Department of Psychology, Center on Aging, California State University San Bernardino, San Bernardino, CA, USA.
Department of Psychology, Center on Aging, California State University San Bernardino, San Bernardino, CA, USA.
Parkinsonism Relat Disord. 2020 Mar;72:7-12. doi: 10.1016/j.parkreldis.2020.01.009. Epub 2020 Jan 25.
Non-motor symptoms such as cognitive and gastrointestinal (GI) symptoms are common in Parkinson's disease (PD). In PD, GI-symptoms often present prior to motor symptoms. It is hypothesized that GI-symptoms reflect disruptions of the microbiome-gut-brain axis, which leads to altered immune functioning, chronic neuroinflammation, and subsequent neurodegeneration. Initial evidence links gut-dysbiosis to PD pathology and motor symptom severity. The present study examines the longitudinal relationship between severity of GI-symptoms and cognitive impairment in newly diagnosed PD patients.
A secondary data analysis of the Parkinson's Progression Markers Initiative (PPMI) included 423 newly diagnosed PD patients who were followed for up to 5 years. Participants underwent neuropsychological tests of processing speed, attention, visuospatial functioning, verbal learning and verbal delayed recall. Participant were classified as cognitive intact, mild cognitive impairment or Parkinson's disease dementia. Frequency of GI-symptoms were assessed with the Scales for Outcomes in Parkinson's Disease Autonomic (SCOPA-AUT). Multi-level models (MLM) examined the longitudinal relationship between GI symptoms and cognitive impairment.
All cognitive outcomes were predicted by the main effect of GI symptoms, or the GI-symptom X Occasion interaction term. Specifically, more severe GI-symptoms were predictive of a less favorable trajectory of performance on tests of letter fluency, visuospatial, learning and memory. Cognitive performance was uniquely associated with GI-symptoms and unrelated to non-GI autonomic symptoms.
The presence of GI symptoms may serve as an early marker of cognitive impairment in PD. Future studies should examine specific mechanisms underlying the relationship between gut-dysbiosis and cognitive impairment.
非运动症状,如认知和胃肠道(GI)症状,在帕金森病(PD)中很常见。在 PD 中,GI 症状通常先于运动症状出现。据推测,GI 症状反映了微生物群-肠道-大脑轴的紊乱,这导致免疫功能改变、慢性神经炎症和随后的神经退行性变。最初的证据将肠道失调与 PD 病理和运动症状严重程度联系起来。本研究检查了新诊断的 PD 患者中 GI 症状严重程度与认知障碍的纵向关系。
对帕金森病进展标志物倡议(PPMI)的二次数据分析包括 423 名新诊断的 PD 患者,他们的随访时间长达 5 年。参与者接受了处理速度、注意力、视空间功能、语言学习和语言延迟回忆的神经心理学测试。参与者被分类为认知正常、轻度认知障碍或帕金森病痴呆。使用帕金森病自主神经量表(SCOPA-AUT)评估 GI 症状的频率。多层次模型(MLM)检查了 GI 症状与认知障碍的纵向关系。
所有认知结果均由 GI 症状的主要效应或 GI 症状与发作的交互项预测。具体来说,更严重的 GI 症状预示着字母流畅性、视空间、学习和记忆测试的表现轨迹更差。认知表现与 GI 症状相关,与非 GI 自主神经症状无关。
GI 症状的存在可能是 PD 认知障碍的早期标志物。未来的研究应检查肠道失调与认知障碍之间关系的具体机制。