Cargando…

Subjective reward processing and catechol-O- methyltransferase Val158Met polymorphism as potential research domain criteria in addiction: A pilot study

The Research Domain Criteria (RDoC) approach seeks to understand mental functioning in continuous valid dimensions ranging from functional to pathological. Reward processing is a transdiagnostic functioning domain of the RDoC. Due to prototypical abnormalities, addictions are especially applicable f...

Descripción completa

Detalles Bibliográficos
Autores principales:	Rohlfing, Nico, Bonnet, Udo, Tendolkar, Indira, Hinney, Anke, Scherbaum, Norbert
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2022
Materias:	Psychiatry
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9613938/ https://www.ncbi.nlm.nih.gov/pubmed/36311493 http://dx.doi.org/10.3389/fpsyt.2022.992657

Ejemplares similares

Catechol-O-Methyltransferase Val158Met Polymorphism Is Associated with Somatosensory Amplification and Nocebo Responses
por: Wendt, Laura, et al.
Publicado: (2014)

The Influence of the Val158Met Catechol-O-Methyltransferase Polymorphism on the Personality Traits of Bipolar Patients
por: Dávila, Wendy, et al.
Publicado: (2013)

Catechol‐O‐methyltransferase Val158Met polymorphism associates with affect and cortisol levels in women
por: Hill, Lauren D., et al.
Publicado: (2018)

Investigation of Catechol-O-methyltransferase (COMT) gene Val158Met polymorphism in ovarian cancer
por: Abaoğlu, İpek Yağmur, et al.
Publicado: (2021)

Catechol-O-Methyltransferase Val158Met and brain-derived neurotrophic factor Val66Met gene polymorphisms in paraphilic sexual offenders
por: Cengiz, Mujgan, et al.
Publicado: (2019)

The impact of the Catechol-O-methyltransferase Val158Met polymorphism on survival in the general population – the HUNT study
por: Hagen, Knut, et al.
Publicado: (2007)

The Relationship between the Val158Met Catechol-o-Methyltransferase (COMT) Polymorphism and Irritable Bowel Syndrome
por: Karling, Pontus, et al.
Publicado: (2011)

The association between headache and Val158Met polymorphism in the catechol–O–methyltransferase gene: the HUNT Study
por: Hagen, K., et al.
Publicado: (2006)

Association between the Catechol O-Methyltransferase (COMT) Val158met Polymorphism and Different Dimensions of Impulsivity
por: Malloy-Diniz, Leandro Fernandes, et al.
Publicado: (2013)

Catechol-O-Methyltransferase val158met Polymorphism Predicts Placebo Effect in Irritable Bowel Syndrome
por: Hall, Kathryn T., et al.
Publicado: (2012)

Catechol-O-methyltransferase val(158)met Polymorphism Interacts with Sex to Affect Face Recognition Ability
por: Lamb, Yvette N., et al.
Publicado: (2016)

Catechol-O-Methyltransferase Val158Met Polymorphism on Striatum Structural Covariance Networks in Alzheimer’s Disease
por: Chang, Chiung-Chih, et al.
Publicado: (2017)

Role of Catechol-O-methyltransferase Val158Met Polymorphism on Transcranial Direct Current Stimulation in Swallowing
por: Hwang, Hyemi, et al.
Publicado: (2022)

Association between Catechol-O-Methyltransferase Val158Met (158G/A) Polymorphism and Suicide Susceptibility: A Meta-analysis
por: Sadeghiyeh, Tahereh, et al.
Publicado: (2017)

COMT Val(158)Met Genotype Determines the Direction of Cognitive Effects Produced by Catechol-O-Methyltransferase Inhibition
por: Farrell, Sarah M., et al.
Publicado: (2012)

The Catechol-O-Methyltransferase (COMT) val(158)met Polymorphism Affects Brain Responses to Repeated Painful Stimuli
por: Loggia, Marco L., et al.
Publicado: (2011)

Affect-Modulated Startle: Interactive Influence of Catechol-O-Methyltransferase Val158Met Genotype and Childhood Trauma
por: Klauke, Benedikt, et al.
Publicado: (2012)

Association between the catechol-o-methyltransferase val158met polymorphism with susceptibility and severity of carpal tunnel syndrome
por: Erkol İnal, E, et al.
Publicado: (2016)

No association between chronic musculoskeletal complaints and Val158Met polymorphism in the Catechol-O-methyltransferase gene. The HUNT study
por: Hagen, Knut, et al.
Publicado: (2006)

