Mabrouk Rostom
Department of Computer Science, Bishop's University, Sherbrooke, QC J1M 1Z7, Canada.
J Imaging. 2022 Feb 25;8(3):56. doi: 10.3390/jimaging8030056.
Dysfunction of neurons in the central nervous system is the primary pathological feature of Parkinson's disease (PD). Despite different triggering, emerging evidence indicates that neuroinflammation revealed through microglia activation is critical for PD. Moreover, recent investigations sought a potential relationship between Lrrk2 genetic mutation and microglia activation. In this paper, neuroinflammation in sporadic PD, Lrrk2-PD and unaffected Lrrk2 mutation carriers were investigated. The principal component analysis (PCA) and the subject's residual profile (SRP) techniques were performed on multiple groups and regions of interest in 22 brain-regions. The C-PBR28 binding profiles were compared in four genotypes depending on groups, i.e., HC, sPD, Lrrk2-PD and UC, using the PCA and SPR scores. The genotype effect was found as a principal feature of group-dependent C-PBR28 binding, and preliminary evidence of a MAB-Lrrk2 mutation interaction in manifest Parkinson's and subjects at risk was found.
中枢神经系统中神经元功能障碍是帕金森病(PD)的主要病理特征。尽管触发因素不同,但新出现的证据表明,通过小胶质细胞激活所揭示的神经炎症对帕金森病至关重要。此外,最近的研究探寻了Lrrk2基因突变与小胶质细胞激活之间的潜在关系。在本文中,对散发性帕金森病、Lrrk2基因相关帕金森病以及未受影响的Lrrk2基因突变携带者中的神经炎症进行了研究。对22个脑区的多个组和感兴趣区域进行了主成分分析(PCA)和受试者残余轮廓(SRP)技术分析。根据组别,即健康对照(HC)、散发性帕金森病(sPD)、Lrrk2基因相关帕金森病(Lrrk2-PD)和未受影响的携带者(UC),利用PCA和SRP评分比较了四种基因型中的C-PBR28结合谱。发现基因型效应是组依赖性C-PBR28结合的主要特征,并发现了在明显帕金森病患者和有患病风险的受试者中MAB-Lrrk2突变相互作用的初步证据。