TY - JOUR
T1 - A multisite study of the clinical diagnosis of different autism spectrum disorders
AU - Lord, Catherine
AU - Petkova, Eva
AU - Hus, Vanessa
AU - Gan, Weijin
AU - Lu, Feihan
AU - Martin, Donna M.
AU - Ousley, Opal
AU - Guy, Lisa
AU - Bernier, Raphael
AU - Gerdts, Jennifer
AU - Algermissen, Molly
AU - Whitaker, Agnes
AU - Sutcliffe, James S.
AU - Warren, Zachary
AU - Klin, Ami
AU - Saulnier, Celine
AU - Hanson, Ellen
AU - Hundley, Rachel
AU - Piggot, Judith
AU - Fombonne, Eric
AU - Steiman, Mandy
AU - Miles, Judith
AU - Kanne, Stephen M.
AU - Goin-Kochel, Robin P.
AU - Peters, Sarika U.
AU - Cook, Edwin H.
AU - Guter, Stephen
AU - Tjernagel, Jennifer
AU - Green-Snyder, Lee Anne
AU - Bishop, Somer
AU - Esler, Amy
AU - Gotham, Katherine
AU - Luyster, Rhiannon
AU - Miller, Fiona
AU - Olson, Jennifer
AU - Richler, Jennifer
AU - Risi, Susan
PY - 2012/3
Y1 - 2012/3
N2 - Context: Best-estimate clinical diagnoses of specific autism spectrum disorders (autistic disorder, pervasive developmental disorder-not otherwise specified, and Asperger syndrome) have been used as the diagnostic gold standard, even when information from standardized instruments is available. Objective: To determine whether the relationships between behavioral phenotypes and clinical diagnoses of different autism spectrum disorders vary across 12 university- based sites. Design: Multisite observational study collecting clinical phenotype data (diagnostic, developmental, and demographic) for genetic research. Classification trees were used to identify characteristics that predicted diagnosis across and within sites. Setting: Participants were recruited through 12 university- based autism service providers into a genetic study of autism. Participants: A total of 2102 probands (1814 male probands) between 4 and 18 years of age (mean [SD] age, 8.93 [3.5] years) who met autism spectrum criteria on the Autism Diagnostic Interview-Revised and the Autism Diagnostic Observation Schedule and who had a clinical diagnosis of an autism spectrum disorder. Main Outcome Measure: Best-estimate clinical diagnoses predicted by standardized scores from diagnostic, cognitive, and behavioral measures. Results: Although distributions of scores on standardized measures were similar across sites, significant site differences emerged in best-estimate clinical diagnoses of specific autism spectrum disorders. Relationships between clinical diagnoses and standardized scores, particularly verbal IQ, language level, and core diagnostic features, varied across sites in weighting of information and cutoffs. Conclusions: Clinical distinctions among categorical diagnostic subtypes of autism spectrum disorders were not reliable even across sites with well-documented fidelity using standardized diagnostic instruments. Results support the move from existing subgroupings of autism spectrum disorders to dimensional descriptions of core features of social affect and fixated, repetitive behaviors, together with characteristics such as language level and cognitive function.
AB - Context: Best-estimate clinical diagnoses of specific autism spectrum disorders (autistic disorder, pervasive developmental disorder-not otherwise specified, and Asperger syndrome) have been used as the diagnostic gold standard, even when information from standardized instruments is available. Objective: To determine whether the relationships between behavioral phenotypes and clinical diagnoses of different autism spectrum disorders vary across 12 university- based sites. Design: Multisite observational study collecting clinical phenotype data (diagnostic, developmental, and demographic) for genetic research. Classification trees were used to identify characteristics that predicted diagnosis across and within sites. Setting: Participants were recruited through 12 university- based autism service providers into a genetic study of autism. Participants: A total of 2102 probands (1814 male probands) between 4 and 18 years of age (mean [SD] age, 8.93 [3.5] years) who met autism spectrum criteria on the Autism Diagnostic Interview-Revised and the Autism Diagnostic Observation Schedule and who had a clinical diagnosis of an autism spectrum disorder. Main Outcome Measure: Best-estimate clinical diagnoses predicted by standardized scores from diagnostic, cognitive, and behavioral measures. Results: Although distributions of scores on standardized measures were similar across sites, significant site differences emerged in best-estimate clinical diagnoses of specific autism spectrum disorders. Relationships between clinical diagnoses and standardized scores, particularly verbal IQ, language level, and core diagnostic features, varied across sites in weighting of information and cutoffs. Conclusions: Clinical distinctions among categorical diagnostic subtypes of autism spectrum disorders were not reliable even across sites with well-documented fidelity using standardized diagnostic instruments. Results support the move from existing subgroupings of autism spectrum disorders to dimensional descriptions of core features of social affect and fixated, repetitive behaviors, together with characteristics such as language level and cognitive function.
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U2 - 10.1001/archgenpsychiatry.2011.148
DO - 10.1001/archgenpsychiatry.2011.148
M3 - Article
C2 - 22065253
AN - SCOPUS:84857943542
SN - 0003-990X
VL - 69
SP - 306
EP - 313
JO - Archives of General Psychiatry
JF - Archives of General Psychiatry
IS - 3
ER -