Genetic gating of human fear learning and extinction
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Genetic gating of human fear learning and extinction : possible implications for gene-environment interaction in anxiety disorder. / Lonsdorf, Tina B; Weike, Almut I; Nikamo, Pernilla; Schalling, Martin; Hamm, Alfons O; Ohman, Arne.
In: PSYCHOL SCI, Vol. 20, No. 2, 01.02.2009, p. 198-206.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - Genetic gating of human fear learning and extinction
T2 - possible implications for gene-environment interaction in anxiety disorder
AU - Lonsdorf, Tina B
AU - Weike, Almut I
AU - Nikamo, Pernilla
AU - Schalling, Martin
AU - Hamm, Alfons O
AU - Ohman, Arne
PY - 2009/2/1
Y1 - 2009/2/1
N2 - Pavlovian fear conditioning is a widely used model of the acquisition and extinction of fear. Neural findings suggest that the amygdala is the core structure for fear acquisition, whereas prefrontal cortical areas are given pivotal roles in fear extinction. Forty-eight volunteers participated in a fear-conditioning experiment, which used fear potentiation of the startle reflex as the primary measure to investigate the effect of two genetic polymorphisms (5-HTTLPR and COMTval158met) on conditioning and extinction of fear. The 5-HTTLPR polymorphism, located in the serotonin transporter gene, is associated with amygdala reactivity and neuroticism, whereas the COMTval158met polymorphism, which is located in the gene coding for catechol-O-methyltransferase (COMT), a dopamine-degrading enzyme, affects prefrontal executive functions. Our results show that only carriers of the 5-HTTLPR s allele exhibited conditioned startle potentiation, whereas carriers of the COMT met/met genotype failed to extinguish conditioned fear. These results may have interesting implications for understanding gene-environment interactions in the development and treatment of anxiety disorders.
AB - Pavlovian fear conditioning is a widely used model of the acquisition and extinction of fear. Neural findings suggest that the amygdala is the core structure for fear acquisition, whereas prefrontal cortical areas are given pivotal roles in fear extinction. Forty-eight volunteers participated in a fear-conditioning experiment, which used fear potentiation of the startle reflex as the primary measure to investigate the effect of two genetic polymorphisms (5-HTTLPR and COMTval158met) on conditioning and extinction of fear. The 5-HTTLPR polymorphism, located in the serotonin transporter gene, is associated with amygdala reactivity and neuroticism, whereas the COMTval158met polymorphism, which is located in the gene coding for catechol-O-methyltransferase (COMT), a dopamine-degrading enzyme, affects prefrontal executive functions. Our results show that only carriers of the 5-HTTLPR s allele exhibited conditioned startle potentiation, whereas carriers of the COMT met/met genotype failed to extinguish conditioned fear. These results may have interesting implications for understanding gene-environment interactions in the development and treatment of anxiety disorders.
KW - Adult
KW - Alleles
KW - Anxiety Disorders
KW - Catechol O-Methyltransferase
KW - Conditioning (Psychology)
KW - Environment
KW - Extinction, Psychological
KW - Fear
KW - Female
KW - Genotype
KW - Humans
KW - Learning
KW - Male
KW - Prefrontal Cortex
KW - Serotonin Plasma Membrane Transport Proteins
U2 - 10.1111/j.1467-9280.2009.02280.x
DO - 10.1111/j.1467-9280.2009.02280.x
M3 - SCORING: Journal article
C2 - 19175757
VL - 20
SP - 198
EP - 206
JO - PSYCHOL SCI
JF - PSYCHOL SCI
SN - 0956-7976
IS - 2
ER -