双侧STN-DBS治疗帕金森病患者脑淀粉样蛋白-β沉积、轴向特征和认知改变:一项长期队列研究

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Francesco Cavallieri, Alessandro Fraternali, Annachiara Arnone, Isabella Campanini, Alessandro Marti, Annalisa Gessani, Valentina Fioravanti, Maria Angela Molinari, Giulia Di Rauso, Francesca Antonelli, Vittorio Rispoli, Alberto Feletti, Riccardo Stanzani, Benedetta Damiano, Sara Scaltriti, Lorenzo Cavazzuti, Elisa Bardi, Maria Giulia Corni, Francesca Cavalleri, Giuseppe Biagini, Giacomo Pavesi, Mirco Lusuardi, Carla Budriesi, Andrea Merlo, Annibale Versari, Franco Valzania
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引用次数: 0

摘要

目的:我们的目的是评估接受丘脑下核深部脑刺激(STN-DBS)治疗的PD患者可能的长期脑内淀粉样蛋白-β沉积及其对轴向和认知变量的可能影响。方法:纳入双侧STN-DBS治疗的连续PD患者,并进行长期随访。术后通过18f -氟替美莫正电子发射断层扫描(PET)评估淀粉样蛋白-β沉积。轴向症状采用标准化的临床仪器方法进行评估。语音通过感知和声学分析进行评估,步态通过仪器计时Up and Go测试(iTUG)进行评估。运动严重程度通过应用UPDRS第三部分评分和子评分进行评估,而认知功能通过完整的神经心理学评估进行评估。评估了不同的刺激和药物条件:刺激/停药,非刺激/停药,刺激/停药(单任务和双任务)。结果:共19例PD患者(男性11例;年龄:63.52岁;UPDRS-III: 17.05),术后随访5年。淀粉样蛋白-β沉积在21%(4/19)的患者中发现,普遍累及前额叶、边缘和顶叶区。与没有淀粉样蛋白-β沉积的患者相比,PET研究中18f -氟替他莫阳性的PD患者术前UPDRS-I评分更高(p = 0.037)。结论:我们的研究结果表明,从长期来看,在STN-DBS后,很大比例的PD患者可能出现脑淀粉样蛋白-β沉积。然而,需要更大的样本来评估淀粉样蛋白-β沉积在手术后轴向和认知改变发展中的可能作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cerebral Amyloid-β Deposition, Axial Features, and Cognitive Alterations in Patients with Parkinson's Disease Treated with Bilateral STN-DBS: A Long-Term Cohort Study.

Objectives: Our aim was to evaluate the possible long-term cerebral deposition of amyloid-β in patients with PD treated with subthalamic nucleus deep brain stimulation (STN-DBS) and its possible influence on axial and cognitive variables. Methods: Consecutive PD patients treated with bilateral STN-DBS with a long-term follow-up were included. The amyloid-β deposition was evaluated postoperatively through an 18F-flutemetamol positron emission tomography (PET) study. Axial symptoms were assessed using a standardized clinical-instrumental approach. The speech was assessed by perceptual and acoustic analysis, while gait was assessed by means of the instrumented Timed Up and Go test (iTUG). Motor severity was evaluated by applying the UPDRS part III score and subscores, while cognitive functions were assessed through a complete neuropsychological assessment. Different stimulation and drug conditions were assessed: on-stimulation/off-medication, off-stimulation/off-medication, and on-stimulation/on-medication conditions (single- and dual-task). Results: In total, 19 PD patients (male: 11; age: 63.52 years; on-stimulation/on-medication UPDRS-III: 17.05) with a five-year postoperative follow-up were included. The amyloid-β deposition was found in 21% of patients (4/19) with a prevalent involvement of prefrontal, limbic, and parietal areas. Compared with patients without amyloid-β deposition, PD patients with positive 18F-flutemetamol in the PET study showed a higher preoperative UPDRS-I (p = 0.037) score. Conclusions: Our results suggest that in the long term, after STN-DBS, a significant percentage of PD patients may present brain amyloid-β deposition. However, larger samples are needed to evaluate the possible role of amyloid-β deposition in the development of axial and cognitive alterations after surgery.

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来源期刊
Journal of Personalized Medicine
Journal of Personalized Medicine Medicine-Medicine (miscellaneous)
CiteScore
4.10
自引率
0.00%
发文量
1878
审稿时长
11 weeks
期刊介绍: Journal of Personalized Medicine (JPM; ISSN 2075-4426) is an international, open access journal aimed at bringing all aspects of personalized medicine to one platform. JPM publishes cutting edge, innovative preclinical and translational scientific research and technologies related to personalized medicine (e.g., pharmacogenomics/proteomics, systems biology). JPM recognizes that personalized medicine—the assessment of genetic, environmental and host factors that cause variability of individuals—is a challenging, transdisciplinary topic that requires discussions from a range of experts. For a comprehensive perspective of personalized medicine, JPM aims to integrate expertise from the molecular and translational sciences, therapeutics and diagnostics, as well as discussions of regulatory, social, ethical and policy aspects. We provide a forum to bring together academic and clinical researchers, biotechnology, diagnostic and pharmaceutical companies, health professionals, regulatory and ethical experts, and government and regulatory authorities.
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