4.6 Article

Host lipidome and tuberculosis treatment failure

Journal

EUROPEAN RESPIRATORY JOURNAL
Volume 59, Issue 1, Pages -

Publisher

EUROPEAN RESPIRATORY SOC JOURNALS LTD
DOI: 10.1183/13993003.04532-2020

Keywords

-

Funding

  1. Government of India's (GOI) Department of Biotechnology (DBT), Indian Council of Medical Research (ICMR)
  2. US National Institutes of Health (NIH)
  3. US National Institutes of Health (NIH), National Institute of Allergy and Infectious Diseases (NIAID), Office of AIDS Research
  4. NIAID [UM1AI069465, R01AI097494]
  5. NICHD [R00HD089753]
  6. Gilead Foundation
  7. Ujala Foundation
  8. Fogarty International Center BJGMC-JHU HIV-TB Program [D43TW009574]
  9. Johns Hopkins University School of Medicine funds
  10. Columbia University Department of Epidemiology funds
  11. Intramural research program from FIOCRUZ
  12. National Institutes of Health [U01AI115940]
  13. NIH/CRDF RePORT International Supplemental Funds
  14. NIH Research Training Grant - NIH Fogarty International Center [D43 TW009340]
  15. NIH [U24 DK097154]
  16. USDA [2032-51530-022-00D, 2032-51530-025-00D]
  17. CRDF Global [USB1-31147-XX13]

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This study investigated the association between host lipids and treatment failure in tuberculosis (TB) using unbiased lipidomics. The results showed that treatment failure was associated with lower levels of cholesteryl esters and oxylipin, and higher levels of ceramides and triglycerides at the baseline. A lipid signature with predictive accuracy for TB treatment failure was also identified.
Introduction Host lipids play important roles in tuberculosis (TB) pathogenesis. Whether host lipids at TB treatment initiation (baseline) affect subsequent treatment outcomes has not been well characterised. We used unbiased lipidomics to study the prospective association of host lipids with TB treatment failure. Methods A case-control study (n=192), nested within a prospective cohort study, was used to investigate the association of baseline plasma lipids with TB treatment failure among adults with pulmonary TB. Cases (n=46) were defined as TB treatment failure, while controls (n=146) were those without failure. Complex lipids and inflammatory lipid mediators were measured using liquid chromatography mass spectrometry techniques. Adjusted least-square regression was used to assess differences in groups. In addition, machine learning identified lipids with highest area under the curve (AUC) to classify cases and controls. Results Baseline levels of 32 lipids differed between controls and those with treatment failure after false discovery rate adjustment. Treatment failure was associated with lower baseline levels of cholesteryl esters and oxylipin, and higher baseline levels of ceramides and triglycerides compared to controls. Two cholesteryl ester lipids combined in a unique classifier model provided an AUC of 0.79 (95% CI 0.65-0.93) in the test dataset for prediction of TB treatment failure. Conclusions We identified lipids, some with known roles in TB pathogenesis, associated with TB treatment failure. In addition, a lipid signature with prognostic accuracy for TB treatment failure was identified. These lipids could be potential targets for risk-stratification, adjunct therapy and treatment monitoring.

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