AI Article Synopsis

  • Recent research indicates that calcium channel blockers (CCBs) can lower the risk of developing active tuberculosis (TB) by 29%, although they do not impact TB-related mortality rates.
  • The study synthesized data from eight observational studies involving over 4 million patients, showing similar benefits for both those with and without diabetes mellitus.
  • The findings suggest more significant protective effects in the general population and among patients treated with certain types of CCBs, but further studies are needed for conclusive evidence.

Article Abstract

Recent studies suggest that calcium channel blockers (CCBs) could reduce the risk of active tuberculosis and improve clinical outcomes. We aimed to synthesize the evidence regarding the effect of CCBs on the risk of developing active tuberculosis and mortality. We systematically searched for observational studies and clinical trials published in six databases until 31 August 2023, following a PECO/PICO strategy. We included eight observational studies, 4,020,830 patients, among whom 241,761 had diabetes mellitus and 30,397 had active tuberculosis. According to our results, CCBs reduce the risk of developing active tuberculosis by 29% (RR 0.71; 95% CI 0.67-0.75) in patients with and without diabetes mellitus. However, CCBs do not show any benefit in terms of tuberculosis-related mortality (RR 1.00; 95% CI 0.98-1.02). For both outcomes, no statistical heterogeneity was found (I = 0, > 0.10). This protective effect of CCBs on the risk of active tuberculosis remained independent of the type of patient (with diabetes mellitus vs. general population) or the class of CCB administered (DHP-CCB vs. non-DHP-CCB) (test for subgroup differences I = 0, > 0.10). However, this beneficial effect was more significant among the general population (RR 0.70; 95% CI 0.66-0.74) compared to patients with diabetes mellitus (RR 0.72; 95% CI 0.61-0.86) and among those patients treated with DHP-CCBs (RR 0.69; 95% CI 0.63-0.74) compared to patients treated with non-DHP-CCBs (RR 0.72; 95% CI 0.67-0.78). CCBs may reduce the risk of active TB in patients with diabetes and the general population. On the contrary, CCBs do not seem to have a protective effect on tuberculosis-related mortality. However, more evidence is still needed. We recommend developing clinical trials to verify these findings, including more diverse populations. [https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=352129].

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10830796PMC
http://dx.doi.org/10.3389/fphar.2024.1298919DOI Listing

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