Department of Neurology, Antwerp University Hospital, Drie Eikenstraat 655, 2650, Edegem, Belgium; Faculty of Medicine and Health Sciences, Translational Neurosciences, University of Antwerp, Universiteitsplein 1, 2610, Wilrijk, Belgium; Laboratory for Sleep Disorders and Department of Neurology, St.-Dimpna Regional Hospital, J.-B. Stessensstraat 2, 2440, Geel, Belgium.
Department of Neurology, Antwerp University Hospital, Drie Eikenstraat 655, 2650, Edegem, Belgium; Faculty of Medicine and Health Sciences, Translational Neurosciences, University of Antwerp, Universiteitsplein 1, 2610, Wilrijk, Belgium; Department of Psychiatry, Antwerp University Hospital, Drie Eikenstraat 655, 2650, Edegem, Belgium; Multidisciplinary Sleep Disorders Center, Antwerp University Hospital, Drie Eikenstraat 655, 2650, Edegem, Belgium.
Parkinsonism Relat Disord. 2022 May;98:47-52. doi: 10.1016/j.parkreldis.2022.04.007. Epub 2022 Apr 21.
Wearable technology research suggests that nocturnal movements are disturbed in early Parkinson's disease (PD). In this study, we investigate if patients also already experience impaired bed mobility before PD diagnosis. Furthermore, we explore its association with motor and nonmotor features and its value for phenoconversion and disease progression prediction.
PPMI data were downloaded for de novo PD subjects, subjects at-risk for developing a synucleinopathy (with isolated REM sleep behavior disorder, hyposmia or a pathogenic genetic variant) and controls. Impaired bed mobility was assessed with the MDS-UPDRS part 2 item 9. A frequency analysis was performed. Multivariable logistic regression analyses were used to investigate the association with other PD variables. Cox proportional-hazards models were used to test if difficulties with turning in bed could predict phenoconversion. Linear mixed models were used to evaluate if difficulties with turning in bed could predict disease progression.
Of the at-risk subjects, 9.2-12.5% experienced difficulties with turning in bed vs. 25.0% of de novo PD subjects and 2.5% of controls. Impaired turning ability was associated with MDS-UPDRS motorscore (axial signs in the at-risk group, bradykinesia in the de novo PD group) and SCOPA-AUT score (gastrointestinal symptoms). In addition, difficulties with turning in bed were a significant predictor for phenoconversion in the at-risk group and for development of motor complications in the de novo PD group.
Our findings suggest that difficulties with turning in bed can be helpful as clinical symptom for a prodromal PD screening and for motor complication prediction in early PD.
可穿戴技术研究表明,帕金森病(PD)早期患者的夜间运动受到干扰。在这项研究中,我们调查患者在 PD 诊断前是否已经存在睡眠中床移动能力受损的情况。此外,我们还探讨了这种情况与运动和非运动特征的关系,以及它对表型转化和疾病进展预测的价值。
下载 PPMI 数据,用于研究新诊断的 PD 患者、有发生突触核蛋白病风险的患者(有孤立 REM 睡眠行为障碍、嗅觉减退或致病性遗传变异)和对照组。使用 MDS-UPDRS 第 2 部分项目 9 评估睡眠中床移动能力受损情况。进行了频率分析。使用多变量逻辑回归分析调查与其他 PD 变量的关系。使用 Cox 比例风险模型检验在床翻身困难是否可以预测表型转化。使用线性混合模型评估在床翻身困难是否可以预测疾病进展。
在有风险的患者中,9.2%-12.5%出现了在床翻身困难的情况,而新诊断的 PD 患者中为 25.0%,对照组中为 2.5%。转动能力受损与 MDS-UPDRS 运动评分(有风险的患者中为轴性症状,新诊断的 PD 患者中为运动迟缓)和 SCOPA-AUT 评分(胃肠道症状)相关。此外,在床翻身困难是有风险的患者发生表型转化和新诊断的 PD 患者发生运动并发症的显著预测因子。
我们的研究结果表明,在床翻身困难可能有助于作为 PD 早期的前驱期筛查的临床症状,以及对运动并发症的预测。