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

Author:

Keijser Rebecka12ORCID,Åsberg Johnels Jakob34,Habbe Marika12,Lichtenstein Paul5,Larsson Henrik56,Lundström Sebastian3,Taylor Mark J.5ORCID,Tammimies Kristiina12ORCID

Affiliation:

1. The 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

2. Astrid Lindgren Children's Hospital Karolinska University Hospital Solna Sweden

3. Gillberg Neuropsychiatry Centre Institute of Neuroscience and Physiology University of Gothenburg Gothenburg Sweden

4. Speech and Language Pathology Unit Institute of Neuroscience and Physiology University of Gothenburg Gothenburg Sweden

5. Department of Medical Epidemiology and Biostatistics Karolinska Institutet Stockholm Sweden

6. School of Medical Sciences Örebro University Örebro Sweden

Abstract

AbstractBackgroundResearch 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.MethodsData 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.ResultsThe 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.ConclusionsWe 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.

Publisher

Wiley

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