BDNF Val66Met and DRD2 Taq1A polymorphisms interact to influence PTSD symptom severity: a preliminary investigation in a South African population. Hemmings, S. M. J., Martin, L. I., Klopper, M., van der Merwe, L., Aitken, L., de Wit, E., Black, G. F., Hoal, E. G., Walzl, G., & Seedat, S. Progress in Neuro-Psychopharmacology & Biological Psychiatry, 40:273–280, January, 2013. 00012 doi abstract bibtex BACKGROUND: We evaluated the role that selected variants in serotonin transporter (5-HTT), dopamine receptor 2 (DRD2) and brain-derived neurotrophic factor (BDNF) genes play in PTSD symptom severity in an at-risk population. We also investigated the interaction between the genetic variants to determine whether these variables and the interactions between the variables influenced the severity of PTSD symptoms. METHODS: PTSD symptoms were quantitatively assessed using the Davidson Trauma Scale (DTS) in 150 participants from an at-risk South African population. All participants were genotyped for the 5-HTTLPR, DRD2 Taq1A and BDNF Val66Met polymorphisms. Gene-gene interactions were investigated using various linear models. All analyses were adjusted for age, gender, major depressive disorder diagnosis, level of resilience, level of social support and alcohol dependence. RESULTS: A significant interaction effect between DRD2 Taq1A and BDNF Val66Met variants on DTS score was observed. On the background of the BDNF Val66Val genotype, DTS score increased significantly with the addition of a DRD2 Taq1A A1 allele. However, on the BDNF Met66 allele background, the addition of an A1 allele was found to reduce total DTS score. CONCLUSIONS: This study provides preliminary evidence for an epistatic interaction between BDNF Val66Met and DRD2 Taq1A polymorphisms on the severity of PTSD symptoms, where both too little and too much dopamine can result in increased PTSD symptom severity.
@article{hemmings_bdnf_2013,
title = {{BDNF} {Val66Met} and {DRD2} {Taq1A} polymorphisms interact to influence {PTSD} symptom severity: a preliminary investigation in a {South} {African} population},
volume = {40},
issn = {1878-4216},
shorttitle = {{BDNF} {Val66Met} and {DRD2} {Taq1A} polymorphisms interact to influence {PTSD} symptom severity},
doi = {10.1016/j.pnpbp.2012.10.011},
abstract = {BACKGROUND: We evaluated the role that selected variants in serotonin transporter (5-HTT), dopamine receptor 2 (DRD2) and brain-derived neurotrophic factor (BDNF) genes play in PTSD symptom severity in an at-risk population. We also investigated the interaction between the genetic variants to determine whether these variables and the interactions between the variables influenced the severity of PTSD symptoms.
METHODS: PTSD symptoms were quantitatively assessed using the Davidson Trauma Scale (DTS) in 150 participants from an at-risk South African population. All participants were genotyped for the 5-HTTLPR, DRD2 Taq1A and BDNF Val66Met polymorphisms. Gene-gene interactions were investigated using various linear models. All analyses were adjusted for age, gender, major depressive disorder diagnosis, level of resilience, level of social support and alcohol dependence.
RESULTS: A significant interaction effect between DRD2 Taq1A and BDNF Val66Met variants on DTS score was observed. On the background of the BDNF Val66Val genotype, DTS score increased significantly with the addition of a DRD2 Taq1A A1 allele. However, on the BDNF Met66 allele background, the addition of an A1 allele was found to reduce total DTS score.
