The primary aim of this study is to determine whether the cholesterol-lowering efficacy of barley b- glucan varied as function of molecular weight (MW) and the total daily amount consumed. Our second aim is to investigate the mechanism responsible for the action, specifically, whether β-glucan lowers circulating cholesterol concentration via inhibiting cholesterol absorption and synthesis. Thirdly, we aim to determine if any gene-diet interactions are associated with cholesterol lowering by barley β-glucan. In addition, we aim to investigate the alteration of the gut microbiota after β-glucan consumption and the correlation between the altered gut microbiota and cardiovascular disease risk factors.
This study consists of four dietary phases which are separated by \>28 days wash-out period. During the treatment phase, participants will be provided with all meals for the 35 day period. Breakfast meals will be consumed under the supervision of the research staff and lunch, dinner and snacks will be provided to take home in take-out packaging. While subjects are on the wash-out period they will return to their normal diet. The meals are on a 7 day rotating schedule that reflect an average Canadian diet. Changes in blood lipids, body weight, and waist circumference will be measured during each treatment phase. Cholesterol absorption and synthesis will be examined by stable isotope method. Single nucleotide polymorphisms (SNPs), rs3808607 of gene CYP7A1and rs429358 and rs7412 will be determined byTaqMan® SNP Genotyping assay following the manufacturer's protocol. Fecal samples will be collected at the end of each intervention phase and will be subjected to Illumina sequencing of 16S rRNA genes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Enrollment
45
Minimal beta-glucan
3grams beta-glucan
5 grams beta-glucan
3 grams of high molecular weight beta-glucan
Richardson Centre for Functional Foods and Neutraceuticals
Winnipeg, Manitoba, Canada
Changs in Total Cholesterol
Fasted total cholesterol concentration will be measured using the automated enzymatic methods.
Time frame: Beginning and end of each phase
Changes in LDL Cholesterol
Serum LDL cholesterol will be estimated using the Friedewald equation.
Time frame: Beginning and end of each phase
Cholesterol Absorption/Synthesis
The rate of cholesterol absorption and synthesis will be measured in each intervention phase using single stable isotope labelling technique.
Time frame: End of each phase
Potential Gene-nutrient Interactions: CYP7A1 and APOE
The Single Nucleotide Polymorphism (SNP) rs3808607 of CYP7A1 gene, rs429358 and rs7412 of APOE gene, and their associations with different blood lipid responses to beta-glucan interventions will be determined.
Time frame: Once for each participant
Changes in Body Weight and Waist Circumference(WC)
Body weight will be monitored every day when subject visits the Richardson Centre. Waist circumference will be measured at the beginning and end of each study phase.
Time frame: Every day for body weight; beginning and end of each phase for WC
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