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Does the addition of high-dose vitamin D3 reduce the period of time required for the treatment of pulmonary tuberculosis?
  1. Jessica Reed
  1. Correspondence to Dr Jessica Reed, FY1, South Tees Hospitals NHS Trust, Middlesbrough, UK; jessica.reed{at}nhs.net

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This double-blind randomised placebo control trial investigated the addition of four doses of 2.5 mg of vitamin D3 to intensive phase antimicrobial therapy (isoniazid, rifampicin, pyrazinamide and ethambutol) for tuberculosis and the effect upon culture conversion rates. Time to conversion was measured at 14, 28, 42 and 56 days compared with placebo with intensive antimicrobial therapy. The primary outcome was also characterised with respect to the expression of vitamin D3 genotypes Tak1 and Fok1.

The authors recruited one hundred and forty-six patients from 10 NHS London Trusts, of which one hundred and twenty-six were included. The median age of the patients was 30.6 years. The authors demonstrated a reduced median culture time in the vitamin D3 group of 36 days (95% CI 31.8 to 40.2) compared with the placebo group of 43.5 days (95% CI 36.5 to 50.5). Subgroup analysis of the Taq1 and Fok1 vitamin D receptor types showed that patients homozygous for the Taq1 polymorphism had reduced time to culture conversion.

In conclusion, the addition of vitamin D3 to intensive anti-tuberculosis treatment did not confer a significant advantage compared with placebo in the time taken for sputum culture conversion except in individuals who were homozygous for the Taq1 polymorphism. Investigation of this gene interaction and its possible clinical advantage is therefore warranted.

▶  Martineau AR, Timms PM, Bothamley GH, et al. High-dose vitamin D3 during intensive-phase antimicrobial treatment of pulmonary tuberculosis: a double-blind randomised controlled trial. Lancet 2011;377:242–50.

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