一些患者在最初的SARS-CoV-2感染后超过2年,在没有病理生理机制的情况下持续疲劳。

IF 2.8 4区 医学 Q2 PHYSIOLOGY
Giovanni Baldassarre, Lucrezia Zuccarelli, Thomas Favaretto, Caterina Ursella, Andrea Palomba, Paulo Cesar do Nascimento Salvador, Emanuela Sozio, Ernesto Crisafulli, Massimo Imazio, Carlo Tascini, Bruno Grassi
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引用次数: 0

摘要

在急性感染严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)后,相当大比例的患者报告持续出现虚弱症状,这些症状通常被归类为“长冠状病毒”综合征。我们试图确定一些长期COVID患者在原始感染后2年以上持续存在与疲劳/运动不耐受(过度或早期疲劳、过度或早期呼吸困难、肌肉无力和肌痛)相关症状的潜在病理生理机制。12例患者报告持续症状(长COVID组;57±6年,平均±SD),无症状14例(对照组;57±8年)。进行了一系列广泛的测量,以确定可能导致这些症状的病理生理机制。在长期COVID患者中,所有评估生活质量的项目(SF-36问卷)得分均较低(P V²${\dot V_{{\ maththrm {O}}_2}}}}$动力学、微血管/内皮功能(被动腿部运动时股总动脉充血反应)、骨骼肌氧化代谢(峰值分数O2提取和肌肉V²${\dot V_{{\ maththrm {O}}_2}}}$恢复动力学)。近红外光谱分析)两组间差异无统计学意义。在长COVID患者亚组中描述了通气效率低下的证据。在最初的SARS-CoV-2感染2年多后,观察到疲劳/运动不耐受的衰弱症状的持续存在与缺乏几种已研究的病理生理机制之间存在差异。这种差异可能是由于一些尚未阐明的因素造成的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Persistence of fatigue in the absence of pathophysiological mechanisms in some patients more than 2 years after the original SARS-CoV-2 infection.

Following an acute infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a substantial percentage of patients report the persistence of debilitating symptoms, often grouped in a syndrome termed 'long COVID'. We sought to identify potential pathophysiological mechanisms responsible for the persistence, in some long COVID patients, of symptoms related to fatigue/exercise intolerance (excessive or early fatigue, excessive or early dyspnoea, muscle weakness, and myalgias) more than 2 years after the original infection. Twelve patients who reported persistent symptoms (Long COVID group; 57 ± 6 years, mean ± SD), and 14 patients without the symptoms (Control group; 57 ± 8 years) were evaluated. An extensive series of measurements were performed to identify pathophysiological mechanisms potentially responsible for the symptoms. In long COVID patients, all items evaluating quality of life (SF-36 questionnaire) had lower scores (P < 0.01) compared to control. The habitual level of physical activity, muscle size and strength, maximal aerobic power and the ventilatory thresholds, peak cardiac function, the mechanical efficiency of cycling, pulmonary V ̇ O 2 ${\dot V_{{{\mathrm{O}}_2}}}$ kinetics, microvascular/endothelial function (hyperemic response in the common femoral artery during passive leg movements), skeletal muscle oxidative metabolism (peak fractional O2 extraction and muscle V ̇ O 2 ${\dot V_{{{\mathrm{O}}_2}}}$ recovery kinetics by the repeated occlusions test, by near-infrared spectroscopy) were not different in the two groups. Evidence of ventilatory inefficiency was described in a subgroup of long COVID patients. More than 2 years after the original SARS-CoV-2 infection, a discrepancy was observed between the persistence of debilitating symptoms of fatigue/exercise intolerance and the absence of several investigated pathophysiological mechanisms. The discrepancy may be due to factors that remain to be elucidated.

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来源期刊
Experimental Physiology
Experimental Physiology 医学-生理学
CiteScore
5.10
自引率
3.70%
发文量
262
审稿时长
1 months
期刊介绍: Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged. Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.
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