Rissardo Jamir Pitton, Gadelmawla Ahmed Farid, Khalil Ibrahim, Abdulgadir Ayah, Bhatti Karandeep Singh, Fornari Caprara Ana Letícia
Department of Neurology, Cooper University Hospital, Camden, NJ 08103, USA.
Faculty of Medicine, Menoufia University, Menoufia 6132720, Egypt.
Med Int (Lond). 2025 Sep 1;5(6):68. doi: 10.3892/mi.2025.267. eCollection 2025 Nov-Dec.
Although autonomic dysfunction symptoms are commonly reported by patients with Parkinson's disease (PD) (70-90%), they are frequently under-recognized. Dysautonomia often precedes motor symptoms and can affect the quality of life (QoL) of patients with PD. The present review provides a summary of evidence on prevalence patterns, risk factors and clinical presentations from organ systems related to autonomic dysfunction. Cardiovascular symptoms include orthostatic hypotension (30-50%), supine hypertension (34-50%) and non-dipping patterns of blood pressure (83-88%). Constipation is commonly observed during the prodromal period (60%), and is observed in up to 100% of patients with PD. Genitourinary (89%) and sexual dysfunctions (52-75%) are common, although under-reported. An older age, male sex, duration of disease, severity of the disease and akinetic-rigid phenotype are directly related to overall worse dysautonomia. Genotypic variants have varying degrees of relation with autonomic symptoms; for example, the SNCA gene mutation is associated with cardiac sympathetic denervation, and PARK2 or PARK9 are related to mild effect in autonomic function. Autonomic symptoms are associated with more rapid progression of disease, the attainment of disease milestones, cognitive decline and a poorer QoL. The true prevalence of dysautonomia may be higher due to of the variability of presentation and reporting biases, and current diagnostic definitions may underestimate these non-motor symptoms. The early detection of autonomic impairment may provide time points for intervention that could modify the natural history of the disease. Future studies are required to be directed towards PD-related treatment strategies, autonomic-cognitive relationships, and the development of better animal models covering the complex pathophysiology of PD.
尽管帕金森病(PD)患者中常报告有自主神经功能障碍症状(70 - 90%),但这些症状常未得到充分认识。自主神经功能障碍通常先于运动症状出现,并可影响PD患者的生活质量(QoL)。本综述总结了与自主神经功能障碍相关的器官系统在患病率模式、危险因素和临床表现方面的证据。心血管症状包括直立性低血压(30 - 50%)、卧位高血压(34 - 50%)和血压非勺型模式(83 - 88%)。便秘在前驱期很常见(60%),在高达100%的PD患者中可观察到。泌尿生殖系统功能障碍(89%)和性功能障碍(52 - 75%)很常见,尽管报告不足。年龄较大、男性、病程、疾病严重程度和运动不能 - 强直型表型与总体更严重的自主神经功能障碍直接相关。基因变异与自主神经症状有不同程度的关联;例如,SNCA基因突变与心脏交感神经去神经支配有关,而PARK2或PARK9与自主神经功能的轻度影响有关。自主神经症状与疾病进展更快、达到疾病里程碑、认知衰退和较差的生活质量相关。由于表现的变异性和报告偏差,自主神经功能障碍的真实患病率可能更高,并且当前的诊断定义可能低估了这些非运动症状。自主神经损伤的早期检测可能为干预提供时间点,从而改变疾病的自然病程。未来的研究需要针对与PD相关的治疗策略、自主神经 - 认知关系以及开发涵盖PD复杂病理生理学的更好动物模型。