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1
Efavirenz is associated with severe vitamin D deficiency and increased alkaline phosphatase.依非韦伦可导致严重维生素 D 缺乏和碱性磷酸酶升高。
AIDS. 2010 Jul 31;24(12):1923-8. doi: 10.1097/QAD.0b013e32833c3281.
2
Antiretroviral therapy and bone mineral measurements in HIV-infected youths.抗逆转录病毒疗法与 HIV 感染青少年的骨矿物质测量。
Bone. 2010 Jun;46(6):1633-8. doi: 10.1016/j.bone.2010.02.029. Epub 2010 Mar 6.
3
Global vitamin D status and determinants of hypovitaminosis D.全球维生素 D 状况及维生素 D 缺乏症的决定因素。
Osteoporos Int. 2009 Nov;20(11):1807-20. doi: 10.1007/s00198-009-0954-6. Epub 2009 Jun 19.
4
First line zidovudine/lamivudine/lopinavir/ritonavir leads to greater bone loss compared to nevirapine/lopinavir/ritonavir.与奈韦拉平/洛匹那韦/利托那韦相比,一线治疗药物齐多夫定/拉米夫定/洛匹那韦/利托那韦会导致更多的骨质流失。
AIDS. 2009 Jul 17;23(11):1367-76. doi: 10.1097/QAD.0b013e32832c4947.
5
Effect of bimonthly supplementation with oral cholecalciferol on serum 25-hydroxyvitamin D concentrations in HIV-infected children and adolescents.每两个月口服补充胆钙化醇对感染HIV的儿童和青少年血清25-羟维生素D浓度的影响。
Pediatrics. 2009 Jan;123(1):e121-6. doi: 10.1542/peds.2008-0176.
6
The tolerability and biochemical effects of high-dose bolus vitamin D2 and D3 supplementation in patients with vitamin D insufficiency.大剂量冲击补充维生素D2和D3对维生素D缺乏患者的耐受性及生化影响
Scand J Rheumatol. 2009 Mar-Apr;38(2):149-53. doi: 10.1080/03009740802419081.
7
HIV-1 triggers apoptosis in primary osteoblasts and HOBIT cells through TNFalpha activation.HIV-1通过激活肿瘤坏死因子α(TNFα)触发原代成骨细胞和HOBIT细胞凋亡。
J Med Virol. 2008 Sep;80(9):1507-14. doi: 10.1002/jmv.21266.
8
25-Hydroxylation of vitamin D3: relation to circulating vitamin D3 under various input conditions.维生素D3的25-羟化作用:在各种输入条件下与循环维生素D3的关系。
Am J Clin Nutr. 2008 Jun;87(6):1738-42. doi: 10.1093/ajcn/87.6.1738.
9
Optimal serum 25-hydroxyvitamin D levels for multiple health outcomes.多种健康结局的最佳血清25-羟维生素D水平。
Adv Exp Med Biol. 2008;624:55-71. doi: 10.1007/978-0-387-77574-6_5.
10
Pharmacokinetics of a single, large dose of cholecalciferol.单次大剂量胆钙化醇的药代动力学。
Am J Clin Nutr. 2008 Mar;87(3):688-91. doi: 10.1093/ajcn/87.3.688.

补充胆钙化醇和钙对 HIV 感染的儿童和青少年 2 年骨量积累的影响:一项随机临床试验。

Effect of supplementation with cholecalciferol and calcium on 2-y bone mass accrual in HIV-infected children and adolescents: a randomized clinical trial.

机构信息

Sergievsky Center, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.

出版信息

Am J Clin Nutr. 2012 Mar;95(3):678-85. doi: 10.3945/ajcn.111.024786. Epub 2012 Jan 18.

DOI:10.3945/ajcn.111.024786
PMID:22258265
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3278244/
Abstract

BACKGROUND

Skeletal abnormalities have been reported in HIV-infected children and adolescents. Although the etiology is not well understood, vitamin D deficiency may be involved.

OBJECTIVE

The study objective was to evaluate the effect of vitamin D and calcium supplementation on bone mass accrual in HIV-infected youth.

DESIGN

Perinatally HIV-infected children were randomly assigned to receive vitamin D (100,000 IU cholecalciferol given every 2 mo) and calcium (1 g/d) (supplemented group) or double placebo (placebo group) for 2 y. The total-body bone mineral content (TBBMC), total-body bone mineral density (TBBMD), spine bone mineral content (SBMC), and spine bone mineral density (SBMD) were assessed by using dual-energy X-ray absorptiometry at baseline and at 2 annual follow-up visits.

RESULTS

Fifty-nine participants, aged 6-16 y, were randomly assigned to either the supplemented (n = 30) or the placebo (n = 29) group. At enrollment, supplemented and placebo groups did not differ with respect to age, sex, dietary intakes of vitamin D and calcium, mean baseline serum 25-hydroxyvitamin D [25(OH)D] concentration, TBBMC, TBBMD, SBMC, or SBMD. Significant increases in serum 25(OH)D were observed in the supplemented group but not in the placebo group. TBBMC, TBBMD, SBMC, and SBMD increased significantly at 1 and 2 y in both groups. No between-group differences were observed at any time before or after adjustment for stage of sexual maturation by mixed linear model analysis.

CONCLUSION

One gram of calcium per day and oral cholecalciferol at a dosage of 100,000 IU every 2 mo administered to HIV-infected children and adolescents did not affect bone mass accrual despite significant increases in serum 25(OH)D concentrations. This trial was registered at clinicaltrials.gov as NCT00724178.

摘要

背景

HIV 感染的儿童和青少年会出现骨骼异常。虽然病因尚不清楚,但维生素 D 缺乏可能与此相关。

目的

本研究旨在评估补充维生素 D 和钙对 HIV 感染青少年骨量积累的影响。

设计

采用随机分组方法,将经胎盘感染 HIV 的儿童分为补充组(维生素 D10 万 IU,每 2 月 1 次,同时补充 1 g/d 钙)和安慰剂组(接受双倍安慰剂),两组均接受为期 2 年的治疗。在基线和 2 年随访时,采用双能 X 射线吸收法测量全身骨矿物质含量(TBBMC)、全身骨矿物质密度(TBBMD)、脊柱骨矿物质含量(SBMC)和脊柱骨矿物质密度(SBMD)。

结果

59 名 6-16 岁的参与者被随机分配至补充组(n = 30)或安慰剂组(n = 29)。入组时,两组在年龄、性别、维生素 D 和钙的饮食摄入量、基线时的血清 25-羟维生素 D [25(OH)D]浓度、TBBMC、TBBMD、SBMC 或 SBMD 等方面无差异。补充组的血清 25(OH)D 显著升高,而安慰剂组无此变化。两组在 1 年和 2 年时 TBBMC、TBBMD、SBMC 和 SBMD 均显著增加。经混合线性模型分析,在未调整和调整性成熟分期后,两组间任何时间点的上述指标均无差异。

结论

对于 HIV 感染的儿童和青少年,每天补充 1 克钙和每 2 月 1 次口服 10 万 IU 胆钙化醇,尽管血清 25(OH)D 浓度显著升高,但并未影响骨量积累。本试验已在 clinicaltrials.gov 登记,编号为 NCT00724178。