<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Damodar T</submitter><funding>DBT/Wellcome Trust India Alliance Fellowship IA/E/15/1/503960</funding><funding>Indian Council of Medical Research (ICMR) (Project ID: 2021- 3668)</funding><funding>National Institute for Health Research (NIHR)</funding><funding>DBT/Wellcome Trust India Alliance</funding><funding>Wellcome Trust</funding><pagination>e29666</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7616670</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>96(5)</volume><pubmed_abstract>Acute encephalitis syndrome (AES) in children poses a significant public health challenge in India. This study aims to explore the utility of host inflammatory mediators and neurofilament (NfL) levels in distinguishing etiologies, assessing disease severity, and predicting outcomes in AES. We assessed 12 mediators in serum (n = 58) and 11 in cerebrospinal fluid (CSF) (n = 42) from 62 children with AES due to scrub typhus, viral etiologies, and COVID-associated multisystem inflammatory syndrome (MIS-C) in Southern India. Additionally, NfL levels in serum (n = 20) and CSF (n = 18) were examined. Clinical data, including Glasgow coma scale (GCS) and Liverpool outcome scores, were recorded. Examining serum and CSF markers in the three AES etiology groups revealed notable distinctions, with scr</pubmed_abstract><journal>Journal of medical virology</journal><pubmed_title>Diagnostic markers of acute encephalitis syndrome and COVID-associated multisystem inflammatory syndrome in children from Southern India.</pubmed_title><pmcid>PMC7616670</pmcid><funding_grant_id>IA/CPHE/18/1/503960</funding_grant_id><funding_grant_id>NIHR200907</funding_grant_id><pubmed_authors>Dunai C</pubmed_authors><pubmed_authors>Dsouza FS</pubmed_authors><pubmed_authors>Basavaraja GV</pubmed_authors><pubmed_authors>Ravi V</pubmed_authors><pubmed_authors>Sajjan SV</pubmed_authors><pubmed_authors>Kinhal UV</pubmed_authors><pubmed_authors>Marate S</pubmed_authors><pubmed_authors>Singh B</pubmed_authors><pubmed_authors>Gowda VK</pubmed_authors><pubmed_authors>Solomon T</pubmed_authors><pubmed_authors>Michael BD</pubmed_authors><pubmed_authors>Turtle L</pubmed_authors><pubmed_authors>Tharmaratnam K</pubmed_authors><pubmed_authors>Damodar T</pubmed_authors><pubmed_authors>Akhila L</pubmed_authors><pubmed_authors>Mani RS</pubmed_authors><pubmed_authors>Anusha Raj K</pubmed_authors><pubmed_authors>Lalitha AV</pubmed_authors><pubmed_authors>Jose M</pubmed_authors><pubmed_authors>Yadav R</pubmed_authors><pubmed_authors>Prathyusha PV</pubmed_authors><pubmed_authors>Prabhu N</pubmed_authors><pubmed_authors>Kolamunnage-Dona R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Diagnostic markers of acute encephalitis syndrome and COVID-associated multisystem inflammatory syndrome in children from Southern India.</name><description>Acute encephalitis syndrome (AES) in children poses a significant public health challenge in India. This study aims to explore the utility of host inflammatory mediators and neurofilament (NfL) levels in distinguishing etiologies, assessing disease severity, and predicting outcomes in AES. We assessed 12 mediators in serum (n = 58) and 11 in cerebrospinal fluid (CSF) (n = 42) from 62 children with AES due to scrub typhus, viral etiologies, and COVID-associated multisystem inflammatory syndrome (MIS-C) in Southern India. Additionally, NfL levels in serum (n = 20) and CSF (n = 18) were examined. Clinical data, including Glasgow coma scale (GCS) and Liverpool outcome scores, were recorded. Examining serum and CSF markers in the three AES etiology groups revealed notable distinctions, with scr</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2025-04-06T15:27:59.561Z</modification><creation>2025-04-06T15:27:59.561Z</creation></dates><accession>S-EPMC7616670</accession><cross_references><pubmed>38738569</pubmed><doi>10.1002/jmv.29666</doi></cross_references></HashMap>