Schneier Franklin R, Abi-Dargham Anissa, Martinez Diana, Slifstein Mark, Hwang Dah-Ren, Liebowitz Michael R, Laruelle Marc
Anxiety Disorders Clinic, New York State Psychiatric Institute, Unit 69, 1051 Riverside Drive, New York, NY 10032, USA.
Depress Anxiety. 2009;26(5):411-8. doi: 10.1002/da.20543.
Dopamine D2 receptor and dopamine transporter (DAT) availability in the striatum (STR) have each been reported abnormal in generalized social anxiety disorder (GSAD) in studies using single photon emission computerized tomography (SPECT). D2 receptors and DAT have not previously been studied within the same GSAD subjects, however, and prior GSAD studies have not assessed dopamine release or subdivided the STR into functional subregions.
Unmedicated adults with GSAD (N=17) and matched healthy comparison (HC) subjects (N=13) participated in this study. Of these, 15 GSAD and 13 HC subjects completed baseline assessment of D2 receptor availability using positron emission tomography (PET) with the radiotracer [11C]raclopride. Twelve GSAD and 13 HC subjects completed a repeat scan after intravenous administration of d-amphetamine to study dopamine release. Twelve of the GSAD subjects and 10 of the HC subjects also completed SPECT with the radiotracer [123I] methyl 3beta-(4-iodophenyl) tropane-2beta-carboxylate ([123I]beta-CIT) to assess DAT availability.
GSAD and HC groups did not differ significantly in striatal DAT availability, the overall striatal or striatal subregion D2 receptor availability at baseline, or change in D(2) receptor availability after d-amphetamine. Receptor availability and change after d-amphetamine were not significantly associated with severity of social anxiety or trait detachment.
These findings do not replicate previous findings of altered striatal DAT and D2 receptor availability in GSAD subjects assessed with SPECT. The differences from results of prior studies may be due to differences in imaging methods or characteristics of samples.
在使用单光子发射计算机断层扫描(SPECT)的研究中,已报道广泛性社交焦虑障碍(GSAD)患者纹状体(STR)中的多巴胺D2受体和多巴胺转运体(DAT)可用性均异常。然而,此前尚未在同一GSAD受试者中对D2受体和DAT进行研究,并且先前的GSAD研究未评估多巴胺释放情况,也未将STR细分为功能亚区。
未用药的GSAD成年患者(N = 17)和匹配的健康对照(HC)受试者(N = 13)参与了本研究。其中,15名GSAD患者和13名HC受试者使用放射性示踪剂[11C]雷氯必利通过正电子发射断层扫描(PET)完成了D2受体可用性的基线评估。12名GSAD患者和13名HC受试者在静脉注射d-苯丙胺后完成了重复扫描,以研究多巴胺释放情况。12名GSAD患者和10名HC受试者还使用放射性示踪剂[123I]3β-(4-碘苯基)托烷-2β-羧酸甲酯([123I]β-CIT)完成了SPECT检查,以评估DAT可用性。
GSAD组和HC组在纹状体DAT可用性、基线时整体纹状体或纹状体亚区D2受体可用性或d-苯丙胺后D(2)受体可用性变化方面无显著差异。d-苯丙胺后的受体可用性和变化与社交焦虑严重程度或特质分离无显著相关性。
这些发现未能重复先前使用SPECT评估的GSAD受试者纹状体DAT和D2受体可用性改变的研究结果。与先前研究结果的差异可能归因于成像方法或样本特征的不同。