Cristin-resultat-ID: 1929629
Sist endret: 2. februar 2022, 15:12
NVI-rapporteringsår: 2021
Resultat
Vitenskapelig artikkel
2021

A map of metabolic phenotypes in patients with myalgic encephalomyelitis/chronic fatigue syndrome

Bidragsytere:
  • Fredrik Hoel
  • August Hoel
  • Ina Katrine Nitschke Pettersen
  • Ingrid Gurvin Rekeland
  • Kristin Risa
  • Kine Alme
  • mfl.

Tidsskrift

JCI Insight
ISSN 2379-3708
e-ISSN 2379-3708
NVI-nivå 1

Om resultatet

Vitenskapelig artikkel
Publiseringsår: 2021
Volum: 6:e149217
Hefte: 16
Sider: 1 - 19
Open Access

Importkilder

Scopus-ID: 2-s2.0-85113396148

Beskrivelse Beskrivelse

Tittel

A map of metabolic phenotypes in patients with myalgic encephalomyelitis/chronic fatigue syndrome

Sammendrag

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a debilitating disease usually presenting after infection. Emerging evidence supports that energy metabolism is affected in ME/CFS, but a unifying metabolic phenotype has not been firmly established. We performed global metabolomics, lipidomics, and hormone measurements, and we used exploratory data analyses to compare serum from 83 patients with ME/CFS and 35 healthy controls. Some changes were common in the patient group, and these were compatible with effects of elevated energy strain and altered utilization of fatty acids and amino acids as catabolic fuels. In addition, a set of heterogeneous effects reflected specific changes in 3 subsets of patients, and 2 of these expressed characteristic contexts of deregulated energy metabolism. The biological relevance of these metabolic phenotypes (metabotypes) was supported by clinical data and independent blood analyses. In summary, we report a map of common and context-dependent metabolic changes in ME/CFS, and some of them presented possible associations with clinical patient profiles. We suggest that elevated energy strain may result from exertion-triggered tissue hypoxia and lead to systemic metabolic adaptation and compensation. Through various mechanisms, such metabolic dysfunction represents a likely mediator of key symptoms in ME/CFS and possibly a target for supportive intervention.

Bidragsytere

Fredrik Hoel

  • Tilknyttet:
    Forfatter
    ved Institutt for biomedisin ved Universitetet i Bergen

August Hoel

  • Tilknyttet:
    Forfatter
    ved Klinisk institutt 1 ved Universitetet i Bergen
  • Tilknyttet:
    Forfatter
    ved Institutt for biomedisin ved Universitetet i Bergen

Ina Katrine Nitschke Pettersen

  • Tilknyttet:
    Forfatter
    ved Institutt for biomedisin ved Universitetet i Bergen

Ingrid Gurvin Rekeland

  • Tilknyttet:
    Forfatter
    ved Avdeling for kreftbehandling og medisinsk fysikk ved Helse Bergen HF - Haukeland universitetssykehus

Kristin Risa

  • Tilknyttet:
    Forfatter
    ved Avdeling for kreftbehandling og medisinsk fysikk ved Helse Bergen HF - Haukeland universitetssykehus
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