1. Genetic Variations in Elements of the Oxytocinergic Pathway are Associated with Attention/Hyperactivity Problems and Anxiety Problems in Childhood.
- Author
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Camerini, Laísa, Zurchimitten, Gabriel, Bock, Bertha, Xavier, Janaína, Bastos, Clarissa Ribeiro, Martins, Evânia, Ardais, Ana Paula, dos Santos Motta, Janaína Vieira, Pires, Andressa Jacondino, de Matos, Mariana Bonati, de Ávila Quevedo, Luciana, Pinheiro, Ricardo Tavares, and Ghisleni, Gabriele
- Subjects
GENETIC variation ,ATTENTION-deficit hyperactivity disorder ,HYPERACTIVITY ,SOCIAL anxiety ,ANXIETY ,CD38 antigen - Abstract
Genetic alterations related to oxytocin system seem to influence the neurobiology of attention-deficit hyperactivity disorder and anxiety problems leading to greater functional, social and emotional impairment. Here, we analyzed the association of OXTR rs2254298 and CD38 rs6449182 variants with attention/hyperactivity problems and anxiety problems in children. The study enrolled 292 children and adjusted regression model revealed OXTR rs2254298 AA genotype as a risk factor for attention deficit/hyperactivity problems (PR: 2.37; P
adjFDR = 0.006), attention problems (PR: 2.71; PadjFDR = 0.003) and anxiety problems (PR: 1.92; PadjFDR = 0.018). CD38 rs6449182 G allele showed as a risk factor for attention deficit/hyperactivity problems (PR: 1.56; PadjFDR = 0.028). Moreover, in silico approach for regulatory roles found markers that influence chromatin accessibility and transcription capacity. Together, these data provide genetic information of oxytocin in developmental and behavioral disorders opening a range of opportunities for future studies that clarify their neurobiology in childhood. [ABSTRACT FROM AUTHOR]- Published
- 2024
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