Preserved Serotonin Transporter Availability in Parkinson Disease Measured with Either [11C]MADAM or [11C]DASB: A Study Including 2 Separate Cohorts of Nondepressed Patients

Minyoung Oh, Joachim Brumberg, Vesna Sossi, Andrea Varrone
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Abstract

Serotonin transporter (SERT) availability was assessed using 2 tracers, [11C]N,N-dimethyl-2-(2-amino-4-cyanophenylthio)benzylamine ([11C]DASB) and [11C]N,N-dimethyl-2-(2-amino-4-fluoromethylphenylthio)benzylamine) ([11C]MADAM), in independent cohorts of patients and controls. This study aimed to independently confirm whether SERT remains intact in nondepressed individuals with early-stage Parkinson disease (PD), because the use of diverse methodologies could potentially yield disparate results. Methods: Seventeen PD patients (5 women and 12 men; age, 64 ± 7 y; Unified Parkinson’s Disease Rating Scale motor score, 23 ± 5; Beck Depression Inventory score, 5 ± 4) and 20 age- and sex-matched healthy controls underwent [11C]MADAM PET at Karolinska Institutet. Fifteen PD patients (5 women and 10 men; age, 59 ± 9 y; Unified Parkinson’s Disease Rating Scale motor score, 15 ± 7; Beck Depression Inventory score, 4 ± 4) and 8 controls were examined with [11C]DASB PET at the University of British Columbia. PET scans were performed at both institutions using a high-resolution research tomograph. A simplified reference tissue model and Logan graphical analysis were used to calculate the regional nondisplaceable binding potential (BPND), using the cerebellum as the reference. Parametric BPND images were generated using wavelet-aided parametric imaging. MRI-defined volumes of interest included cortical and subcortical regions, as well as brain stem nuclei. Results: There were no significant differences between controls and early-stage PD patients in either the [11C]DASB or the [11C]MADAM cohort, regardless of the analysis method. Group differences (Cohen d) in the [11C]DASB cohort ranged from 0.34 to 0.86 in brain stem nuclei, 0.09 to 0.61 in subcortical regions, and 0.28 to 0.70 in cortical regions. In the [11C]MADAM cohort, they ranged from 0.16 to 0.40, 0.19 to 0.55, and 0.32 to 0.61, respectively. Logan BPND highly correlated with simplified reference tissue model BPND for both tracers in each group (P < 0.001). Conclusion: SERT availability is relatively preserved in nondepressed patients with PD. This study suggests that serotonergic degeneration is not a major feature of the disease in nondepressed patients with nonadvanced disease.

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用[11C]MADAM或[11C]DASB测量帕金森病中保留的血清素转运体可用性:一项包括2个独立队列的非抑郁患者的研究
5 -羟色胺转运体(SERT)可用性评估采用两种示踪剂,[11C]N,N-二甲基-2-(2-氨基-4-氰苯基硫)苄胺([11C]DASB)和[11C]N,N-二甲基-2-(2-氨基-4-氟甲基苯基硫)苄胺([11C]MADAM),在独立的患者和对照组队列中进行。本研究旨在独立确认SERT是否在早期帕金森病(PD)的非抑郁个体中保持完整,因为使用不同的方法可能会产生不同的结果。方法:17例PD患者(女性5例,男性12例;年龄:64±7y;统一帕金森病评定量表运动评分,23±5分;贝克抑郁量表评分(5±4)和20名年龄和性别匹配的健康对照者在卡罗林斯卡研究所接受了[11C]MADAM PET检查。PD患者15例(女性5例,男性10例;年龄:59±9岁;统一帕金森病评定量表运动评分,15±7分;采用英属哥伦比亚大学的[11C]DASB PET检测Beck抑郁量表评分(4±4)和8名对照者。PET扫描在两个机构使用高分辨率的研究层析成像进行。以小脑为参照,采用简化的参考组织模型和Logan图形分析计算区域不可置换结合电位(BPND)。采用小波辅助参数成像技术生成参数化BPND图像。mri定义的感兴趣的体积包括皮层和皮层下区域,以及脑干核。结果:无论采用何种分析方法,在[11C]DASB或[11C]MADAM队列中,对照组与早期PD患者之间均无显著差异。在[11C]DASB队列中,脑干核组差异(Cohen d)为0.34 ~ 0.86,皮质下区为0.09 ~ 0.61,皮质区为0.28 ~ 0.70。在[11C]MADAM队列中,它们的范围分别为0.16 ~ 0.40、0.19 ~ 0.55和0.32 ~ 0.61。两组示踪剂的Logan BPND与简化参考组织模型BPND高度相关(P <;0.001)。结论:非抑郁PD患者的SERT可用性相对保留。这项研究表明,血清素能变性不是非抑郁症患者非晚期疾病的主要特征。
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