Malek Naveed, Lawton Michael A, Grosset Katherine A, Bajaj Nin, Barker Roger A, Burn David J, Foltynie Tom, Hardy John, Morris Huw R, Williams Nigel M, Ben-Shlomo Yoav, Wood Nicholas W, Grosset Donald G
Department of Neurology Ipswich Hospital NHS Trust Ipswich United Kingdom.
School of Social and Community Medicine University of Bristol Bristol United Kingdom.
Mov Disord Clin Pract. 2016 Nov 24;4(4):509-516. doi: 10.1002/mdc3.12454. eCollection 2017 Jul-Aug.
Autonomic dysfunction is common in the later stages of Parkinson's disease (PD), but less is known about its presence and severity in early disease.
To analyze features of autonomic dysfunction in recent onset PD cases, and their relationship to motor severity, medication use, other nonmotor symptoms (NMS), and quality-of-life scores.
Detailed patient-reported symptoms of autonomic dysfunction were assessed in a multicenter cohort study in PD cases that had been diagnosed within the preceding 3.5 years.
There were 1746 patients (1132 males, 65.2%), mean age 67.6 years (SD 9.3), mean disease duration 1.3 years (SD 0.9), mean Movement Disorder Society Unified Parkinson's Disease Rating Scale motor score 22.5 (SD 12.1). Orthostatic symptoms were reported by 39.6%, male erectile dysfunction by 56.1%, and female anorgasmia by 57.4%. Sialorrhea was an issue in 51.4% of patients, constipation in 43.6%, and dysphagia in 20.1%. Autonomic features increased with higher modified Hoehn and Yahr stages ( < 0.001). The severity of autonomic dysfunction was associated with the postural instability gait difficulty motor phenotype [β-coefficient 1.7, 95% confidence interval (CI) 0.7, 2.6, < 0.001], depression (β-coefficient 4.1, CI 3.0, 5.2, < 0.001), and excess daytime sleepiness (β-coefficient 3.1, CI 1.9, 4.2, < 0.001). Dopamine agonists were the only drug class associated with greater autonomic dysfunction ( = 0.019). The severity of autonomic dysfunction strongly correlated with the presence of other NMS (ρ = 0.717, < 0.001), and with poorer quality-of-life scores (ρ = 0.483, < 0.001).
Autonomic dysfunction is common in early PD. Autonomic dysfunction correlates with the presence of other NMS, and with worse quality of life.
自主神经功能障碍在帕金森病(PD)晚期较为常见,但在疾病早期其存在情况及严重程度鲜为人知。
分析近期发病的PD病例中自主神经功能障碍的特征,及其与运动严重程度、药物使用、其他非运动症状(NMS)和生活质量评分的关系。
在一项多中心队列研究中,对在之前3.5年内确诊的PD病例中患者报告的自主神经功能障碍详细症状进行评估。
共有1746例患者(1132例男性,占65.2%),平均年龄67.6岁(标准差9.3),平均病程1.3年(标准差0.9),平均运动障碍协会统一帕金森病评定量表运动评分22.5(标准差12.1)。39.6%的患者报告有体位性症状,56.1%的男性有勃起功能障碍,57.4%的女性有性高潮缺失。51.4%的患者存在流涎问题,43.6%的患者有便秘,20.1%的患者有吞咽困难。自主神经特征随改良Hoehn和Yahr分期升高而增加(<0.001)。自主神经功能障碍的严重程度与姿势不稳步态困难运动表型相关[β系数1.7,95%置信区间(CI)0.7,2.6,<0.001]、抑郁(β系数4.1,CI 3.0,5.2,<0.001)和日间过度嗜睡(β系数3.1,CI 1.9,4.2,<0.001)。多巴胺激动剂是唯一与更严重自主神经功能障碍相关的药物类别(P = 0.019)。自主神经功能障碍的严重程度与其他NMS的存在密切相关(ρ = 0.717,<0.001),且与较差的生活质量评分相关(ρ = 0.483,<0.001)。
自主神经功能障碍在早期PD中很常见。自主神经功能障碍与其他NMS的存在相关,且与较差的生活质量相关。