Evidence map›Paper›PMID 34240550›Full record

ArticleAmerican journal of medical genetics. Part A2021

Early developmental impact of sex chromosome trisomies on attention deficit-hyperactivity disorder symptomology in young children.

Kimberly Kuiper, Hanna Swaab, Nicole Tartaglia, Sophie van Rijn

Open access · hybridAbstract read
In one paragraph

Article in American journal of medical genetics. Part A, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  4. Emotional reactivity and expressivity in young children with sex chromosome trisomies: evidence from psychophysiological and observational data.Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence · 2023
    Article
  5. Review
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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

4 authors at 2 institutions in 2 countries.

Kimberly KuiperClinical Neurodevelopmental Sciences, Leiden University, Leiden, The Netherlands.ORCID 0000-0002-6429-5835
Hanna SwaabClinical Neurodevelopmental Sciences, Leiden University, Leiden, The Netherlands.
Nicole TartagliaeXtraordinarY Kids Clinic, Developmental Pediatrics, Children's Hospital Colorado, Aurora, Colorado, USA.
Sophie van RijnClinical Neurodevelopmental Sciences, Leiden University, Leiden, The Netherlands.
Leiden University · NLChildren's Hospital Colorado · US

Funding

NIH Prior Approval Process ProfessionalUL1TR002535 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2018 to 2022
$51.1M
The eXtraordinarY Babies Study: Natural History of Health and Neurodevelopment in Infants with Sex Chromosome TrisomyR01HD091251 · NICHD · UNIVERSITY OF COLORADO DENVER · PI Nicole Renee Tartaglia · 2017 to 2026
$5.6M
NCATS NIH HHS UL1 TR002535NCBDD CDC HHS U01 DD001298NICHD NIH HHS R01 HD091251NIH HHS UL1 TR002535
6 · The paper itself

Abstract

Individuals with sex chromosome trisomies ([SCT], XXX, XXY, and XYY)) are at increased risk for neurodevelopmental problems, given that a significant portion of the sex chromosome genes impact brain functioning. An elevated risk for psychopathology has also been described, including attention deficit-hyperactivity disorder (ADHD). The present study aimed at identifying early markers of ADHD, providing the first investigation of ADHD symptomology in very young children with SCT. The variety, type, and severity of ADHD symptomology in 1-6-year-old children with SCT (n = 104) were compared with population-based controls (n = 101) using the strengths and weaknesses of ADHD symptoms and normal-behavior (SWAN) parent-report questionnaire. ADHD symptomology was significantly more prevalent in SCT and already present from toddlerhood on, compared to controls. ADHD inattention symptoms were significantly increased in all karyotypes (XXX, XXY, and XYY), boys with XYY also showed significantly more hyperactivity/impulsivity symptoms than controls. Inattentiveness was more pronounced with increasing age for SCT, in contrast to controls. Within the SCT group, 24% of the children had significantly elevated ADHD symptoms at a clinical level. Already from an early age on, SCT is associated with a risk for ADHD, suggesting that its neurodevelopmental risk lies anchored in early brain maturation. Studying this genetically vulnerable population allows for the prospective study of risk markers to facilitate early and preventive interventions.

Indexed as

Sex Chromosome AberrationsAbnormal KaryotypeAttention Deficit Disorder with HyperactivityChildChild, PreschoolCognition DisordersFemaleHumansInfantMaleSex ChromosomesTrisomyXYY KaryotypeADHDdevelopmental psychopathologyKlinefelter syndromesex chromosomestrisomy X syndrome

Identifiers

PMID34240550
PMCPMC9292447
OpenAlexW3181419249

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.