Suppr超能文献

帕金森病相关认知障碍。

Parkinson disease-associated cognitive impairment.

机构信息

Department of Old Age Psychiatry, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.

Centre for Age-Related Medicine, Stavanger University Hospital, Stavanger, Norway.

出版信息

Nat Rev Dis Primers. 2021 Jul 1;7(1):47. doi: 10.1038/s41572-021-00280-3.

Abstract

Parkinson disease (PD) is the second most common neurodegenerative disorder, affecting >1% of the population ≥65 years of age and with a prevalence set to double by 2030. In addition to the defining motor symptoms of PD, multiple non-motor symptoms occur; among them, cognitive impairment is common and can potentially occur at any disease stage. Cognitive decline is usually slow and insidious, but rapid in some cases. Recently, the focus has been on the early cognitive changes, where executive and visuospatial impairments are typical and can be accompanied by memory impairment, increasing the risk for early progression to dementia. Other risk factors for early progression to dementia include visual hallucinations, older age and biomarker changes such as cortical atrophy, as well as Alzheimer-type changes on functional imaging and in cerebrospinal fluid, and slowing and frequency variation on EEG. However, the mechanisms underlying cognitive decline in PD remain largely unclear. Cortical involvement of Lewy body and Alzheimer-type pathologies are key features, but multiple mechanisms are likely involved. Cholinesterase inhibition is the only high-level evidence-based treatment available, but other pharmacological and non-pharmacological strategies are being tested. Challenges include the identification of disease-modifying therapies as well as finding biomarkers to better predict cognitive decline and identify patients at high risk for early and rapid cognitive impairment.

摘要

帕金森病(PD)是第二常见的神经退行性疾病,影响超过 1%的 65 岁及以上人群,预计到 2030 年患病率将翻一番。除了 PD 的明确运动症状外,还会出现多种非运动症状;其中,认知障碍很常见,并且可能发生在任何疾病阶段。认知能力下降通常缓慢而隐匿,但在某些情况下可能会迅速发生。最近,人们的关注点集中在早期认知变化上,执行功能和视空间损害是典型的,并且可能伴有记忆障碍,从而增加早期进展为痴呆的风险。导致早期进展为痴呆的其他风险因素包括幻视、年龄较大以及生物标志物改变,如皮质萎缩,以及功能成像和脑脊液中的阿尔茨海默病样改变,以及脑电图的减慢和频率变化。然而,PD 患者认知下降的机制在很大程度上仍不清楚。路易体和阿尔茨海默病样病理的皮质受累是关键特征,但可能涉及多种机制。乙酰胆碱酯酶抑制是唯一具有高级别循证证据的治疗方法,但其他药理学和非药理学策略正在测试中。挑战包括确定疾病修饰疗法以及寻找生物标志物来更好地预测认知下降并识别出高风险的早期和快速认知障碍患者。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验