Mij
Senior Member (Voting Rights)
Opinion piece:
Highlights
Long COVID occurs when symptoms persist for more than 3 months after acute SARS-CoV-2 infection. Symptoms include fatigue, brain fog, myalgia, and post-exertional malaise (PEM), which worsens with physical, mental, or cognitive exertion.
Long COVID shares many characteristics with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), particularly PEM, which is necessary for ME/CFS diagnosis.
Long COVID is associated with intrinsic skeletal muscle mitochondrial dysfunction, endothelial abnormalities, and a shift towards more glycolytic muscle fibers, which contribute to a lower exercise capacity.
Several potential mechanisms may explain skeletal muscle abnormalities in long COVID, including local hypoxia, deconditioning, autoimmunity, electrophysiological changes, and central fatigue.
There are no treatments for long COVID or PEM, but ongoing trials include immunoadsorption, dietary supplements, and anti-inflammatory/antiviral drugs.
Abstract
When acute SARS-CoV-2 infections cause symptoms that persist longer than 3 months, this condition is termed long COVID. Symptoms experienced by patients often include myalgia, fatigue, brain fog, cognitive impairments, and post-exertional malaise (PEM), which is the worsening of symptoms following mental or physical exertion. There is little consensus on the pathophysiology of exercise-induced PEM and skeletal-muscle-related symptoms. In this opinion article we highlight intrinsic mitochondrial dysfunction, endothelial abnormalities, and a muscle fiber type shift towards a more glycolytic phenotype as main contributors to the reduced exercise capacity in long COVID. The mechanistic trigger for physical exercise to induce PEM is unknown, but rapid skeletal muscle tissue damage and intramuscular infiltration of immune cells contribute to PEM-related symptoms.
LINK
Highlights
Long COVID occurs when symptoms persist for more than 3 months after acute SARS-CoV-2 infection. Symptoms include fatigue, brain fog, myalgia, and post-exertional malaise (PEM), which worsens with physical, mental, or cognitive exertion.
Long COVID shares many characteristics with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), particularly PEM, which is necessary for ME/CFS diagnosis.
Long COVID is associated with intrinsic skeletal muscle mitochondrial dysfunction, endothelial abnormalities, and a shift towards more glycolytic muscle fibers, which contribute to a lower exercise capacity.
Several potential mechanisms may explain skeletal muscle abnormalities in long COVID, including local hypoxia, deconditioning, autoimmunity, electrophysiological changes, and central fatigue.
There are no treatments for long COVID or PEM, but ongoing trials include immunoadsorption, dietary supplements, and anti-inflammatory/antiviral drugs.
Abstract
When acute SARS-CoV-2 infections cause symptoms that persist longer than 3 months, this condition is termed long COVID. Symptoms experienced by patients often include myalgia, fatigue, brain fog, cognitive impairments, and post-exertional malaise (PEM), which is the worsening of symptoms following mental or physical exertion. There is little consensus on the pathophysiology of exercise-induced PEM and skeletal-muscle-related symptoms. In this opinion article we highlight intrinsic mitochondrial dysfunction, endothelial abnormalities, and a muscle fiber type shift towards a more glycolytic phenotype as main contributors to the reduced exercise capacity in long COVID. The mechanistic trigger for physical exercise to induce PEM is unknown, but rapid skeletal muscle tissue damage and intramuscular infiltration of immune cells contribute to PEM-related symptoms.
LINK
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