دانلود مقاله ISI انگلیسی شماره 117102
ترجمه فارسی عنوان مقاله

بررسی توموگرافی انتشاری پوزیترون از سیستم سروتونرژیک در ارتباط با اضطراب در افسردگی

عنوان انگلیسی
A positron emission tomography study of the serotonergic system in relation to anxiety in depression
کد مقاله سال انتشار تعداد صفحات مقاله انگلیسی
117102 2017 11 صفحه PDF
منبع

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

Journal : European Neuropsychopharmacology, Volume 27, Issue 10, October 2017, Pages 1011-1021

ترجمه کلمات کلیدی
اضطراب، سروتونین، توموگرافی گسیل پوزیترون، افسردگی،
کلمات کلیدی انگلیسی
Anxiety; Serotonin; Positron emission tomography; Depression;
پیش نمایش مقاله
پیش نمایش مقاله  بررسی توموگرافی انتشاری پوزیترون از سیستم سروتونرژیک در ارتباط با اضطراب در افسردگی

چکیده انگلیسی

Symptoms of anxiety are highly comorbid with major depressive disorder (MDD) and are known to alter the course of the disease. To help elucidate the biological underpinnings of these prevalent disorders, we previously examined the relationship between components of anxiety (somatic, psychic and motoric) and serotonin 1A receptor (5-HT1A) binding in MDD and found that higher psychic and lower somatic anxiety was associated with greater 5-HT1A binding. In this work, we sought to examine the correlation between these anxiety symptom dimensions and 5-HTT binding. Positron emission tomography with [11C]-3-amino-4-(3-dimethylamino-methylphenylsulfanyl)-benzonitrile ([11C]DASB) and a metabolite-corrected arterial input function were used to estimate regional 5-HTT binding in 55 subjects with MDD and anxiety symptoms. Somatic anxiety was negatively correlated with 5-HTT binding in the thalamus (β=−.33, p=.025), amygdala (β=−.31, p=.007) and midbrain (β=−.72, p<.001). Psychic anxiety was positively correlated with 5-HTT binding in midbrain only (β=.46, p=.0025). To relate to our previous study, correlation between 5-HT1A and 5-HTT binding was examined, and none was found. We also examined how much of the variance in anxiety symptom dimensions could be explained by both 5-HTT and 5-HT1A binding. The developed model was able to explain 68% (p<.001), 38% (p=.012) and 32% (p=.038) of the total variance in somatic, psychic, and motoric anxiety, respectively. Results indicate the tight coupling between the serotonergic system and anxiety components, which may be confounded when using aggregate anxiety measures. Uncovering serotonin's role in anxiety and depression in this way may give way to a new generation of therapeutics and treatment strategies.