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Value of lipocalin 2 as a potential biomarker for bacterial meningitis.
Thanh, T T; Casals-Pascual, C; Ny, N T H; Ngoc, N M; Geskus, R; Nhu, L N T; Hong, N T T; Duc, D T; Thu, D D A; Uyen, P N; Ngoc, V B; Chau, L T M; Quynh, V X; Hanh, N H H; Thuong, N T T; Diem, L T; Hanh, B T B; Hang, V T T; Oanh, P K N; Fischer, R; Phu, N H; Nghia, H D T; Chau, N V V; Hoa, N T; Kessler, B M; Thwaites, G; Tan, L V.
Afiliação
  • Thanh TT; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
  • Casals-Pascual C; Department of Clinical Microbiology, Hospital Clínic de Barcelona, CDB, Barcelona, Spain; ISGlobal Barcelona, Institute for Global Health, Barcelona, Spain.
  • Ny NTH; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
  • Ngoc NM; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam; Hospital for Tropical Diseases, Ho Chi Minh City, Viet Nam.
  • Geskus R; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, Oxford, United Kingdom.
  • Nhu LNT; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
  • Hong NTT; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
  • Duc DT; Department of Infectious Diseases, Pham Ngoc Thach University of Medicine, Ho Chi Minh City, Viet Nam.
  • Thu DDA; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
  • Uyen PN; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
  • Ngoc VB; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
  • Chau LTM; Hospital for Tropical Diseases, Ho Chi Minh City, Viet Nam.
  • Quynh VX; Hospital for Tropical Diseases, Ho Chi Minh City, Viet Nam.
  • Hanh NHH; Department of Medicine, Vietnam National University, Ho Chi Minh City, Viet Nam.
  • Thuong NTT; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
  • Diem LT; Department of Medicine, Vietnam National University, Ho Chi Minh City, Viet Nam.
  • Hanh BTB; Department of Infectious Diseases, Pham Ngoc Thach University of Medicine, Ho Chi Minh City, Viet Nam.
  • Hang VTT; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
  • Oanh PKN; Hospital for Tropical Diseases, Ho Chi Minh City, Viet Nam.
  • Fischer R; Target Discovery Institute, Oxford, United Kingdom; University of Oxford, Oxford, United Kingdom.
  • Phu NH; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam; Department of Medicine, Vietnam National University, Ho Chi Minh City, Viet Nam.
  • Nghia HDT; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam; Department of Infectious Diseases, Pham Ngoc Thach University of Medicine, Ho Chi Minh City, Viet Nam; Hospital for Tropical Diseases, Ho Chi Minh City, Viet Nam.
  • Chau NVV; Hospital for Tropical Diseases, Ho Chi Minh City, Viet Nam.
  • Hoa NT; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
  • Kessler BM; Target Discovery Institute, Oxford, United Kingdom; University of Oxford, Oxford, United Kingdom.
  • Thwaites G; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, Oxford, United Kingdom.
  • Tan LV; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam. Electronic address: tanlv@oucru.org.
Article em En | MEDLINE | ID: mdl-32659386
ABSTRACT

OBJECTIVES:

Central nervous system (CNS) infections are common causes of morbidity and mortality worldwide. We aimed to discover protein biomarkers that could rapidly and accurately identify the likely cause of the infections, essential for clinical management and improving outcome.

METHODS:

We applied liquid chromatography tandem mass spectrometry on 45 cerebrospinal fluid (CSF) samples from a cohort of adults with and without CNS infections to discover potential diagnostic biomarkers. We then validated the diagnostic performance of a selected biomarker candidate in an independent cohort of 364 consecutively treated adults with CNS infections admitted to a referral hospital in Vietnam.

RESULTS:

In the discovery cohort, we identified lipocalin 2 (LCN2) as a potential biomarker of bacterial meningitis (BM) other than tuberculous meningitis. The analysis of the validation cohort showed that LCN2 could discriminate BM from other CNS infections (including tuberculous meningitis, cryptococcal meningitis and virus/antibody-mediated encephalitis), with sensitivity of 0.88 (95% confident interval (CI), 0.77-0.94), specificity of 0.91 (95% CI, 0.88-0.94) and diagnostic odds ratio of 73.8 (95% CI, 31.8-171.4). LCN2 outperformed other CSF markers (leukocytes, glucose, protein and lactate) commonly used in routine care worldwide. The combination of LCN2, CSF leukocytes, glucose, protein and lactate resulted in the highest diagnostic performance for BM (area under the receiver operating characteristics curve, 0.96; 95% CI, 0.93-0.99). Data are available via ProteomeXchange with identifier PXD020510.

CONCLUSIONS:

LCN2 is a sensitive and specific biomarker for discriminating BM from a broad spectrum of other CNS infections. A prospective study is needed to assess the diagnostic utility of LCN2 in the diagnosis and management of CNS infections.
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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies Idioma: En Revista: Clin Microbiol Infect Assunto da revista: DOENCAS TRANSMISSIVEIS / MICROBIOLOGIA Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies Idioma: En Revista: Clin Microbiol Infect Assunto da revista: DOENCAS TRANSMISSIVEIS / MICROBIOLOGIA Ano de publicação: 2020 Tipo de documento: Article