Catechol-O-Methyltransferase (COMT) Val(108/158 )Met polymorphism does not modulate executive function in children with ADHD
por: Taerk, Evan, et al.
Publicado: (2004)

Association between the Catechol-O-Methyltransferase (COMT) Val(158)Met Polymorphism and Manual Aiming Control in Healthy Subjects
por: Lage, Guilherme M., et al.
Publicado: (2014)

Catechol-O-Methyltransferase Val158Met Polymorphism on the Relationship between White Matter Hyperintensity and Cognition in Healthy People
por: Liu, Mu-En, et al.
Publicado: (2014)

The Role of the Catechol-o-methyltransferase (COMT) Gene Val158Met in Aggressive Behavior, A Review of Genetic Studies
por: Qayyum, Arqam, et al.
Publicado: (2015)

Association between the Catechol-O-Methyltransferase (COMT) Val(158)Met Polymorphism and Alexithymia in Patients with Obsessive-Compulsive Disorder
por: Koh, Min Jung, et al.
Publicado: (2016)

Impact of Catechol-O-Methyltransferase Val 158Met (rs4680) Polymorphism on Breast Cancer Susceptibility in Asian Population
por: Rai, Vandana, et al.
Publicado: (2017)

Warriors, Worriers, and COVID-19: An Exploratory Study of the Catechol O-Methyltransferase Val158Met Polymorphism Across Populations
por: Rajkumar, Ravi P
Publicado: (2020)

Toxoplasma gondii Seropositivity Interacts with Catechol-O-methyltransferase Val105/158Met Variation Increasing the Risk of Schizophrenia
por: Rovira, Paula, et al.
Publicado: (2022)

Impaired Set-Shifting Ability in Patients with Eating Disorders, Which Is Not Moderated by Their Catechol-O-Methyltransferase Val158Met Genotype
por: Kim, Youl-Ri, et al.
Publicado: (2010)

Catechol-O-Methyltransferase Val158Met Polymorphism Associates with Individual Differences in Sleep Physiologic Responses to Chronic Sleep Loss
por: Goel, Namni, et al.
Publicado: (2011)

Catechol-O-Methyltransferase Val158Met Polymorphism Modulates Gray Matter Volume and Functional Connectivity of the Default Mode Network
por: Tian, Tian, et al.
Publicado: (2013)

The catechol-o-methyltransferase Val(158)Met polymorphism modulates the intrinsic functional network centrality of the parahippocampal cortex in healthy subjects
por: Zhang, Xiaolong, et al.
Publicado: (2015)

Differential Effects of the Catechol-O-Methyltransferase Val158Met Genotype on the Cognitive Function of Schizophrenia Patients and Healthy Japanese Individuals
por: Tsuchimine, Shoko, et al.
Publicado: (2013)

The Catechol-O-Methyltransferase Val158Met Polymorphism Contributes to the Risk of Breast Cancer in the Chinese Population: An Updated Meta-Analysis
por: Wan, Guo-Xing, et al.
Publicado: (2014)

Age-Dependent Effects of Catechol-O-Methyltransferase (COMT) Gene Val(158)Met Polymorphism on Language Function in Developing Children
por: Sugiura, Lisa, et al.
Publicado: (2017)

Meta-Analysis of the Effects of the Catechol-O-Methyltransferase Val158/108Met Polymorphism on Parkinson’s Disease Susceptibility and Cognitive Dysfunction
por: Tang, Chuanxi, et al.
Publicado: (2019)

Contributions of the Catechol-O-Methyltransferase Val158Met Polymorphism to Changes in Brain Iron Across Adulthood and Their Relationships to Working Memory
por: Gustavsson, Jonatan, et al.
Publicado: (2022)

Catechol-O-Methyltransferase (COMT) Gene (Val158Met) and Brain-Derived Neurotropic Factor (BDNF) (Val66Met) Genes Polymorphism in Schizophrenia: A Case-Control Study
por: Saravani, Ramin, et al.
Publicado: (2017)

Depression and anxiety in relation to catechol-O-methyltransferase Val(158)Met genotype in the general population: The Nord-Trøndelag Health Study (HUNT)
por: Bækken, Petter M, et al.
Publicado: (2008)

No association between catechol-o-methyltransferase Val108/158Met polymorphism and schizophrenia or its clinical symptomatology in a Mexican population
por: Tovilla-Zárate, Carlos, et al.
Publicado: (2012)

Association of the Catechol O-Methyltransferase Val158-Met Polymorphism and Reduced Interference Control in Korean Children with Attention-Deficit Hyperactivity Disorder
por: Park, Subin, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_spqku3ljrtd360litnaj3ksu6o