Literature DB >> 23889589

Quantitative FLAIR analysis indicates predominant affection of the amygdala in antibody-associated limbic encephalitis.

Jan Wagner1, Jan-Christoph Schoene-Bake, Michael P Malter, Horst Urbach, Hans-Jürgen Huppertz, Christian E Elger, Bernd Weber.   

Abstract

PURPOSE: Limbic encephalitis is an autoimmune-mediated disease leading to temporal lobe epilepsy, mnestic deficits, and affective disturbances. Magnetic resonance imaging (MRI) usually shows signal and volume changes of the temporomesial structures. However, these abnormalities may be subtle, thereby hampering the diagnosis by conventional visual assessment. In the present study we evaluated the diagnostic value of a fully automated MRI postprocessing technique in limbic encephalitis and hippocampal sclerosis.
METHODS: The MRI postprocessing was based largely on a recently described method allowing for an observer-independent quantification of the fluid-attenuated inversion recovery (FLAIR) signal intensities of amygdala and hippocampus. A 95% confidence region was calculated from the FLAIR intensities of 100 healthy controls. We applied this analysis to the MRI data of 39 patients with antibody-associated limbic encephalitis and 63 patients with hippocampal sclerosis. Moreover, the results were compared to those of visual assessment by an experienced neuroradiologist. KEY
FINDINGS: The method detected limbic encephalitis and hippocampal sclerosis with a high sensitivity of 85% and 95%, respectively. The detection rate of the automated approach in limbic encephalitis was significantly superior to visual analysis (85% vs. 51%; p = 0.001), whereas no statistically significant difference for the detection rate in hippocampal sclerosis was found. Patients with limbic encephalitis had significantly higher absolute intensity values of the amygdala and a significantly higher percentage fell outside of the amygdalar confidence region compared to those with hippocampal sclerosis (79% vs. 27%; p < 0.001), whereas we found opposite results in the hippocampal analysis (38% vs. 95%; p < 0.001). SIGNIFICANCE: The FLAIR analysis applied in this study is a powerful tool to quantify signal changes of the amygdala and hippocampus in limbic encephalitis and hippocampal sclerosis. It significantly increases the diagnostic sensitivity in limbic encephalitis in comparison to conventional visual analysis. Furthermore, the method provides an interesting insight into the distinct properties of these two disease entities on MRI, indicating a predominant affection of the amygdala in limbic encephalitis, whereas the affection of the hippocampus is far less pronounced when compared to hippocampal sclerosis. Wiley Periodicals, Inc.
© 2013 International League Against Epilepsy.

Entities:  

Keywords:  Epilepsy; Hippocampal sclerosis; Magnetic resonance imaging; Postprocessing

Mesh:

Year:  2013        PMID: 23889589     DOI: 10.1111/epi.12320

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  15 in total

1.  Supratentorial white matter blurring associated with voltage-gated potassium channel-complex limbic encephalitis.

Authors:  H Urbach; S Rauer; I Mader; S Paus; J Wagner; M P Malter; H Prüss; J Lewerenz; J Kassubek; H Hegen; M Auer; F Deisenhammer; F Ufer; C G Bien; A Baumgartner
Journal:  Neuroradiology       Date:  2015-08-21       Impact factor: 2.804

Review 2.  Recent advances in epilepsy.

Authors:  Mark Manford
Journal:  J Neurol       Date:  2017-01-24       Impact factor: 4.849

3.  Limbic Encephalitis in Patients with Epilepsy-is Quantitative MRI Diagnostic?

Authors:  Arndt-Hendrik Schievelkamp; Alina Jurcoane; Theodor Rüber; Leon Ernst; Andreas Müller; Burkhard Mädler; Hans Heinz Schild; Elke Hattingen
Journal:  Clin Neuroradiol       Date:  2018-07-16       Impact factor: 3.649

4.  Impaired Autonomic Responses to Emotional Stimuli in Autoimmune Limbic Encephalitis.

Authors:  Olga Schröder; Elisabeth Schriewer; Kristin S Golombeck; Julia Kürten; Hubertus Lohmann; Wolfram Schwindt; Heinz Wiendl; Maximilian Bruchmann; Nico Melzer; Thomas Straube
Journal:  Front Neurol       Date:  2015-11-30       Impact factor: 4.003

5.  Seizure semiology: an important clinical clue to the diagnosis of autoimmune epilepsy.

Authors:  Rui-Juan Lv; Hai-Tao Ren; Hong-Zhi Guan; Tao Cui; Xiao-Qiu Shao
Journal:  Ann Clin Transl Neurol       Date:  2018-01-22       Impact factor: 4.511

6.  Selective Limbic Blood-Brain Barrier Breakdown in a Feline Model of Limbic Encephalitis with LGI1 Antibodies.

Authors:  Anna R Tröscher; Andrea Klang; Maria French; Lucía Quemada-Garrido; Sibylle Maria Kneissl; Christian G Bien; Ákos Pákozdy; Jan Bauer
Journal:  Front Immunol       Date:  2017-10-18       Impact factor: 7.561

Review 7.  CD8(+) T Cell-Mediated Neuronal Dysfunction and Degeneration in Limbic Encephalitis.

Authors:  Petra Ehling; Nico Melzer; Thomas Budde; Sven G Meuth
Journal:  Front Neurol       Date:  2015-07-15       Impact factor: 4.003

Review 8.  Limbic Encephalitis: Potential Impact of Adaptive Autoimmune Inflammation on Neuronal Circuits of the Amygdala.

Authors:  Nico Melzer; Thomas Budde; Oliver Stork; Sven G Meuth
Journal:  Front Neurol       Date:  2015-08-03       Impact factor: 4.003

9.  Hippocampus and Insula Are Targets in Epileptic Patients With Glutamic Acid Decarboxylase Antibodies.

Authors:  Mercè Falip; Laura Rodriguez-Bel; Sara Castañer; Jacint Sala-Padró; Júlia Miro; Sónia Jaraba; Carlos Casasnovas; Francisco Morandeira; Javier Berdejo; Mar Carreño
Journal:  Front Neurol       Date:  2019-01-09       Impact factor: 4.003

10.  18F-FDG-PET/MRI in the diagnostic work-up of limbic encephalitis.

Authors:  Cornelius Deuschl; Theodor Rüber; Leon Ernst; Wolfgang P Fendler; Julian Kirchner; Christoph Mönninghoff; Ken Herrmann; Carlos M Quesada; Michael Forsting; Christian E Elger; Lale Umutlu
Journal:  PLoS One       Date:  2020-01-17       Impact factor: 3.240

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