Publication date: Feb 01, 2025
Chronic fatigue syndrome (CFS) remains a subject of scientific research specifically with regards to its association with infections, including the more recently described Long COVID condition. Chronic fatigue and sleep disturbances in Long COVID are intricately linked to disruptions in circadian rhythms, driven by distinct molecular and cellular mechanisms triggered by SARS-CoV-2 infection. This can be driven by various mechanisms including dysregulation of key clock genes (CLOCK, BMAL1, PER2), mitochondrial dysfunction impairing oxidative phosphorylation, and cytokine-induced neuroinflammation (e. g., interleukin-6, tumor necrosis factor-alpha). Epigenetic changes, including DNA methylation at clock-related loci, particularly in peripheral tissues, further contribute to systemic circadian dysregulation. This work underscores the multifaceted molecular and systemic disruptions to circadian regulation in relation to fatigue and sleep disturbances identified as post-infectious sequelae, focusing on the Long COVID condition.
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| Concepts | Keywords |
|---|---|
| Circadian | Chronic fatigue syndrome |
| Covid | Circadian rhythms |
| Eclinicalmedicine | Long COVID |
| Fatigue | Post-infectious fatigue |
| Tumor |
Semantics
| Type | Source | Name |
|---|---|---|
| pathway | KEGG | Circadian rhythm |
| disease | MESH | infections |
| disease | MESH | Chronic fatigue syndrome |
| disease | MESH | Long COVID |
| disease | MESH | SARS-CoV-2 infection |
| pathway | REACTOME | SARS-CoV-2 Infection |
| disease | MESH | mitochondrial dysfunction |
| pathway | KEGG | Oxidative phosphorylation |
| disease | MESH | neuroinflammation |
| pathway | REACTOME | DNA methylation |
| disease | MESH | circadian dysregulation |
| disease | MESH | sequelae |