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dc.contributor.authorSommersten, Cathrine Horn
dc.contributor.authorLaupsa-Borge, Johnny
dc.contributor.authorAndersen, Amanda Iselin Olesen
dc.contributor.authorFasmer, Kristine Eldevik
dc.contributor.authorHolmefjord, Mari-Anna Frydenlund
dc.contributor.authorRevheim, Ingrid
dc.contributor.authorJohannessen, Kristine Kjerpeseth
dc.contributor.authorNæsheim, Nicole Tandrevold
dc.contributor.authorStorås, Inghild
dc.contributor.authorLeikanger, Trine
dc.contributor.authorAmundsen, Kristin
dc.contributor.authorSkjerve, Karoline Lyngstad
dc.contributor.authorLawrence-Archer, Laurence
dc.contributor.authorSpjelkavik, Camilla
dc.contributor.authorHaldorsen, Ingfrid S.
dc.contributor.authorLindseth, Inge Andreas
dc.contributor.authorDierkes, Jutta
dc.contributor.authorMellgren, Gunnar
dc.contributor.authorDankel, Simon N
dc.date.accessioned2022-10-28T11:37:10Z
dc.date.available2022-10-28T11:37:10Z
dc.date.created2022-10-24T13:36:20Z
dc.date.issued2022
dc.identifier.issn0261-5614
dc.identifier.urihttps://hdl.handle.net/11250/3028850
dc.description.abstractBackground & aims: Visceral adipose tissue (VAT) volume is associated with common lifestyle diseases. Dietary quality, including food matrix and degree of carbohydrate cellularity, as well as the carbohydrate/fat ratio, may influence VAT volume. We aimed to determine the effects of isocaloric diets differing in either “cellularity”, a novel marker of dietary carbohydrate quality, or carbohydrate amount on visceral fat volume and anthropometric measures in adults with obesity. Methods: In a randomized controlled trial of 193 people with obesity/central adiposity, we compared changes in VAT volume after 6 and 12 months, measured by abdominal computed tomography, on three isocaloric eating patterns based on “acellular” carbohydrate sources (e.g., flour-based whole-grain products; comparator arm), “cellular” carbohydrate sources (minimally processed foods with intact cellular structures such as fruits, potatoes/tubers, and rice), or low-carbohydrate high-fat (LCHF) principles. Outcomes were compared by an intention-to-treat (ITT) analysis using constrained linear mixed-effects modelling (cLMM) providing baseline-adjusted change scores and proper missing data handling without imputation. Results: 78 and 57 participants completed 6 and 12 months, respectively, with similar intakes of energy (females: 1820−2060 kcal, males: 2480−2550 kcal) and protein (16–17 energy percent, E%) throughout the intervention, and only modest reductions in energy from baseline. Reported dietary intakes were 42–44, 41–42, and 11–15 E% carbohydrate and 36–38, 37–38, and 66–70 E% fat in the acellular, cellular and LCHF groups, respectively. There were no significant between-group differences in VAT volume after 6 months (cellular vs. acellular [95% CI]: −55 cm³ [−545, 436]; LCHF vs. acellular [95% CI]: −225 cm³ [−703, 253]) or after 12 months (cellular vs. acellular [95% CI]: −122 cm³ [−757, 514]; LCHF vs. acellular [95% CI]: −317 cm³ [−943, 309]). VAT volume decreased significantly within all groups by 14–18% and 12–17% after 6 and 12 months, respectively. Waist circumference was reduced to a significantly greater degree in the LCHF vs. acellular group at 6 months (LCHF vs. acellular [95% CI]: −2.78 cm [−5.54, −0.017]). Conclusions: Despite modest energy restriction, the three isocaloric eating patterns, differing in carbohydrate cellularity and amount, decreased visceral fat volume significantly and to a similar clinically relevant degree.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleDiets differing in carbohydrate cellularity and amount similarly reduced visceral fat in people with obesity - a randomized controlled trial (CARBFUNC)en_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2022 The Author(s)en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.doi10.1016/j.clnu.2022.08.028
dc.identifier.cristin2064437
dc.source.journalClinical Nutritionen_US
dc.source.pagenumber2345-2355en_US
dc.identifier.citationClinical Nutrition. 2022, 41 (10), 2345-2355.en_US
dc.source.volume41en_US
dc.source.issue10en_US


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