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维生素D代谢物、抗逆转录病毒疗法与HIV感染者骨矿物质密度之间的关联。

Associations between vitamin D metabolites, antiretroviral therapy and bone mineral density in people with HIV.

作者信息

Klassen K M, Kimlin M G, Fairley C K, Emery S, Anderson P H, Ebeling P R

机构信息

Department of Medicine, University of Melbourne, Victoria, 3021, Australia.

Melbourne Sexual Health Centre, Alfred Health, 580 Swanston Street, Carlton, Melbourne, Victoria, Australia.

出版信息

Osteoporos Int. 2016 May;27(5):1737-45. doi: 10.1007/s00198-015-3432-3. Epub 2015 Dec 11.

Abstract

RATIONALE

To see if vitamin D and antiretroviral therapy are associated with bone mineral density (BMD) in people with HIV.

RESULT

Lower hip BMD was associated with tenofovir (an antiretroviral medicine) in those with 25(OH)D ≥50 nmol/L.

SIGNIFICANCE

The relationship between antiretroviral therapy and hip BMD differs depending on vitamin D status.

INTRODUCTION

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.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

原理

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。

结果

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。

意义

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。

引言

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。

方法

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。

结果

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。

结论

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。

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