Intravenous immunoglobulin treatment improves multiple neuropsychiatric outcomes in patients with pediatric acute-onset neuropsychiatric syndrome
Affiliation
Division of Allergy, Immunology and Rheumatology, Department of Pediatrics, University of ArizonaDepartment of Internal Medicine, Arizona College of Osteopathic Medicine, Midwestern University
Division of Developmental and Behavioral Pediatrics, Department of Pediatrics, University of Arizona
Issue Date
2023-10-16Keywords
immune deficiencyimmunomodulation
intravenous immunoglobulins (IVIG)
neuropsychological testing
pediatric acute-onset neuropsychiatric syndrome (PANS)
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections (PANDAS)
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Frontiers Media SACitation
Eremija J, Patel S, Rice S and Daines M (2023) Intravenous immunoglobulin treatment improves multiple neuropsychiatric outcomes in patients with pediatric acute-onset neuropsychiatric syndrome. Front. Pediatr. 11:1229150. doi: 10.3389/fped.2023.1229150Journal
Frontiers in PediatricsRights
© 2023 Eremija, Patel, Rice and Daines. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Pediatric Acute-Onset Neuropsychiatric Syndrome (PANS) is defined by acute onset of diverse neuropsychiatric manifestations, presumably in the setting of underlying immune dysfunction. We used standardized neuropsychological testing to assess how intravenous immunoglobulins (IVIG) impact neurological and cognitive functions in PANS patients by comparing pretreatment with post-treatment scores. A 5-year retrospective study was undertaken in Children's Postinfectious Autoimmune Encephalopathy Center at University of Arizona. We identified 12 children diagnosed with PANS and treated with immunomodulatory IVIG doses, who also completed neuropsychological testing before and after treatment. We tracked multiple patient characteristics, type/timeline of testing, and number of IVIG courses. Score change of 1 standard deviation in any tested domain/subdomain was considered improvement. We further reviewed records for laboratory signs of triggering infection and immune dysfunction. Improvement occurred in 11/12 patients, in one or multiple domains/subdomains, independently of time between disease onset and IVIG initiation (0–7 years). Participants received 1–7 IVIG courses. Improvement was primarily seen in memory (58%), sensory-motor (37%) and visual-motor integration (30%). In 5/12 patients we detected hypogammaglobulinemia requiring ongoing IVIG replacement, one patient had isolated low IgA. Only one patient had to discontinue IVIG therapy due to severe adverse effects. Standardized neuropsychological testing represents an important tool to objectively measure improvement in PANS patients. IVIG was tolerated well and showed efficacy in the vast majority of participants, independently from timelapse since disease onset, emphasizing impact of immunomodulation in PANS. Significant presence of baseline hypogammaglobulinemia in children with PANS emphasizes the presumed role of immune dysfunction in disease pathogenesis. 2023 Eremija, Patel, Rice and Daines.Note
Open access journalISSN
2296-2360PubMed ID
37908968Version
Final Published Versionae974a485f413a2113503eed53cd6c53
10.3389/fped.2023.1229150
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Except where otherwise noted, this item's license is described as © 2023 Eremija, Patel, Rice and Daines. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).
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