ArticleFrontiers in public health2026
Glucose driven bacterial persistence in extensively drug-resistant tuberculosis with diabetes.
Article in Frontiers in public health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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7 authors.
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Abstract
Background: Diabetes mellitus (DM) disrupts the metabolic environment of extensively drug-resistant tuberculosis (XDR) patients, promoting mycobacterial persistence. Key factors influencing bacterial clearance remain unclear. This study aimed to identify critical host factors and assess the therapeutic value of intensive glucose control. Method: A 48-month single-center retrospective cohort study compared sputum smear conversion (bacterial clearance) between 57 XDR-only (XDR) and 84 XDR with DM (XDR + DM) patients (similar treatment, consistent Results: Compared with XDR patients, the XDR + DM group exhibited a significantly lower bacterial clearance rate (80.7% vs. 45.2%) and longer median clearance time (6 vs. 12 months), despite comparable baseline smear grades. Crucially, XDR + DM patients displayed distinct immunometabolic dysregulation, characterized by elevated inflammatory markers (CRP) and a disrupted CD4+ /CD8+ T-cell balance (increased CD4+, decreased CD8+ counts). Multivariable analysis identified hyperglycemia as the primary driver of delayed clearance (aHR = 1.48, 95% CI: 1.23-1.77, Conclusion: Dysregulated glucose metabolism and subsequent immune imbalance in diabetes are key drivers of delayed bacterial clearance in XDR patients, independent of the anti-tuberculosis regimen. Precise glucose control should be regarded as a core strategy, on a par with anti-XDR treatment.
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