Haskelberg Hila, Mallon Patrick W G, Hoy Jennifer, Amin Janaki, Moore Cecilia, Phanuphak Praphan, Ferret Samuel, Belloso Waldo H, Boyd Mark A, Cooper David A, Emery Sean
*The Kirby Institute, University of New South Wales, Sydney, Australia; †UCD School of Medicine and Medical Science, Dublin, Ireland; ‡The Alfred Hospital, Melbourne, Australia; §Thai Red Cross AIDS Research Center, Bangkok, Thailand; ‖Hopital Saint-Louis, Paris, France; and ¶CICAL, Buenos Aires, Argentina.
J Acquir Immune Defic Syndr. 2014 Oct 1;67(2):161-8. doi: 10.1097/QAI.0000000000000288.
To compare bone mineral density (BMD) changes over 96 weeks in adults virologically failing standard first-line therapy, randomized to raltegravir plus lopinavir/ritonavir (RAL + LPV/r) or conventional 2-3 nucleoside/nucleotide reverse transcriptase inhibitors [N(t)RTIs] + LPV/r second-line therapy.
Participants underwent dual-energy x-ray absorptiometry at baseline and weeks 48 and 96 to measure total hip and lumbar spine BMD. Analyses were adjusted for gender, body mass index, and smoking. Linear regression was used to compare between-group differences, logistic regression for low BMD (hip or spine Z-score ≤ -2) incidence, and multivariate linear regression to determine predictors of BMD change. This work represents the extension and final results of the previously published initial 48 weeks of the study.
The population included 210 adults from 5 middle-income countries: 52% females, 52% Asians, 43% Africans, mean age, 39 years (SD, 8 years). In the 2-3 N(t)RTI group (vs. RAL), BMD reduction was greater at the spine (mean change, -4.9% vs. -3.5%; adjusted difference, -1.9%; 95% confidence interval: -3.3 to -0.5%, P = 0.009) and hip (-4.1% vs. -2.2%; -1.9%; -3.4 to -0.4; P = 0.012). BMD decrease was greatest at 48 weeks with stabilization to week 96. Overall, low BMD occurred in 15 participants (7.9%), with no between-group differences. Independent predictors for bone loss included lower body mass index (regression coefficient: hip, -0.18% and spine, -0.26% per 1 kg/m), longer tenofovir exposure (hip, -0.74% and spine, -1.0% per year), greater change in CD4 to week 12 (hip, -5.11% per 10-fold higher), and higher baseline HIV-RNA (spine, -0.7% per 10-fold higher).
Over 96 weeks, there was greater BMD decrease with 2-3 N(t)RTI + LPV/r compared with RAL + LPV/r; the relative decrease at the spine was greater than the hip. BMD decreases with second-line antiretroviral therapy largely occurred in the first 48 weeks with stabilization, but no recovery thereafter.
比较病毒学上一线标准治疗失败的成年人在随机接受raltegravir联合洛匹那韦/利托那韦(RAL + LPV/r)或传统的2 - 3种核苷/核苷酸逆转录酶抑制剂[N(t)RTIs] + LPV/r二线治疗后96周内的骨矿物质密度(BMD)变化。
参与者在基线、第48周和第96周接受双能X线吸收测定法,以测量全髋和腰椎的BMD。分析针对性别、体重指数和吸烟情况进行了调整。采用线性回归比较组间差异,采用逻辑回归分析低BMD(髋部或脊柱Z评分≤ -2)的发生率,并采用多元线性回归确定BMD变化的预测因素。这项工作代表了先前发表的该研究最初48周的扩展和最终结果。
该人群包括来自5个中等收入国家的210名成年人:52%为女性,52%为亚洲人,43%为非洲人,平均年龄39岁(标准差8岁)。在2 - 3种N(t)RTI组(与RAL组相比),脊柱的BMD降低幅度更大(平均变化,-4.9%对-3.5%;调整后差异,-1.9%;95%置信区间:-3.3至-0.5%,P = 0.009),髋部也是如此(-4.1%对-2.2%;-1.9%;-3.4至-0.4;P = 0.012)。BMD下降在第48周时最大,到第96周稳定下来。总体而言,15名参与者(7.9%)出现低BMD,组间无差异。骨质流失的独立预测因素包括较低的体重指数(回归系数:髋部,每1 kg/m降低-0.18%,脊柱降低-0.26%)、替诺福韦暴露时间更长(髋部,每年降低-0.74%,脊柱降低-1.0%)、到第12周时CD4变化更大(髋部,每高10倍降低-5.11%)以及更高的基线HIV - RNA(脊柱,每高10倍降低-0.7%)。
在96周内,与RAL + LPV/r相比,2 - 3种N(t)RTI + LPV/r导致的BMD下降幅度更大;脊柱的相对下降幅度大于髋部。二线抗逆转录病毒治疗导致的BMD下降主要发生在最初48周内,之后稳定下来,但此后没有恢复。