic fractures than population-based controls despite normal BMD. Research is needed to assess bone microarchitecture and develop a reliable fracture risk assessment tool for HIV+ women.
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