IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
Department of Computer Science and Technology, University of Cambridge, Cambridge, United Kingdom.
Mech Ageing Dev. 2021 Mar;194:111426. doi: 10.1016/j.mad.2020.111426. Epub 2020 Dec 29.
Advanced age is the major risk factor for idiopathic Parkinson's disease (PD), but to date the biological relationship between PD and ageing remains elusive. Here we describe the rationale and the design of the H2020 funded project "PROPAG-AGEING", whose aim is to characterize the contribution of the ageing process to PD development. We summarize current evidences that support the existence of a continuum between ageing and PD and justify the use of a Geroscience approach to study PD. We focus in particular on the role of inflammaging, the chronic, low-grade inflammation characteristic of elderly physiology, which can propagate and transmit both locally and systemically. We then describe PROPAG-AGEING design, which is based on the multi-omic characterization of peripheral samples from clinically characterized drug-naïve and advanced PD, PD discordant twins, healthy controls and "super-controls", i.e. centenarians, who never showed clinical signs of motor disability, and their offspring. Omic results are then validated in a large number of samples, including in vitro models of dopaminergic neurons and healthy siblings of PD patients, who are at higher risk of developing PD, with the final aim of identifying the molecular perturbations that can deviate the trajectories of healthy ageing towards PD development.
年龄增长是特发性帕金森病(PD)的主要危险因素,但迄今为止,PD 与衰老之间的生物学关系仍难以捉摸。在这里,我们描述了 H2020 资助项目“PROPAG-AGEING”的原理和设计,该项目的目的是描述衰老过程对 PD 发展的贡献。我们总结了目前支持衰老和 PD 之间存在连续体的证据,并证明了使用老年科学方法来研究 PD 的合理性。我们特别关注炎症衰老的作用,即老年生理学中慢性、低水平炎症的特征,这种炎症可以在局部和全身传播和传递。然后,我们描述了 PROPAG-AGEING 的设计,该设计基于对临床特征明确的药物初治和晚期 PD、PD 不一致双胞胎、健康对照和“超级对照”(即从未出现过运动障碍临床症状的百岁老人)及其后代的外周样本进行多组学特征描述。然后在大量样本中验证了组学结果,包括多巴胺能神经元的体外模型和 PD 患者的健康兄弟姐妹,他们患 PD 的风险更高,最终目的是确定可以改变健康衰老轨迹向 PD 发展的分子扰动。