Evidence map›Paper›PMID 40549282›Full record

ArticleJournal of autism and developmental disorders2025

Sleep in Infants with Down Syndrome or Familial Likelihood of Autism in the First Year of Life.

Emma R Coco, Jeffrey Munson, Tanya St John, Stephen R Dager, Kelly Botteron, Jed Elison, Dea Garic, Heather Hazlett, Chimei Lee, Natasha Marrus and 6 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of autism and developmental disorders, 2025. 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

16 authors.

Emma R CocoInstitute on Human Development and Disability, University of Washington, Seattle, WA, 98195, USA.
Jeffrey MunsonInstitute on Human Development and Disability, University of Washington, Seattle, WA, 98195, USA.
Tanya St JohnInstitute on Human Development and Disability, University of Washington, Seattle, WA, 98195, USA.
Stephen R DagerInstitute on Human Development and Disability, University of Washington, Seattle, WA, 98195, USA.
Kelly BotteronDepartment of Psychiatry, Washington University School of Medicine in St. Louis, St. Louis, MI, 63110, USA.
Jed ElisonDepartment of Educational Psychology, University of Minnesota, Minneapolis, MN, 55455, USA.
Dea GaricDepartment of Psychiatry, University of North Carolina, Chapel Hill, NC, 27599, USA.
Heather HazlettDepartment of Psychiatry, University of North Carolina, Chapel Hill, NC, 27599, USA.
Chimei LeeDepartment of Educational Psychology, University of Minnesota, Minneapolis, MN, 55455, USA.
Natasha MarrusDepartment of Psychiatry, Washington University School of Medicine in St. Louis, St. Louis, MI, 63110, USA.
John R PruettDepartment of Psychiatry, Washington University School of Medicine in St. Louis, St. Louis, MI, 63110, USA.
Robert SchultzCenter for Autism Research, The Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA, 19104, USA.
Mark ShenDepartment of Psychiatry, University of North Carolina, Chapel Hill, NC, 27599, USA.
Lonnie ZwaigenbaumDepartment of Pediatrics, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, AB, Canada.
Joseph PivenDepartment of Psychiatry, University of North Carolina, Chapel Hill, NC, 27599, USA.
Annette EstesInstitute on Human Development and Disability, University of Washington, Seattle, WA, 98195, USA. estesa@uw.edu.ORCID http://orcid.org/0000-0003-2687-4155

Funding

Cellular and molecular mechanisms governing cortical surface area overgrowth in iPSC-derived neural cells from longitudinally characterized individuals with autismR01HD055741 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Joseph Piven · 2007 to 2026
$52.6M
MRI-Based Presymptomatic Prediction of ASD, and Early Infant to School-Age Brain-Behavior Trajectories, Mechanisms, and Related OutcomesR01MH118362 · NIMH · WASHINGTON UNIVERSITY · PI John R Pruett · 2019 to 2026
$16.3M
WUIDDRC Supplement-Supporting the health and well-being of children with intellectual and developmental disability during COVID-19 pandemicP50HD103525 · NICHD · WASHINGTON UNIVERSITY · PI JEFFREY D MILBRANDT · 2020 to 2026
$15.5M
A Longitudinal MRI Study Characterizing Very Early Brain Development in Infants with Down SyndromeR01HD088125 · NICHD · WASHINGTON UNIVERSITY · PI MARRUS, NATASHA · 2018 to 2024
$13.9M
Sleep, Brain Development, and Behavioral Correlates in a Longitudinal Cohort of Children at Risk for ASDR01HD101578 · NICHD · UNIVERSITY OF WASHINGTON · PI ESTES, ANNETTE · 2021 to 2025
$3.4M
NICHD NIH HHS P50 HD103525NICHD NIH HHS R01 HD055741NICHD NIH HHS R01 HD088125NICHD NIH HHS R01 HD101578NIMH NIH HHS R01 MH118362
6 · The paper itself

Abstract

Sleep problems have been associated with atypical development, but there is limited understanding of when sleep problems arise and how they differ across clinical populations. We aimed to evaluate sleep characteristics of infants with Down syndrome (DS), higher familial likelihood of autism (HL) and lower familial likelihood of autism (LL) at 6 and 12 months of age. Participants were from two longitudinal, multi-site, studies. Sleep was estimated by parent report on the Brief Infant Sleep Questionnaire at 6 months (59 DS, 173 HL, 54 LL); 12 months (58 DS, 129 HL, 30 LL); and in a longitudinal subset at both 6 and 12 months (100 HL; 23 LL; 33 DS). At 6-months, DS parents reported less concern about infant sleep and less night wakefulness than LL parents; HL parents reported longer sleep onset latency (SOL). At 12 months DS parents reported less night sleep and more night wakefulness; HL parents reported less night sleep, more night wakefulness and longer SOL compared to LL. Night wakefulness increased significantly in the DS and HL groups from 6 to 12 months of age. A higher proportion of DS and HL infants decreased Night Sleep and increased Night Wakefulness compared with the LL group. A higher proportion of DS infants increased SOL compared with the LL group. Sleep alterations are present in the first year of life and may differ in DS and HL infants. The mechanisms behind these sleep alterations may be an important early intervention target.

Indexed as

Autistic DisorderDown SyndromeSleepSleep Wake DisordersFemaleHumansInfantLongitudinal StudiesMaleParentsSurveys and QuestionnairesWakefulnessAutismDown syndromeInfantSleep

Identifiers

PMID40549282
PMCPMC12589275

What OpenQuestion 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 OpenQuestion graph.