AI Article Synopsis

  • * A study involving 40 individuals (20 with newly diagnosed DM and 20 without) analyzed serum samples to quantify pro-inflammatory and pro-resolving lipid mediators, identifying specific lipid families that are abundant in each group.
  • * Findings revealed that individuals with TB-DM exhibited stronger connections between pro-inflammatory and pro-resolving lipid mediators than those with TB alone, suggesting a complex molecular balance at play in this comorbidity.

Article Abstract

Individuals with concurrent tuberculosis (TB) and Type 2 diabetes (DM) have a higher risk of adverse outcomes. To better understand potential immunological differences, we utilized a comprehensive panel to characterize pro-inflammatory and pro-resolving (i.e., mediators involved in the resolution of inflammation) lipid mediators in individuals with TB and TB-DM. A nested cross-sectional study of 40 individuals (20 newly diagnosed DM and 20 without DM) was conducted within a cohort of individuals with active drug-susceptible treatment-naïve pulmonary TB. Lipid mediators were quantified in serum samples through lipid mediator profiling. We conducted correlation-based analysis of these mediators. Overall, the arachidonic acid-derived leukotriene and prostaglandin families were the most abundant pro-inflammatory lipid mediators, while lipoxins and maresins families were the most abundant pro-resolving lipid mediators in individuals with TB and TB-DM. Individuals with TB-DM had increased correlations and connectivity with both pro-inflammatory and pro-resolving lipid mediators compared to those with TB alone. We identified the most abundant lipid mediator metabolomes in circulation among individuals with TB and TB-DM; in addition, our data shows a substantial number of significant correlations between both pro-inflammatory and pro-resolving lipid mediators in individuals with TB-DM, delineating a molecular balance that potentially defines this comorbidity.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067657PMC
http://dx.doi.org/10.1016/j.prostaglandins.2019.106398DOI Listing

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