2017
DOI: 10.1080/15622975.2017.1282175
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Common and specific genes and peripheral biomarkers in children and adults with attention-deficit/hyperactivity disorder

Abstract: Through a convergent functional genomics, this review contributes to clarification of which genetic/biological mechanisms differ with age. The effects of some genes do not change throughout the lifetime, whereas others are linked to age-specific stages. Additional research and further studies are needed to generate firmer conclusions that might someday be useful for predicting the remission and persistence of the disorder. Despite the limitations, some of these genes/proteins could be potential useful biomarke… Show more

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Cited by 68 publications
(45 citation statements)
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“…Previous studies have shown that symptoms and neurocognitive deficits of ADHD patients are related to abnormalities in cortex development and functional and structural connectivity among several brain regions ( 53 ). Several peripheral (e.g., norepinephrine, 3-methoxy-4-hydroxyphenylethylene glycol, monoamine oxidase, zinc) ( 4 ) and genetic biomarkers (e.g., genes belonging to dopaminergic, circadian rhythms and neurodevelopmental systems) ( 54 ) have been associated with ADHD both in diagnosis and in treatment response. miRNAs participate in modulating gene expression, resulting in the influence on the transcription of hereditary messages ( 18 ), and miRNAs are particularly associated with the abnormal differentiation and maldevelopment of neurons ( 19 , 20 ).…”
Section: Discussionmentioning
confidence: 99%
“…Previous studies have shown that symptoms and neurocognitive deficits of ADHD patients are related to abnormalities in cortex development and functional and structural connectivity among several brain regions ( 53 ). Several peripheral (e.g., norepinephrine, 3-methoxy-4-hydroxyphenylethylene glycol, monoamine oxidase, zinc) ( 4 ) and genetic biomarkers (e.g., genes belonging to dopaminergic, circadian rhythms and neurodevelopmental systems) ( 54 ) have been associated with ADHD both in diagnosis and in treatment response. miRNAs participate in modulating gene expression, resulting in the influence on the transcription of hereditary messages ( 18 ), and miRNAs are particularly associated with the abnormal differentiation and maldevelopment of neurons ( 19 , 20 ).…”
Section: Discussionmentioning
confidence: 99%
“… 272 273 274 Recent population-based studies from Brazil, the United Kingdom, and New Zealand have claimed that a large portion of de novo ADHD cases emerge at adult age, 275 276 277 but these results can probably be explained by methodological artifacts and missed subthreshold cases. 76 278 279 However, meta-analytic findings by Bonvicini et al 280 indicate that in part, different genes and polymorphisms seem to contribute to childhood ADHD and adulthood ADHD, lending some genetic plausibility to findings of a late manifestation of the disorder. According to the MTA study, the contribution of interventions administered during childhood to outcome in adulthood is negligible, but controlled intervention was limited to a relatively short period of time (14 months).…”
Section: Long-term Outcomementioning
confidence: 99%
“…However, specific genetic factors differentiating childhood and persistent ADHD into adulthood are not well understood due to the lack of longitudinal studies. Molecular studies, including the most recent GWAS-MA of ADHD [6], have been performed in children and adults either separately or jointly [6,[31][32][33][34][35][36][37][38][39][40], but large-scale analyses comparing their genetic basis are yet to be conducted.…”
Section: Introductionmentioning
confidence: 99%