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Prevalence and heritability of parental-reported speech and/or language difficulties in a Swedish population-based twin sample
he 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 2Astrid Lindgren Children's Hospital, Karolinska University Hospital, Solna, Sweden.
Gillberg Neuropsychiatry Centre, Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden; Speech and Language Pathology Unit, Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden .
he 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 2Astrid Lindgren Children's Hospital, Karolinska University Hospital, Solna, Sweden.
DDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
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2024 (English)In: JCPP Advances, E-ISSN 2692-9384, Vol. 4, no 3, article id e12221Article in journal (Refereed) Published
Abstract [en]

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.

Place, publisher, year, edition, pages
John Wiley & Sons, 2024. Vol. 4, no 3, article id e12221
Keywords [en]
Heritability, language disorder, prevalence, speech disorder, twin study
National Category
Public Health, Global Health and Social Medicine
Identifiers
URN: urn:nbn:se:oru:diva-116872DOI: 10.1002/jcv2.12221ISI: 001336635900013PubMedID: 39411473OAI: oai:DiVA.org:oru-116872DiVA, id: diva2:1906666
Funder
Forte, Swedish Research Council for Health, Working Life and Welfare, 2021‐00110The Swedish Brain Foundation, FO2021‐0073Swedish Psychiatric Foundation, 2022/2023
Note

The study was financed by The Swedish Research Councilfor Health, Working Life and Welfare – Forte (2021‐00110), the Swedish Brain Foundation (FO2021‐0073), Fonden för Psykisk Hälsa (2022/2023), and the Strategic Research Area Neuroscience at Karolinska Institutet (StratNeuro).

Available from: 2024-10-18 Created: 2024-10-18 Last updated: 2025-02-20Bibliographically approved

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