Topography of Cholinergic Nerve Terminal Vulnerability and Balance Self-Efficacy in Parkinson's Disease.

IF 2.5 4区 医学 Q3 NEUROSCIENCES Journal of integrative neuroscience Pub Date : 2024-09-24 DOI:10.31083/j.jin2309178
Jaimie Barr, Robert Vangel, Prabesh Kanel, Stiven Roytman, Chatkaew Pongmala, Roger L Albin, Peter J H Scott, Nicolaas I Bohnen
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Abstract

Background: Postural instability and gait disturbances (PIGD) represent a significant cause of disability in Parkinson's disease (PD). Cholinergic system dysfunction has been implicated in falls in PD. The occurrence of falls typically results in fear of falling (FoF) that in turn may lead to poorer balance self-efficacy. Balance self-efficacy refers to one's level of confidence in their ability to balance while completing activities of daily living like getting dressed, bathing, and walking. Lower self-efficacy, or greater FoF during these activities is a function of motor, cognitive, and emotional impairments and may impact quality of life in PD. Unlike known cholinergic reduction, especially in the right lateral geniculate and caudate nuclei, little is known about the role of cholinergic transporters in FoF or mobility self-efficacy in PD.

Methods: [18F]fluoroethoxybenzovesamicol ([18F]FEOBV) positron emission tomography (PET) studies were conducted to assess vesicular acetylcholine transporter (VAChT) expression in 126 patients with PD (male (m) = 95, female (f) = 31). Participants had a mean age of 67.3 years (standard deviation (SD) = 7.1) and median Hoehn Yahr stage of 2.5. Patients also completed the Short Falls Efficacy Scale (sFES-I) as a survey measure of concerns about falling. [18F]FEOBV data were processed in Statistical Parametric Mapping (SPM) using a voxel-wise regression model with sFES-I scores as the outcome measure.

Results: Reduced [18F]FEOBV binding in tectum, metathalamic (lateral more than medial geniculate nuclei), thalamus proper, bilateral mesiotemporal (hippocampal, parahippocampal, fusiform gyri and fimbriae), and right cerebellar lobule VI significantly associated with higher sFES-I scores (p < 0.05, family-wise error (FWE) correction after Threshold-Free Cluster Enhancement (TFCE)).

Conclusions: Unlike the more limited involvement of the brainstem-thalamic complex and caudate nuclei cholinergic topography associated with falls in PD, cholinergic reductions in the extended connectivity between the thalamic complex and the temporal limbic system via the fimbriae associates with FoF. Additional cholinergic changes were seen in the cerebellum. The temporal limbic system plays a role not only in episodic memory but also in spatial navigation, scene and contextual (e.g., emotional) processing. Findings may augur novel therapeutic approaches to treat poor mobility self-efficacy in PD.

Clinical trial registration: No: NCT02458430. Registered 18 March, 2015, https://www.

Clinicaltrials: gov/study/NCT02458430; No: NCT05459753. Registered 01 July, 2022, https://www.

Clinicaltrials: gov/study/NCT05459753.

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帕金森病患者胆碱能神经末梢易损性和平衡自我效能的地形图。
背景:姿势不稳和步态障碍(PIGD)是帕金森病(PD)致残的一个重要原因。胆碱能系统功能障碍与帕金森病患者跌倒有关。跌倒的发生通常会导致对跌倒的恐惧(FoF),进而可能导致平衡自我效能感降低。平衡自我效能指的是一个人在完成穿衣、洗澡和行走等日常生活活动时对自己平衡能力的自信程度。在这些活动中,自我效能感较低或FoF较大是运动、认知和情感障碍的一种表现,可能会影响帕金森病患者的生活质量。与已知的胆碱能减少(尤其是右侧膝状核和尾状核)不同,人们对胆碱能转运体在帕金森氏症患者FoF或行动自我效能中的作用知之甚少。方法:在126名帕金森氏症患者(男性(m)=95人,女性(f)=31人)中进行了[18F]氟乙氧基苯并ovesamicol([18F]FEOBV)正电子发射断层扫描(PET)研究,以评估囊泡乙酰胆碱转运体(VAChT)的表达。参与者的平均年龄为 67.3 岁(标准差 (SD) = 7.1),中位 Hoehn Yahr 分期为 2.5。患者还填写了 "短跌倒效能量表"(sFES-I),作为对跌倒问题的调查测量。[18F]FEOBV数据在统计参数映射(SPM)中进行处理,使用体素回归模型,以sFES-I评分作为结果测量指标:结果:在视网膜、丘脑(外侧膝状核多于内侧膝状核)、丘脑本部、双侧中颞叶(海马、海马旁、纺锤形回和边缘)和右侧小脑VI中,[18F]FEOBV结合率降低与sFES-I评分升高显著相关(p < 0.05,无阈值簇增强(TFCE)后的族向误差(FWE)校正):与脑干-丘脑复合体和尾状核胆碱能地形图与帕金森病患者跌倒相关的有限参与不同,丘脑复合体与颞叶边缘系统之间通过缘膜的扩展连接中的胆碱能减少与FoF相关。小脑中也出现了其他胆碱能变化。颞边缘系统不仅在情节记忆中发挥作用,而且还在空间导航、场景和情境(如情感)处理中发挥作用。研究结果可能预示着治疗帕金森病行动自我效能低下的新型治疗方法:临床试验注册:NCT02458430。2015年3月18日注册,https://www.Clinicaltrials: gov/study/NCT02458430;编号:NCT05459753。注册日期为 2022 年 7 月 1 日,https://www.Clinicaltrials: gov/study/NCT05459753。
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来源期刊
CiteScore
2.80
自引率
5.60%
发文量
173
审稿时长
2 months
期刊介绍: JIN is an international peer-reviewed, open access journal. JIN publishes leading-edge research at the interface of theoretical and experimental neuroscience, focusing across hierarchical levels of brain organization to better understand how diverse functions are integrated. We encourage submissions from scientists of all specialties that relate to brain functioning.
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