<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Binks SNM</submitter><funding>Petre Foundation</funding><funding>Epilepsy Research UK</funding><funding>Medical Research Council</funding><funding>NIHR Oxford Biomedical Research Centre</funding><funding>National Institute for Health Research (NIHR)</funding><funding>National Health and Medical Research Council</funding><funding>University of Sydney</funding><funding>National Institute for Health and Care Research</funding><funding>British Medical Association</funding><funding>Wellcome Trust</funding><funding>Royal Australasian College of Physicians</funding><funding>US-UK Fulbright Commission</funding><pagination>1053-1058</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11021603</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(4)</volume><pubmed_abstract>Patient-reported quality-of-life (QoL) and carer impacts are not reported after leucine-rich glioma-inactivated 1-antibody encephalitis (LGI1-Ab-E). From 60 patients, 85% (51 out of 60) showed one abnormal score across QoL assessments and 11 multimodal validated questionnaires. Compared to the premorbid state, QoL significantly deteriorated (p &lt; 0.001) and, at a median of 41 months, fatigue was its most important predictor (p = 0.025). In total, 51% (26 out of 51) of carers reported significant burden. An abbreviated five-item battery explained most variance in QoL. Wide-ranging impacts post-LGI1-Ab-E include decreased QoL and high caregiver strain. We identify a rapid method to capture QoL in routine clinic or clinical trial settings.</pubmed_abstract><journal>Annals of clinical and translational neurology</journal><pubmed_title>Fatigue predicts quality of life after leucine-rich glioma-inactivated 1-antibody encephalitis.</pubmed_title><pmcid>PMC11021603</pmcid><funding_grant_id>MR/V007173/1</funding_grant_id><funding_grant_id>CL-2022-13-007</funding_grant_id><funding_grant_id>Margaret Temple 2017</funding_grant_id><funding_grant_id>206330/Z/17/Z</funding_grant_id><funding_grant_id>P1201</funding_grant_id><funding_grant_id>MR/X022013/1</funding_grant_id><funding_grant_id>Vera Down grant 2013</funding_grant_id><funding_grant_id>104079/Z/14/Z</funding_grant_id><funding_grant_id>GNT2008339</funding_grant_id><pubmed_authors>Michael S</pubmed_authors><pubmed_authors>Nissen MS</pubmed_authors><pubmed_authors>Jacob S</pubmed_authors><pubmed_authors>Okai D</pubmed_authors><pubmed_authors>Binks SNM</pubmed_authors><pubmed_authors>Handel AE</pubmed_authors><pubmed_authors>Irani SR</pubmed_authors><pubmed_authors>Coebergh J</pubmed_authors><pubmed_authors>Blaabjerg M</pubmed_authors><pubmed_authors>Maddison P</pubmed_authors><pubmed_authors>Ramanathan S</pubmed_authors><pubmed_authors>Leite MI</pubmed_authors><pubmed_authors>Easton A</pubmed_authors><pubmed_authors>Husain M</pubmed_authors><pubmed_authors>Veldsman M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Fatigue predicts quality of life after leucine-rich glioma-inactivated 1-antibody encephalitis.</name><description>Patient-reported quality-of-life (QoL) and carer impacts are not reported after leucine-rich glioma-inactivated 1-antibody encephalitis (LGI1-Ab-E). From 60 patients, 85% (51 out of 60) showed one abnormal score across QoL assessments and 11 multimodal validated questionnaires. Compared to the premorbid state, QoL significantly deteriorated (p &lt; 0.001) and, at a median of 41 months, fatigue was its most important predictor (p = 0.025). In total, 51% (26 out of 51) of carers reported significant burden. An abbreviated five-item battery explained most variance in QoL. Wide-ranging impacts post-LGI1-Ab-E include decreased QoL and high caregiver strain. We identify a rapid method to capture QoL in routine clinic or clinical trial settings.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2025-04-04T12:58:21.216Z</modification><creation>2025-04-04T12:58:21.216Z</creation></dates><accession>S-EPMC11021603</accession><cross_references><pubmed>38303486</pubmed><doi>10.1002/acn3.52006</doi></cross_references></HashMap>