Temporal profile of brain response to alprazolam in patients with generalized anxiety disorder

被引:19
|
作者
Brown, Gregory G. [1 ]
Ostrowitzki, Susanne [2 ]
Stein, Murray B. [1 ]
von Kienlin, Markus [2 ]
Liu, Thomas T. [3 ]
Simmons, Alan [1 ]
Wierenga, Christina [1 ]
Stein, Orah Y. [1 ]
Bruns, Andreas [2 ]
Bischoff-Grethe, Amanda [1 ]
Paulus, Martin [1 ,4 ]
机构
[1] Univ Calif San Diego, Dept Psychiat, San Diego, CA 92093 USA
[2] F Hoffmann La Roche Ltd, Roche Innovat Ctr Basel, Neurosci, Basel, Switzerland
[3] Univ Calif San Diego, Dept Radiol, San Diego, CA 92093 USA
[4] Laureate Inst Brain Res, Tulsa, OK USA
关键词
Alprazolam; Functional magnetic resonance imaging; Emotional faces; Affective anticipation; Double-blind placebo-controlled trial; Generalized anxiety disorder; COGNITIVE-BEHAVIORAL THERAPY; ACTIVATION; AMYGDALA; INSULA; WORRY; VALIDATION; TOLERANCE; EMOTION; ANTICIPATION; METAANALYSIS;
D O I
10.1016/j.pscychresns.2015.06.016
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
This study investigated the temporal pattern of brain response to emotional stimuli during 28 days of alprazolam treatment among patients with generalized anxiety disorder (GAD) randomized 2:1 to drug or placebo in a double-blind design. Functional magnetic resonance imaging scans obtained during an emotion face matching task (EFMT) and an affective stimulus expectancy task (STIMEX) were performed at baseline, one hour after initial drug administration and 28 clays later Alprazolam significantly reduced scores on the Hamilton Anxiety Scale and the Penn State Worry Questionnaire after one week and 28 days of treatment. Brain activation in the amygclala during the [EMT and in the insula during the STIMEX was reduced one hour after alprazolam administration but returned to baseline levels at Day 28. Exploratory analyses revealed significant treatment differences in brain activity during the STIMEX on Day 28 in frontal lobe, caudate nucleus, middle temporal gyrus, secondary visual cortex, and supramarginal gyms. These results are consistent with the notion that the neural mechanisms supporting sustained treatment effects of benzodiazepines in GAD differ from those underlying their acute effects. Published by Elsevier Ireland Ltd
引用
收藏
页码:394 / 401
页数:8
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