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Tryptophan metabolism determines outcome in tuberculous meningitis: a targeted metabolomic analysis
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Background:Cellular metabolism is critical for the host immune function against pathogens, and metabolomic analysis may help understand the characteristic immunopathology of tuberculosis. We performed targeted metabolomic analyses in a large cohort of patients with tuberculous meningitis (TBM), the most severe manifestation of tuberculosis, focusing on tryptophan metabolism.Methods:We studied 1069 Indonesian and Vietnamese adults with TBM (26.6% HIV-positive), 54 non-infectious controls, 50 with bacterial meningitis, and 60 with cryptococcal meningitis. Tryptophan and downstream metabolites were measured in cerebrospinal fluid (CSF) and plasma using targeted liquid chromatography–mass spectrometry. Individual metabolite levels were associated with survival, clinical parameters, CSF bacterial load and 92 CSF inflammatory proteins.Results:CSF tryptophan was associated with 60-day mortality from TBM (hazard ratio [HR] = 1.16, 95% confidence interval [CI] = 1.10–1.24, for each doubling in CSF tryptophan) both in HIV-negative and -positive patients. CSF tryptophan concentrations did not correlate with CSF bacterial load nor CSF inflammation but were negatively correlated with CSF interferon-gamma concentrations. Unlike tryptophan, CSF concentrations of an intercorrelating cluster of downstream kynurenine metabolites did not predict mortality. These CSF kynurenine metabolites did however correlate with CSF inflammation and markers of blood–CSF leakage, and plasma kynurenine predicted death (HR 1.54, 95% CI = 1.22–1.93). These findings were mostly specific for TBM, although high CSF tryptophan was also associated with mortality from cryptococcal meningitis.Conclusions:TBM patients with a high baseline CSF tryptophan or high systemic (plasma) kynurenine are at increased risk of death. These findings may reveal new targets for host-directed therapy.Funding:This study was supported by National Institutes of Health (R01AI145781) and the Wellcome Trust (110179/Z/15/Z and 206724/Z/17/Z).
eLife Sciences Publications, Ltd
Edwin Ardiansyah
Julian Avila-Pacheco
Le Thanh Hoang Nhat
Sofiati Dian
Dao Nguyen Vinh
Hoang Thanh Hai
Kevin Bullock
Bachti Alisjahbana
Mihai G Netea
Riwanti Estiasari
Trinh Thi Bich Tram
Joseph Donovan
Dorothee Heemskerk
Tran Thi Hong Chau
Nguyen Duc Bang
Ahmad Rizal Ganiem
Rovina Ruslami
Valerie ACM Koeken
Raph L Hamers
Darma Imran
Kartika Maharani
Vinod Kumar
Clary B Clish
Reinout van Crevel
Guy Thwaites
Arjan van Laarhoven
Nguyen Thuy Thuong Thuong
Title: Tryptophan metabolism determines outcome in tuberculous meningitis: a targeted metabolomic analysis
Description:
Background:Cellular metabolism is critical for the host immune function against pathogens, and metabolomic analysis may help understand the characteristic immunopathology of tuberculosis.
We performed targeted metabolomic analyses in a large cohort of patients with tuberculous meningitis (TBM), the most severe manifestation of tuberculosis, focusing on tryptophan metabolism.
Methods:We studied 1069 Indonesian and Vietnamese adults with TBM (26.
6% HIV-positive), 54 non-infectious controls, 50 with bacterial meningitis, and 60 with cryptococcal meningitis.
Tryptophan and downstream metabolites were measured in cerebrospinal fluid (CSF) and plasma using targeted liquid chromatography–mass spectrometry.
Individual metabolite levels were associated with survival, clinical parameters, CSF bacterial load and 92 CSF inflammatory proteins.
Results:CSF tryptophan was associated with 60-day mortality from TBM (hazard ratio [HR] = 1.
16, 95% confidence interval [CI] = 1.
10–1.
24, for each doubling in CSF tryptophan) both in HIV-negative and -positive patients.
CSF tryptophan concentrations did not correlate with CSF bacterial load nor CSF inflammation but were negatively correlated with CSF interferon-gamma concentrations.
Unlike tryptophan, CSF concentrations of an intercorrelating cluster of downstream kynurenine metabolites did not predict mortality.
These CSF kynurenine metabolites did however correlate with CSF inflammation and markers of blood–CSF leakage, and plasma kynurenine predicted death (HR 1.
54, 95% CI = 1.
22–1.
93).
These findings were mostly specific for TBM, although high CSF tryptophan was also associated with mortality from cryptococcal meningitis.
Conclusions:TBM patients with a high baseline CSF tryptophan or high systemic (plasma) kynurenine are at increased risk of death.
These findings may reveal new targets for host-directed therapy.
Funding:This study was supported by National Institutes of Health (R01AI145781) and the Wellcome Trust (110179/Z/15/Z and 206724/Z/17/Z).
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