Journal of the American Academy of Child & Adolescent Psychiatry
Volume 47, Issue 10 , Pages 1151-1157, October 2008

CBCL Pediatric Bipolar Disorder Profile and ADHD: Comorbidity and Quantitative Trait Loci Analysis

Drs. McGough and McCracken are with the Division of Child and Adolescent Psychiatry at the UCLA Semel Institute for Neuroscience and Human Behavior and David Geffen School of Medicine; Drs. Loo and Smalley and Mr. Dang are with the Center for Neurobehavioral Genetics at the UCLA Semel Institute; and Dr. Nelson and Ms. Clark are with the Center for Neurobehavioral Genetics at the UCLA Semel Institute and Department of Human Genetics in the David Geffen School of Medicine

Accepted 21 May 2008.

Disclosure: Dr. McGough has served as a consultant to Eli Lilly, Janssen Pharmaceuticals, and Shire Pharmaceuticals and has received research support from Eli Lilly, Janssen, and Shire. Dr. McCracken has served as a consultant to Abbott, Janssen, Pfizer, Sanofi-Aventis, and Wyeth and has received research support from Aspect, Bristol-Myers Squibb, Eli Lilly, and Janssen and speaker honoraria from UCB. The other authors report no conflicts of interest.

Abstract 

Objective

The pediatric bipolar disorder profilme of the Child Behavior Checklist (CBCL-PBD), a parent-completed measure that avoids clinician ideological bias, has proven useful in differentiating patients with attention-deficit/hyperactivity disorder (ADHD). We used CBCL-PBD profiles to distinguish patterns of comorbidity and to search for quantitative trait loci in a genomewide scan in a sample of multiple affected ADHD sibling pairs.

Method

A total of 540 ADHD subjects ages 5 to 18 years were assessed with the Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime version and CBCL. Parents were assessed with the Schedule for Affective Disorders and Schizophrenia-Lifetime version supplemented by the Schedule for Affective Disorders and Schizophrenia for School-Age Children for disruptive behavioral disorders. Patterns of psychiatric comorbidity were contrasted based on the CBCL-PBD profile. A quantitative trait loci variance component analysis was used to identify potential genomic regions that may harbor susceptibility genes for the CBCL-PBD quantitative phenotype.

Results

Bipolar spectrum disorders represented less than 2% of the overall sample. The CBCL-PBD classification was associated with increased generalized anxiety disorder (p = .001), oppositional defiant disorder (p = .008), conduct disorder (p = .003), and parental substance abuse (p = .005). A moderately significant linkage signal (multipoint maximum lod score = 2.5) was found on chromosome 2q.

Conclusions

The CBCL-PBD profile distinguishes a subset of ADHD patients with significant comorbidity. Linkage analysis of the CBCL-PBD phenotype suggests certain genomic regions that merit further investigation for genes predisposing to severe psychopathology.

Key Words:  attention-deficit/hyperactivity disorder , bipolar disorder , Child Behavior Checklist , quantitative trait loci , linkage analysis

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 This work was supported by National Institute of Mental Health grants MH01969 (to J.J.M.), HD40275 (to S.K.L.), MH01805 (to J.T.M.), MH071852 (to S.F.N.), and MH58277 (to S.L.S.).The authors dedicate this article to the memory of Richard D. Todd, M.D., Ph.D. (1951–2008).

PII: S0890-8567(08)60100-8

doi:10.1097/CHI.0b013e3181825a68

Journal of the American Academy of Child & Adolescent Psychiatry
Volume 47, Issue 10 , Pages 1151-1157, October 2008