Department of Neurology, Zaans Medisch Centrum, 1502 DV Zaandam, The Netherlands.
Department of Neurology, University Medical Centre, 9713 GZ Groningen, The Netherlands.
Biomolecules. 2020 Jun 8;10(6):880. doi: 10.3390/biom10060880.
The pathophysiology of cervical dystonia (CD) is thought to be related to changes in dopamine and serotonin levels in the brain. We performed a double-blind trial with escitalopram (selective serotonin reuptake inhibitor; SSRI) in patients with CD. Here, we report on changes in dopamine D receptor (D2/3R), dopamine transporter (DAT) and serotonin transporter (SERT) binding potential (BP) after a six-week treatment course with escitalopram or placebo. CD patients had [123I]FP-CIT SPECT (I-123 fluoropropyl carbomethoxy-3 beta-(4-iodophenyltropane) single-photon emission computed tomography) scans, to quantify extrastriatal SERT and striatal DAT, and [123I]IBZM SPECT (I-123 iodobenzamide SPECT) scans to quantify striatal D2/3R BPND before and after six weeks of treatment with either escitalopram or placebo. Treatment effect was evaluated with the Clinical Global Impression scale for dystonia, jerks and psychiatric symptoms, both by physicians and patients. In both patients treated with escitalopram and placebo there were no significant differences after treatment in SERT, DAT or D2/3R BP. Comparing scans after treatment with escitalopram (n = 8) to placebo (n = 8) showed a trend ( = 0.13) towards lower extrastriatal SERT BPND in the SSRI group (median SERT occupancy of 64.6%). After treatment with escitalopram, patients who reported a positive effect on dystonia or psychiatric symptoms had significantly higher SERT occupancy compared to patients who did not experience an effect. Higher extrastriatal SERT occupancy after treatment with escitalopram is associated with a trend towards a positive subjective effect on dystonia and psychiatric symptoms in CD patients.
颈源性肌张力障碍 (CD) 的病理生理学被认为与大脑中多巴胺和 5-羟色胺水平的变化有关。我们对 CD 患者进行了艾司西酞普兰(选择性 5-羟色胺再摄取抑制剂;SSRIs)的双盲试验。在这里,我们报告了六周艾司西酞普兰或安慰剂治疗后多巴胺 D 受体 (D2/3R)、多巴胺转运体 (DAT) 和 5-羟色胺转运体 (SERT) 结合潜能 (BP) 的变化。CD 患者进行了[123I]FP-CIT SPECT(I-123 氟丙基卡巴氧-3β-(4-碘苯托烷)单光子发射计算机断层扫描)扫描,以定量评估纹状体外 SERT 和纹状体 DAT,以及[123I]IBZM SPECT(I-123 碘苯酰胺 SPECT)扫描以定量评估纹状体 D2/3R BPND,然后在接受艾司西酞普兰或安慰剂治疗六周前后。使用临床总体印象量表对肌张力障碍、抽搐和精神症状进行评估,由医生和患者共同评估治疗效果。 在接受艾司西酞普兰和安慰剂治疗的患者中,治疗后 SERT、DAT 或 D2/3R BP 均无显著差异。与安慰剂相比,接受艾司西酞普兰治疗的患者的扫描结果(n = 8)显示(= 0.13)SSRI 组的纹状体外 SERT BPND 呈下降趋势(SERT 占有率中位数为 64.6%)。接受艾司西酞普兰治疗后,报告对肌张力障碍或精神症状有积极影响的患者的 SERT 占有率明显高于无影响的患者。 接受艾司西酞普兰治疗后,SERT 占有率较高与 CD 患者对肌张力障碍和精神症状的主观疗效呈正相关趋势。