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dc.contributor.authorHarneshaug, Magnus
dc.contributor.authorSaltyte Benth, Jurate
dc.contributor.authorKirkhus, Lene
dc.contributor.authorGrønberg, Bjørn Henning
dc.contributor.authorBergh, Sverre
dc.contributor.authorRostoft, Siri
dc.contributor.authorJordhøy, Marit Slaaen
dc.date.accessioned2020-11-18T14:23:48Z
dc.date.available2020-11-18T14:23:48Z
dc.date.created2020-11-09T12:59:16Z
dc.date.issued2020
dc.identifier.citationIn Vivo. 2020, 34 3565-3572.en_US
dc.identifier.issn0258-851X
dc.identifier.urihttps://hdl.handle.net/11250/2688524
dc.description.abstractBackground/Aim: Muscle loss, inflammation, and frailty are prevalent among older cancer patients. We aimed to evaluate whether inflammatory markers could identify muscle loss, and if muscle measures differed between frail and non-frail patients. Patients and Methods: A total of 115 patients ≥70 years old with solid tumors were included. Inflammation was measured using the Glasgow Prognostic Score (GPS), which is based on C-reactive protein (CRP) and albumin levels, and CRP alone. Frailty was evaluated using a modified geriatric assessment (mGA) of eight domains affecting older patients' health status. Computed tomography-derived muscle measures were collected at the level of the third lumbar vertebra. Results: Patients with GPS=2 and CRP>27 mg/l exhibited poorer muscle measures compared to patients with lower levels. No associations between mGA-based frailty and muscle mass were found. Conclusion: Inflammation has detrimental effects on muscle mass. However, GPS or CRP alone cannot be used to identify muscle loss, and muscle measures were not associated with frailty in this series.en_US
dc.language.isoengen_US
dc.publisherInternational Institute of Anticancer Researchen_US
dc.titleCT Derived Muscle Measures, Inflammation, and Frailty in a Cohort of Older Cancer Patientsen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber3565-3572en_US
dc.source.volume34en_US
dc.source.journalIn Vivoen_US
dc.identifier.doi10.21873/invivo.12200
dc.identifier.cristin1846137
dc.description.localcodeDOI: doi:10.21873/invivo.12200. This article is freely accessible online. Copyright© 2020, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserveden_US
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cristin.fulltextoriginal
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