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The role of the prefrontal Cortex (PFC) in higher cognitive functions - including working memory, conflict resolution, set shifting and semantic processing - has been demonstrated unequivocally. Despite the great heterogeneity among tasks measuring these phenotypes, due in part to the different cognitive sub-processes implied and the specificity of the stimulus material used, there is agreement that all of these tasks recruit an executive control system located in the PFC. On a biochemical level it is known that the dopaminergic system plays an important role in executive control functions. Evidence comes from molecular genetics relating the functional COMT Val158Met polymorphism to working memory and set shifting. In order determine whether this pattern of findings generalises to linguistic and semantic processing, we investigated the effects of the COMT Val158Met polymorphism in lexical decision making using masked and unmasked versions of the semantic priming paradigm on N = 104 healthy subjects. Although we observed strong priming effects in all conditions (masked priming, unmasked priming with short/long stimulus asynchronies (SOAs), direct and indirect priming), COMT was not significantly related to priming, suggesting no reliable influence on semantic processing. However, COMT Val158Met was strongly associated with lexical decision latencies in all priming conditions if considered separately, explaining between 9 and 14.5% of the variance. Therefore, the findings indicate that COMT mainly influences more general executive control functions in the PFC supporting the speed of lexical decisions.
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http://dx.doi.org/10.3389/neuro.09.020.2009 | DOI Listing |
J Coll Physicians Surg Pak
August 2025
Department of Public Health, Army Medical College, Rawalpindi, Pakistan.
Objective: To examine the association between the catechol-O-methyltransferase (COMT) rs4680 polymorphism - a common genetic variation in the gene, which regulates dopamine metabolism in the prefrontal cortex - and academic performance among medical students at a public-sector medical college in Rawalpindi, Pakistan.
Study Design: A cross-sectional analytical study. Place and Duration of the Study: Department of Pharmacology, Army Medical College, Rawalpindi, in collaboration with the Institute of Biomedical and Genetic Engineering, Islamabad, Pakistan, from January to March 2025.
Front Biosci (Landmark Ed)
July 2025
Studio Indagini Mediche E Forensi (SIMEF), 89128 Reggio Calabria, Italy.
Background: Methamphetamine (METH) addiction is a global concern due to its severe impact on public health, including heightened aggression and neurotoxic effects. Genetic and epigenetic factors, particularly involving the and genes, are implicated in individual vulnerability to METH addiction. Thus, understanding the molecular mechanisms involved is crucial for developing targeted prevention and treatment strategies.
View Article and Find Full Text PDFClin J Pain
July 2025
Department of Rheumatology, Rehabilitation and Physical Medicine, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Objectives: We aimed to explore the potential contribution of small fiber pathology (SFP) and COMT enzyme gene Val/158/Met functional polymorphism to neuropathic pain (NP) in FMS female patients.
Methods: This case-control study was conducted on 60 women with FMS and 60 matched healthy women. All patients were subjected to detailed clinical assessment.
Dev Psychobiol
July 2025
School of Psychology, Key Laboratory of Behavioral and Mental Health of Gansu Province, Northwest Normal University, Lanzhou, China.
The present study investigated the interaction effects of family socioeconomic status (SES), parent-child relationship, and COMT Val158Met polymorphism on the executive function (EF) of Chinese preschool-aged children. The sample comprised 748 preschoolers (M = 5.02 years, SD = 0.
View Article and Find Full Text PDFNeurorehabil Neural Repair
August 2025
Stroke Biological Recovery Laboratory, Spaulding Rehabilitation Hospital, Teaching Affiliate of Harvard Medical School, Charlestown, MA, USA.
. A single nucleotide polymorphism (SNP) in the catechol-o-methyltransferase () gene, Val158Met (rs4680), influences cognition in the general population. However, its role in stroke recovery is unclear.
View Article and Find Full Text PDF