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抗逆转录病毒治疗起始后的骨折。

Fractures after antiretroviral initiation.

机构信息

Department of Medicine, Columbia University Medical Center, New York, NY 10032, USA.

出版信息

AIDS. 2012 Nov 13;26(17):2175-84. doi: 10.1097/QAD.0b013e328359a8ca.

Abstract

BACKGROUND

Bone mineral density declines by 2-6% within 1-2 years after initiation of antiretroviral therapy (ART); however, it is uncertain whether this results in an immediate or cumulative increase in fracture rates.

METHODS

We evaluated the incidence and predictors of fracture in 4640 HIV-positive participants from 26 randomized ART studies followed in the AIDS Clinical Trials Group (ACTG) Longitudinal-Linked Randomized Trial study for a median of 5 years. Fragility and nonfragility fractures were recorded prospectively at semiannual visits. Incidence was calculated as fractures/total person-years. Cox proportional hazards models evaluated effects of traditional fracture risks, HIV disease characteristics, and ART exposure on fracture incidence.

RESULTS

Median (interquartile range) age was 39 (33, 45) years; 83% were men, 48% white, and median nadir CD4 cell count was 187 (65, 308) cells/μl. Overall, 116 fractures were reported in 106 participants with median time-to-first fracture of 2.3 years. Fracture incidence was 0.40 of 100 person-years among all participants and 0.38 of 100 person-years among 3398 participants who were ART naive at enrollment into ACTG parent studies. Among ART-naive participants, fracture rates were higher within the first 2 years after ART initiation (0.53/100 person-years) than subsequent years (0.30/100 person-years). In a multivariate analysis of ART-naive participants, increased hazard of fracture was associated with current smoking and glucocorticoid use but not with exposure to specific antiretrovirals.

CONCLUSION

Fracture rates were higher within the first 2 years after ART initiation, relative to subsequent years. However, continuation of ART was not associated with increasing fracture rates in these relatively young HIV-positive individuals.

摘要

背景

开始抗逆转录病毒治疗(ART)后 1-2 年内,骨矿物质密度会下降 2-6%;然而,目前尚不清楚这是否会导致骨折发生率的即刻或累积增加。

方法

我们评估了 4640 名来自 26 项随机 ART 研究的 HIV 阳性参与者在 AIDS 临床试验组(ACTG)纵向链接随机试验研究中的骨折发生率和预测因素,中位随访时间为 5 年。在半年一次的就诊时前瞻性记录脆性和非脆性骨折。发生率以骨折/总人年计算。Cox 比例风险模型评估了传统骨折风险、HIV 疾病特征和 ART 暴露对骨折发生率的影响。

结果

中位(四分位距)年龄为 39(33,45)岁;83%为男性,48%为白人,中位最低 CD4 细胞计数为 187(65,308)细胞/μl。总体而言,106 名参与者中有 116 名报告了骨折,首次骨折的中位时间为 2.3 年。所有参与者的骨折发生率为 0.40/100 人年,而在 ACTG 母研究入组时即未接受 ART 的 3398 名参与者中,骨折发生率为 0.38/100 人年。在未接受 ART 的参与者中,ART 起始后前 2 年的骨折发生率(0.53/100 人年)高于随后几年(0.30/100 人年)。在未接受 ART 的参与者的多变量分析中,骨折风险增加与当前吸烟和使用糖皮质激素有关,但与特定抗逆转录病毒药物的暴露无关。

结论

与随后几年相比,ART 起始后前 2 年骨折发生率较高。然而,在这些相对年轻的 HIV 阳性个体中,继续接受 ART 治疗与骨折发生率的增加无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d59/3652631/8668cf0ac962/nihms456532f1.jpg

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Fractures after antiretroviral initiation.抗逆转录病毒治疗起始后的骨折。
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