Evidence map›Paper›PMID 37094999›Full record

ArticleNeurology(R) neuroimmunology & neuroinflammation2023

Arterial Spin Labeling Changes Parallel Asymmetric Perisylvian and Perirolandic Symptoms in 3 Pediatric Cases of Anti-NMDAR Encephalitis.

Alexander J Sandweiss, Varun Kannan, Nilesh K Desai, Stephen F Kralik, Eyal Muscal, Kristen S Fisher

Open access · goldAbstract read
In one paragraph

Article in Neurology(R) neuroimmunology & neuroinflammation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 6 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 2 countries.

Alexander J SandweissFrom the Division of Pediatric Neurology and Developmental Neuroscience (A.J.S., V.K., K.S.F.), Department of Pediatrics; Department of Radiology (N.K.D., S.F.K.); and Department of Pediatrics (E.M.), Section of Rheumatology, Baylor College of Medicine and Texas Children's Hospital.ORCID 0000-0002-8213-2941
Varun KannanFrom the Division of Pediatric Neurology and Developmental Neuroscience (A.J.S., V.K., K.S.F.), Department of Pediatrics; Department of Radiology (N.K.D., S.F.K.); and Department of Pediatrics (E.M.), Section of Rheumatology, Baylor College of Medicine and Texas Children's Hospital.ORCID 0000-0002-9783-4401
Nilesh K DesaiFrom the Division of Pediatric Neurology and Developmental Neuroscience (A.J.S., V.K., K.S.F.), Department of Pediatrics; Department of Radiology (N.K.D., S.F.K.); and Department of Pediatrics (E.M.), Section of Rheumatology, Baylor College of Medicine and Texas Children's Hospital.
Stephen F KralikFrom the Division of Pediatric Neurology and Developmental Neuroscience (A.J.S., V.K., K.S.F.), Department of Pediatrics; Department of Radiology (N.K.D., S.F.K.); and Department of Pediatrics (E.M.), Section of Rheumatology, Baylor College of Medicine and Texas Children's Hospital.
Eyal MuscalFrom the Division of Pediatric Neurology and Developmental Neuroscience (A.J.S., V.K., K.S.F.), Department of Pediatrics; Department of Radiology (N.K.D., S.F.K.); and Department of Pediatrics (E.M.), Section of Rheumatology, Baylor College of Medicine and Texas Children's Hospital.
Kristen S FisherFrom the Division of Pediatric Neurology and Developmental Neuroscience (A.J.S., V.K., K.S.F.), Department of Pediatrics; Department of Radiology (N.K.D., S.F.K.); and Department of Pediatrics (E.M.), Section of Rheumatology, Baylor College of Medicine and Texas Children's Hospital. kristenf@bcm.edu.ORCID 0000-0002-1598-8571
Norwegian Womens Public Health Association · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesAnti-NMDA receptor autoimmune encephalitis (NMDAR AE) is an autoantibody-mediated disorder characterized by seizures, neuropsychiatric symptoms, movement disorder, and focal neurologic deficits. Conventionally defined broadly as an inflammatory brain disease, the heterotopic localization is rarely discussed in children. Imaging findings are often nonspecific, and there are no early biomarkers of disease other than the presence of anti-NMDAR antibodies.

methodsWe conducted a retrospective analysis of our pediatric NMDAR AE cases (as determined by either positive serum or CSF antibodies or both) at Texas Children's Hospital between 2020-2021 and extracted medical record data of those patients who had arterial spin labeling (ASL) as part of their imaging workup for encephalitis. The ASL findings were described in the context of their symptoms and disease courses.

resultsWe identified 3 children on our inpatient floor, intensive care unit (ICU), and emergency department (ED) settings who were diagnosed with NMDAR AE and had ASL performed as part of their focal neurologic symptom workup. All 3 patients presented with focal neurologic deficits, expressive aphasia, and focal seizures before the onset of other well-characterized NMDAR AE symptoms. Their initial MRI revealed no diffusion abnormalities but uncovered asymmetric and predominantly unilateral multifocal hyperperfusion of perisylvian/perirolandic regions on ASL that correlated with focal EEG abnormalities and their focal examination findings. All 3 patients were treated with first-line and second-line therapies, and their symptoms improved. DISCUSSION: We found that ASL may be a suitable early imaging biomarker to highlight perfusion changes corresponding to the functional localization of NMDAR AE in pediatric patients. We briefly highlight the neuroanatomic parallels between working models of schizophrenia, chronic NMDAR antagonist administration (ketamine abuse), and NMDAR AE affecting primarily language centers. The regional specificity seen in NMDAR hypofunction may make ASL a reasonable early and specific biomarker of NMDAR AE disease activity. Future studies are necessary to evaluate regional changes in those patients who present with primarily psychiatric phenotypes rather than classical focal neurologic deficits.

Indexed as

Anti-N-Methyl-D-Aspartate Receptor EncephalitisBrainEncephalitisHashimoto DiseaseHumansReceptors, N-Methyl-D-AspartateRetrospective StudiesSeizuresSpin LabelsReceptors, N-Methyl-D-AspartateSpin Labels

Identifiers

PMID37094999
PMCPMC10136681
OpenAlexW4366815657

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.