Berkebile John A, Inan Omer T, Beach Paul A
School of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, GA, United States.
Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA, United States.
Front Netw Physiol. 2025 Apr 24;5:1543838. doi: 10.3389/fnetp.2025.1543838. eCollection 2025.
Levodopa is the most common therapy to reduce motor symptoms of parkinsonism. However, levodopa has potential to exacerbate cardiovascular autonomic (CVA) dysfunction that may co-occur in patients. Heart rate variability (HRV) is the most common method for assessing CVA function, but broader monitoring of CVA function and levodopa effects is typically limited to clinical settings and symptom reporting, which fail to capture its holistic nature. In this study, we evaluated the feasibility of a multimodal wearable chest patch for monitoring changes in CVA function during clinical and 24-h ambulatory (at home) conditions in 14 patients: 11 with Parkinson's disease (PD) and 3 with multiple system atrophy (MSA). In-clinic data were analyzed to examine the effects of orally administered levodopa on CVA function using a pre (OFF) and 60-min (ON) post-exposure protocol. Wearable-derived physiological markers related to the electrical and mechanical activity of the heart alongside vascular function were extracted. Pre-ejection period (PEP) and ratio of PEP to left ventricular ejection time index (LVETi) increased significantly (p 0.05) following levodopa, indicating a decrease in cardiac contractility. We further explored dose-response relationships and how CVA responses differed between participants with orthostatic hypotension (OH) from those without OH. Heart rate variability, specifically root-mean-square-of-successive-differences (RMSSD), following levodopa decreased significantly more in participants with OH (n = 7) compared to those without (no-OH, n = 7). The results suggest that the wearable patch's measures are sensitive to CVA dynamics and provide exploratory insights into levodopa's potential role in inducing a negative inotropic effect and exacerbating CVA dysfunction. This work encourages further evaluation of these wearable-derived physiomarkers for quantifying CVA and informing individualized care of individuals with parkinsonism.
左旋多巴是减轻帕金森症运动症状最常用的疗法。然而,左旋多巴有可能加剧患者可能同时出现的心血管自主神经(CVA)功能障碍。心率变异性(HRV)是评估CVA功能最常用的方法,但对CVA功能和左旋多巴作用的更广泛监测通常仅限于临床环境和症状报告,而这些无法全面反映其整体情况。在本研究中,我们评估了一种多模式可穿戴式胸贴在14例患者的临床和24小时动态(在家)情况下监测CVA功能变化的可行性:11例帕金森病(PD)患者和3例多系统萎缩(MSA)患者。分析临床数据,采用暴露前(关期)和暴露后60分钟(开期)方案,研究口服左旋多巴对CVA功能的影响。提取了与心脏电活动和机械活动以及血管功能相关的可穿戴设备衍生的生理标志物。左旋多巴给药后,射血前期(PEP)和PEP与左心室射血时间指数(LVETi)的比值显著增加(p<0.05),表明心脏收缩力下降。我们进一步探讨了剂量反应关系,以及体位性低血压(OH)患者与非OH患者之间CVA反应的差异。与无OH的参与者(n = 7)相比,左旋多巴给药后,OH参与者(n = 7)的心率变异性,特别是逐次差值均方根(RMSSD)显著降低。结果表明,可穿戴胸贴的测量对CVA动态变化敏感,并为左旋多巴在诱导负性肌力作用和加剧CVA功能障碍方面的潜在作用提供了探索性见解。这项工作鼓励进一步评估这些可穿戴设备衍生的生理标志物,以量化CVA并为帕金森症患者的个体化护理提供依据。