Klassen K M, Kimlin M G, Fairley C K, Emery S, Anderson P H, Ebeling P R
Department of Medicine, University of Melbourne, Victoria, 3021, Australia.
Melbourne Sexual Health Centre, Alfred Health, 580 Swanston Street, Carlton, Melbourne, Victoria, Australia.
Osteoporos Int. 2016 May;27(5):1737-45. doi: 10.1007/s00198-015-3432-3. Epub 2015 Dec 11.
To see if vitamin D and antiretroviral therapy are associated with bone mineral density (BMD) in people with HIV.
Lower hip BMD was associated with tenofovir (an antiretroviral medicine) in those with 25(OH)D ≥50 nmol/L.
The relationship between antiretroviral therapy and hip BMD differs depending on vitamin D status.
People with HIV have an increased risk of low BMD and fractures. Antiretroviral therapy contributes to this increased risk. The aim of this study was to evaluate associations between vitamin D metabolites and antiretroviral therapy on BMD.
The simplification of antiretroviral therapy with tenofovir-emtricitabine or abacavir-lamivudine trial (STEAL) was an open-label, prospective randomised non-inferiority study that compared simplification of current nucleoside reverse transcriptase inhibitors (NRTIs) to fixed-dose combination tenofovir-emtricitabine (TDF-FTC) or abacavir-lamivudine. Serum 25(OH)D and 1,25(OH)2D were measured in 160 individuals (90 receiving TDF-FTC, 70 receiving other NRTIs) at baseline from this study. Multivariable linear regression models were constructed to evaluate the covariates of 1,25(OH)2D and BMD.
Protease inhibitor use (p = 0.02) and higher body mass index (BMI) (p = 0.002) were associated with lower 1,25(OH)2D levels in those with 25(OH)D <50 nmol/L. However, TDF-FTC use (p = 0.01) was associated with higher 1,25(OH)2D levels, but only in those with 25(OH)D ≥50 nmol/L. White ethnicity (p = 0.02) and lower BMI (p < 0.001) in those with 25(OH)D <50 nmol/L and with TDF-FTC use (p = 0.008) in those with 25(OH)D ≥50 nmol/L were associated with lower hip BMD. TDF-FTC use, higher serum calcium and serum βCTX, winter, and lower bone-specific alkaline phosphatase (BALP) and BMI were associated with lower lumbar spine BMD.
TDF-FTC use (versus non-TDF-FTC use) was associated with lower hip BMD, and this difference was more pronounced in those with 25(OH)D ≥50 nmol/L. Serum 25(OH)D <50 nmol/L was associated with lower hip BMD in all participants. Therefore, the associations between antiretroviral therapy and hip BMD differ depending on vitamin D status.
研究维生素D和抗逆转录病毒疗法是否与HIV感染者的骨矿物质密度(BMD)相关。
在25(OH)D≥50 nmol/L的人群中,较低的髋部骨密度与替诺福韦(一种抗逆转录病毒药物)相关。
抗逆转录病毒疗法与髋部骨密度之间的关系因维生素D状态而异。
HIV感染者发生低骨密度和骨折的风险增加。抗逆转录病毒疗法导致了这种风险的增加。本研究的目的是评估维生素D代谢物与抗逆转录病毒疗法对骨密度的关联。
替诺福韦-恩曲他滨或阿巴卡韦-拉米夫定简化抗逆转录病毒疗法试验(STEAL)是一项开放标签、前瞻性随机非劣效性研究,该研究比较了将当前核苷类逆转录酶抑制剂(NRTIs)简化为固定剂量组合的替诺福韦-恩曲他滨(TDF-FTC)或阿巴卡韦-拉米夫定。在本研究基线时,对160名个体(90名接受TDF-FTC治疗,70名接受其他NRTIs治疗)进行血清25(OH)D和1,25(OH)2D检测。构建多变量线性回归模型以评估1,25(OH)2D和骨密度的协变量。
在25(OH)D<50 nmol/L的人群中,使用蛋白酶抑制剂(p = 0.02)和较高的体重指数(BMI)(p = 0.002)与较低的1,25(OH)2D水平相关。然而,仅在25(OH)D≥50 nmol/L的人群中,使用TDF-FTC(p = 0.01)与较高的1,25(OH)2D水平相关。在25(OH)D<50 nmol/L的人群中,白人种族(p = 0.02)和较低的BMI(p<0.001)以及在25(OH)D≥50 nmol/L的人群中使用TDF-FTC(p = 0.008)与较低的髋部骨密度相关。使用TDF-FTC、较高的血清钙和血清βCTX、冬季以及较低的骨特异性碱性磷酸酶(BALP)和BMI与较低的腰椎骨密度相关。
使用TDF-FTC(与不使用TDF-FTC相比)与较低的髋部骨密度相关,并且这种差异在25(OH)D≥50 nmol/L的人群中更为明显。在所有参与者中,血清25(OH)D<50 nmol/L与较低的髋部骨密度相关。因此,抗逆转录病毒疗法与髋部骨密度之间的关联因维生素D状态而异。