Association between COMT methylation and response to treatment in children with ADHD. (March 2021)

• Record Type: Journal Article
• Authors: Fageera, Weam; Chaumette, Boris; Fortier, Marie-Ève; Grizenko, Natalie; Labbe, Aurelie; Sengupta, Sarojini M.; Joober, Ridha
• Is Part Of: Journal of psychiatric research. Volume 135(2021)
• Page Start: 86
• Page End: 93
• Publication Date: 2021-03
• Subjects: Attention-deficit/hyperactivity disorder (ADHD) -- Methylation -- Pharmacoepigenetics -- Treatment response -- Conners' -- COMT; Psychiatry -- Periodicals; Mental Disorders -- Periodicals; Maladies mentales -- Périodiques; Psychiatry; Electronic journals; Periodicals; 616.89005
• DOI: 10.1016/j.jpsychires.2021.01.008
• Languages: English
• ISSNs: 0022-3956

Abstract

Abstract: Background: COMT had been considered a promising candidate gene in pharmacogenetic studies in ADHD; yet the findings from these studies have been inconsistent. Part of these inconsistencies could be related to epigenetic mechanisms (including DNA methylation). Here we investigated the role of genetic variants of the COMT gene on the methylation levels of CpG sites in the same gene and explored the effect of methylation on methylphenidate (MPH) and placebo (PBO) response in children with ADHD. Methods: Two hundred and thirty children with ADHD (6–12 years) participated in a randomized, double-blind, placebo-controlled crossover trial with MPH. Univariate analysis was performed to examine the associations between genotypes in the COMT gene and DNA methylation in the same genetic loci. Association between the DNA methylation of 11 CpG sites and PBO/MPH responses were then assessed using spearman's correlation analysis in 212 children. Multiple linear regression analyses were performed to test the interaction between these factors while accounting for sex. Results: Associations were observed between specific genetic variants and methylation level of cg20709110. Homozygous genotypes of GG (rs6269), CC (rs4633), GG (rs4818), Val/Val (rs4680) and the haplotype (ACCVal/GCGVal) were significantly associated with higher level of methylation. This CpG showed a significant correlation with placebo response (r = −0.15, P = 0.045) according to the teachers' evaluation, and a close-to significance correlation with response to MPH according to parents' evaluation (r = −0.134, p = 0.051). Regression analysis showed that in the model including rs4818, sex and DNA methylation of cg20709110 contributed significantly to treatment response. Conclusions: These preliminary results could provide evidence for the effect of genetic variations on methylation level and the involvement of the epigenetic variation of COMT loci in modulating the response to treatment in ADHD. Trial registration: clinicaltrials.gov, number NCT00483106 .