Continuous antiretroviral therapy decreases bone mineral density

被引:178
作者
Grund, Birgit [1 ]
Peng, Grace
Gibert, Cynthia L. [2 ,3 ]
Hoy, Jennifer F. [4 ,5 ]
Isaksson, Rachel L.
Shlay, Judith C. [6 ]
Martinez, Esteban [7 ]
Reiss, Peter [8 ]
Visnegarwala, Fehmida [9 ]
Carr, Andrew D. [10 ,11 ]
机构
[1] Univ Minnesota, Coordinating Ctr Biometr Res, Minneapolis, MN 55414 USA
[2] George Washington Univ, Med Ctr, Washington, DC 20037 USA
[3] Vet Affairs Med Ctr, Washington, DC 20422 USA
[4] Alfred Hosp, Melbourne, Vic, Australia
[5] Monash Univ, Melbourne, Vic 3004, Australia
[6] Denver Publ Hlth, Denver, CO USA
[7] Univ Barcelona, Hosp Clin, Inst Invest Biomed August Pi & Sunyer, Barcelona, Spain
[8] Univ Amsterdam, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
[9] AbsoluteCare Med Ctr & Morehouse Sch Med, Atlanta, GA USA
[10] St Vincents Hosp, Sydney, NSW 2010, Australia
[11] Univ New S Wales, Sydney, NSW, Australia
基金
美国国家卫生研究院;
关键词
antiretroviral therapy; bone mineral density; fracture; HIV; osteoporosis; HIV-INFECTED PATIENTS; RANDOMIZED-TRIAL; BODY-COMPOSITION; NAIVE PATIENTS; FRACTURE RISK; CELL COUNT; MEN; OSTEOPOROSIS; WOMEN; INTERRUPTION;
D O I
10.1097/QAD.0b013e32832c1792
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objectives: To assess the effects of anti retroviral therapy (ART) on bone mineral density (BMD) Design: Randomized comparison of continuous ART (viral suppression group; VS) with intermittent ART (drug conservation group; DC) Setting: Outpatient clinics in the United States, Australia, and Spain. Participants: Participants in the Strategies for Management of Antiretroviral Therapy (SMART) Body Composition substudy. Main outcome measures: Annual hip and spine BMD by dual-energy radiographic absorptiometry (DXA) and spine BMD by quantitative computed tomography (qCT). Methods: Comparisons were by intention-to-treat analysis, using longitudinal models for change in BMD. Risk factors for BMD loss were evaluated. Results: The 214 participants (median 44 years, 19% female participants, 73% on ART; median T-scores -0.5 total hip, -0.7 spine DXA, -0.9 spine qCT; 98 randomized to VS and 116 to DC) were followed for a mean 2.4 years. With continuous ART, BMD declined per year by 0.8% (hip), 0.41% (spine DXA), and 2.41% (spine qCT). BMD declined significantly less with intermittent ART. Estimated DC minus VS group differences in mean BMD change through follow-up were 1.4% [hip; 95% confidence interval (CI) 0.6-2.3; P=0.0021, 1.3% (spine DXA; 95% Cl 0.1-2.4, P=0.03), and 3.0% (spine qCT; 959% Cl 0.8-5.2, P=0.007). No consistent drug-specific association with BMD decline was found. In the parent study, 10 of 2753 participants in the VS group and two of 2720 in the DC group reported serious fractures (hazard ratio 4.9; 95% Cl 1.1-22.5; P=0.04). Conclusion: Continuous ART is associated with decline in BMD and possibly more fractures relative to intermittent, CD4 cell count-guided ART. (C) 2009 Wolters Kluwer Health | Lippincott Williams & Wilkins
引用
收藏
页码:1519 / 1529
页数:11
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