Abstract

Attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorders (ASDs) frequently co-occur. However, due to previous exclusionary diagnostic criteria, little is known about the underlying causes of this covariation. Twin studies assessing ADHD symptoms and autistic-like traits (ALTs) suggest substantial genetic overlap, but have largely failed to take into account the genetic heterogeneity of symptom subscales. This study aimed to clarify the phenotypic and genetic relations between ADHD and ASD by distinguishing between symptom subscales that characterise the two disorders. Moreover, we aimed to investigate whether ADHD-related cognitive impairments show a relationship with ALT symptom subscales; and whether potential shared cognitive impairments underlie the genetic risk shared between the ADHD and ALT symptoms. Multivariate structural equation modelling was conducted on a population-based sample of 1312 twins aged 7–10. Social-communication ALTs correlated moderately with both ADHD symptom domains (phenotypic correlations around 0.30) and showed substantial genetic overlap with both inattention and hyperactivity-impulsivity (genetic correlation = 0.52 and 0.44, respectively). In addition to previously reported associations with ADHD traits, reaction time variability (RTV) showed significant phenotypic (0.18) and genetic (0.32) association with social-communication ALTs. RTV captured a significant proportion (24 %) of the genetic influences shared between inattention and social-communication ALTs. Our findings suggest that social-communication ALTs underlie the previously observed phenotypic and genetic covariation between ALTs and ADHD symptoms. RTV is not specific to ADHD symptoms, but is also associated with social-communication ALTs and can, in part, contribute to an explanation of the co-occurrence of ASD and ADHD.

Highlights

  • Attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorders (ASDs) frequently co-occur

  • reaction time variability (RTV) captured a significant proportion (24 %) of the genetic influences shared between inattention and social-communication autistic-like traits (ALTs)

  • commission errors (CE) showed less differentiation between the ADHD symptom domains, the genetic correlations were overall low. Given these findings and the genetic heterogeneity of ALTs (Dworzynski et al 2009; Robinson et al 2012; Ronald et al 2005, 2006a, b, 2011), we extended the previous model with an aim to investigate if the phenotypic and genetic covariation between ADHD symptoms and ALTS are driven by specific symptom subscales, and if cognitive impairments (CE and RTV) represent unique etiological pathways for ADHD symptoms or are shared with ALTs, and show different patterns of co-occurrence across ALT subscales

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Summary

Introduction

Attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorders (ASDs) frequently co-occur. Twin studies assessing ADHD symptoms and autistic-like traits (ALTs) suggest substantial genetic overlap, but have largely failed to take into account the genetic heterogeneity of symptom subscales. As a result of the diagnostic exclusionary criteria, little is known about the underlying causes of the covariation of these disorders (Ronald et al 2008). Both ADHD and autism symptoms can be viewed as continuously distributed traits (Chen et al 2008; Dawson et al 2002; Lubke et al 2009; Robinson et al 2011). Twin studies have explored shared and specific etiological influences of quantitative assessments of autistic-like traits (ALTs) and ADHD symptoms

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