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dc.contributor.authorAlehagen, Urban
dc.contributor.authorJohansson, Peter
dc.contributor.authorAaseth, Jan
dc.contributor.authorAlexander, Jan
dc.contributor.authorSurowiec, Izabella
dc.contributor.authorLundstedt-Enkel, Katrin
dc.contributor.authorLundstedt, Torbjörn
dc.date.accessioned2020-05-29T12:58:45Z
dc.date.available2020-05-29T12:58:45Z
dc.date.created2019-12-31T14:16:41Z
dc.date.issued2019
dc.identifier.citationBiomolecules . 2019 Sep 30;9(10):553. doi: 10.3390/biom9100553.en_US
dc.identifier.issn2218-273X
dc.identifier.urihttps://hdl.handle.net/11250/2656050
dc.description.abstractSelenium and coenzyme Q10 (SeQ10) are important for normal cellular function. Low selenium intake leads to increased cardiovascular mortality. Intervention with these substances with healthy elderly persons over a period of four years in a double-blind, randomised placebo-controlled prospective study showed reduced cardiovascular mortality, increased cardiac function, and a lower level of NT-proBNP. Therefore, we wanted to evaluate changes in biochemical pathways as a result of the intervention with SeQ10 using metabolic profiling. From a population of 443 healthy elderly individuals that were given 200 µg selenium and 200 mg coenzyme Q10, or placebo daily for four years, we selected nine males on active intervention and nine males on placebo for metabolic profiling in the main study. To confirm the results, two validation studies (study 1 n = 60 males, study 2 n = 37 males) were conducted. Principal component analyses were used on clinical and demographic data to select representative sets of samples for analysis and to divide the samples into batches for analysis. Gas chromatography time-of-flight mass spectrometry-based metabolomics was applied. The metabolite data were evaluated using univariate and multivariate approaches, mainly T-tests and orthogonal projections to latent structures (OPLS) analyses. Out of 95 identified metabolites, 19 were significantly decreased due to the intervention after 18 months of intervention. Significant changes could be seen in the pentose phosphate, the mevalonate, the beta-oxidation and the xanthine oxidase pathways. The intervention also resulted in changes in the urea cycle, and increases in the levels of the precursors to neurotransmitters of the brain. This adds information to previous published results reporting decreased oxidative stress and inflammation. This is the first-time metabolic profiling has been applied to elucidate the mechanisms behind an intervention with SeQ10. The study is small and should be regarded as hypothesis-generating; however, the results are interesting and, therefore, further research in the area is needed. This study was registered at Clinicaltrials.gov, with the identifier NCT01443780.en_US
dc.description.sponsorshipThe analysis costs were partially supported by grants from Pharma Nord Aps, Denmark, the County Council of Östergötland, Linköping University. The funding organisations had no role in the design, management, analysis, or interpretation of the data, nor in the preparation, review or approval of the manuscript. No economic compensation was distributed.en_US
dc.language.isoengen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectcoenzyme Q10;en_US
dc.subjectelderly;en_US
dc.subjectmetabolic profiling;en_US
dc.subjectseleniumen_US
dc.titleSignificant changes in metabolic profiles after intervention with selenium and coenzyme q10 in an elderly populationen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).en_US
dc.source.volume9en_US
dc.source.journalBiomoleculesen_US
dc.source.issue10en_US
dc.identifier.doi10.3390/biom9100553
dc.identifier.cristin1764559
cristin.unitcode1991,5,6,0
cristin.unitnameAvd Indremedisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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