MUC5AC Genetic Variation Is Associated With Tuberculous Meningitis Cerebral Spinal Fluid Cytokine Responses and Mortality

Author:

Sabo Michelle C1ORCID,Thuong Nguyen T T23,Chang Xuling4,Ardiansyah Edwin5,Tram Trinh T B2,Hai Hoang T2,Nghia Ho D T26,Bang Nguyen D67,Dian Sofiati5,Ganiem A Rizal58,Shaporifar Shima1,Kumar Vinod5,Li Zheng9,Hibberd Martin10,Khor Chiea Chuen9,Thwaites Guy E23,Heemskerk Dorothee2311,van Laarhoven Arjan5,van Crevel Reinout5ORCID,Dunstan Sarah J4,Shah Javeed A112ORCID

Affiliation:

1. Department of Medicine, University of Washington , Seattle, Washington , USA

2. Oxford University Clinical Research Unit , Ho Chi Minh , Vietnam

3. Nuffield Department of Medicine, University of Oxford , Oxford , United Kingdom

4. Department of Infectious Diseases, Peter Doherty Institute for Infection and Immunity, University of Melbourne , Melbourne , Australia

5. Radboud University Medical Center , Nijmegen , The Netherlands

6. Hospital for Tropical Diseases , Ho Chi Minh City , Vietnam

7. Pham Ngoc Thach Hospital , Ho Chi Minh , Vietnam

8. Department of Neurology, Universitas Padjadjaran/Hasan Sadikin Hospital , Bandung , Indonesia

9. Genome Institute of Singapore , Singapore , Singapore

10. London School of Tropical Medicine and Hygiene , London , United Kingdom

11. Amsterdam University Medical Centre , Amsterdam , The Netherlands

12. Veterans Affairs Puget Sound Healthcare System , Seattle, Washington , USA

Abstract

Abstract Background The purpose of this study was to assess if single nucleotide polymorphisms (SNPs) in lung mucins MUC5B and MUC5AC are associated with Mycobacterium tuberculosis outcomes. Methods Independent SNPs in MUC5B and MUC5AC (genotyped by Illumina HumanOmniExpress array) were assessed for associations with tumor necrosis factor (TNF) concentrations (measured by immunoassay) in cerebral spinal fluid (CSF) from tuberculous meningitis (TBM) patients. SNPs associated with CSF TNF concentrations were carried forward for analyses of pulmonary and meningeal tuberculosis susceptibility and TBM mortality. Results MUC5AC SNP rs28737416 T allele was associated with lower CSF concentrations of TNF (P = 1.8 × 10−8) and IFN-γ (P = 2.3 × 10−6). In an additive genetic model, rs28737416 T/T genotype was associated with higher susceptibility to TBM (odds ratio [OR], 1.24; 95% confidence interval [CI], 1.03–1.49; P = .02), but not pulmonary tuberculosis (OR, 1.11, 95% CI, .98–1.25; P = .10). TBM mortality was higher among participants with the rs28737416 T/T and T/C genotypes (35/119, 30.4%) versus the C/C genotype (11/89, 12.4%; log-rank P = .005) in a Vietnam discovery cohort (n = 210), an independent Vietnam validation cohort (n = 87; 9/87, 19.1% vs 1/20, 2.5%; log-rank P = .02), and an Indonesia validation cohort (n = 468, 127/287, 44.3% vs 65/181, 35.9%; log-rank P = .06). Conclusions MUC5AC variants may contribute to immune changes that influence TBM outcomes.

Funder

National Institute of Child Health and Human Development

National Institute of Allergy and Infectious Diseases

University of Washington Center for AIDS Research

Wellcome Trust

National Health and Medical Research Council

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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