Literature DB >> 30908652

SWAN scale for ADHD trait-based genetic research: a validity and polygenic risk study.

Christie L Burton1, Leah Wright1, Janet Shan1, Bowei Xiao2, Annie Dupuis3,4, Tara Goodale1, S-M Shaheen5,6, Elizabeth C Corfield1,7, Paul D Arnold2,5,6, Russell J Schachar1,7,8, Jennifer Crosbie1,7.   

Abstract

BACKGROUND: Population-based samples with valid, quantitative and genetically informative trait measures of psychopathology could be a powerful complement to case/control genetic designs. We report the convergent and predictive validity of the parent- and self-report versions of the Strengths and Weaknesses of ADHD Symptoms and Normal Behavior Rating Scale (SWAN). We tested if SWAN scores were associated with ADHD diagnosis, ADHD polygenic risk, as well as traits and polygenic risk for disorders that co-occur with ADHD: anxiety and obsessive-compulsive disorder (OCD).
METHODS: We collected parent- and self-report SWAN scores in a sample of 15,560 children and adolescents (6-17 years) recruited at a science museum (Spit for Science sample). We established age and sex norms for the SWAN. Sensitivity-specificity analyses determined SWAN cut-points that discriminated those with and without a reported ADHD diagnosis. These cut-points were validated in a clinic sample (266 ADHD cases; 36 controls). Convergent validity was established using the Conners' parent- and self-report scales. Using Spit for Science participants with genome-wide data (n = 5,154), we tested if low, medium and high SWAN scores were associated with polygenic risk for ADHD, OCD and anxiety disorders.
RESULTS: Parent- and self-report SWAN scores showed high convergent validity with Conners' scales and distinguished ADHD participants with high sensitivity and specificity in the Spit for Science sample. In a clinic sample, the Spit for Science cut-points discriminated ADHD cases from controls with a sensitivity of 84% and specificity of 92%. High SWAN scores and scores above the Spit for Science cut-points were significantly associated with polygenic risk for ADHD. SWAN scores were not associated with polygenic risk for OCD or anxiety disorders.
CONCLUSIONS: Our study supports the validity of the parent- and self-report SWAN scales and their potential in ADHD population-based genetic research.
© 2019 Association for Child and Adolescent Mental Health.

Entities:  

Keywords:  zzm321990ADHDzzm321990; zzm321990SWANzzm321990; polygenic risk score; psychometric validity; standardized norms

Year:  2019        PMID: 30908652     DOI: 10.1111/jcpp.13032

Source DB:  PubMed          Journal:  J Child Psychol Psychiatry        ISSN: 0021-9630            Impact factor:   8.982


  10 in total

1.  Autism Spectrum Disorder and Attention-Deficit/Hyperactivity Disorder: Shared or Unique Neurocognitive Profiles?

Authors:  Russell J Schachar; Annie Dupuis; Paul D Arnold; Evdokia Anagnostou; Elizabeth Kelley; Stelios Georgiades; Robert Nicolson; Parker Townes; Christie L Burton; Jennifer Crosbie
Journal:  Res Child Adolesc Psychopathol       Date:  2022-08-25

2.  Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sample.

Authors:  Aurina Arnatkeviciute; Mark A Bellgrove; Mia Moses; Jeggan Tiego; Ditte Demontis; G Bragi Walters; Hreinn Stefansson; Kari Stefansson; Anders D Børglum
Journal:  Mol Psychiatry       Date:  2022-09-23       Impact factor: 13.437

3.  Cortical Gyrification Morphology in ASD and ADHD: Implication for Further Similarities or Disorder-Specific Features?

Authors:  Avideh Gharehgazlou; Marlee Vandewouw; Justine Ziolkowski; Jimmy Wong; Jennifer Crosbie; Russell Schachar; Rob Nicolson; Stelios Georgiades; Elizabeth Kelley; Muhammad Ayub; Christopher Hammill; Stephanie H Ameis; Margot J Taylor; Jason P Lerch; Evdokia Anagnostou
Journal:  Cereb Cortex       Date:  2022-05-30       Impact factor: 4.861

4.  Shared genetic etiology between obsessive-compulsive disorder, obsessive-compulsive symptoms in the population, and insulin signaling.

Authors:  Janita Bralten; Joanna Widomska; Barbara Franke; Geert Poelmans; Ward De Witte; Dongmei Yu; Carol A Mathews; Jeremiah M Scharf; Jan Buitelaar; Jennifer Crosbie; Russell Schachar; Paul Arnold; Mathieu Lemire; Christie L Burton
Journal:  Transl Psychiatry       Date:  2020-04-27       Impact factor: 6.222

5.  A suicide prevention strategy for youth presenting to the emergency department with suicide related behaviour: protocol for a randomized controlled trial.

Authors:  Daphne J Korczak; Yaron Finkelstein; Melanie Barwick; Gloria Chaim; Kristin Cleverley; Joanna Henderson; Suneeta Monga; Myla E Moretti; Andrew Willan; Peter Szatmari
Journal:  BMC Psychiatry       Date:  2020-01-14       Impact factor: 3.630

6.  Tracking Inhibitory Control in Youth With ADHD: A Multi-Modal Neuroimaging Approach.

Authors:  Lescia K Tremblay; Christopher Hammill; Stephanie H Ameis; Mehereen Bhaijiwala; Donald J Mabbott; Evdokia Anagnostou; Jason P Lerch; Russell J Schachar
Journal:  Front Psychiatry       Date:  2020-11-19       Impact factor: 4.157

Review 7.  Genetics in the ADHD Clinic: How Can Genetic Testing Support the Current Clinical Practice?

Authors:  Lívia Balogh; Attila J Pulay; János M Réthelyi
Journal:  Front Psychol       Date:  2022-03-08

8.  Age-Related Variance in Performance versus Ratings of Attention and Impulse Regulation in Children: Implications for the Assessment of ADHD.

Authors:  Rachael E Lyon; Jala Rizeq; David B Flora; Rhonda Martinussen; Brendan F Andrade; Maggie E Toplak
Journal:  Brain Sci       Date:  2022-08-04

9.  Training inhibitory control in adolescents with elevated attention deficit hyperactivity disorder traits: a randomised controlled trial of the Alfi Virtual Reality programme.

Authors:  Erin McKay; Hannah Kirk; James Coxon; Danielle Courtney; Mark Bellgrove; Aurina Arnatkeviciute; Kim Cornish
Journal:  BMJ Open       Date:  2022-09-20       Impact factor: 3.006

10.  Obsessive-compulsive disorder and attention-deficit/hyperactivity disorder: distinct associations with DNA methylation and genetic variation.

Authors:  Sarah J Goodman; Christie L Burton; Darci T Butcher; Michelle T Siu; Mathieu Lemire; Eric Chater-Diehl; Andrei L Turinsky; Michael Brudno; Noam Soreni; David Rosenberg; Kate D Fitzgerald; Gregory L Hanna; Evdokia Anagnostou; Paul D Arnold; Jennifer Crosbie; Russell Schachar; Rosanna Weksberg
Journal:  J Neurodev Disord       Date:  2020-08-16       Impact factor: 4.025

  10 in total

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