NCAM1‐TTC12‐ANKK1‐DRD2 gene cluster and the clinical and genetic heterogeneity of adults with ADHD. Issue 6 (18th May 2015)

• Record Type: Journal Article
• Authors: Mota, Nina R.; Rovaris, Diego L.; Kappel, Djenifer B.; Picon, Felipe A.; Vitola, Eduardo S.; Salgado, Carlos A. I.; Karam, Rafael G.; Rohde, Luis A.; Grevet, Eugenio H.; Bau, Claiton H. D.
• Other Names: Franke Barbara guestEditor.
• Is Part Of: American journal of medical genetics. Volume 168:Issue 6(2015)
• Page Start: 433
• Page End: 444
• Publication Date: 2015-05-18
• Subjects: dopamine receptor -- attention deficit/hyperactivity disorder -- comorbidity -- personality; Neuropsychiatry -- Periodicals; Medical genetics -- Periodicals; 616.8904205
• DOI: 10.1002/ajmg.b.32317
• Languages: English
• ISSNs: 1552-4841

Abstract

Abstract : Dysfunctions of the dopaminergic system have been implicated on the etiology of Attention Deficit/Hyperactivity Disorder (ADHD). Meta‐analyses addressing the association of the dopamine receptor D2 ( DRD2 ) gene and ADHD were inconclusive due to excessive heterogeneity across studies. Both the great phenotypic heterogeneity of ADHD and the complexity of the genomic region where DRD2 is located could contribute to the inconsistent findings. Most previous DRD2 studies focused on the well‐known Taq1A (rs1800497) SNP, which is actually placed in a neighbor gene ( ANKK1 ). These two genes, together with NCAM1 and TTC12, form the NTAD gene cluster on Chr11q22–23. In order to address the reasons for the high heterogeneity previously reported on DRD2 effects on ADHD, this study investigates the role of NTAD variants on ADHD susceptibility in adults and on the modulation of comorbidity and personality profiles in these patients. Functional polymorphisms from NTAD were analyzed, both individually and in haplotypes, on a sample of 520 adults with ADHD and 630 non‐ADHD controls. No direct association of NTAD variants with ADHD susceptibility itself was observed. However, different NTAD polymorphisms and haplotypes were associated to various phenotypes relevant to the clinical heterogeneity of ADHD, including Major Depressive Disorder, Generalized Anxiety Disorder, and Harm Avoidance and Persistence temperament scores. Therefore, these findings represent a possible explanation for the multiple conflicting findings regarding polymorphisms in this genomic region in psychiatry. The NTAD cluster may comprise a variety of independent molecular influences on various brain and behavior characteristics eventually associated with ADHD comorbidities and personality traits. © 2015 Wiley Periodicals, Inc.