Haskelberg Hila, Pocock Nicholas, Amin Janaki, Ebeling Peter Robert, Emery Sean, Carr Andrew, Allworth Anthony
The Kirby Institute, University of New South Wales, Sydney, Australia.
St. Vincent's Hospital, Sydney, Australia.
PLoS One. 2014 Apr 10;9(4):e94858. doi: 10.1371/journal.pone.0094858. eCollection 2014.
Therapy with tenofovir is associated with lower bone mineral density (BMD), higher markers of bone turnover and increased fracture risk in HIV-infected adults. Bone structural parameters generated by hip structural analysis may represent a separate measure of bone strength, but have not been assessed in HIV.
Dual-energy X-ray absorptiometry (DXA) scans from 254 HIV-infected adults randomised to simplify their existing dual nucleoside analogue reverse transcriptase inhibitor therapy to coformulated tenofovir-emtricitabine or abacavir-lamivudine were analysed using DXA-derived hip structural analysis software. Hip structural parameters included femoral strength index, section modulus, cross-sectional area, and cross-sectional moment of inertia. We used one-way ANOVA to test the relationship between nucleoside analogue type at baseline and structural parameters, multivariable analysis to assess baseline covariates associated with femoral strength index, and t-tests to compare mean change in structural parameters over 96 weeks between randomised groups.
Participants taking tenofovir at baseline had lower section modulus (-107.3 mm2, p = 0.001), lower cross-sectional area (-15.01 mm3, p = 0.001), and lower cross-sectional moment of inertia (-2,036.8 mm4, p = 0.007) than those receiving other nucleoside analogues. After adjustment for baseline risk factors, the association remained significant for section modulus (p = 0.008) and cross-sectional area (p = 0.002). Baseline covariates significantly associated with higher femoral strength index were higher spine T-score (p = 0.001), lower body fat mass (p<0.001), lower bone alkaline phosphatase (p = 0.025), and higher osteoprotegerin (p = 0.024). Hip structural parameters did not change significantly over 96 weeks and none was significantly affected by treatment simplification to tenofovir-emtricitabine or abacavir-lamivudine.
In this population, tenofovir use was associated with reduced composite indices of bone strength as measured by hip structural analysis, but none of the structural parameters improved significantly over 96 weeks with tenofovir cessation.
ClinicalTrials.gov NCT00192634.
在感染HIV的成年人中,替诺福韦治疗与较低的骨矿物质密度(BMD)、较高的骨转换标志物以及骨折风险增加有关。通过髋部结构分析得出的骨结构参数可能代表了一种独立的骨强度测量方法,但尚未在HIV患者中进行评估。
使用基于双能X线吸收法(DXA)的髋部结构分析软件,对254名感染HIV的成年人的DXA扫描结果进行分析。这些成年人被随机分组,将现有的双核苷类似物逆转录酶抑制剂治疗简化为复方替诺福韦-恩曲他滨或阿巴卡韦-拉米夫定。髋部结构参数包括股骨强度指数、截面模量、横截面积和截面惯性矩。我们使用单因素方差分析来检验基线时核苷类似物类型与结构参数之间的关系,使用多变量分析来评估与股骨强度指数相关的基线协变量,并使用t检验来比较随机分组之间96周内结构参数的平均变化。
与接受其他核苷类似物的参与者相比,基线时服用替诺福韦的参与者的截面模量较低(-107.3平方毫米,p = 0.001)、横截面积较低(-15.01立方毫米,p = 0.001)以及截面惯性矩较低(-2036.8四次方毫米,p = 0.007)。在对基线风险因素进行调整后,截面模量(p = 0.008)和横截面积(p = 0.002)的关联仍然显著。与较高的股骨强度指数显著相关的基线协变量包括较高的脊柱T值(p = 0.001)、较低的体脂肪量(p<0.001)、较低的骨碱性磷酸酶(p = 0.025)以及较高的骨保护素(p = 0.024)。髋部结构参数在96周内没有显著变化,简化为替诺福韦-恩曲他滨或阿巴卡韦-拉米夫定的治疗对其均无显著影响。
在该人群中,通过髋部结构分析测量,使用替诺福韦与骨强度复合指数降低有关,但在停用替诺福韦的96周内,没有一个结构参数有显著改善。
ClinicalTrials.gov NCT00192634。