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CSF neopterin and quinolinic acid are biomarkers of neuroinflammation and neurotoxicity in FIRES and other infection-triggered encephalopathy syndromes.
Dale, Russell C; Thomas, Terrence; Patel, Shrujna; Han, Velda X; Kothur, Kavitha; Troedson, Christopher; Gupta, Sachin; Gill, Deepak; Malone, Stephen; Waak, Michaela; Calvert, Sophie; Subramanian, Gopinath; Andrews, P Ian; Kandula, Tejaswi; Menezes, Manoj P; Ardern-Holmes, Simone; Mohammad, Shekeeb; Bandodkar, Sushil; Yan, Jingya.
Afiliação
  • Dale RC; Kids Neuroscience Centre, The Children's Hospital at Westmead, Faculty of Medicine and Health, University of Sydney, Westmead, New South Wales, Australia.
  • Thomas T; Clinical School, The Children's Hospital at Westmead, Faculty of Medicine and Health, University of Sydney, Westmead, New South Wales, Australia.
  • Patel S; Department of Paediatrics, Neurology Service, KK Women's and Children's Hospital, Singapore, Singapore.
  • Han VX; Kids Neuroscience Centre, The Children's Hospital at Westmead, Faculty of Medicine and Health, University of Sydney, Westmead, New South Wales, Australia.
  • Kothur K; Clinical School, The Children's Hospital at Westmead, Faculty of Medicine and Health, University of Sydney, Westmead, New South Wales, Australia.
  • Troedson C; Khoo Teck Puat-National University Children's Medical Institute, National University Health System, Singapore, Singapore.
  • Gupta S; Kids Neuroscience Centre, The Children's Hospital at Westmead, Faculty of Medicine and Health, University of Sydney, Westmead, New South Wales, Australia.
  • Gill D; Clinical School, The Children's Hospital at Westmead, Faculty of Medicine and Health, University of Sydney, Westmead, New South Wales, Australia.
  • Malone S; TY Nelson Department of Neurology and Neurosurgery, The Children's Hospital at Westmead, The University of Sydney, Westmead, New South Wales, Australia.
  • Waak M; TY Nelson Department of Neurology and Neurosurgery, The Children's Hospital at Westmead, The University of Sydney, Westmead, New South Wales, Australia.
  • Calvert S; TY Nelson Department of Neurology and Neurosurgery, The Children's Hospital at Westmead, The University of Sydney, Westmead, New South Wales, Australia.
  • Subramanian G; Kids Neuroscience Centre, The Children's Hospital at Westmead, Faculty of Medicine and Health, University of Sydney, Westmead, New South Wales, Australia.
  • Andrews PI; TY Nelson Department of Neurology and Neurosurgery, The Children's Hospital at Westmead, The University of Sydney, Westmead, New South Wales, Australia.
  • Kandula T; Department of Neuroscience, Queensland Children's Hospital, South Brisbane, Queensland, Australia.
  • Menezes MP; Department of Neuroscience, Queensland Children's Hospital, South Brisbane, Queensland, Australia.
  • Ardern-Holmes S; Department of Neuroscience, Queensland Children's Hospital, South Brisbane, Queensland, Australia.
  • Mohammad S; Department of Paediatrics, John Hunter Children's Hospital, Newcastle, New South Wales, Australia.
  • Bandodkar S; Department of Neurology, Sydney Children's Hospital Network, Sydney, New South Wales, Australia.
  • Yan J; Department of Neurology, Sydney Children's Hospital Network, Sydney, New South Wales, Australia.
Ann Clin Transl Neurol ; 10(8): 1417-1432, 2023 08.
Article em En | MEDLINE | ID: mdl-37340737
ABSTRACT

OBJECTIVE:

Infection-triggered encephalopathy syndromes (ITES) are potentially devastating neuroinflammatory conditions. Although some ITES syndromes have recognisable MRI neuroimaging phenotypes, there are otherwise few biomarkers of disease. Early detection to enable immune modulatory treatments could improve outcomes.

METHODS:

We measured CSF neopterin, quinolinic acid, kynurenine and kynurenine/tryptophan ratio using a liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) system. The CSF of 18 children with ITES were compared with acute encephalitis (n = 20), and three control groups, namely epilepsy (n = 20), status epilepticus (n = 18) and neurogenetic controls (n = 20).

RESULTS:

The main ITES phenotypes in 18 patients were acute encephalopathy with biphasic seizures and late restricted diffusion (AESD, n = 4), febrile infection-related epilepsy syndrome (FIRES n = 4) and other ITES phenotypes. Influenza A was the most common infectious trigger (n = 5), and 50% of patients had a preceding notable neurodevelopmental or family history. CSF neopterin, quinolinic acid and kynurenine were elevated in ITES group compared to the three control groups (all p < 0.0002). The ROC (area under curve) for CSF neopterin (99.3%, CI 98.1-100) was significantly better than CSF pleocytosis (87.3% CI 76.4-98.2) (p = 0.028). Elevated CSF neopterin could discriminate ITES from other causes of seizures, status epilepticus and febrile status epilepticus (all p < 0.0002). The elevated CSF metabolites normalised during longitudinal testing in two patients with FIRES.

INTERPRETATION:

CSF neopterin and quinolinic acid are neuroinflammatory and excitotoxic metabolites. This CSF metabolomic inflammatory panel can discriminate ITES from other causes of new onset seizures or status epilepticus, and rapid results (4 h) may facilitate early immune modulatory therapy.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estado Epiléptico / Encefalopatias / Encefalite Tipo de estudo: Diagnostic_studies / Etiology_studies / Screening_studies Limite: Humans Idioma: En Revista: Ann Clin Transl Neurol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estado Epiléptico / Encefalopatias / Encefalite Tipo de estudo: Diagnostic_studies / Etiology_studies / Screening_studies Limite: Humans Idioma: En Revista: Ann Clin Transl Neurol Ano de publicação: 2023 Tipo de documento: Article