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dc.contributor.authorSarin, Heikki V.
dc.contributor.authorHulmi, Juha J.
dc.contributor.authorQin, Youwen
dc.contributor.authorInouye, Michael
dc.contributor.authorRitchie, Scott C.
dc.contributor.authorCheng, Susan
dc.contributor.authorWatrous, Jeramie D.
dc.contributor.authorNguyen, Thien-Tu C.
dc.contributor.authorLee, Joseph H.
dc.contributor.authorJin, Zhezhen
dc.contributor.authorTerwilliger, Joseph D.
dc.contributor.authorNiiranen, Teemu
dc.contributor.authorHavulinna, Aki
dc.contributor.authorSalomaa, Veikko
dc.contributor.authorPietiläinen, Kirsi H.
dc.contributor.authorIsola, Ville
dc.contributor.authorAhtiainen, Juha P.
dc.contributor.authorHäkkinen, Keijo
dc.contributor.authorJain, Mohit
dc.contributor.authorPerola, Markus
dc.date.accessioned2022-10-11T07:40:15Z
dc.date.available2022-10-11T07:40:15Z
dc.date.issued2022
dc.identifier.citationSarin, H. V., Hulmi, J. J., Qin, Y., Inouye, M., Ritchie, S. C., Cheng, S., Watrous, J. D., Nguyen, T.-T. C., Lee, J. H., Jin, Z., Terwilliger, J. D., Niiranen, T., Havulinna, A., Salomaa, V., Pietiläinen, K. H., Isola, V., Ahtiainen, J. P., Häkkinen, K., Jain, M., & Perola, M. (2022). Substantial Fat Loss in Physique Competitors Is Characterized by Increased Levels of Bile Acids, Very-Long Chain Fatty Acids, and Oxylipins. <i>Metabolites</i>, <i>12</i>(10), Article 928. <a href="https://doi.org/10.3390/metabo12100928" target="_blank">https://doi.org/10.3390/metabo12100928</a>
dc.identifier.otherCONVID_157013953
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/83513
dc.description.abstractWeight loss and increased physical activity may promote beneficial modulation of the metabolome, but limited evidence exists about how very low-level weight loss affects the metabolome in previously non-obese active individuals. Following a weight loss period (21.1 ± 3.1 weeks) leading to substantial fat mass loss of 52% (−7.9 ± 1.5 kg) and low body fat (12.7 ± 4.1%), the liquid chromatography-mass spectrometry-based metabolic signature of 24 previously young, healthy, and normal weight female physique athletes was investigated. We observed uniform increases (FDR < 0.05) in bile acids, very-long-chain free fatty acids (FFA), and oxylipins, together with reductions in unsaturated FFAs after weight loss. These widespread changes, especially in the bile acid profile, were most strongly explained (FDR < 0.05) by changes in android (visceral) fat mass. The reported changes did not persist, as all of them were reversed after the subsequent voluntary weight regain period (18.4 ± 2.9 weeks) and were unchanged in non-dieting controls (n = 16). Overall, we suggest that the reported changes in FFA, bile acid, and oxylipin profiles reflect metabolic adaptation to very low levels of fat mass after prolonged periods of intense exercise and low-energy availability. However, the effects of the aforementioned metabolome subclass alteration on metabolic homeostasis remain controversial, and more studies are warranted to unravel the complex physiology and potentially associated health implications. In the end, our study reinforced the view that transient weight loss seems to have little to no long-lasting molecular and physiological effects.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofseriesMetabolites
dc.rightsCC BY 4.0
dc.subject.otherweight loss
dc.subject.otherexercise
dc.subject.othervisceral fat mass
dc.subject.otherLC-MS metabolome
dc.subject.otherbioactive metabolites
dc.titleSubstantial Fat Loss in Physique Competitors Is Characterized by Increased Levels of Bile Acids, Very-Long Chain Fatty Acids, and Oxylipins
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202210114839
dc.contributor.laitosLiikuntatieteellinen tiedekuntafi
dc.contributor.laitosFaculty of Sport and Health Sciencesen
dc.contributor.oppiaineBiomekaniikkafi
dc.contributor.oppiaineValmennus- ja testausoppifi
dc.contributor.oppiaineLiikuntafysiologiafi
dc.contributor.oppiaineBiomechanicsen
dc.contributor.oppiaineScience of Sport Coaching and Fitness Testingen
dc.contributor.oppiaineExercise Physiologyen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn2218-1989
dc.relation.numberinseries10
dc.relation.volume12
dc.type.versionpublishedVersion
dc.rights.copyright© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
dc.rights.accesslevelopenAccessfi
dc.relation.grantnumber275922
dc.subject.ysoliikunta
dc.subject.ysofyysinen aktiivisuus
dc.subject.ysopainonhallinta
dc.subject.ysokuntoliikunta
dc.subject.ysoaineenvaihdunta
dc.subject.ysolaihdutus
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p916
jyx.subject.urihttp://www.yso.fi/onto/yso/p23102
jyx.subject.urihttp://www.yso.fi/onto/yso/p822
jyx.subject.urihttp://www.yso.fi/onto/yso/p3708
jyx.subject.urihttp://www.yso.fi/onto/yso/p3066
jyx.subject.urihttp://www.yso.fi/onto/yso/p825
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.3390/metabo12100928
dc.relation.funderResearch Council of Finlanden
dc.relation.funderSuomen Akatemiafi
jyx.fundingprogramAcademy Research Fellow, AoFen
jyx.fundingprogramAkatemiatutkija, SAfi
jyx.fundinginformationThis study was supported by grants from the Finnish Foundation for Cardiovascular Research (M.P. and V.S.), The Finnish Medical Foundation (H.V.S.), and the US National Institutes of Health (K01DK116917 to J.D.W.; S10OD020025, R01ES027595 to M.J.; R01HL143227 to S.C.R.) and by the Academy of Finland (269517 [M.P.]; 275922 [J.J.H.]). K.H.P. was funded by the Academy of Finland, grant numbers 335443, 314383, 272376, 266286; Finnish Medical Foundation; Gyllenberg Foundation; Novo Nordisk Foundation, grant numbers NNF20OC0060547, NNF17OC0027232, NNF10OC1013354; Finnish Diabetes Research Foundation; University of Helsinki and Helsinki University Hospital Government Research Funds. S.C.R. was funded by the National Institute for Health Research (NIHR) Cambridge Biomedical Research Centre (BRC-1215-20014). A.H. was supported by the Academy of Finland, grant #321356.
dc.type.okmA1


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