Evidence map›Paper›PMID 30097568›Full record

Observational studyTranslational psychiatry2018

Intravenous immunoglobulin for the treatment of autoimmune encephalopathy in children with autism.

Kathleen Connery, Marie Tippett, Leanna M Delhey, Shannon Rose, John C Slattery, Stephen G Kahler, Juergen Hahn, Uwe Kruger, Madeleine W Cunningham, Craig Shimasaki and 1 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Translational psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.6field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 60 citations in OpenAlex.

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  19. Viruses and autism: A Bi-mutual cause and effect.World journal of virology · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 1 country.

Kathleen ConneryUniversity of Arkansas for Medical Sciences, Little Rock, AR, 77205, USA.
Marie TippettUniversity of Arkansas for Medical Sciences, Little Rock, AR, 77205, USA.
Leanna M DelheyUniversity of Arkansas for Medical Sciences, Little Rock, AR, 77205, USA.
Shannon RoseUniversity of Arkansas for Medical Sciences, Little Rock, AR, 77205, USA.ORCID http://orcid.org/0000-0003-0595-4367
John C SlatteryBioROSA Technologies Inc, San Francisco, CA, 94103, USA.
Stephen G KahlerUniversity of Arkansas for Medical Sciences, Little Rock, AR, 77205, USA.
Juergen HahnDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, NY, 12180, USA.ORCID http://orcid.org/0000-0002-1078-4203
Uwe KrugerDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, NY, 12180, USA.
Madeleine W CunninghamDepartment of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 73104, USA.
Craig ShimasakiMoleculera Labs, Inc, Oklahoma City, OK, USA.
Richard E FryeBarrow Neurological Institute at Phoenix Children's Hospital, Phoenix, AZ, USA. rfrye@phoenixchildrens.com.ORCID http://orcid.org/0000-0003-4442-2937
University of Arkansas for Medical Sciences · USRensselaer Polytechnic Institute · USBarrow Neurological Institute · USMolecule Works (United States) · USSA Technologies (United States) · USUniversity of Oklahoma Health Sciences Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The identification of brain-targeted autoantibodies in children with autism spectrum disorder (ASD) raises the possibility of autoimmune encephalopathy (AIE). Intravenous immunoglobulin (IVIG) is effective for AIE and for some children with ASD. Here, we present the largest case series of children with ASD treated with IVIG. Through an ASD clinic, we screened 82 children for AIE, 80 of them with ASD. IVIG was recommended for 49 (60%) with 31 (38%) receiving the treatment under our care team. The majority of parents (90%) reported some improvement with 71% reporting improvements in two or more symptoms. In a subset of patients, Aberrant Behavior Checklist (ABC) and/or Social Responsiveness Scale (SRS) were completed before and during IVIG treatment. Statistically significant improvement occurred in the SRS and ABC. The antidopamine D2L receptor antibody, the anti-tubulin antibody and the ratio of the antidopamine D2L to D1 receptor antibodies were related to changes in the ABC. The Cunningham Panel predicted SRS, ABC, parent-based treatment responses with good accuracy. Adverse effects were common (62%) but mostly limited to the infusion period. Only two (6%) patients discontinued IVIG because of adverse effects. Overall, our open-label case series provides support for the possibility that some children with ASD may benefit from IVIG. Given that adverse effects are not uncommon, IVIG treatment needs to be considered cautiously. We identified immune biomarkers in select IVIG responders but larger cohorts are needed to study immune biomarkers in more detail. Our small open-label exploratory trial provides evidence supporting a neuroimmune subgroup in patients with ASD.

Indexed as

Administration, IntravenousAdolescentAmbulatory Care FacilitiesArkansasAutism Spectrum DisorderCase-Control StudiesChildChild, PreschoolEncephalitisFemaleHashimoto DiseaseHumansImmunoglobulins, IntravenousMaleReceptors, Dopamine D1Immunoglobulins, IntravenousReceptors, Dopamine D1

Identifiers

PMID30097568
PMCPMC6086890
OpenAlexW2885292966

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.