CONCLUSIONS: This study provides preliminary evidence for an epistatic interaction between BDNF Val66Met and DRD2 Taq1A polymorphisms on the severity of PTSD symptoms, where both too little and too much dopamine can result in increased PTSD symptom severity.},
language = {eng},
journal = {Progress in Neuro-Psychopharmacology \& Biological Psychiatry},
author = {Hemmings, Sian M. J. and Martin, Lindi I. and Klopper, Marisa and van der Merwe, Lize and Aitken, Lisa and de Wit, Erika and Black, Gillian F. and Hoal, Eileen G. and Walzl, Gerhard and Seedat, Soraya},
month = jan,
year = {2013},
pmid = {23103549},
note = {00012 },
keywords = {Adult, Alleles, Brain-Derived Neurotrophic Factor, Epistasis, Genetic, Female, Genetic Predisposition to Disease, Genotype, Humans, Male, Polymorphism, Single Nucleotide, Questionnaires, Receptors, Dopamine D2, Resilience, Psychological, Serotonin Plasma Membrane Transport Proteins, Severity of Illness Index, Social Support, Stress Disorders, Post-Traumatic},
pages = {273--280},
}
Downloads: 0
{"_id":"wRvsZRYJj43DbEm6q","bibbaseid":"hemmings-martin-klopper-vandermerwe-aitken-dewit-black-hoal-etal-bdnfval66metanddrd2taq1apolymorphismsinteracttoinfluenceptsdsymptomseverityapreliminaryinvestigationinasouthafricanpopulation-2013","author_short":["Hemmings, S. M. J.","Martin, L. I.","Klopper, M.","van der Merwe, L.","Aitken, L.","de Wit, E.","Black, G. F.","Hoal, E. G.","Walzl, G.","Seedat, S."],"bibdata":{"bibtype":"article","type":"article","title":"BDNF Val66Met and DRD2 Taq1A polymorphisms interact to influence PTSD symptom severity: a preliminary investigation in a South African population","volume":"40","issn":"1878-4216","shorttitle":"BDNF Val66Met and DRD2 Taq1A polymorphisms interact to influence PTSD symptom severity","doi":"10.1016/j.pnpbp.2012.10.011","abstract":"BACKGROUND: We evaluated the role that selected variants in serotonin transporter (5-HTT), dopamine receptor 2 (DRD2) and brain-derived neurotrophic factor (BDNF) genes play in PTSD symptom severity in an at-risk population. We also investigated the interaction between the genetic variants to determine whether these variables and the interactions between the variables influenced the severity of PTSD symptoms. METHODS: PTSD symptoms were quantitatively assessed using the Davidson Trauma Scale (DTS) in 150 participants from an at-risk South African population. All participants were genotyped for the 5-HTTLPR, DRD2 Taq1A and BDNF Val66Met polymorphisms. Gene-gene interactions were investigated using various linear models. All analyses were adjusted for age, gender, major depressive disorder diagnosis, level of resilience, level of social support and alcohol dependence. RESULTS: A significant interaction effect between DRD2 Taq1A and BDNF Val66Met variants on DTS score was observed. On the background of the BDNF Val66Val genotype, DTS score increased significantly with the addition of a DRD2 Taq1A A1 allele. However, on the BDNF Met66 allele background, the addition of an A1 allele was found to reduce total DTS score. CONCLUSIONS: This study provides preliminary evidence for an epistatic interaction between BDNF Val66Met and DRD2 Taq1A polymorphisms on the severity of PTSD symptoms, where both too little and too much dopamine can result in increased PTSD symptom severity.","language":"eng","journal":"Progress in Neuro-Psychopharmacology & Biological Psychiatry","author":[{"propositions":[],"lastnames":["Hemmings"],"firstnames":["Sian","M.","J."],"suffixes":[]},{"propositions":[],"lastnames":["Martin"],"firstnames":["Lindi","I."],"suffixes":[]},{"propositions":[],"lastnames":["Klopper"],"firstnames":["Marisa"],"suffixes":[]},{"propositions":["van","der"],"lastnames":["Merwe"],"firstnames":["Lize"],"suffixes":[]},{"propositions":[],"lastnames":["Aitken"],"firstnames":["Lisa"],"suffixes":[]},{"propositions":["de"],"lastnames":["Wit"],"firstnames":["Erika"],"suffixes":[]},{"propositions":[],"lastnames":["Black"],"firstnames":["Gillian","F."],"suffixes":[]},{"propositions":[],"lastnames":["Hoal"],"firstnames":["Eileen","G."],"suffixes":[]},{"propositions":[],"lastnames":["Walzl"],"firstnames":["Gerhard"],"suffixes":[]},{"propositions":[],"lastnames":["Seedat"],"firstnames":["Soraya"],"suffixes":[]}],"month":"January","year":"2013","pmid":"23103549","note":"00012 ","keywords":"Adult, Alleles, Brain-Derived Neurotrophic Factor, Epistasis, Genetic, Female, Genetic Predisposition to Disease, Genotype, Humans, Male, Polymorphism, Single Nucleotide, Questionnaires, Receptors, Dopamine D2, Resilience, Psychological, Serotonin Plasma Membrane Transport Proteins, Severity of Illness