Sharma Anjali, Shi Qiuhu, Hoover Donald R, Anastos Kathryn, Tien Phyllis C, Young Mary A, Cohen Mardge H, Golub Elizabeth T, Gustafson Deborah, Yin Michael T
*Department of Medicine, Albert Einstein College of Medicine, Bronx, NY; †Department of Epidemiology and Community Health, New York Medical College, Valhalla, NY; ‡Department of Statistics and Biostatistics, Rutgers University, Piscataway, NJ; §Division of Infectious Diseases, University of California at San Francisco and San Francisco Veterans Affairs Medical Center, San Francisco, CA; ‖Department of Medicine, Georgetown University School of Medicine, Washington, DC; ¶Department of Medicine, Stroger (formerly Cook County) Hospital and Rush University, Chicago, IL; #Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; **Department of Neurology, State University of New York Downstate Medical Center, Brooklyn, NY; and ††Division of Infectious Diseases, Columbia University Medical Center, New York, NY.
J Acquir Immune Defic Syndr. 2015 Sep 1;70(1):54-61. doi: 10.1097/QAI.0000000000000674.
We previously reported that fracture incidence rates did not differ by HIV status among predominantly premenopausal Women's Interagency HIV Study participants. We now conduct a follow-up study with 5 additional observation years to further characterize fracture risk associated with HIV infection in women as they age.
We measured time to first new fracture at any site in 2375 (1713 HIV-infected and 662 HIV-uninfected) Women's Interagency HIV Study participants, with median 10-year follow-up. Fractures were self-reported semiannually. Proportional hazards models assessed predictors of incident fracture.
At index visit, HIV-infected women were older [median age of 40 years (IQR: 34-46) vs. 35 (27-43), P < 0.0001] and more likely to be postmenopausal, hepatitis C virus infected, and weigh less than HIV-uninfected women. Among HIV-infected women, mean CD4 count was 480 cells per microliter and 63% were taking highly active antiretroviral therapy. Unadjusted incidence rates of any fracture were higher in HIV-infected than in HIV-uninfected women [2.19/100 person-years (py) vs. 1.54/100 py, P = 0.002]. In multivariate models, HIV status, older age, white (vs. black) race, prior fracture, history of cocaine use, and history of injection drug use were significant predictors of incident fracture. Among HIV-infected women, age, white race, prior fracture, smoking, and prior AIDS were predictors of new fracture.
Middle-aged HIV-infected women had a higher adjusted fracture rate than HIV-uninfected women. Cocaine use and injection drug use were also associated with a greater risk of incident fracture. Further research is needed to understand whether the risk of fracture associated with cocaine use relates to increased rate of falls or direct effects on bone metabolism.
我们之前报道过,在主要为绝经前女性的机构间HIV研究参与者中,骨折发生率在HIV感染状态不同的人群间并无差异。我们现在开展一项后续研究,增加5年的观察期,以进一步描述随着年龄增长,HIV感染女性的骨折风险特征。
我们在2375名(1713名HIV感染女性和662名未感染HIV女性)机构间HIV研究参与者中测量了首次出现任何部位新骨折的时间,随访时间中位数为10年。骨折情况每半年由参与者自行报告一次。比例风险模型评估了骨折发生的预测因素。
在首次就诊时,HIV感染女性年龄更大[中位年龄40岁(四分位间距:34 - 46岁),而未感染HIV女性为35岁(27 - 43岁),P < 0.0001],更可能处于绝经后状态、感染丙型肝炎病毒,且体重低于未感染HIV的女性。在HIV感染女性中,平均CD4细胞计数为每微升480个细胞,63%的女性正在接受高效抗逆转录病毒治疗。HIV感染女性中任何骨折的未调整发生率高于未感染HIV的女性[2.19/100人年(py)对1.54/100 py,P = 0.002]。在多变量模型中,HIV感染状态、年龄较大、白人(与黑人相比)种族、既往骨折史、使用可卡因史以及注射吸毒史是骨折发生的显著预测因素。在HIV感染女性中,年龄、白人种族、既往骨折史、吸烟以及既往艾滋病史是新骨折的预测因素。
中年HIV感染女性经调整后的骨折发生率高于未感染HIV的女性。使用可卡因和注射吸毒也与骨折发生风险增加有关。需要进一步研究以了解与使用可卡因相关的骨折风险是否与跌倒发生率增加或对骨代谢的直接影响有关。