Department of Neurology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Department of Pharmacology, Vanderbilt University, Nashville, TN 37232, USA.
Brain. 2024 Jul 5;147(7):2440-2448. doi: 10.1093/brain/awae033.
We aimed to describe the clinical features of patients with pure autonomic failure (PAF) preceding phenoconversion that could be useful as predictive markers for advancing α-synuclein-associated neurodegeneration of the brain. Patients diagnosed with PAF were evaluated at eight centres (seven US-based and one European) and enrolled in a longitudinal observational cohort study (NCT01799915). Subjects underwent detailed assessments of motor, sleep, olfactory, cognitive and autonomic function and were followed prospectively to determine whether they developed parkinsonism or dementia for up to 10 years. We identified incident cases of Parkinson's disease (PD), dementia with Lewy bodies (DLB) or multiple system atrophy (MSA) and computed hazard ratios for phenoconversion as functions of clinical features. A total of 209 participants with PAF with a median disease duration of 6 years (IQR: 3-10) were enrolled. Of those, 149 provided follow-up information at an office or telemedicine visit. After a mean follow-up duration of 3 years, 48 (33%) participants phenoconverted (42% to PD, 35% to DLB and 23% to MSA). Faster phenoconversion from study enrolment to any diagnosis was associated with urinary and sexual dysfunction [hazard ratio (HR) 5.9, 95% confidence interval (CI): 1.6-22 and HR: 3.6, 95% CI: 1.1-12] followed by subtle motor signs (HR: 2.7, 95% CI: 1.2-6), trouble swallowing (HR 2.5, 95% CI: 1.4-4.5) and changes in speech (HR:2.4, 95% CI:1.1-4.8) at enrolment. Subjects reporting deterioration of handwriting were more likely to phenoconvert to PD (HR: 2.6, 95% CI: 1.1-5.9) and those reporting difficulty handling utensils were more likely to phenoconvert to DLB (HR: 6.8, 95% CI: 1.2-38). Patients with a younger age of PAF onset (HR: 11, 95% CI: 2.6-46), preserved olfaction (HR: 8.7, 95% CI: 1.7-45), anhidrosis (HR: 1.8, 95% CI: 1-3.1, P = 0.042) and severe urinary problems (HR 1.6, 95% CI: 1-2.5, P = 0.033) were more likely to phenoconvert to MSA. The best autonomic predictor of PD was a blunted heart rate increase during the tilt-table test (HR: 6.1, 95% CI: 1.4-26). Patients with PAF have an estimated 12% (95% CI: 9-15%) per year annual risk following study entry of phenoconverting to a manifest CNS synucleinopathy.
我们旨在描述纯自主神经衰竭(PAF)患者发生表型转化前的临床特征,这些特征可能成为预测脑α-突触核蛋白相关神经退行性变进展的标志物。在八个中心(七个美国和一个欧洲)评估诊断为 PAF 的患者,并将其纳入一项纵向观察队列研究(NCT01799915)。受试者接受了运动、睡眠、嗅觉、认知和自主功能的详细评估,并前瞻性随访,以确定他们是否在长达 10 年内发展为帕金森病、路易体痴呆(DLB)或多系统萎缩(MSA)。我们确定了帕金森病(PD)、路易体痴呆(DLB)或多系统萎缩(MSA)的新发病例,并计算了表型转化的风险比作为临床特征的函数。共纳入 209 例 PAF 患者,中位病程为 6 年(IQR:3-10)。其中,149 例在办公室或远程医疗就诊时提供了随访信息。在平均 3 年的随访后,48 例(33%)患者发生表型转化(42%转化为 PD,35%转化为 DLB,23%转化为 MSA)。从研究入组到任何诊断的表型转化速度越快,与尿失禁和性功能障碍相关(风险比[HR]5.9,95%置信区间[CI]:1.6-22 和 HR:3.6,95%CI:1.1-12),随后是细微的运动迹象(HR:2.7,95%CI:1.2-6)、吞咽困难(HR 2.5,95%CI:1.4-4.5)和言语变化(HR:2.4,95%CI:1.1-4.8)在入组时。报告手部书写恶化的受试者更有可能向 PD 表型转化(HR:2.6,95%CI:1.1-5.9),而报告难以处理餐具的受试者更有可能向 DLB 表型转化(HR:6.8,95%CI:1.2-38)。PAF 发病年龄较小的患者(HR:11,95%CI:2.6-46)、嗅觉保存(HR:8.7,95%CI:1.7-45)、无汗(HR:1.8,95%CI:1-3.1,P = 0.042)和严重的尿失禁问题(HR 1.6,95%CI:1-2.5,P = 0.033)更有可能向 MSA 表型转化。PD 的最佳自主神经预测因子是倾斜试验中心率增加不明显(HR:6.1,95%CI:1.4-26)。PAF 患者在研究入组后,每年有 12%(95%CI:9-15%)的估计风险会出现显性中枢神经系统突触核蛋白病表型转化。