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DOI 10.1371/journal.pone.0070032

Медицинская библиотека · PloS one · 2013

L-arginine and vitamin D adjunctive therapies in pulmonary tuberculosis: a randomised, double-blind, placebo-controlled trial.

Ralph Anna P, Waramori Govert, Pontororing Gysje J, Kenangalem Enny, Wiguna Andri, Tjitra Emiliana, Sandjaja, Lolong Dina B, Yeo Tsin W, Chatfield Mark D, Soemanto Retno K, Bastian Ivan, Lumb Richard, Maguire Graeme P, Eisman John, Price Ric N, Morris Peter S, Kelly Paul M, Anstey Nicholas M

СтатьяРандомизированное исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

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).

METHODS

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.

RESULTS

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.

CONCLUSION

Neither vitD nor L-arginine supplementation, at the doses administered and with the power attained, affected TB outcomes.

REGISTRY: ClinicalTrials.gov. Registry number: NCT00677339.

Для цитирования: Ralph Anna P, Waramori Govert, Pontororing Gysje J, Kenangalem Enny, Wiguna Andri, Tjitra Emiliana, Sandjaja, Lolong Dina B, Yeo Tsin W, Chatfield Mark D, Soemanto Retno K, Bastian Ivan, Lumb Richard, Maguire Graeme P, Eisman John, Price Ric N, Morris Peter S, Kelly Paul M, Anstey Nicholas M. L-arginine and vitamin D adjunctive therapies in pulmonary tuberculosis: a randomised, double-blind, placebo-controlled trial.. PloS one. 2013. DOI: 10.1371/journal.pone.0070032.

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