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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/52382
Title: Do intracerebral cytokine responses explain the harmful effects of dexamethasone in human immunodeficiency virus–associated cryptococcal meningitis?
Authors: Justin Beardsley
Nhat L.T. Hoang
Freddie M. Kibengo
Nguyen L.N. Tung
Tran Q. Binh
Le Q. Hung
Wirongrong Chierakul
Guy E. Thwaites
Nguyen V.V. Chau
Thuong T.T. Nguyen
Ronald B. Geskus
Jeremy N. Day
Cho Ray Hospital
The University of Sydney
UCL
Mahidol University
Nuffield Department of Clinical Medicine
LSHTM Uganda Research Unit
Oxford University Clinical Research Unit
Keywords: Medicine
Issue Date: 1-Jan-2019
Citation: Clinical Infectious Diseases. Vol.68, No.9 (2019), 1494-1501
Abstract: © The Author(s) 2018. Background. The CryptoDex trial showed that dexamethasone caused poorer clinical outcomes and slowed fungal clearance in human immunodeficiency virus–associated cryptococcal meningitis. We analyzed cerebrospinal fluid (CSF) cytokine concentrations from participants over the first week of treatment to investigate mechanisms of harm and test 2 hypotheses: (1) dexamethasone reduced proinflammatory cytokine concentrations, leading to poorer outcomes and (2) leukotriene A4 hydrolase (LTA4H) genotype influenced the clinical impact of dexamethasone, as observed in tuberculous meningitis. Methods. We included participants from Vietnam, Thailand, and Uganda. Using the Luminex system, we measured CSF concentrations of the following: interferon γ, tumor necrosis factor (TNF) α, granulocyte-macrophage colony-stimulating factor, monocyte chemoattractant 1, macrophage inflammatory protein 1α, and interleukin 6, 12p70, 8, 4, 10, and 17. We determined the LTA4H genotype based on the promoter region single-nucleotide polymorphism rs17525495. We assessed the impact of dexamethasone on cytokine concentration dynamics and the association between cytokine concentration dynamics and fungal clearance with mixed effect models. We measured the influence of LTA4H genotype on outcomes with Cox regression models. Results. Dexamethasone increased the rate TNF-α concentration’s decline in (−0.13 log2pg/mL/d (95% confidence interval, −.22 to −.06 log2pg/mL/d; P = .03), which was associated with slower fungal clearance (correlation, −0.62; 95% confidence interval, −.83 to −.26). LTA4H genotype had no statistically significant impact on outcome or response to dexamethasone therapy. Better clinical outcomes were associated with higher baseline concentrations of interferon γ. Conclusions. Dexamethasone may slow fungal clearance and worsen outcomes by increasing TNF-α concentration’s rate of decline.
URI: http://repository.li.mahidol.ac.th/dspace/handle/123456789/52382
metadata.dc.identifier.url: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85067391314&origin=inward
ISSN: 15376591
10584838
Appears in Collections:Scopus 2019

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