ABSTRACT
Introduction
Tuberculosis (TB) is a transnational public health concern, which requires more precise treatment strategies than the existing approaches. Vitamin D modulates the inflammatory and immune response to the disease. Robust evidence shows that vitamin D deficiency and its receptor gene polymorphism influence the susceptibility to TB and the outcome of the anti-tubercular treatment (ATT). However, in the different populations, these findings were inconsistent and even contradictory.
Areas covered
The current review focuses on the association between vitamin D receptor (VDR) gene polymorphism with the risk of development of TB disease and response to the ATT. Additionally, it reviews various systematic reviews and meta-analyses on the impact of vitamin D supplements on both clinical and treatment outcomes in TB patients.
Expert opinion
Although the majority of the findings rule out the benefits of the supplementation, sufficient evidence is available to warrant larger epidemiological research that should be aimed to generate possible interaction among the VDR polymorphism, vitamin D status, and the outcome in TB. We conclude that establishing such an association in different ethnic populations will help design nutrigenomics- or pharmacogenomics-based vitamin D supplementation to develop a personalized medicine approach to flatten the curve of TB disease.
Article highlights
Evidence shows that deficiency of vitamin D and its receptor gene polymorphism influences the susceptibility to tuberculosis and the treatment outcome
Despite many of the findings that rule out the benefits of the vitamin D supplementation in tuberculosis, sufficient evidence is available to warrant extensive epidemiological research to generate possible interaction among the VDR polymorphism, vitamin D status, and the outcome in tuberculosis
The robust evidence on such interplay will help to develop a more personalized medicine approach for vitamin D supplementation in tuberculosis patients
Declaration of interest
The authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.
Reviewer disclosures
Peer reviewers on this manuscript have no relevant financial or other relationships to disclose.
Author contributions
SS and MR conceptualized the review. SSM, NV, SJK, TB, and LT wrote the manuscript. SSM and BSR are involved in visualization. MM, MB, and MR critically evaluated the manuscript. All the authors participated in the literature collection and review. All the authors approved the final draft of the article.