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Individual differences in neural correlates of fear conditioning as a function of 5-HTTLPR and stressful life events
被引:46
|作者:
Klucken, Tim
[1
]
Alexander, Nina
[2
]
Schweckendiek, Jan
[1
]
Merz, Christian J.
[1
,3
]
Kagerer, Sabine
[1
]
Osinsky, Roman
[4
]
Walter, Bertram
[1
]
Vaitl, Dieter
[1
]
Hennig, Juergen
[5
]
Stark, Rudolf
[1
]
机构:
[1] Univ Giessen, Bender Inst Neuroimaging, D-35394 Giessen, Germany
[2] Tech Univ Dresden, Dept Biol Psychol, D-01069 Dresden, Germany
[3] Ruhr Univ Bochum, Dept Cognit Psychol, D-44780 Bochum, Germany
[4] Univ Wurzburg, Dept Psychol 1, D-97070 Wurzburg, Germany
[5] Univ Giessen, Dept Psychobiol & Behav Med, D-35394 Giessen, Germany
关键词:
imaging genetics;
classical conditioning;
fear;
5-HTTLPR;
amygdala;
SEROTONIN TRANSPORTER GENE;
ANXIETY SENSITIVITY;
HUMAN AMYGDALA;
PROMOTER POLYMORPHISM;
PREFRONTAL CORTEX;
DEPRESSION;
HUMANS;
METAANALYSIS;
ACTIVATION;
BRAIN;
D O I:
10.1093/scan/nss005
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Fear learning is a crucial process in the pathogeneses of psychiatric disorders, which highlights the need to identify specific factors contributing to interindividual variation. We hypothesized variation in the serotonin transporter gene (5-HTTLPR) and stressful life events (SLEs) to be associated with neural correlates of fear conditioning in a sample of healthy male adults (n = 47). Subjects were exposed to a differential fear conditioning paradigm after being preselected regarding 5-HTTLPR genotype and SLEs. Individual differences in brain activity as measured by functional magnetic resonance imaging (fMRI), skin conductance responses and preference ratings were assessed. We report significant variation in neural correlates of fear conditioning as a function of 5-HTTLPR genotype. Specifically, the conditioned stimulus (CS+) elicited elevated activity within the fear-network (amygdala, insula, thalamus, occipital cortex) in subjects carrying two copies of the 5-HTTLPR S' allele. Moreover, our results revealed preliminary evidence for a significant gene-by-environment interaction, such as homozygous carriers of the 5-HTTLPR S' allele with a history of SLEs demonstrated elevated reactivity to the CS+ in the occipital cortex and the insula. Our findings contribute to the current debate on 5-HTTLPR x SLEs interaction by investigating crucial alterations on an intermediate phenotype level which may convey an elevated vulnerability for the development of psychopathology.
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页码:318 / 325
页数:8
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