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dc.contributor.authorHoel, Fredrik
dc.contributor.authorHoel, August
dc.contributor.authorPettersen, Ina Katrine Nitschke
dc.contributor.authorRekeland, Ingrid Gurvin
dc.contributor.authorRisa, Kristin
dc.contributor.authorAlme, Kine
dc.contributor.authorSørland, Kari
dc.contributor.authorFosså, Alexander
dc.contributor.authorLien, Katarina
dc.contributor.authorHerder, Ingrid
dc.contributor.authorThurmer, Hanne
dc.contributor.authorGotaas, Merethe Otelie Eide
dc.contributor.authorSchäfer, Christoph
dc.contributor.authorBerge, Rolf K.
dc.contributor.authorSommerfelt, Kristian
dc.contributor.authorMarti, Hans Peter
dc.contributor.authorDahl, Olav
dc.contributor.authorMella, Olav
dc.contributor.authorFluge, Øystein
dc.contributor.authorTronstad, Karl Johan
dc.date.accessioned2021-09-29T11:43:48Z
dc.date.available2021-09-29T11:43:48Z
dc.date.created2021-08-30T09:47:08Z
dc.date.issued2021
dc.identifier.issn2379-3708
dc.identifier.urihttps://hdl.handle.net/11250/2786016
dc.description.abstractMyalgic 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.en_US
dc.language.isoengen_US
dc.publisherAmerican Society for Clinical Investigationen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleA map of metabolic phenotypes in patients with myalgic encephalomyelitis/chronic fatigue syndromeen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2021 the authorsen_US
dc.source.articlenumbere149217en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1172/jci.insight.149217
dc.identifier.cristin1929629
dc.source.journalJCI Insighten_US
dc.identifier.citationJCI Insight. 2021, 6 (16), e149217.en_US
dc.source.volume6en_US
dc.source.issue16en_US


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