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Hidden burden of leprosy in incarcerated populations in northeast Brazil: active case detection and serological assessment
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Hidden burden of leprosy in incarcerated populations in northeast Brazil: active case detection and serological assessment

European Journal of Clinical Microbiology & Infectious Diseases·July 13Open Access
Infectious DiseasesSafety signalLeprosyCross-Sectional StudySerological Diagnostic TestingAdultAnti-Mce1A Antibody ELISAAnti-PGL-I IgM ELISA

Summary

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What was studied

This cross-sectional study screened 915 male inmates at a penitentiary in Maceió, Alagoas, Brazil using the Leprosy Suspicion Questionnaire (LSQ), neurodermatological examination (n=260), and serological testing for anti-PGL-I (IgM) and anti-Mce1A antibodies (IgA, IgM, IgG) via indirect ELISA (n=244) to assess leprosy burden and screening strategies in an incarcerated population.

Key findings

8 new leprosy cases were found among 260 examined inmates, yielding an overall new case detection rate (NCDR) of 3.08% (6.52% among LSQ-positive/symptomatic individuals). All 8 cases were multibacillary, and 100% had some degree of physical disability at diagnosis. Anti-Mce1A IgA was positive in 100% of diagnosed cases vs. anti-PGL-I positivity in only 19.9% of clinically unaffected individuals; 75% of leprosy cases had a positive LSQ vs. 34.1% in the non-leprosy group (p=0.0249).

Study limitations

- Single-site, single-sex (male) facility limits generalizability to other prison settings or female populations. - Not all 915 inmates underwent clinical examination (only 260 evaluated), introducing selection bias. - Cross-sectional design precludes causal inference or assessment of transmission dynamics over time.

Clinical implications

Clinicians and public health teams should consider active leprosy screening with LSQ plus clinical examination in overcrowded incarcerated settings in endemic regions, as NCDR exceeded 3% with all detected cases being multibacillary and presenting physical disability. Anti-Mce1A serology—especially IgA—may improve detection of early-stage and neural leprosy compared to anti-PGL-I alone.

Caveats

  • Anti-PGL-I and anti-Mce1A are described as diagnostic modalities rather than therapeutic agents; tagged under 'generic' as a best approximation given available tag types.
  • Level of evidence assigned as 4 (cross-sectional observational study); no comparator group or randomization was used.
  • The full text retrieved appears to be a Brazilian Ministry of Health epidemiological bulletin (Boletim Epidemiológico 2025) rather than the original research article described in the abstract. The abstract and results sections match the DOI paper, but the full text body contains national surveillance data, not the primary study methods/discussion. Summary is based on the abstract and results sections only.

Related Questions

Explore related topics

What leprosy screening tools are most effective in high-risk congregate settings like prisons?How does anti-Mce1A serology compare to anti-PGL-I for early leprosy detection?What is the prevalence and disease burden of leprosy in incarcerated populations in Brazil?

Publication Details

Year
2026
Journal
European Journal of Clinical Microbiology & Infectious Diseases
Sample Size
n=915
Source
View article
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