2019
DOI: 10.1016/j.biopsych.2019.05.014
|View full text |Cite
|
Sign up to set email alerts
|

Which Dopamine Polymorphisms Are Functional? Systematic Review and Meta-analysis of COMT, DAT, DBH, DDC, DRD1–5, MAOA, MAOB, TH, VMAT1, and VMAT2

Abstract: BACKGROUND: Many polymorphisms in dopamine genes are reported to affect cognitive, imaging, or clinical phenotypes. It is often inferred or assumed that such associations are causal, mediated by a direct effect of the polymorphism on the gene product itself. However, the supporting evidence is not always clear. METHODS: We conducted systematic reviews and meta-analyses to assess the empirical evidence for functional polymorphisms in genes encoding dopaminergic enzymes (COMT, DBH, DDC, MAOA, MAOB, and TH), dopa… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

3
39
2
1

Year Published

2019
2019
2022
2022

Publication Types

Select...
4
3
3

Relationship

0
10

Authors

Journals

citations
Cited by 72 publications
(45 citation statements)
references
References 72 publications
(69 reference statements)
3
39
2
1
Order By: Relevance
“…The precise mechanism by which COMT regulates reward-driven behavioral flexibility remains unclear, as there were no consistent changes in behavioral strategy or reinforcement learning that emerged from the analyses. However, although acute pharmacological inhibition is different than the chronic changes in enzymatic activity arising from the human COMT Val/Met polymorphism (58), our findings are concordant with reports of increased sensitivity to rewards and faster reinforcement learning in Met allele carriers, who have lower COMT activity than Val allele homozygotes (59,60).…”
Section: Discussionsupporting
confidence: 89%
“…The precise mechanism by which COMT regulates reward-driven behavioral flexibility remains unclear, as there were no consistent changes in behavioral strategy or reinforcement learning that emerged from the analyses. However, although acute pharmacological inhibition is different than the chronic changes in enzymatic activity arising from the human COMT Val/Met polymorphism (58), our findings are concordant with reports of increased sensitivity to rewards and faster reinforcement learning in Met allele carriers, who have lower COMT activity than Val allele homozygotes (59,60).…”
Section: Discussionsupporting
confidence: 89%
“…Because the populations, research designs, and DNAm measures varied, we conducted a narrative synthesis, rather than a meta-analysis, of this literature to characterize the heterogeneity of studies and summarize patterns across studies (36, 37). We did not assess risk of publication bias, because most standard systematic review indices evaluating risk of bias are not applicable to the observational study types included here (38).…”
Section: Methodsmentioning
confidence: 99%
“…Likewise, we acknowledge that the candidate gene concept in schizophrenia has been largely replaced by genome wide association studies—the former has largely failed to yield insights into the genetic basis of schizophrenia ( Collins et al, 2012 , Farrell et al, 2015 ). Critically, COMT polymorphisms appear to be reliably associated with differential higher order processing ( Mier et al, 2010 ), and appear to be a valid marker of dopaminergic function relative to other candidate genes ( Tunbridge et al, 2019 ). In this context, our present findings of differential effects of COMT variation on neural functions related to higher-order processing in individuals with liability for schizophrenia and bipolar disorder are interesting, though must be interpreted with caution.…”
Section: Limitationsmentioning
confidence: 99%