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dc.contributor.advisorMartins, Catia
dc.contributor.advisorRøknes, Jessica Ann
dc.contributor.authorStakvik, Karina
dc.date.accessioned2021-09-25T16:17:59Z
dc.date.available2021-09-25T16:17:59Z
dc.date.issued2021
dc.identifierno.ntnu:inspera:81396206:46703930
dc.identifier.urihttps://hdl.handle.net/11250/2782722
dc.description.abstract
dc.description.abstractIntroduction: Ketogenic diets (KDs) have the ability to suppress the increase in appetite otherwise seen with diet-induced weight loss (WL). The exact mechanisms involved remains unknown, but changes in gut microbiota (GM)/short-chain fatty acids (SCFA) have been suggested as a potential link. Therefore, the main aim of this thesis was to evaluate if changes in fecal SCFA concentrations are associated with appetite suppression during WL induced by a ketogenic low energy diet (LED). A secondary aim was to investigate the impact of WL induced by a ketogenic LED on GM and SCFA. Method: This study is a longitudinal study with repeated measurements. 83 healthy adults with obesity (BMI: 34.93.5 kg/m2) underwent an 8-week powder-based LED (1000 kcal/day), with a carbohydrate content ranging from 70-130 g/day, followed by a 4-week refeeding and weight stabilization phase. Body weight (BW) and composition, subjective appetite feelings and plasma concentration of appetite hormones (both fasting and postprandial), fasting B-hydroxybutyric acid (BHB) plasma concentration, GM and fecal SCFA were measured at three timepoints (baseline (BL), week 9 (W9) and week 13 (W13)). Data are shown as estimated marginal means  SEM. Results: Participants lost 141.3 kg at W9 (P<0.001) and maintained it at W13. Plasma BHB increased from BL to W9 (0.80.0 mmol/L) and was no longer different from BL at W13. Fasting and postprandial feelings of hunger did not change at W9, but both were higher than BL at W13 (P<0.01, P<0.001, respectively). Basal, but not postprandial AG increased from BL to W9 (P<0.001), and both basal and postprandial AG were higher than BL at W13 (P<0.001, P<0,01, respectively). Alistipes and Ruminococcaceae both increased from BL to W9 (P<0.001, P<0.01, respectively), and Ruminococcaceae decreased from W9 to W13 (P<0.05). Eubacterium rectale decreased from BL to W9 (P<0.001) and increased from W9 to W13 (P<0.001), however the relative composition of this group was lower at W13 compered to BL (P<0.01). Fecal concentration of acetic, propionic and butyric acids decreased from BL to W9 (P<0.001, for all) and increased from W9 to W13 (P<0.05, P<0.01, P<0.001, respectively), but values at W13 were still below BL (P<0.01, for all). The greater the decrease in butyric acid the higher the increase, or smaller the reduction, in basal AG (r=-0.260, P=0.043, n=61) under ketogenic conditions (W9). Conclusions: This study suggest that WL induced by KD alters GM and SCFA production. However, fecal SCFA do not seem to play a role in the appetite suppression seen under ketogenic conditions. The exact molecular mechanisms mediating appetite suppression under KD remain unknown and more research is clearly needed in this field.
dc.languageeng
dc.publisherNTNU
dc.titleAppetite suppression during ketogenic diets: Do fecal short-chain fatty acids play a role?
dc.typeMaster thesis


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