Haemodynamic compensations for exercise tissue oxygenation in early stages of COPD: an integrated cardiorespiratory assessment study.

IF 3.6 3区 医学 Q1 RESPIRATORY SYSTEM
Ruddy Richard, Dennis Jensen, Julianne Touron, Costes Frederic, Aurélien Mulliez, Bruno Pereira, Laura Filaire, Darcy Marciniuk, François Maltais, Wan Tan, Jean Bourbeau, Hélène Perrault
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引用次数: 0

Abstract

Background: Cardiovascular comorbidities are increasingly being recognised in early stages of chronic obstructive pulmonary disease (COPD) yet complete cardiorespiratory functional assessments of individuals with mild COPD or presenting with COPD risk factors are lacking. This paper reports on the effectiveness of the cardiocirculatory-limb muscles oxygen delivery and utilisation axis in smokers exhibiting no, or mild to moderate degrees of airflow obstruction using standardised cardiopulmonary exercise testing (CPET).

Methods: Post-bronchodilator spirometry was used to classify participants as 'ever smokers without' (n=88), with 'mild' (n=63) or 'mild-moderate' COPD (n=56). All underwent CPET with continuous concurrent monitoring of oxygen uptake (V'O2) and of bioimpedance cardiac output (Qc) enabling computation of arteriovenous differences (a-vO2). Mean values of Qc and a-vO2 were mapped across set ranges of V'O2 and Qc isolines to allow for meaningful group comparisons, at same metabolic and circulatory requirements.

Results: Peak exercise capacity was significantly reduced in the 'mild-moderate COPD' as compared with the two other groups who showed similar pulmonary function and exercise capacity. Self-reported cardiovascular and skeletal muscle comorbidities were not different between groups, yet disease impact and exercise intolerance scores were three times higher in the 'mild-moderate COPD' compared with the other groups. Mapping of exercise Qc and a-vO2 also showed a leftward shift of values in this group, indicative of a deficit in peripheral O2 extraction even for submaximal exercise demands. Concurrent with lung hyperinflation, a distinctive blunting of exercise stroke volume expansion was also observed in this group.

Conclusion: Contrary to the traditional view that cardiovascular complications were the hallmark of advanced disease, this study of early COPD spectrum showed a reduced exercise O2 delivery and utilisation in individuals meeting spirometry criteria for stage II COPD. These findings reinforce the preventive clinical management approach to preserve peripheral muscle circulatory and oxidative capacities.

慢性阻塞性肺病早期运动组织氧合的血流动力学补偿:心肺功能综合评估研究。
背景:越来越多的慢性阻塞性肺病(COPD)患者在早期阶段就被发现有心血管合并症,但目前还缺乏对轻度慢性阻塞性肺病患者或有慢性阻塞性肺病危险因素的患者进行完整的心肺功能评估。本文利用标准化心肺运动测试(CPET)报告了无气流阻塞或轻度至中度气流阻塞的吸烟者的心血管-肢体肌肉氧输送和利用轴的有效性:方法:使用支气管扩张剂后肺活量测定法将参与者分为 "无气流阻塞"(88 人)、"轻度"(63 人)或 "轻中度 "慢性阻塞性肺疾病(56 人)的吸烟者。所有参与者都接受了 CPET,并同时连续监测摄氧量(V'O2)和生物阻抗心输出量(Qc),以便计算动静脉差(a-vO2)。Qc 和 a-vO2 的平均值被映射到 V'O2 和 Qc 隔离线的设定范围内,以便在代谢和循环要求相同的情况下进行有意义的分组比较:结果:与肺功能和运动能力相似的其他两组相比,"轻中度慢性阻塞性肺病 "组的峰值运动能力明显下降。各组间自我报告的心血管和骨骼肌合并症没有差异,但 "轻度-中度慢性阻塞性肺病 "组的疾病影响和运动不耐受评分是其他组的三倍。运动 Qc 和 a-vO2 图谱也显示该组的数值左移,这表明即使在亚极限运动需求下,外周氧气汲取也会出现不足。与肺过度充气同时,在该组中还观察到运动中每搏容积扩张明显减弱:与心血管并发症是晚期疾病标志的传统观点相反,这项对早期慢性阻塞性肺疾病谱的研究显示,在符合肺活量测定标准的慢性阻塞性肺疾病 II 期患者中,运动氧气输送和利用率降低。这些发现强化了预防性临床管理方法,以保护外周肌肉循环和氧化能力。
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来源期刊
BMJ Open Respiratory Research
BMJ Open Respiratory Research RESPIRATORY SYSTEM-
CiteScore
6.60
自引率
2.40%
发文量
95
审稿时长
12 weeks
期刊介绍: BMJ Open Respiratory Research is a peer-reviewed, open access journal publishing respiratory and critical care medicine. It is the sister journal to Thorax and co-owned by the British Thoracic Society and BMJ. The journal focuses on robustness of methodology and scientific rigour with less emphasis on novelty or perceived impact. BMJ Open Respiratory Research operates a rapid review process, with continuous publication online, ensuring timely, up-to-date research is available worldwide. The journal publishes review articles and all research study types: Basic science including laboratory based experiments and animal models, Pilot studies or proof of concept, Observational studies, Study protocols, Registries, Clinical trials from phase I to multicentre randomised clinical trials, Systematic reviews and meta-analyses.
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