Evidence map›Paper›PMID 37293056›Full record

ArticleResearch square2023

Sensorimotor Behavior in Individuals with Autism Spectrum Disorder and Their Unaffected Biological Parents.

Erin K Bojanek, Shannon E Kelly, Lauren M Schmitt, Stormi P White, John A Sweeney, Andreas Sprenger, Kathryn E Unruh, Matthew W Mosconi

Open access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2023. 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, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 6 institutions in 2 countries.

Erin K BojanekUniversity of Rochester, University of Rochester Medical Center.
Shannon E KellyScholars Strategy Network.
Lauren M SchmittCincinnati Children's Hospital Medical Center.
Stormi P WhiteEmory University School of Medicine.
John A SweeneyUniversity of Cincinnati College of Medicine.
Andreas SprengerUniversity of Lübeck.
Kathryn E UnruhUniversity of Kansas.
Matthew W MosconiUniversity of Kansas.
University of Kansas · USCincinnati Children's Hospital Medical Center · USEmory University · USUniversity of Cincinnati Medical Center · USUniversity of Lübeck · DEUniversity of Rochester Medical Center · US

Funding

Using PCORnet to Expand the DS-CONNECT Cohort Through Healthcare System Recruitment, Incorporating Electronic Health Records, and Assessing Self-DeterminationU54HD090216 · NICHD · UNIVERSITY OF KANSAS LAWRENCE · PI BRADY, NANCY CAROLINE · 2016 to 2020
$6.2M
Motor abnormalities and functional brain mechanisms in autism spectrum disorderR01MH112734 · NIMH · UNIVERSITY OF KANSAS LAWRENCE · PI MOSCONI, MATTHEW W · 2017 to 2021
$2.3M
NICHD NIH HHS U54 HD090216NIMH NIH HHS R01 MH112734
6 · The paper itself

Abstract

Background: Sensorimotor impairments are common in autism spectrum disorder (ASD) and evident in unaffected first-degree relatives, suggesting that they may serve as important endophenotypes associated with inherited risk. We tested the familiality of sensorimotor impairments in ASD across multiple motor behaviors and effector systems and in relation to parental broader autism phenotypic (BAP) characteristics. Methods: Fifty-eight autistic individuals (probands), 109 parents, and 89 control participants completed tests of manual motor and oculomotor control. Sensorimotor tests varied in their involvement of Results: Probands with BAP- parents (BAP- probands) showed rapid manual motor and oculomotor deficits, while BAP+ probands showed sustained motor impairments compared to controls. BAP- parents showed impaired rapid oculomotor and sustained manual motor abilities relative to BAP+ parents and controls. Atypical rapid oculomotor impairments also were familial. Limitations: Larger samples of ASD families including greater samples of probands with BAP+ parents are needed. Genetic studies also are needed to link sensorimotor endophenotype findings directly to genes. Conclusions: Results indicate rapid sensorimotor behaviors are selectively impacted in BAP- probands and their parents and may reflect familial liabilities for ASD that are independent of familial autistic traits. Sustained sensorimotor behaviors were affected in BAP+ probands and BAP- parents re ecting familial traits that may only confer risk when combined with parental autistic trait liabilities. These findings provide new evidence that rapid and sustained sensorimotor alterations represent strong but separate familial pathways of ASD risk that demonstrate unique interactions with mechanisms related to parental autistic traits.

Indexed as

autism spectrum disorderbroader autism phenotypeendophenotypefamilialityheritable risksensorimotor

Identifiers

PMID37293056
PMCPMC10246285
OpenAlexW4378174949

What OpenQuestion holds

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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.