The association between baseline fructose consumption and baseline biomarkers of inflammation in a randomized controlled feeding trial.

dc.contributor.advisorNeuhouser, Marian Len_US
dc.contributor.authorLuo, Keen_US
dc.date.accessioned2015-05-11T21:00:17Z
dc.date.available2015-05-11T21:00:17Z
dc.date.issued2015-05-11
dc.date.submitted2015en_US
dc.descriptionThesis (Master's)--University of Washington, 2015en_US
dc.description.abstractBackground: High fructose intake, especially through sugar-sweetened beverage consumption, has been associated with increased risk of chronic diseases, such as obesity, type 2 diabetes mellitus, cardiovascular disease, hypertension, and cancer. Biomarkers of inflammation are useful indicators of low-grade chronic inflammation caused by chronic diseases. Objective: To examine the association between baseline fructose consumption and baseline biomarkers of inflammation in the Carbohydrates and Related Biomarkers (CARB) Study participants. Methods: Data are from the CARB Study conducted at the Fred Hutchinson Cancer Research Center (FHCRC), with healthy adult participants. Baseline 12-hour fasting serum samples were collected to measure biomarkers of inflammation, which were high-sensitivity C-reactive protein (hs-CRP), serum amyloid A (SAA), and interleukin-6 (IL-6). At baseline, participants completed 3-day food records and food frequency questionnaires (FFQ) to estimate their dietary intake. Each participant also received a full-body dual-energy X-ray absorptiometry (DXA) scan to assess percent body fat. Participants were then stratified into two subgroups, based on their percent body fat. Statistical Analysis: Ordinary least squares (OLS) linear regression models were utilized to quantify the association between fructose consumption and biomarkers of inflammation. Effect modification assessment was performed to examine the difference between associations of fructose consumption and biomarkers in the two subgroups. Adjustments were made for participants' age, sex, percent body fat, glycemic load, and energy intake. Results: Eighty participants were included in this analysis. Participants with high percent body fat (>32% for female and >25% for male) tended to be older and more likely to be female than those with low percent body fat (<32% for female and <25% for male). On average, participants with low percent body fat consumed more energy, fructose, glucose, added sugar, sweetened soft drinks, and had higher glycemic load diets than participants with high percent body fat. Using both univariate- and multivariate-adjusted models, there was no significant associations between fructose consumption and biomarkers of inflammation. Conclusion: In CARB Study participants, we found no significant association between fructose consumption and hs-CRP, SAA, or IL-6 concentrations. Further investigation of this association could be designed with a larger sample size and greater difference in fructose consumption among participants.en_US
dc.embargo.termsOpen Accessen_US
dc.format.mimetypeapplication/pdfen_US
dc.identifier.otherLuo_washington_0250O_14204.pdfen_US
dc.identifier.urihttp://hdl.handle.net/1773/33225
dc.language.isoen_USen_US
dc.rightsCopyright is held by the individual authors.en_US
dc.subjectbiomarkers of inflammation; fructoseen_US
dc.subject.otherNutritionen_US
dc.subject.othernutritional sciencesen_US
dc.titleThe association between baseline fructose consumption and baseline biomarkers of inflammation in a randomized controlled feeding trial.en_US
dc.typeThesisen_US

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