Department of Biomedical Sciences, University of Cagliari, 09042 Monserrato, Italy.
Department of Neurology, Azienda Ospedaliero Universitaria, Policlinico 'D. Casula', 09042 Monserrato, Italy.
Biomolecules. 2021 Jan 22;11(2):144. doi: 10.3390/biom11020144.
Parkinson's disease (PD) is a clinically heterogenic disorder characterized by distinct clinical entities. Most studies on motor deficits dichotomize PD into tremor dominant (TD) or non-tremor dominant (non-TD) with akinetic-rigid features (AR). Different pathophysiological mechanisms may affect the onset of motor manifestations. Recent studies have suggested that gut microbes may be involved in PD pathogenesis. The aim of this study was to investigate the gut microbiota and metabolome composition in PD patients in relation to TD and non-TD phenotypes. In order to address this issue, gut microbiota and the metabolome structure of PD patients were determined from faecal samples using 16S next generation sequencing and gas chromatography-mass spectrometry approaches. The results showed a reduction in the relative abundance of Lachnospiraceae, , , , and an increase in Enterobacteriaceae, and linked to non-TD subtypes. Moreover, the levels of important molecules (i.e., nicotinic acid, cadaverine, glucuronic acid) were altered in relation to the severity of phenotype. We hypothesize that the microbiota/metabolome enterotypes associated to non-TD subtypes may favor the development of gut inflammatory environment and gastrointestinal dysfunctions and therefore a more severe α-synucleinopathy. This study adds important information to PD pathogenesis and emphasizes the potential pathophysiological link between gut microbiota/metabolites and PD motor subtypes.
帕金森病(PD)是一种临床异质性疾病,其特征为不同的临床实体。大多数关于运动缺陷的研究将 PD 分为震颤为主(TD)或非震颤为主(非 TD)伴运动不能-僵硬特征(AR)。不同的病理生理机制可能会影响运动表现的发作。最近的研究表明,肠道微生物可能与 PD 的发病机制有关。本研究旨在调查与 TD 和非 TD 表型相关的 PD 患者的肠道微生物群和代谢组组成。为了解决这个问题,我们使用 16S 下一代测序和气相色谱-质谱分析方法从粪便样本中确定了 PD 患者的肠道微生物群和代谢组结构。结果表明,与非 TD 亚型相关的lachnospiraceae、、、和 enterobacteriaceae、和的相对丰度降低。此外,与表型严重程度相关的重要分子(如烟酸、尸胺、葡萄糖醛酸)水平发生改变。我们假设与非 TD 亚型相关的微生物群/代谢物 enterotypes 可能有利于肠道炎症环境和胃肠道功能障碍的发展,从而导致更严重的α-突触核蛋白病。本研究为 PD 的发病机制增加了重要信息,并强调了肠道微生物群/代谢物与 PD 运动亚型之间的潜在病理生理联系。