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People with Long COVID and Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Exhibit Similarly Impaired Vascular Function - 11/02/25

Doi : 10.1016/j.amjmed.2023.09.013 
Marie Mclaughlin, PhD a, b, , Nilihan E.M. Sanal-Hayes, PhD a, c, Lawrence D. Hayes, PhD a, Ethan C. Berry, BSc a, Nicholas F. Sculthorpe, PhD a
a Sport and Physical Activity Research Institute, School of Health and Life Sciences, University of the West of Scotland, Glasgow, United Kingdom 
b School of Sport, Exercise & Rehabilitation Sciences, Faculty of Health Sciences, University of Hull, United Kingdom 
c School of Health and Society, University of Salford, United Kingdom 

Requests for reprints should be addressed to Marie Mclaughlin, PhD, School of Sport, Exercise & Rehabilitation Sciences, Faculty of Health Sciences, University of Hull, United Kingdom.School of SportExercise & Rehabilitation SciencesFaculty of Health SciencesUniversity of HullUnited Kingdom

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Abstract

Background

This study aimed to compare flow-mediated dilation values between individuals with long COVID, individuals with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), and healthy age-matched controls to assess the potential implications for clinical management and long-term health outcomes.

Methods

A case-case-control approach was employed, and flow-mediated dilation measurements were obtained from 51 participants (17 long COVID patients, 17 ME/CFS patients, and 17 healthy age-matched controls). Flow-mediated dilation values were analyzed using 1-way analysis of variance for between-group comparisons.

Results

Results revealed significantly impaired endothelial function in both long COVID and ME/CFS groups compared with healthy age-matched controls as determined by maximum % brachial artery diameter post-occlusion compared with pre-occlusion resting diameter (6.99 ± 4.33% and 6.60 ± 3.48% vs 11.30 ± 4.44%, respectively, both P < .05). Notably, there was no difference in flow-mediated dilation between long COVID and ME/CFS groups (P = .949), despite significantly longer illness duration in the ME/CFS group (ME/CFS: 16 ± 11.15 years vs long COVID: 1.36 ± 0.51 years, P < .0001).

Conclusion

The study demonstrates that both long COVID and ME/CFS patients exhibit similarly impaired endothelial function, indicating potential vascular involvement in the pathogenesis of these post-viral illnesses. The significant reduction in flow-mediated dilation values suggests an increased cardiovascular risk in these populations, warranting careful monitoring and the development of targeted interventions to improve endothelial function and mitigate long-term health implications.

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Keywords : Chronic fatigue syndrome, Flow-mediated dilation, Long COVID, Myalgic encephalomyelitis


Esquema


 Funding: This work was supported by grants from the Chief Scientist Office for Scotland (COV/LTE/20/08) and the National Institute for Health and Care Research (COV-LT2-0010).
 Conflict of Interest: None.
 Authorship: All authors had access to the data and a role in writing this manuscript.


© 2023  The Authors. Publicado por Elsevier Masson SAS. Todos los derechos reservados.
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Vol 138 - N° 3

P. 560-566 - mars 2025 Regresar al número
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