Eckard Allison Ross, OʼRiordan Mary Ann, Rosebush Julia C, Ruff Joshua H, Chahroudi Ann, Labbato Danielle, Daniels Julie E, Uribe-Leitz Monika, Tangpricha Vin, McComsey Grace A
*Department of Pediatrics and Medicine, Divisions of Infectious Diseases, Medical University of South Carolina, Charleston, SC; †Department of Pediatrics, Division of Infectious Diseases, Emory University School of Medicine, Atlanta, GA; ‡Department of Pediatrics, Division of Infectious Diseases, Case Western Reserve University, Rainbow Babies & Children's Hospital, Cleveland, OH; and §Department of Medicine, Division of Endocrinology, Metabolism and Lipids.
J Acquir Immune Defic Syndr. 2017 Dec 15;76(5):539-546. doi: 10.1097/QAI.0000000000001545.
Low bone mineral density (BMD) is a significant comorbidity in HIV. However, studies evaluating vitamin D supplementation on bone health in this population are limited. This study investigates changes in bone health parameters after 12 months of supplementation in HIV-infected youth with vitamin D insufficiency.
This is a randomized, active-control, double-blind trial investigating changes in bone parameters with 3 different vitamin D3 doses [18,000 (standard/control dose), 60,000 (moderate dose), and 120,000 IU/monthly (high dose)] in HIV-infected youth 8-25 years old with baseline serum 25-hydroxyvitamin D (25(OH)D) concentrations <30 ng/mL. BMD and bone turnover markers were measured at baseline and 12 months.
One hundred two subjects enrolled. Over 12 months, serum 25(OH)D concentrations increased with all doses, but the high dose (ie, 120,000 IU/monthly) maintained serum 25(OH)D concentrations in an optimal range (≥30 or ≥20 ng/mL) throughout the study period for more subjects (85% and 93%, respectively) compared with either the moderate (54% and 88%, respectively) or standard dose (63% and 80%, respectively). All dosing groups showed some improvement in BMD; however, only the high-dose arm showed significant decreases in bone turnover markers for both procollagen type 1 aminoterminal propeptide (-3.7 ng/mL; P = 0.001) and Β-CrossLaps (-0.13 ng/mL; P = 0.0005).
High-dose vitamin D supplementation (120,000 IU/mo) given over 12 months decreases bone turnover markers in HIV-infected youth with vitamin D insufficiency, which may represent an early, beneficial effect on bone health. High vitamin D doses are needed to maintain optimal serum 25(OH)D concentrations.
低骨矿物质密度(BMD)是HIV患者的一种重要合并症。然而,评估维生素D补充剂对该人群骨骼健康影响的研究有限。本研究调查了维生素D不足的HIV感染青年补充维生素D 12个月后骨骼健康参数的变化。
这是一项随机、活性对照、双盲试验,研究8至25岁、基线血清25-羟基维生素D(25(OH)D)浓度<30 ng/mL的HIV感染青年使用3种不同剂量的维生素D3[18,000(标准/对照剂量)、60,000(中等剂量)和120,000 IU/月(高剂量)]后骨骼参数的变化。在基线和12个月时测量骨密度和骨转换标志物。
102名受试者入组。在12个月期间,所有剂量的血清25(OH)D浓度均升高,但高剂量组(即120,000 IU/月)在整个研究期间使更多受试者(分别为85%和93%)的血清25(OH)D浓度维持在最佳范围(≥30或≥20 ng/mL),相比中等剂量组(分别为54%和88%)或标准剂量组(分别为63%和80%)。所有给药组的骨密度均有一定改善;然而,只有高剂量组的I型前胶原氨基端前肽(-3.7 ng/mL;P = 0.001)和β-交联C端肽(-0.13 ng/mL;P = 0.0005)这两种骨转换标志物显著下降。
维生素D不足的HIV感染青年补充高剂量维生素D(120,000 IU/月)12个月可降低骨转换标志物,这可能对骨骼健康具有早期有益作用。需要高剂量维生素D来维持最佳血清25(OH)D浓度。