Neurodegeneration Imaging Group, Institute of Psychiatry, Psychology & Neuroscience (IoPPN), King's College London, United Kingdom.
School of Psychology and Cardiff University Brain Research Imaging Centre, Cardiff University, United Kingdom; Division of Neuroscience & Experimental Psychology, University of Manchester, United Kingdom.
Parkinsonism Relat Disord. 2020 Aug;77:163-169. doi: 10.1016/j.parkreldis.2019.02.027. Epub 2019 Feb 22.
Preclinical studies suggest a link between cAMP/PKA signalling, phosphodiesterase 4 (PDE4) expression and excessive daytime sleepiness (EDS). Here, we investigated in vivo the association between PDE4 expression and EDS in Parkinson's disease (PD) patients using [C]rolipram PET and MR imaging.
Eighteen participants, 12 PD and 6 healthy controls, underwent one [C]rolipram PET and a multi-modal MRI scan. Probabilistic tractography was performed on subjects' diffusion data to functionally parcellate the striatum according with projections to limbic cortical areas. The severity of EDS was assessed using the Epworth Sleepiness Scale (ESS). To assess PDE4 expression in PD patients with EDS, the PD cohort was divided according to the presence (n = 5) or absence (n = 7) of EDS, defined using validated cut-off of score ≥10 on the ESS as score ≥10 on the ESS.
PD patients with EDS showed significantly increased [C]rolipram volume of distribution (V) in the caudate (P = 0.029), hypothalamus (P = 0.013), hippocampus (P = 0.036) and limbic striatum (P = 0.030) compared to patients without EDS. Furthermore, higher ESS scores correlated with increased [C]rolipram V in the caudate (r = 0.77; P = 0.003), hypothalamus (r = 0.84; P = 0.001), hippocampus (r = 0.81; P = 0.001) and limbic subdivisions of the striatum (r = 0.80; P = 0.003).
Our findings translate into humans preclinical data indicating that EDS is associated with elevated PDE4 in regions regulating sleep. The severity of EDS in PD was associated with elevated PDE4 expression; thus, suggesting a role of PDE4 in the pathophysiology of EDS in PD.
临床前研究表明环磷酸腺苷/蛋白激酶 A(cAMP/PKA)信号转导、磷酸二酯酶 4(PDE4)表达与日间过度嗜睡(EDS)之间存在关联。在此,我们使用 [C]rolipram PET 和磁共振成像(MRI)研究了帕金森病(PD)患者中 PDE4 表达与 EDS 之间的内在联系。
18 名参与者,包括 12 名 PD 患者和 6 名健康对照者,接受了一次 [C]rolipram PET 和多模态 MRI 扫描。对受试者的扩散数据进行概率性束追踪,根据与边缘皮质区域的投射将纹状体进行功能分区。采用 Epworth 嗜睡量表(ESS)评估 EDS 的严重程度。为了评估 PD 伴 EDS 患者的 PDE4 表达,根据 ESS 评分≥10(定义为 ESS 评分≥10)将 PD 队列分为伴 EDS(n=5)和不伴 EDS(n=7)。
与不伴 EDS 的 PD 患者相比,伴 EDS 的 PD 患者的尾状核(P=0.029)、下丘脑(P=0.013)、海马体(P=0.036)和边缘纹状体(P=0.030)的 [C]rolipram 分布容积(V)明显增加。此外,ESS 评分越高,尾状核(r=0.77;P=0.003)、下丘脑(r=0.84;P=0.001)、海马体(r=0.81;P=0.001)和边缘纹状体(r=0.80;P=0.003)的 [C]rolipram V 也越高。
本研究将临床前数据转化为人类研究,表明 EDS 与调节睡眠的区域中 PDE4 升高有关。PD 患者 EDS 的严重程度与 PDE4 表达升高相关,这表明 PDE4 在 PD 中 EDS 的病理生理学中起作用。