Evidence map›Paper›PMID 40943215›Full record

ArticleInternational journal of molecular sciences2025

Transgenerational Effects and Heritability of Folate Receptor Alpha Autoantibodies in Autism Spectrum Disorder.

Richard E Frye, Ira L Cohen, Jeffrey M Sequeira, Zoe Hill, Alina Espinoza, W Ted Brown, Clifford Mevs, Elaine Marchi, Michael Flory, Edmund C Jenkins and 2 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. 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
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

Richard E FryeAutism Discovery and Treatment Foundation, Phoenix, AZ 85050, USA.ORCID 0000-0003-4442-2937
Ira L CohenDepartment of Psychology, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY 10314, USA.
Jeffrey M SequeiraDepartment of Medicine, SUNY Downstate Medical Center, Brooklyn, NY 11203, USA.
Zoe HillAutism Discovery and Treatment Foundation, Phoenix, AZ 85050, USA.
Alina EspinozaAutism Discovery and Treatment Foundation, Phoenix, AZ 85050, USA.
W Ted BrownDepartment of Human Genetics, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY 10314, USA.
Clifford MevsPediatric Health Care, Staten Island, NY 10311, USA.
Elaine MarchiDepartment of Human Genetics, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY 10314, USA.
Michael FloryResearch Design and Analysis Core, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY 10314, USA.
Edmund C JenkinsDepartment of Human Genetics, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY 10314, USA.
Milen T VelinovDepartment of Genetics, Rutgers University, Piscataway, NJ 08854, USA.ORCID 0000-0002-0551-2019
Edward V QuadrosDepartment of Medicine, SUNY Downstate Medical Center, Brooklyn, NY 11203, USA.

Funding

Arizona Department of Health Services RFGA2022-010-31Autism Speaks 8202New York State OPWDD NAXEL Foundation NA
6 · The paper itself

Abstract

Autism Spectrum Disorder (ASD) affects an estimated prevalence of 1 in 31 children but the cause in most cases is unknown. Human and animal studies have linked ASD to Folate Receptor Alpha Autoantibodies (FRAAs). Our previous studies demonstrated that FRAAs are more common, on average, in families with children with ASD. This study reanalyzed data from a previous study which included 82 children diagnosed with ASD, 53 unaffected siblings, 70 mothers, 65 fathers, and 52 typically developing controls who did not have a history of ASD in their family. This study investigates the association of FRAA titers with ASD risk factors and explores the relationship of FRAA titers across generations. Several known risk factors for ASD, including multiplex ASD families, multiple birth pregnancies, and increased maternal and paternal ages at birth, were related to offspring FRAA titers. Multiplex ASD families demonstrated higher FRAA titers. Significant correlation were found between maternal and offspring blocking FRAA titers. FRAA titers increased across generations, although the increase in blocking FRAA titers was only seen in multiplex families. The proband with ASD showed higher blocking but not higher binding, FRAA titers compared to their non-affected siblings. Paternal FRAA titers are associated with several measures of offspring behavior and cognitive development. This research highlights the potential transgenerational transmission of FRAAs and their role in ASD. This supports the notion that heritable non-genetic factors may be important in the etiology of ASD and that FRAAs may demonstrate anticipation (worsening across generations), especially in multiplex families. FRAAs may provide one example of the possibility that susceptibility to autoimmune processes may contribute to disrupted brain development and function in ASD.

Indexed as

Autism Spectrum DisorderAutoantibodiesFolate Receptor 1AdultChildChild, PreschoolFemaleGenetic Predisposition to DiseaseHumansMaleRisk FactorsSiblingsAutoantibodiesFolate Receptor 1FOLR1 protein, humananticipationautism spectrum disordercerebral folate deficiencyfolate receptor alphafolate receptor alpha autoantibodiesheritability

Identifiers

PMID40943215
PMCPMC12428755

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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.