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Original article
Ethnicity and mycobacterial lineage as determinants of tuberculosis disease phenotype
  1. Manish Pareek1,2,3,
  2. Jason Evans4,
  3. John Innes5,
  4. Grace Smith4,
  5. Suzie Hingley-Wilson1,
  6. Kathryn E Lougheed6,
  7. Saranya Sridhar1,
  8. Martin Dedicoat5,
  9. Peter Hawkey4,7,
  10. Ajit Lalvani1
  1. 1Tuberculosis Research Unit, National Heart and Lung Institute, Imperial College London, London, UK
  2. 2Department of Infectious Disease Epidemiology, Imperial College London, London, UK
  3. 3Department of Infection, Immunity and Inflammation, University of Leicester, Leicester, UK
  4. 4Health Protection Agency Midlands Laboratory, Heart of England NHS Foundation Trust, Bordesley Green East, Birmingham, UK
  5. 5Department of Infection and Tropical Medicine, Heart of England NHS Foundation Trust, Bordesley Green East, Birmingham, UK
  6. 6Department of Integrative Cell Biology, Division of Cell & Molecular Biology, Imperial College London, London, UK
  7. 7School of Immunity and Infection, The Medical School, University of Birmingham, Edgbaston, Birmingham, UK
  1. Correspondence to Prof Ajit Lalvani, Tuberculosis Research Unit, National Heart and Lung Institute, Imperial College London, London W21PG, UK; a.lalvani{at}imperial.ac.uk

Abstract

Background Emerging evidence suggests that Mycobacterium tuberculosis (Mtb) lineage and host ethnicity can determine tuberculosis (TB) clinical disease patterns but their relative importance and interaction are unknown.

Methods We evaluated prospectively collected TB surveillance and Mtb strain typing data in an ethnically heterogeneous UK population. Lineage assignment was denoted using 15-loci mycobacterial interspersed repetitive units containing variable numbers of tandem repeats (MIRU-VNTR) and MIRU-VNTRplus. Geographical and ethnic associations of the six global Mtb lineages were identified and the influence of lineage and demographic factors on clinical phenotype were assessed using multivariate logistic regression.

Results Data were available for 1070 individuals with active TB which was pulmonary only, extrapulmonary only and concurrent pulmonary–extrapulmonary in 52.1%, 36.9% and 11.0% respectively. The most prevalent lineages were Euro-American (43.7%), East African Indian (30.2%), Indo-Oceanic (13.6%) and East Asian (12.2%) and were geo-ethnically restricted with, for example, Indian subcontinent ethnicity inversely associated with Euro-American lineage (OR 0.23; 95% CI 0.14 to 0.39) and positively associated with the East African-Indian lineage (OR 4.04; 95% CI 2.19 to 7.45). Disease phenotype was most strongly associated with ethnicity (OR for extrathoracic disease 21.14 (95% CI 6.08 to 73.48) for Indian subcontinent and 14.05 (3.97 to 49.65) for Afro-Caribbean), after adjusting for lineage. With East Asian lineage as the reference category, the Euro-American (OR 0.54; 95% CI 0.32 to 0.91) and East-African Indian (OR 0.50; 95% CI 0.29 to 0.86) lineages were negatively associated with extrathoracic disease, compared with pulmonary disease, after adjusting for ethnicity.

Conclusions Ethnicity is a powerful determinant of clinical TB phenotype independently of mycobacterial lineage and the role of ethnicity-associated factors in pathogenesis warrants investigation.

  • Tuberculosis

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