Evidence map›Paper›PMID 39411473›Full record

ArticleJCPP advances2024

Prevalence and heritability of parental-reported speech and/or language difficulties in a Swedish population-based twin sample.

Rebecka Keijser, Jakob Åsberg Johnels, Marika Habbe, Paul Lichtenstein, Henrik Larsson, Sebastian Lundström, Mark J Taylor, Kristiina Tammimies

Abstract read
In one paragraph

Article in JCPP advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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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

8 authors.

Rebecka KeijserThe Center of Neurodevelopmental Disorders (KIND) Centre for Psychiatry Research Department of Women's and Children's Health Karolinska Institutet and Child and Adolescent Psychiatry Stockholm Health Care Services Stockholm County Council Stockholm Sweden.ORCID https://orcid.org/0000-0003-1711-9748
Jakob Åsberg JohnelsGillberg Neuropsychiatry Centre Institute of Neuroscience and Physiology University of Gothenburg Gothenburg Sweden.
Marika HabbeThe Center of Neurodevelopmental Disorders (KIND) Centre for Psychiatry Research Department of Women's and Children's Health Karolinska Institutet and Child and Adolescent Psychiatry Stockholm Health Care Services Stockholm County Council Stockholm Sweden.
Paul LichtensteinDepartment of Medical Epidemiology and Biostatistics Karolinska Institutet Stockholm Sweden.
Henrik LarssonDepartment of Medical Epidemiology and Biostatistics Karolinska Institutet Stockholm Sweden.
Sebastian LundströmGillberg Neuropsychiatry Centre Institute of Neuroscience and Physiology University of Gothenburg Gothenburg Sweden.
Mark J TaylorDepartment of Medical Epidemiology and Biostatistics Karolinska Institutet Stockholm Sweden.ORCID https://orcid.org/0000-0001-5161-4182
Kristiina TammimiesThe Center of Neurodevelopmental Disorders (KIND) Centre for Psychiatry Research Department of Women's and Children's Health Karolinska Institutet and Child and Adolescent Psychiatry Stockholm Health Care Services Stockholm County Council Stockholm Sweden.ORCID https://orcid.org/0000-0002-8324-4697

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Research on genetic and environmental influences on speech and/or language difficulties (SaLD) is sparse, with inconsistent heritability estimates. We aimed to estimate the prevalence of parental reported SaLD and the relative contributions of genetic and environmental factors for the phenotype using a Swedish population-based twin sample. We hypothesized that there would be a stronger genetic than environmental effect on SaLD. Methods: Data were collected from The Child and Adolescent Twin Study in Sweden. The study sample included 16,774 twin pairs (16,946 males, 16,602 females), of which 5141 were monozygotic, 5861 dizygotic (DZ), and 5772 opposite-sex DZ pairs. The language items in the Autism-Tics, Attention-Deficit Hyperactivity Disorder, and other Comorbidities inventory were used to categorize individuals as having parental-reported SaLD. A classical twin design was used to estimate the relative contribution of genetic and environmental factors to the liability of SaLD. Results: The prevalence of SaLD was 7.85% (95% confidence interval (CI) [7.57%-8.15%]) and 7.27% (95% CI [6.99%-7.55%]) when excluding individuals with autism and intellectual disability (ID). We also found that SaLD were significantly more prevalent in males than females with a ratio of 2:1. The heritability was estimated to be 75% (95% CI [67%-83%]) for SaLD. Shared environment played a significant role with an estimated contribution of 22% (95% CI [14%-30%]). The heritability estimate was reduced to 70% but with overlapping CI when excluding individuals with autism and ID. Conclusions: We provide evidence that SaLD is common in the population and under strong genetic influence. Future studies should focus on mapping the genetic architecture of SaLD and related disorders.

Indexed as

heritabilitylanguage disorderprevalencespeech disordertwin study

Identifiers

PMID39411473
PMCPMC11472810

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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.