Global and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australia.
PLoS One. 2013 Aug 14;8(8):e70032. doi: 10.1371/journal.pone.0070032. eCollection 2013.
Vitamin D (vitD) and L-arginine have important antimycobacterial effects in humans. Adjunctive therapy with these agents has the potential to improve outcomes in active tuberculosis (TB).
In a 4-arm randomised, double-blind, placebo-controlled factorial trial in adults with smear-positive pulmonary tuberculosis (PTB) in Timika, Indonesia, we tested the effect of oral adjunctive vitD 50,000 IU 4-weekly or matching placebo, and L-arginine 6.0 g daily or matching placebo, for 8 weeks, on proportions of participants with negative 4-week sputum culture, and on an 8-week clinical score (weight, FEV1, cough, sputum, haemoptysis). All participants with available endpoints were included in analyses according to the study arm to which they were originally assigned. Adults with new smear-positive PTB were eligible. The trial was registered at ClinicalTrials.gov NCT00677339.
200 participants were enrolled, less than the intended sample size: 50 received L-arginine + active vitD, 49 received L-arginine + placebo vit D, 51 received placebo L-arginine + active vitD and 50 received placebo L-arginine + placebo vitD. According to the factorial model, 99 people received arginine, 101 placebo arginine, 101 vitamin D, 99 placebo vitamin D. Results for the primary endpoints were available in 155 (4-week culture) and 167 (clinical score) participants. Sputum culture conversion was achieved by week 4 in 48/76 (63%) participants in the active L-arginine versus 48/79 (61%) in placebo L-arginine arms (risk difference -3%, 95% CI -19 to 13%), and in 44/75 (59%) in the active vitD versus 52/80 (65%) in the placebo vitD arms (risk difference 7%, 95% CI -9 to 22%). The mean clinical outcome score also did not differ between study arms. There were no effects of the interventions on adverse event rates including hypercalcaemia, or other secondary outcomes.
Neither vitD nor L-arginine supplementation, at the doses administered and with the power attained, affected TB outcomes.
ClinicalTrials.gov. Registry number: NCT00677339.
维生素 D(vitD)和 L-精氨酸对人类具有重要的抗分枝杆菌作用。辅助这些药物治疗有可能改善活动性肺结核(TB)的结局。
在印度尼西亚蒂米卡的一项 4 臂随机、双盲、安慰剂对照的因子试验中,我们测试了口服辅助 vitD 50,000 IU 每 4 周一次或匹配安慰剂,以及 L-精氨酸 6.0 g 每日或匹配安慰剂,持续 8 周,对痰培养 4 周阴性的参与者比例,以及 8 周的临床评分(体重、FEV1、咳嗽、咳痰、咯血)的影响。所有有可用终点的参与者均根据其最初分配的研究臂进行分析。患有新的痰涂片阳性肺结核的成年人符合条件。该试验在 ClinicalTrials.gov 注册,编号为 NCT00677339。
共有 200 名参与者入组,少于预期的样本量:50 名接受 L-精氨酸+活性 vitD,49 名接受 L-精氨酸+安慰剂 vitD,51 名接受安慰剂 L-精氨酸+活性 vitD,50 名接受安慰剂 L-精氨酸+安慰剂 vitD。根据因子模型,99 人接受精氨酸,101 人接受安慰剂精氨酸,101 人接受维生素 D,99 人接受安慰剂维生素 D。155 名(4 周培养)和 167 名(临床评分)参与者可获得主要终点结果。在活性 L-精氨酸组中,48/76(63%)的参与者在第 4 周时痰培养转为阴性,而安慰剂 L-精氨酸组中 48/79(61%)的参与者痰培养转为阴性(风险差 -3%,95%CI-19 至 13%),在活性 vitD 组中,44/75(59%)的参与者痰培养转为阴性,而安慰剂 vitD 组中 52/80(65%)的参与者痰培养转为阴性(风险差 7%,95%CI-9 至 22%)。研究组之间的临床结局评分也没有差异。干预措施对不良事件发生率(包括高钙血症)或其他次要结局均无影响。
在给予的剂量和达到的效力下,vitD 或 L-精氨酸补充剂均未影响结核病结局。
ClinicalTrials.gov。注册号:NCT00677339。