Key result
Foamy granulomas (OR 15.55, p=0.0005), neural/perineural infiltrate (OR 4.67), hBI ≥3+, and elevated anti-PGL-I levels significantly predicted leprosy relapse after multi-drug therapy.
Why the study?
This study aimed to identify laboratory factors predicting leprosy relapse after multi-drug therapy.
Do histopathological and serological assessments predict leprosy relapse in patients treated with multi-drug therapy?
Case-Control (n=80)
No
Do histopathological and serological assessments predict leprosy relapse in patients treated with multi-drug therapy?
Odds Ratio: 15.55
p-value: p=0.0005
Histopathological and serological factors, including neural/perineural infiltrate, foamy granulomas, hBI, and anti-PGL-I levels, can identify individuals at high probability of leprosy relapse after multi-drug therapy.
May flag higher relapse risk post-MDT; leaves open prospective validation before guiding surveillance.
This study aimed to identify laboratory factors predicting leprosy relapse (LR) after multi-drug therapy (MDT). A case-control study included 80 patients treated with MDT at a national reference center over 12 years. The Relapse Group had 40 patients who relapsed after an average of 89.2 months post-MDT, while the Control Group had 40 patients who remained asymptomatic for an average of 113.1 months. Significant predictors of LR included neural/perineural lymphocytic infiltrate (OR = 4.67; p = 0.0076) and foamy granulomas (OR = 15.55; p = 0.0005), increasing odds by 4.7 and 15.6 times, respectively. The Relapse Group had a mean histological bacillary index (hBI) of 3.23+ compared to 1.8 in the Control Group (p = 0.004). An hBI ≥3+ had 72% sensitivity and 65% specificity for detecting LR (AUC = 0.72; p = 0.0002). Elevated anti-phenolic glycolipid I (anti-PGL-I) IgM antibody levels (ELISA index, EI ≥1) were also associated with LR (OR = 4.67; p = 0.0031). An EI ≥3.6 had 71% sensitivity and 62% specificity (AUC = 0.70; p = 0.0012). Multivariate analysis indicated that neural/perineural infiltrate, foamy granulomas, hBI ≥ 1+, and EI ≥ 1 significantly predicted LR, with up to 94.32% probability. Conclusively, these factors can identify individuals at high probability of LR after MDT.
No takes yet. Share an insight, caveat, or question.
Dornelas et al. (2024) conducted a case-control in Leprosy relapse (n=80). Histopathological and serological factors (e.g., foamy granulomas, neural infiltrate, elevated hBI and anti-PGL-I) vs. Absence of these factors was evaluated on Leprosy relapse (OR 15.55, p=0.0005). Foamy granulomas (OR 15.55, p=0.0005), neural/perineural infiltrate (OR 4.67), hBI ≥3+, and elevated anti-PGL-I levels significantly predicted leprosy relapse after multi-drug therapy.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: