Laboratory of Sports Medicine, Aristotle University of Thessaloniki, 57001 Thermi, Greece.
Pediatric Pulmonology and Cystic Fibrosis Unit, Hippokration Hospital, Aristotle University of Thessaloniki, 54642 Thessaloniki, Greece.
Sensors (Basel). 2022 Jun 28;22(13):4884. doi: 10.3390/s22134884.
Several studies have shown that patients with cystic fibrosis (CF), even at a young age, have pulmonary and cardiac abnormalities. The main complications are cardiac right ventricular (RV) systolic and/or diastolic dysfunction and pulmonary hypertension, which affects their prognosis. Exercise training (ET) is recommended in patients with CF as a therapeutic modality to improve physical fitness and health-related quality of life. However, questions remain regarding its optimal effective and safe dose and its effects on the patients’ cardiac function. The study aimed to provide a wearable activity tracker (WAT)-based ET to promote physical activity in CF patients and assess its effects on cardiac morphology and function. Forty-two stable CF individuals (aged 16.8 ± 3.6 years) were randomly assigned to either the intervention (Group A) or the control group (Group B). Group A participated in a 1-year WAT-based ET program three times per week. All patients underwent a 6-min walking test (6-MWT) and an echocardiographic assessment focused mainly on RV anatomy and function at the baseline and the end of the study. RV systolic function was evaluated by measuring the tricuspid annular plane systolic excursion (TAPSE), the systolic tricuspid annular velocity (TVS’), the RV free-wall longitudinal strain (RVFWSL), and the right ventricular four-chamber longitudinal strain (RV4CSL). RV diastolic function was assessed using early (TVE) and late (TVA) diastolic transtricuspid flow velocity and their ratio TVE/A. Pulmonary artery systolic pressure (PASP) was also estimated. In Group A after ET, the 6MWT distance improved by 20.6% (p < 0.05), TVA decreased by 17% (p < 0.05), and TVE/A increased by 13.2% (p < 0.05). Moreover, TAPSE, TVS’, RVFWSL, and RV4CSL increased by 8.3% (p < 0.05), 9.0% (p < 0.05), 13.7% (p < 0.05), and 26.7% (p < 0.05), respectively, while PASP decreased by 7.6% (p < 0.05). At the end of the study, there was a significant linear correlation between the number of steps and the PASP (r = −0.727, p < 0.01) as well as the indices of RV systolic function in Group A. In conclusion, WAT is a valuable tool for implementing an effective ET program in CF. Furthermore, ET has a positive effect on RV systolic and diastolic function.
几项研究表明,囊性纤维化 (CF) 患者即使在年幼时也存在肺部和心脏异常。主要并发症是右心室 (RV) 收缩和/或舒张功能障碍以及肺动脉高压,这会影响他们的预后。运动训练 (ET) 被推荐用于 CF 患者作为一种治疗方式,以改善身体适应性和健康相关的生活质量。然而,关于其最佳有效和安全剂量及其对患者心脏功能的影响仍存在疑问。本研究旨在提供一种基于可穿戴活动追踪器 (WAT) 的 ET,以促进 CF 患者的身体活动,并评估其对心脏形态和功能的影响。42 名稳定的 CF 个体(年龄 16.8 ± 3.6 岁)被随机分配到干预组 (A 组) 或对照组 (B 组)。A 组参加了为期 1 年的基于 WAT 的 ET 方案,每周 3 次。所有患者均进行了 6 分钟步行测试 (6-MWT) 和超声心动图评估,主要侧重于 RV 解剖结构和功能。通过测量三尖瓣环平面收缩期位移 (TAPSE)、收缩期三尖瓣环速度 (TVS’)、RV 游离壁纵向应变 (RVFWSL) 和右心室四腔纵向应变 (RV4CSL) 来评估 RV 收缩功能。通过测量早期 (TVE) 和晚期 (TVA) 三尖瓣舒张跨瓣流速及其比值 TVE/A 来评估 RV 舒张功能。还估计了肺动脉收缩压 (PASP)。在 ET 后 A 组中,6MWT 距离增加了 20.6%(p < 0.05),TVA 降低了 17%(p < 0.05),而 TVE/A 增加了 13.2%(p < 0.05)。此外,TAPSE、TVS’、RVFWSL 和 RV4CSL 分别增加了 8.3%(p < 0.05)、9.0%(p < 0.05)、13.7%(p < 0.05)和 26.7%(p < 0.05),而 PASP 降低了 7.6%(p < 0.05)。在研究结束时,A 组的 PASP(r = −0.727,p < 0.01)与 RV 收缩功能指数之间存在显著的线性相关性。总之,WAT 是实施 CF 有效 ET 方案的有价值工具。此外,ET 对 RV 收缩和舒张功能具有积极影响。