Factors Associated with Confirmed and Unconfirmed Autism Spectrum Disorder Diagnosis in Children Volunteering for Research

Diagnostic accuracy of autism spectrum disorder (ASD) is crucial to track and characterize ASD, as well as to guide appropriate interventions at the individual level. However, under-diagnosis, over-diagnosis, and misdiagnosis of ASD are still prevalent. We describe 232 children (M = 10.71 years; 19%...

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Published in:Journal of autism and developmental disorders
Main Authors: Duvall, Susanne W, Greene, Rachel K, Phelps, Randi, Rutter, Tara M, Markwardt, Sheila, Grieser Painter, Julia, Cordova, Michaela, Calame, Beth, Doyle, Olivia, Nigg, Joel T, Fombonne, Eric, Fair, Damien
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Published: United States 12-04-2024
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Abstract Diagnostic accuracy of autism spectrum disorder (ASD) is crucial to track and characterize ASD, as well as to guide appropriate interventions at the individual level. However, under-diagnosis, over-diagnosis, and misdiagnosis of ASD are still prevalent. We describe 232 children (M = 10.71 years; 19% female) with community-based diagnoses of ASD referred for research participation. Extensive assessment procedures were employed to confirm ASD diagnosis before study inclusion. The sample was subsequently divided into two groups with either confirmed ASD diagnoses (ASD+) or unconfirmed/inaccurate diagnoses (ASD-). Clinical characteristics differentiating the groups were further analyzed. 47% of children with community-based ASD diagnoses did not meet ASD criteria by expert consensus. ASD + and ASD- groups did not differ in age, gender, ethnicity, or racial make-up. The ASD + group was more likely to have a history of early language delays compared to the ASD- group; however, no group differences in current functional language use were reported by caregivers. The ASD + group scored significantly higher on ADI-R scores and on the ADOS-2 algorithm composite scores and calibrated severity scores (CSSs). The ASD- group attained higher estimated IQ scores and higher rates of psychiatric disorders, including anxiety disorder, disruptive behavior, and mood disorder diagnoses. Broadly, caregiver questionnaires (SRS-2, CCC-2) did not differentiate groups. Increased reported psychiatric disorders in the ASD- group suggests psychiatric complexity may contribute to community misdiagnosis and possible overdiagnosis of ASD. Clinician-mediated tools (ADI-R, ADOS-2) differentiated ASD + versus ASD- groups, whereas caregiver-reported questionnaires did not.
AbstractList Diagnostic accuracy of autism spectrum disorder (ASD) is crucial to track and characterize ASD, as well as to guide appropriate interventions at the individual level. However, under-diagnosis, over-diagnosis, and misdiagnosis of ASD are still prevalent. We describe 232 children (M = 10.71 years; 19% female) with community-based diagnoses of ASD referred for research participation. Extensive assessment procedures were employed to confirm ASD diagnosis before study inclusion. The sample was subsequently divided into two groups with either confirmed ASD diagnoses (ASD+) or unconfirmed/inaccurate diagnoses (ASD-). Clinical characteristics differentiating the groups were further analyzed. 47% of children with community-based ASD diagnoses did not meet ASD criteria by expert consensus. ASD + and ASD- groups did not differ in age, gender, ethnicity, or racial make-up. The ASD + group was more likely to have a history of early language delays compared to the ASD- group; however, no group differences in current functional language use were reported by caregivers. The ASD + group scored significantly higher on ADI-R scores and on the ADOS-2 algorithm composite scores and calibrated severity scores (CSSs). The ASD- group attained higher estimated IQ scores and higher rates of psychiatric disorders, including anxiety disorder, disruptive behavior, and mood disorder diagnoses. Broadly, caregiver questionnaires (SRS-2, CCC-2) did not differentiate groups. Increased reported psychiatric disorders in the ASD- group suggests psychiatric complexity may contribute to community misdiagnosis and possible overdiagnosis of ASD. Clinician-mediated tools (ADI-R, ADOS-2) differentiated ASD + versus ASD- groups, whereas caregiver-reported questionnaires did not.
