Gonzalez Maria Camila, Dalen Ingvild, Maple-Grødem Jodi, Tysnes Ole-Bjørn, Alves Guido
Department of Quality and Health Technology, Faculty of Health Sciences, University of Stavanger, Stavanger, Norway.
The Norwegian Centre for Movement Disorders, Stavanger University Hospital, Stavanger, Norway.
NPJ Parkinsons Dis. 2022 May 12;8(1):58. doi: 10.1038/s41531-022-00320-z.
Identification of factors predicting and driving mortality in PD is important for patient information, disease management, and design of future clinical trials. This study included newly diagnosed PD patients and normal controls (NC) from a population-based study with repeated assessments over a 10-year period. We used the Kaplan-Meier method to estimate survival, Cox proportional hazards regression models to identify baseline risk factors of mortality, and Cox regression models with time-dependent covariates to evaluate the impact of four clinical milestones of advanced PD (visual hallucinations, recurrent falls, dementia, and nursing home placement) on mortality risk. During the 10-year study, 65 (34.2%) of 190 patients and 25 (12.3%) of 203 NC died, with an unadjusted hazard ratio (HR) of 2.85 (95% CI 1.80-4.52) and a HR of 2.48 (95% CI 1.55-3.95) when adjusted for confounders, including comorbidities. Higher age, more severe motor impairment, and postural instability-gait difficulty (PIGD) phenotype were independent baseline predictors of mortality. Each clinical milestone alone more than doubled the risk of death and had a cumulative effect on mortality, with a HR of 10.83 (95% CI 4.39-26.73) in those experiencing all four milestones. PD patients have an increased mortality risk that is disease-related and becomes evident early during the course of the disease. While motor severity and PIGD phenotype were early risk factors of mortality, clinical milestones signaled a substantially increased risk of death later during the disease course, highlighting their potential significance in clinical disease staging and prognosis.
识别帕金森病(PD)中预测和导致死亡的因素对于患者信息、疾病管理以及未来临床试验的设计至关重要。本研究纳入了来自一项基于人群的研究中的新诊断PD患者和正常对照(NC),并在10年期间进行了重复评估。我们使用Kaplan-Meier方法估计生存率,使用Cox比例风险回归模型识别死亡的基线风险因素,并使用带有时间依存性协变量的Cox回归模型评估晚期PD的四个临床里程碑(视幻觉、反复跌倒、痴呆和入住养老院)对死亡风险的影响。在10年的研究期间,190例患者中有65例(34.2%)死亡,203例NC中有25例(12.3%)死亡,未调整的风险比(HR)为2.85(95%置信区间1.80 - 4.52),在调整包括合并症在内的混杂因素后,HR为2.48(95%置信区间1.55 - 3.95)。年龄较大、运动障碍更严重以及姿势不稳-步态障碍(PIGD)表型是死亡的独立基线预测因素。每个临床里程碑单独使死亡风险增加一倍以上,并且对死亡率有累积影响,在经历所有四个里程碑的患者中,HR为10.83(95%置信区间4.39 - 26.73)。PD患者的死亡风险增加,这与疾病相关,并且在疾病过程早期就很明显。虽然运动严重程度和PIGD表型是早期死亡风险因素,但临床里程碑表明在疾病后期死亡风险大幅增加,突出了它们在临床疾病分期和预后中的潜在重要性。