A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä

Longitudinal brain morphology in anti-NMDA receptor encephalitis: a case report with controls




TekijätLaurikainen H, Isotupa I, Nyman M, Ilonen T, Nummelin T, Salokangas RKR, Hietala J

KustantajaBMC (BioMed Central Ltd.)

KustannuspaikkaLontoo

Julkaisuvuosi2019

JournalBMC Psychiatry

Tietokannassa oleva lehden nimiBMC PSYCHIATRY

Lehden akronyymiBMC PSYCHIATRY

Artikkelin numeroARTN 145

Vuosikerta19

Numero1

Sivujen määrä6

ISSN1471-244X

eISSN1471-244X

DOIhttps://doi.org/10.1186/s12888-019-2141-4

Verkko-osoitehttps://bmcpsychiatry.biomedcentral.com/articles/10.1186/s12888-019-2141-4

Rinnakkaistallenteen osoitehttps://research.utu.fi/converis/portal/detail/Publication/41096888


Tiivistelmä

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.


Ladattava julkaisu

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