Dravid Ameet, Kulkarni Milind, Borkar Amit, Dhande Sachin
HIV Medicine, Ruby Hall Clinic, Pune, India.
J Int AIDS Soc. 2014 Nov 2;17(4 Suppl 3):19567. doi: 10.7448/IAS.17.4.19567. eCollection 2014.
Bone mineral density (BMD) assessment in HIV patients is sparsely done in resource limited settings.
We conducted a cross-sectional study of BMD amongst HIV patients following up in our clinic from 1 June to 1 December 2013 by performing dual-energy X-ray absorptiometry scan (Lunar Prodigy Advanced DXA System, GE Healthcare) of lumbar spine and hip. Patients on long term (≥12 months), virologically suppressive antiretroviral therapy (ART) were included. Patients who were ART naïve were included as control population. Virologic failures were excluded. Low BMD was defined by WHO T-score criteria (normal: T score ≥-1;osteopenia: T score between -1 and -2.5 SD; osteoporosis: T score ≤-2.5 SD). Baseline risk factors associated with low BMD like age, low BMI, lipoatrophy, diabetes mellitus, current smoking, current alcohol intake, steroid exposure and menopause were recorded. ART-related factors associated with low BMD like ART duration, exposure to tenofovir and exposure to protease inhibitors (PI) were studied.
A total of 536 patients (66% males, 496 ART experienced and 40 ART naïve) were included in this analysis. Median age was 42 years, mean BMI 23.35 kg/m(2) and median CD4 count 146 cells/mm(3). All ART experienced patients had plasma viral load<400 copies/ml.
Extremely high prevalence of accelerated BMD loss amongst ART naïve and ART experienced patients in our cohort is a matter of deep concern due to its association with pathological fractures. Bone mineral loss was seen irrespective of ART used. Association of low BMD with low baseline CD4 count strengthens the case for early ART.
在资源有限的环境中,对HIV患者进行骨矿物质密度(BMD)评估的情况很少。
我们于2013年6月1日至12月1日在我们诊所对HIV患者进行了一项BMD横断面研究,通过对腰椎和髋部进行双能X线吸收测定扫描(GE医疗的Lunar Prodigy Advanced DXA系统)。纳入长期(≥12个月)接受病毒学抑制抗逆转录病毒治疗(ART)的患者。将未接受过ART的患者作为对照人群。排除病毒学失败的患者。低BMD根据世界卫生组织T评分标准定义(正常:T评分≥-1;骨量减少:T评分在-1至-2.5标准差之间;骨质疏松症:T评分≤-2.5标准差)。记录与低BMD相关的基线风险因素,如年龄、低体重指数、脂肪萎缩、糖尿病、当前吸烟、当前饮酒、类固醇暴露和绝经情况。研究与低BMD相关的ART因素,如ART疗程、替诺福韦暴露和蛋白酶抑制剂(PI)暴露情况。
本分析共纳入536例患者(66%为男性,496例有ART治疗经历,40例未接受过ART)。中位年龄为42岁,平均体重指数为23.35kg/m²,中位CD4细胞计数为146个/mm³。所有有ART治疗经历的患者血浆病毒载量均<400拷贝/ml。
在我们的队列中,未接受过ART和有ART治疗经历的患者中BMD加速丢失的患病率极高,因其与病理性骨折相关,这是一个令人深感担忧的问题。无论使用何种ART,均观察到骨矿物质丢失。低BMD与低基线CD4细胞计数之间的关联强化了早期进行ART治疗的理由。