Key result
Fibrinaloid microclots may drive long COVID POTS and fatigue by inducing tissue hypoxia and autonomic dysfunction.
Why the study?
Postural orthostatic tachycardia syndrome and fibrinaloid microclots are common accompaniments of chronic inflammatory diseases such as long COVID, motivating an exploration of whether microclots serve as a mechanistic cause of POTS and fatigue.
Provides a mechanistic hypothesis linking fibrinaloid microclots to the development of POTS and fatigue in long COVID via tissue hypoxia and autonomic dysfunction.
Hypothesis-generating for POTS therapies targeting microclots; leaves open clinical utility pending controlled trials.
Postural orthostatic tachycardia syndrome (POTS) is a common accompaniment of a variety of chronic, inflammatory diseases, including long COVID, as are small, insoluble, 'fibrinaloid' microclots. We here develop the argument, with accompanying evidence, that fibrinaloid microclots, through their ability to block the flow of blood through microcapillaries and thus cause tissue hypoxia, are not simply correlated with but in fact, by preceding it, may be a chief intermediary cause of POTS, in which tachycardia is simply the body's exaggerated 'physiological' response to hypoxia. Similar reasoning accounts for the symptoms bundled under the term 'fatigue'. Amyloids are known to be membrane disruptors, and when their targets are nerve membranes, this can explain neurotoxicity and hence the autonomic nervous system dysfunction that contributes to POTS. Taken together as a system view, we indicate that fibrinaloid microclots can serve to link POTS and fatigue in long COVID in a manner that is at once both mechanistic and explanatory. This has clear implications for the treatment of such diseases.
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Kell et al. (2024) conducted a review in Postural orthostatic tachycardia syndrome (POTS) and long COVID. Fibrinaloid microclots was evaluated. Fibrinaloid microclots are proposed as a chief intermediary cause of POTS and fatigue in long COVID by inducing tissue hypoxia and autonomic nervous system dysfunction.
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