4.5 Article

Methylation Dynamics on 5′-UTR of DAT1 Gene as a Bio-Marker to Recognize Therapy Success in ADHD Children

Journal

CHILDREN-BASEL
Volume 10, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/children10030584

Keywords

dopamine transporter (DAT1) gene; attention-deficit; hyperactivity disorder (ADHD); problematic children; CpGs methylation pattern; methylphenidate (MPH); cognitive-behavioral therapy (CBT)

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ADHD affects 5% of children worldwide, and each patient has unique cognitive and motivational characteristics. Our study aims to find clinical biomarkers for ADHD to provide objective guidance for therapy selection. We recruited 60 ADHD children and identified specific methylation patterns in relation to treatment outcomes, which could serve as objective molecular markers for successful cures.
Attention-deficit/hyperactivity disorder (ADHD), a neuropsychiatric condition characterized by inattention, hyperactivity, and impulsivity, afflicts 5% of children worldwide. Each ADHD patient presents with individual cognitive and motivational peculiarities. Furthermore, choice of appropriate therapy is still up to clinicians, who express somewhat qualitative advice on whether a child is being successfully cured or not: it would be more appropriate to use an objective biomarker to indicate whether a treatment led to benefits or not. The aim of our work is to search for such clinical biomarkers. We recruited 60 ADHD kids; psychopathological scales were administered at recruitment and after six weeks of therapy. Out of such a cohort of ADHD children, we rigorously extracted two specific subgroups; regardless of the initial severity of their disease, we compared those who obtained the largest improvement (Delta CGAS > 5) vs. those who were still characterized by a severe condition (CGAS < 40). After such a therapy, methylation levels of DNA extracted from buccal swabs were measured in the 5 '-UTR of the DAT1 gene. CpGs 3 and 5 displayed, in relation to the other CpGs, a particular symmetrical pattern; for improving ADHD children, they were methylated together with CpG 2 and CpG 6; instead, for severe ADHD children, they accompanied a methylated CpG 1. These specific patterns of methylation could be used as objective molecular biomarkers of successful cures, establishing if a certain therapy is akin to a given patient (personalized medicine). Present data support the use of post-therapy molecular data obtained with non-invasive techniques.

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