دانلود مقاله ISI انگلیسی شماره 40083
ترجمه فارسی عنوان مقاله

تاثیر ژنوتیپ کاتکول-O-متیل بر روی آمیگدال و پردازش عاطفی قشر بجلو مغز در اختلال هراس

عنوان انگلیسی
Influence of the catechol-O-methyltransferase val158met genotype on amygdala and prefrontal cortex emotional processing in panic disorder
کد مقاله سال انتشار تعداد صفحات مقاله انگلیسی
40083 2008 8 صفحه PDF
منبع

Publisher : Elsevier - Science Direct (الزویر - ساینس دایرکت)

Journal : Psychiatry Research: Neuroimaging, Volume 163, Issue 1, 30 May 2008, Pages 13–20

ترجمه کلمات کلیدی
اختلال اضطراب - چهره ها
کلمات کلیدی انگلیسی
Anxiety disorder; COMT; fMRI; Emotional faces; Endophenotype
پیش نمایش مقاله
پیش نمایش مقاله  تاثیر ژنوتیپ کاتکول-O-متیل بر روی آمیگدال و پردازش عاطفی قشر بجلو مغز در اختلال هراس

چکیده انگلیسی

Panic disorder is an anxiety disorder with an estimated heritability of up to 48%. The functional val158met polymorphism in the catechol-O-methyltransferase (COMT) gene has been found to be associated with panic disorder and to influence limbic and prefrontal brain activation in response to unpleasant stimuli. In the present study, neuronal activation following emotional stimulation was used as an endophenotype and investigated for association with the COMT val158met polymorphism in panic disorder. Twenty patients with panic disorder were scanned by means of functional magnetic resonance imaging at 3 Tesla under visual presentation of emotional faces and genotyped for the COMT val158met polymorphism. In response to fearful faces, increased activation in the right amygdala was observed in patients carrying at least one 158val allele. Increased activation or less deactivation associated with the 158val allele was seen upon presentation of fearful, angry and happy faces in the orbitofrontal and ventromedial prefrontal cortex, respectively. Our data provide preliminary evidence for a role of the functional val158met COMT polymorphism in amygdala and prefrontal activation in response to emotional faces in panic disorder. This COMT variant might increase the vulnerability to panic disorder by modulating dopaminergic tonus in relevant brain regions and thus altering neuronal processing of anxiety-related emotional cues.