Multidisciplinary Cardiovascular Research Centre and Biomedical Imaging Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, LS2 9JT, UK.
Department of Rehabilitation Medicine, Leeds Teaching Hospitals Trust, Leeds, UK.
J Cardiovasc Magn Reson. 2022 Sep 12;24(1):50. doi: 10.1186/s12968-022-00887-9.
The underlying pathophysiology of post-coronavirus disease 2019 (long-COVID-19) syndrome remains unknown, but increased cardiometabolic demand and state of mitochondrial dysfunction have emerged as candidate mechanisms. Cardiovascular magnetic resonance (CMR) provides insight into pathophysiological mechanisms underlying cardiovascular disease and 31-phosphorus CMR spectroscopy (P-CMRS) allows non-invasive assessment of the myocardial energetic state. The main aim of the study was to assess whether long COVID-19 syndrome is associated with abnormalities of myocardial structure, function, perfusion and energy metabolism.
Prospective case-control study. A total of 20 patients with a clinical diagnosis of long COVID-19 syndrome (seropositive) and no prior underlying cardiovascular disease (CVD) and 10 matching healthy controls underwent P-CMRS and CMR at 3T at a single time point. All patients had been symptomatic with acute COVID-19, but none required hospital admission.
Between the long COVID-19 syndrome patients and matched contemporary healthy controls there were no differences in myocardial energetics (phosphocreatine to ATP ratio), in cardiac structure (biventricular volumes), function (biventricular ejection fractions, global longitudinal strain), tissue characterization (T mapping and late gadolinium enhancement) or perfusion (myocardial rest and stress blood flow, myocardial perfusion reserve). One patient with long COVID-19 syndrome showed subepicardial hyperenhancement on late gadolinium enhancement imaging compatible with prior myocarditis, but no accompanying abnormality in cardiac size, function, perfusion, extracellular volume fraction, native T1, T2 or cardiac energetics.
In this prospective case-control study, the overwhelming majority of patients with a clinical long COVID-19 syndrome with no prior CVD did not exhibit any abnormalities in myocardial energetics, structure, function, blood flow or tissue characteristics.
新冠病毒病 2019 后(post-coronavirus disease 2019,简称 COVID-19)综合征的潜在病理生理学机制尚不清楚,但代谢需求增加和线粒体功能障碍状态已成为候选机制。心血管磁共振(cardiovascular magnetic resonance,简称 CMR)可深入了解心血管疾病的病理生理机制,31 磷磁共振波谱(31-phosphorus CMR spectroscopy,简称 P-CMRS)可对心肌能量状态进行非侵入性评估。本研究的主要目的是评估长 COVID-19 综合征是否与心肌结构、功能、灌注和能量代谢异常有关。
前瞻性病例对照研究。共纳入 20 例临床诊断为长 COVID-19 综合征(血清阳性)且无既往心血管疾病(cardiovascular disease,简称 CVD)的患者和 10 例匹配的健康对照者,在单次 3T 时行 P-CMRS 和 CMR。所有患者均有急性 COVID-19 症状,但均无需住院治疗。
长 COVID-19 综合征患者与同期健康对照者之间,心肌能量学(磷酸肌酸与三磷酸腺苷比值)、心脏结构(双心室容积)、功能(双心室射血分数、整体纵向应变)、组织特征(T 映射和钆延迟增强)或灌注(心肌静息和应激血流、心肌血流储备)均无差异。1 例长 COVID-19 综合征患者的延迟增强图像上出现心外膜下强化,符合既往心肌炎,但心脏大小、功能、灌注、细胞外容积分数、固有 T1、T2 或心肌能量学均无伴随异常。
在这项前瞻性病例对照研究中,绝大多数临床诊断为长 COVID-19 综合征且无既往 CVD 的患者的心肌能量学、结构、功能、血流或组织特征均无异常。