Evidence map›Paper›PMID 42465880›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Maternal Extracellular Vesicles During Pregnancy and Autism Risk in Children.

Delia McGowan, Serena Nencini, William Yakah, Claire-Marie Vacher, Helene Lacaille, David M Haas, William A Grobman, Robert M Silver, Uma M Reddy, Ronald J Wapner and 3 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Delia McGowanBarnard College, Columbia University, New York, NY, United States.
Serena NenciniDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, United States.ORCID 0009-0007-8121-7859
William YakahDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, United States.ORCID 0000-0003-3264-5404
Claire-Marie VacherDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, United States.ORCID 0000-0002-2966-8149
Helene LacailleDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, United States.ORCID 0000-0003-4407-7547
David M HaasDepartment of Obstetrics and Gynecology, School of Medicine, Indiana University, Indianapolis, IN, United States.ORCID 0000-0002-8379-0743
William A GrobmanDepartment of Obstetrics and Gynecology, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Robert M SilverDepartment of Obstetrics and Gynecology, University of Utah, Salt Lake City, UT, United States.ORCID 0000-0002-5794-3152
Uma M ReddyDepartment of Obstetrics, Gynecology and Reproductive Sciences, Yale School of Medicine, New Haven, CT, United States.ORCID 0000-0002-8599-6040
Ronald J WapnerDepartment of Obstetrics and Gynecology, Columbia University Irving Medical Center New York, NY, United States.ORCID 0000-0003-0727-1244
William P FiferDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, United States.ORCID 0000-0002-6936-9303
Anna A PennDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, United States.ORCID 0000-0003-1539-5220
Morgan R FiresteinDepartment of Pediatrics, Child Health Institute of New Jersey, Brain Health Institute, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ, United States.ORCID 0000-0002-3814-8700

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Differences in extracellular vesicles (EVs), bioactive nanoparticles involved in intercellular signaling, have been reported in those with autism. However, little is known about the association between maternal EVs during pregnancy and the likelihood of autism in offspring. This study evaluated the association of the concentration and cargo material of EVs in prenatal maternal plasma with childhood autism likelihood. Methods: Participants in the Nulliparous Pregnancy Outcomes Study provided maternal plasma at 15-23 weeks' gestational age. EVs were isolated by ultracentrifugation, and concentration, mean size, CD63 levels, and RNA cargo were assessed by nanoparticle tracking analysis, ELISA, and small RNA sequencing. At 4.5-6 years of age, parents completed the Social Communication Questionnaire. Thirty-one children at high-risk for autism were matched to 31 low-risk children on sex, age, and gestational age. Differential RNA transcript analysis and over representation analysis were performed. Results: There were no group differences in CD63 levels, mean particle size, or EV concentration ( Limitations: Large studies involving individuals diagnosed with autism are needed to evaluate the role of prenatal EVs in the pathogenesis of the condition. Additionally, prenatal sampling of EVs across multiple timepoints and subsequent deconvolution to determine the source of the EVs will strengthen interpretability and veracity of our findings. Conclusions: These findings provide preliminary evidence that maternal prenatal EV RNA cargo is associated with childhood autism likelihood.

Indexed as

AutismExosomeExtracellular VesicleNeurodevelopmentPregnancyPrenatal

Identifiers

PMID42465880
PMCPMC13370910

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.