Index, Social Support, Stress Disorders, Post-Traumatic","pages":"273–280","bibtex":"@article{hemmings_bdnf_2013,\n\ttitle = {{BDNF} {Val66Met} and {DRD2} {Taq1A} polymorphisms interact to influence {PTSD} symptom severity: a preliminary investigation in a {South} {African} population},\n\tvolume = {40},\n\tissn = {1878-4216},\n\tshorttitle = {{BDNF} {Val66Met} and {DRD2} {Taq1A} polymorphisms interact to influence {PTSD} symptom severity},\n\tdoi = {10.1016/j.pnpbp.2012.10.011},\n\tabstract = {BACKGROUND: We evaluated the role that selected variants in serotonin transporter (5-HTT), dopamine receptor 2 (DRD2) and brain-derived neurotrophic factor (BDNF) genes play in PTSD symptom severity in an at-risk population. We also investigated the interaction between the genetic variants to determine whether these variables and the interactions between the variables influenced the severity of PTSD symptoms.\nMETHODS: PTSD symptoms were quantitatively assessed using the Davidson Trauma Scale (DTS) in 150 participants from an at-risk South African population. All participants were genotyped for the 5-HTTLPR, DRD2 Taq1A and BDNF Val66Met polymorphisms. Gene-gene interactions were investigated using various linear models. All analyses were adjusted for age, gender, major depressive disorder diagnosis, level of resilience, level of social support and alcohol dependence.\nRESULTS: A significant interaction effect between DRD2 Taq1A and BDNF Val66Met variants on DTS score was observed. On the background of the BDNF Val66Val genotype, DTS score increased significantly with the addition of a DRD2 Taq1A A1 allele. However, on the BDNF Met66 allele background, the addition of an A1 allele was found to reduce total DTS score.\nCONCLUSIONS: This study provides preliminary evidence for an epistatic interaction between BDNF Val66Met and DRD2 Taq1A polymorphisms on the severity of PTSD symptoms, where both too little and too much dopamine can result in increased PTSD symptom severity.},\n\tlanguage = {eng},\n\tjournal = {Progress in Neuro-Psychopharmacology \\& Biological Psychiatry},\n\tauthor = {Hemmings, Sian M. J. and Martin, Lindi I. and Klopper, Marisa and van der Merwe, Lize and Aitken, Lisa and de Wit, Erika and Black, Gillian F. and Hoal, Eileen G. and Walzl, Gerhard and Seedat, Soraya},\n\tmonth = jan,\n\tyear = {2013},\n\tpmid = {23103549},\n\tnote = {00012 },\n\tkeywords = {Adult, Alleles, Brain-Derived Neurotrophic Factor, Epistasis, Genetic, Female, Genetic Predisposition to Disease, Genotype, Humans, Male, Polymorphism, Single Nucleotide, Questionnaires, Receptors, Dopamine D2, Resilience, Psychological, Serotonin Plasma Membrane Transport Proteins, Severity of Illness Index, Social Support, Stress Disorders, Post-Traumatic},\n\tpages = {273--280},\n}\n\n\n\n","author_short":["Hemmings, S. M. J.","Martin, L. I.","Klopper, M.","van der Merwe, L.","Aitken, L.","de Wit, E.","Black, G. F.","Hoal, E. G.","Walzl, G.","Seedat, S."],"key":"hemmings_bdnf_2013","id":"hemmings_bdnf_2013","bibbaseid":"hemmings-martin-klopper-vandermerwe-aitken-dewit-black-hoal-etal-bdnfval66metanddrd2taq1apolymorphismsinteracttoinfluenceptsdsymptomseverityapreliminaryinvestigationinasouthafricanpopulation-2013","role":"author","urls":{},"keyword":["Adult","Alleles","Brain-Derived Neurotrophic Factor","Epistasis","Genetic","Female","Genetic Predisposition to Disease","Genotype","Humans","Male","Polymorphism","Single Nucleotide","Questionnaires","Receptors","Dopamine D2","Resilience","Psychological","Serotonin Plasma Membrane Transport Proteins","Severity of Illness Index","Social Support","Stress Disorders","Post-Traumatic"],"metadata":{"authorlinks":{}},"downloads":0,"html":""},"bibtype":"article","biburl":"http://bibbase.org/zotero/TBHostGen","dataSources":["csPxbBZ9RG8CqYnrf"],"keywords":["adult","alleles","brain-derived neurotrophic factor","epistasis","genetic","female","genetic predisposition to disease","genotype","humans","male","polymorphism","single nucleotide","questionnaires","receptors","dopamine d2","resilience","psychological","serotonin plasma membrane transport proteins","severity of illness index","social support","stress disorders","post-traumatic"],"search_terms":["bdnf","val66met","drd2","taq1a","polymorphisms","interact","influence","ptsd","symptom","severity","preliminary","investigation","south","african","population","hemmings","martin","klopper","van der merwe","aitken","de wit","black","hoal","walzl","seedat"],"title":"BDNF Val66Met and DRD2 Taq1A polymorphisms interact to influence PTSD symptom severity: a preliminary investigation in a South African population","year":2013}