Instituto do Cérebro, Instituto de Ensino e Pesquisa do Hospital Israelita Albert Einstein, Sao Paulo, Brazil.
J Neurol Sci. 2011 Nov 15;310(1-2):53-7. doi: 10.1016/j.jns.2011.06.056. Epub 2011 Jul 23.
Social Anxiety Disorder (SAD) is more common among PD patients than in the general population. This association may be explained by psychosocial mechanisms but it is also possible that neurobiological mechanism underlying PD can predispose to SAD. The aim of this study was to investigate a possible dopaminergic mechanism involved in PD patients with SAD, by correlating striatal dopamine transporter binding potential (DAT-BP) with intensity of social anxiety symptoms in PD patients using SPECT with TRODAT-1 as the radiopharmaceutical. Eleven PD patients with generalized SAD and 21 PD patients without SAD were included in this study; groups were matched for age, gender, disease duration and disease severity. SAD diagnosis was determined according to DSM IV criteria assessed with SCID-I and social anxiety symptom severity with the Brief Social Phobia Scale (BSPS). Demographic and clinical data were also collected. DAT-BP was significantly correlated to scores on BSPS for right putamen (r=0.37, p=0.04), left putamen (r=0.43, p=0.02) and left caudate (r=0.39, p=0.03). No significant correlation was found for the right caudate (r=0.23, p=0.21). This finding may reinforce the hypothesis that dopaminergic dysfunction might be implicated in the pathogenesis of social anxiety in PD.
社交焦虑障碍(SAD)在 PD 患者中比普通人群更为常见。这种关联可能可以用心理社会机制来解释,但也有可能是 PD 潜在的神经生物学机制导致了 SAD。本研究的目的是通过使用 TRODAT-1 作为放射性药物的 SPECT 来研究 PD 伴 SAD 患者中可能涉及的多巴胺能机制,以评估纹状体多巴胺转运蛋白结合潜能(DAT-BP)与 PD 患者社交焦虑症状严重程度的相关性。本研究纳入了 11 例广泛性 SAD 的 PD 患者和 21 例无 SAD 的 PD 患者;两组在年龄、性别、病程和疾病严重程度方面相匹配。根据 SCID-I 评估的 DSM-IV 标准和 Brief Social Phobia Scale(BSPS)评估的社交焦虑症状严重程度确定 SAD 诊断。还收集了人口统计学和临床数据。DAT-BP 与右侧壳核(r=0.37,p=0.04)、左侧壳核(r=0.43,p=0.02)和左侧尾状核(r=0.39,p=0.03)的 BSPS 评分显著相关。而右侧尾状核(r=0.23,p=0.21)无显著相关性。这一发现可能进一步证实了多巴胺能功能障碍可能与 PD 患者社交焦虑的发病机制有关的假说。