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Endothelial dysfunction in ME/CFS patients

OBJECTIVE: A few earlier studies have found impaired endothelial function in patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). The present study investigated large-vessel and small-vessel endothelial function in patients with ME/CFS. STUDY DESIGN: The study was a substudy of...

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Autores principales: Sandvik, Miriam Kristine, Sørland, Kari, Leirgul, Elisabeth, Rekeland, Ingrid Gurvin, Stavland, Christina Særsten, Mella, Olav, Fluge, Øystein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9894436/
https://www.ncbi.nlm.nih.gov/pubmed/36730360
http://dx.doi.org/10.1371/journal.pone.0280942
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author Sandvik, Miriam Kristine
Sørland, Kari
Leirgul, Elisabeth
Rekeland, Ingrid Gurvin
Stavland, Christina Særsten
Mella, Olav
Fluge, Øystein
author_facet Sandvik, Miriam Kristine
Sørland, Kari
Leirgul, Elisabeth
Rekeland, Ingrid Gurvin
Stavland, Christina Særsten
Mella, Olav
Fluge, Øystein
author_sort Sandvik, Miriam Kristine
collection PubMed
description OBJECTIVE: A few earlier studies have found impaired endothelial function in patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). The present study investigated large-vessel and small-vessel endothelial function in patients with ME/CFS. STUDY DESIGN: The study was a substudy of the RituxME trial, a national, multicenter, randomized, double-blind, placebo-controlled phase III study on the effect of rituximab vs. placebo in ME/CFS patients in Norway. Flow-mediated dilation (FMD) and post-occlusive reactive hyperemia (PORH) was measured at baseline and after 18 months of treatment in 39 patients and compared with healthy controls. Other outcome measures were symptom severity and various physical function measures. RESULTS: ME/CFS patients had markedly reduced FMD compared to healthy controls at baseline (5.1% vs. 8.2%, p< 0.0001, adjusted for arterial diameter and sex), and significantly lower microvascular regulation measured by PORH than healthy controls (1354 PU vs. 2208 PU, p = 0.002). There were no differences between the treatment and placebo groups in symptom changes or vascular measures. As a group, the ME/CSF patients experienced a slight, but significant improvement in clinical symptoms after 18 months. PORH, but not FMD, was similarly improved (1360 to 1834 PU, p = 0.028). There was no significant correlation between FMD and PORH. There were non-significant tendencies towards associations between symptom severity/physical function measures and lower FMD and PORH, and a significant correlation between PORH and steps per 24 hours at baseline. CONCLUSIONS: ME/CFS patients had reduced macro- and microvascular endothelial function, indicating that vascular homeostasis may play a role in the clinical presentation of this disease.
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spelling pubmed-98944362023-02-03 Endothelial dysfunction in ME/CFS patients Sandvik, Miriam Kristine Sørland, Kari Leirgul, Elisabeth Rekeland, Ingrid Gurvin Stavland, Christina Særsten Mella, Olav Fluge, Øystein PLoS One Research Article OBJECTIVE: A few earlier studies have found impaired endothelial function in patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). The present study investigated large-vessel and small-vessel endothelial function in patients with ME/CFS. STUDY DESIGN: The study was a substudy of the RituxME trial, a national, multicenter, randomized, double-blind, placebo-controlled phase III study on the effect of rituximab vs. placebo in ME/CFS patients in Norway. Flow-mediated dilation (FMD) and post-occlusive reactive hyperemia (PORH) was measured at baseline and after 18 months of treatment in 39 patients and compared with healthy controls. Other outcome measures were symptom severity and various physical function measures. RESULTS: ME/CFS patients had markedly reduced FMD compared to healthy controls at baseline (5.1% vs. 8.2%, p< 0.0001, adjusted for arterial diameter and sex), and significantly lower microvascular regulation measured by PORH than healthy controls (1354 PU vs. 2208 PU, p = 0.002). There were no differences between the treatment and placebo groups in symptom changes or vascular measures. As a group, the ME/CSF patients experienced a slight, but significant improvement in clinical symptoms after 18 months. PORH, but not FMD, was similarly improved (1360 to 1834 PU, p = 0.028). There was no significant correlation between FMD and PORH. There were non-significant tendencies towards associations between symptom severity/physical function measures and lower FMD and PORH, and a significant correlation between PORH and steps per 24 hours at baseline. CONCLUSIONS: ME/CFS patients had reduced macro- and microvascular endothelial function, indicating that vascular homeostasis may play a role in the clinical presentation of this disease. Public Library of Science 2023-02-02 /pmc/articles/PMC9894436/ /pubmed/36730360 http://dx.doi.org/10.1371/journal.pone.0280942 Text en © 2023 Sandvik et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Sandvik, Miriam Kristine
Sørland, Kari
Leirgul, Elisabeth
Rekeland, Ingrid Gurvin
Stavland, Christina Særsten
Mella, Olav
Fluge, Øystein
Endothelial dysfunction in ME/CFS patients
title Endothelial dysfunction in ME/CFS patients
title_full Endothelial dysfunction in ME/CFS patients
title_fullStr Endothelial dysfunction in ME/CFS patients
title_full_unstemmed Endothelial dysfunction in ME/CFS patients
title_short Endothelial dysfunction in ME/CFS patients
title_sort endothelial dysfunction in me/cfs patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9894436/
https://www.ncbi.nlm.nih.gov/pubmed/36730360
http://dx.doi.org/10.1371/journal.pone.0280942
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