Facultad de Biología, Universidad de La Habana, Calle 25 No. 455, Vedado, Plaza de la Revolución, 10400, La Habana, Cuba.
Edmond J Safra Program in Parkinson's Disease and the Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital, 399 Bathurst St, Toronto, ON, M5T 2S8, Canada.
Clin Auton Res. 2019 Dec;29(6):603-614. doi: 10.1007/s10286-019-00632-w. Epub 2019 Aug 23.
Cardiac autonomic dysfunction manifests as reduced heart rate variability (HRV) in idiopathic Parkinson's disease (PD), but no significant reduction has been found in PD patients who carry the LRRK2 mutation. Novel HRV features have not been investigated in these individuals. We aimed to assess cardiac autonomic modulation through standard and novel approaches to HRV analysis in individuals who carry the LRRK2 G2019S mutation.
Short-term electrocardiograms were recorded in 14 LRRK2-associated PD patients, 25 LRRK2-non-manifesting carriers, 32 related non-carriers, 20 idiopathic PD patients, and 27 healthy controls. HRV measures were compared using regression modeling, controlling for age, sex, mean heart rate, and disease duration. Discriminant analysis highlighted the feature combination that best distinguished LRRK2-associated PD from controls.
Beat-to-beat and global HRV measures were significantly increased in LRRK2-associated PD patients compared with controls (e.g., deceleration capacity of heart rate: p = 0.006) and idiopathic PD patients (e.g., 8th standardized moment of the interbeat interval distribution: p = 0.0003), respectively. LRRK2-associated PD patients also showed significantly increased irregularity of heart rate dynamics, as quantified by Rényi entropy, when compared with controls (p = 0.002) and idiopathic PD patients (p = 0.0004). Ordinal pattern statistics permitted the identification of LRRK2-associated PD individuals with 93% sensitivity and 93% specificity. Consistent results were found in a subgroup of LRRK2-non-manifesting carriers when compared with controls.
Increased beat-to-beat HRV in LRRK2 G2019S mutation carriers compared with controls and idiopathic PD patients may indicate augmented cardiac autonomic cholinergic activity, suggesting early impairment of central vagal feedback loops in LRRK2-associated PD.
特发性帕金森病(PD)患者的心脏自主神经功能障碍表现为心率变异性(HRV)降低,但携带 LRRK2 突变的 PD 患者并未发现明显降低。这些个体中尚未研究新的 HRV 特征。我们旨在通过标准和新颖的 HRV 分析方法评估携带 LRRK2 G2019S 突变个体的心脏自主神经调节。
在 14 名 LRRK2 相关 PD 患者、25 名 LRRK2 非表现型携带者、32 名相关非携带者、20 名特发性 PD 患者和 27 名健康对照者中记录短期心电图。使用回归模型比较 HRV 测量值,控制年龄、性别、平均心率和疾病持续时间。判别分析突出了最佳区分 LRRK2 相关 PD 与对照组的特征组合。
与对照组(例如,心率减速能力:p=0.006)和特发性 PD 患者(例如,第 8 个标准化的间期分布矩:p=0.0003)相比,LRRK2 相关 PD 患者的逐搏和整体 HRV 测量值显著增加。与对照组(p=0.002)和特发性 PD 患者(p=0.0004)相比,LRRK2 相关 PD 患者的心率动力学不规则性也显著增加,这是通过 Renyi 熵来量化的。有序模式统计允许以 93%的敏感性和 93%的特异性识别 LRRK2 相关 PD 个体。当与对照组相比时,在 LRRK2 非表现型携带者的亚组中发现了一致的结果。
与对照组和特发性 PD 患者相比,LRRK2 G2019S 突变携带者的逐搏 HRV 增加可能表明心脏自主胆碱能活性增强,提示 LRRK2 相关 PD 中中枢迷走神经反馈回路的早期损伤。