PURPOSEDiagnostic accuracy of autism spectrum disorder (ASD) is crucial to track and characterize ASD, as well as to guide appropriate interventions at the individual level. However, under-diagnosis, over-diagnosis, and misdiagnosis of ASD are still prevalent.METHODSWe describe 232 children (MAge = 10.71 years; 19% female) with community-based diagnoses of ASD referred for research participation. Extensive assessment procedures were employed to confirm ASD diagnosis before study inclusion. The sample was subsequently divided into two groups with either confirmed ASD diagnoses (ASD+) or unconfirmed/inaccurate diagnoses (ASD-). Clinical characteristics differentiating the groups were further analyzed.RESULTS47% of children with community-based ASD diagnoses did not meet ASD criteria by expert consensus. ASD + and ASD- groups did not differ in age, gender, ethnicity, or racial make-up. The ASD + group was more likely to have a history of early language delays compared to the ASD- group; however, no group differences in current functional language use were reported by caregivers. The ASD + group scored significantly higher on ADI-R scores and on the ADOS-2 algorithm composite scores and calibrated severity scores (CSSs). The ASD- group attained higher estimated IQ scores and higher rates of psychiatric disorders, including anxiety disorder, disruptive behavior, and mood disorder diagnoses. Broadly, caregiver questionnaires (SRS-2, CCC-2) did not differentiate groups.CONCLUSIONIncreased reported psychiatric disorders in the ASD- group suggests psychiatric complexity may contribute to community misdiagnosis and possible overdiagnosis of ASD. Clinician-mediated tools (ADI-R, ADOS-2) differentiated ASD + versus ASD- groups, whereas caregiver-reported questionnaires did not.
Author Rutter, Tara M
Markwardt, Sheila
Greene, Rachel K
Duvall, Susanne W
Phelps, Randi
Grieser Painter, Julia
Doyle, Olivia
Fair, Damien
Cordova, Michaela
Calame, Beth
Fombonne, Eric
Nigg, Joel T
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  givenname: Susanne W
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  email: duvall@ohsu.edu
  organization: Departments of Pediatrics and Psychiatry, Institute on Development and Disability, Center for Development and Child Rehabilitation, Oregon Health & Science University, 707 SW Gaines St, Portland, OR, 98239, USA. duvall@ohsu.edu
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  givenname: Rachel K
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  surname: Greene
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  organization: Departments of Pediatrics, Institute on Development and Disability, Center for Development and Child Rehabilitation, Oregon Health & Science University, 707 SW Gaines St, Portland, OR, USA
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  givenname: Randi
  orcidid: 0000-0002-1160-3734
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  organization: Department of Child Health, University of Arizona College of Medicine, 475 N 5th St, Phoenix, AZ, USA
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  givenname: Sheila
  surname: Markwardt
  fullname: Markwardt, Sheila
  organization: Biostatistician III, Biostatistics and Design Program, Oregon Health & Science University, 3181 SW Sam Jackson Rd, Portland, OR, 97217, USA
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  givenname: Julia
  surname: Grieser Painter
  fullname: Grieser Painter, Julia
  organization: Department of Psychiatry, School of Medicine, Oregon Health & Science University, 3181 S.W. Sam Jackson Rd, Portland, OR, USA
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  givenname: Michaela
  orcidid: 0000-0002-6860-5159
  surname: Cordova
  fullname: Cordova, Michaela
  organization: San Diego State University/UC San Diego Joint Doctoral Program in Clinical Psychology, 6363 Alvarado Ct, San Diego, CA, USA
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  givenname: Beth
  surname: Calame
  fullname: Calame, Beth
  organization: Department of Psychiatry, School of Medicine, Oregon Health & Science University, 3181 S.W. Sam Jackson Rd, Portland, OR, USA
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  givenname: Olivia
  orcidid: 0000-0003-3957-2949
  surname: Doyle
  fullname: Doyle, Olivia
  organization: Department of Psychiatry, Oregon Health & Science University, 3181 SW Sam Jackson Rd, Portland, OR, 97217, USA
– sequence: 10
  givenname: Joel T
  orcidid: 0000-0003-0003-3024
  surname: Nigg
  fullname: Nigg, Joel T
  organization: Department of Psychiatry, Oregon Health & Science University, 3181 SW Sam Jackson Rd, Portland, OR, 97239, USA
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  givenname: Eric
  orcidid: 0000-0002-8605-3538
  surname: Fombonne
  fullname: Fombonne, Eric
  organization: Department of Psychiatry, Oregon Health & Science University, 3181 SW Sam Jackson Rd, Portland, OR, 97239, USA
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  givenname: Damien
  orcidid: 0000-0001-8602-393X
  surname: Fair
  fullname: Fair, Damien
  organization: College of Education and Human Development, Department of Pediatrics, Medical School University of Minnesota, Masonic Institute for the Developing Brain, Professor, Institute of Child Development, 2025 E. River Parkway 7962A, Minneapolis, MN, 55414, USA
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Keywords Accuracy
Community-based diagnosis
Diagnosis
Comorbidity
Autism spectrum disorder
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Snippet Diagnostic accuracy of autism spectrum disorder (ASD) is crucial to track and characterize ASD, as well as to guide appropriate interventions at the individual...
PURPOSEDiagnostic accuracy of autism spectrum disorder (ASD) is crucial to track and characterize ASD, as well as to guide appropriate interventions at the...
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Title Factors Associated with Confirmed and Unconfirmed Autism Spectrum Disorder Diagnosis in Children Volunteering for Research
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