A1 Refereed original research article in a scientific journal
Longitudinal brain morphology in anti-NMDA receptor encephalitis: a case report with controls
Authors: Laurikainen H, Isotupa I, Nyman M, Ilonen T, Nummelin T, Salokangas RKR, Hietala J
Publisher: BMC (BioMed Central Ltd.)
Publishing place: Lontoo
Publication year: 2019
Journal: BMC Psychiatry
Journal name in source: BMC PSYCHIATRY
Journal acronym: BMC PSYCHIATRY
Article number: ARTN 145
Volume: 19
Issue: 1
Number of pages: 6
ISSN: 1471-244X
eISSN: 1471-244X
DOI: https://doi.org/10.1186/s12888-019-2141-4
Web address : https://bmcpsychiatry.biomedcentral.com/articles/10.1186/s12888-019-2141-4
Self-archived copy’s web address: https://research.utu.fi/converis/portal/detail/Publication/41096888
Background
Anti-N-methyl-D-aspartate-receptor (NMDAR) encephalitis is a severe autoimmune condition, which typically affects young females. The long-term clinical consequences and brain morphology changes after anti-NMDAR encephalitis are not well known.
Case presentation
We present clinical and neuroimaging follow-up data on a 25-year female patient with typically presenting anti-NMDAR encephalitis. Longitudinal analyses of brain morphology were done using 3T structural magnetic resonance imaging (sMRI) and Freesurfer analysis at the time of diagnosis and after symptomatic remission. The presented case attained good functional recovery after standard immunoglobulin-corticosteroid treatment but elevated serum NMDAR antibody levels persisted. The patient had no symptomatic relapses during a 3-year clinical follow-up. In the baseline brain sMRI scan there were no marked volume changes. However, a follow-up sMRI after 9months indicated clear volume reductions in frontal cortical regions compared to matched controls with identical sMRI scans.
Conclusions
This case report of anti-NMDAR encephalitis suggests that despite clinical recovery long-term brain morphological changes can develop in the frontal cortex. Longer clinical and imaging follow-up studies are needed to see whether these frontocortical alterations are fully reversible and if not, can they result in trait vulnerabilities for e.g. neuropsychiatric disorders.
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