Evidence map›Paper›PMID 31572230›Full record

ArticleFrontiers in psychiatry2019

Inheritance of HLA-Cw7 Associated With Autism Spectrum Disorder (ASD).

Terry Harville, Bobbie Rhodes-Clark, Sirish C Bennuri, Leanna Delhey, John Slattery, Marie Tippett, Rebecca Wynne, Shannon Rose, Stephen Kahler, Richard E Frye

Open access · goldAbstract read
In one paragraph

Article in Frontiers in psychiatry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Immune Dysregulation in Autism Spectrum Disorder: What Do We Know about It?International journal of molecular sciences · 2022
    Review
  6. Article
  7. Review
  8. Article
  9. Review
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

10 authors at 5 institutions in 1 country.

Terry HarvilleDepartment of Pathology, University of Arkansas for Medical Sciences, Little Rock, AR, United States.
Bobbie Rhodes-ClarkDepartment of Pathology, University of Arkansas for Medical Sciences, Little Rock, AR, United States.
Sirish C BennuriDepartment of Pediatrics, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR, United States.
Leanna DelheySchool of Public Health, University of Arkansas for Medical Sciences, Little Rock, AR, United States.
John SlatteryBioRosa Technologies Inc, San Francisco, CA, United States.
Marie TippettDepartment of Pediatrics, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR, United States.
Rebecca WynneNational Center for Toxicological Research, Jefferson, AR, United States.
Shannon RoseDepartment of Pediatrics, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR, United States.
Stephen KahlerDepartment of Pediatrics, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR, United States.
Richard E FryeBarrow Neurological Institute at Phoenix Children's Hospital, Phoenix, AZ, United States.
Arkansas Children's Hospital · USUniversity of Arkansas for Medical Sciences · USNational Center for Toxicological Research · USSA Technologies (United States) · USUniversity of Arizona · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autism spectrum disorder (ASD) is a behaviorally defined disorder that is now thought to affect approximately 1 in 69 children in the United States. In most cases, the etiology is unknown, but several studies point to the interaction of genetic predisposition with environmental factors. The immune system is thought to have a causative role in ASD, and specific studies have implicated T lymphocytes, monocytes, natural killer (NK) cells, and certain cytokines. The human leukocyte antigen (HLA) system is involved in the underlying process for shaping an individual's immune system, and specific HLA alleles are associated with specific diseases as risk factors. In this study, we determine whether a specific HLA allele was associated with ASD in a large cohort of patients with ASD. Identifying such an association could help in the identification of immune system components which may have a causative role in specific cohorts of patients with ASD who share similar specific clinical features. Specimens from 143 patients with ASD were analyzed with respect to race and ethnicity. Overall, HLA-Cw7 was present in a much greater frequency than expected in individuals with ASD as compared to the general population. Further, the cohort of patients who express HLA-Cw7 shares specific immune system/inflammatory clinical features including being more likely to have allergies, food intolerances, and chronic sinusitis as compared to those with ASD who did not express HLA-Cw7. HLA-Cw7 has a role in stimulating NK cells. Thus, this finding may indicate that chronic over-activation of NK cells may have a role in the manifestation of ASD in a cohort of patients with increased immune system/inflammatory features.

Indexed as

autism (ASD)HLAimmune systeminnate immnuitynatural killer cells

Identifiers

PMID31572230
PMCPMC6749146
OpenAlexW2964359950

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.