Effect of Plant Sterols on Inflammatory, Endothelial Function and Oxidative Stress Markers, Microbiota and Sterol Metabolism in a Cardiovascular Risk Population
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 42
- 试验地点
- 2
- 主要终点
- Changes in plasmatic LDL-c
研究概览
简要总结
Potential cholesterol-lowering effect of a regular intake of a plant sterol (PS)-containing food supplement, in overweight/obese type 1 or 2, normoglycemic/pre-diabetic, with LDL-cholesterol values > 115 mg/dl and not pharmacologically treated participants treated with the PS-containing food supplement or placebo supplement.
详细描述
Cardiovascular disease (CVD) is the leading cause of death worldwide, with hypercholesterolemia being one of the main risk factors for CVD. The deposition and oxidation of LDL-cholesterol particles triggers a series of molecular events favoring chronic low-grade inflammation, endothelial dysfunction and oxidative stress. This situation promotes atherogenesis thus increasing cardiovascular risk. Obesity favors the secretion of pro-inflammatory mediators and promotes the recruitment of macrophages to adipose tissue, insulin resistance, hyperglycemia and hyperlipidemia, thus increasing the risk of CVD. In addition, obesity has been associated with gut dysbiosis, which in turn is associated with atherosclerosis in some studies. Beneficial effects of PS on LDL-cholesterol and inflammatory, endothelial dysfunction and oxidative stress markers have been reported by several clinical trials. A meta-analysis suggests a lowering effect of PS on body mass index (BMI) in participants with BMI>25. Furthermore, the consumption of PS has been beneficially associated in in vitro studies with changes in intestinal microbial profile, sterol metabolism and short chain fatty acids (SCFA) production. Therefore, the hypothesis is if the consumption of PS as a food supplementation could reduce cardiovascular risk. The present study aims to evaluate the LDL-cholesterol serum levels after regular intake of a food supplement containing PS (2 g/day) in overweight/obese type 1 or 2 patients, normoglycemic /pre-diabetic and with LDL-cholesterol values > 115 mg/dl not pharmacologically treated. This is a crossover study with 21 participants (intake of a food supplement containing PS) and 21 participants (intake of excipient-based placebo), with a first intervention period of 8 weeks. After a 6-week washout period, the treatments are switched, with a second intervention period of 8 weeks. In addition, to the LDL-cholesterol lowering assessment, other biochemical, hematological, inflammatory, endothelial dysfunction and oxidative stress parameters are assessed in serum samples. Moreover, sterol and metabolite profiling in serum and feces, microbiota modulation, anthropometric measurements and body composition, bioimpedance, dietary intake and physical activity questionnaire are evaluated. All parameters are evaluated at the beginning (weeks 0 and 14) and at the end of each intervention period (weeks 8 and 22).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Basic Science
- 盲法
- Triple (Participant, Care Provider, Investigator)
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •BMI: 27-29.9 or 30-39.9
- •Plasmatic glucose: < 100mg/dl or 100-125mg/dl
- •Glycosylated hemoglobin: < 5.7 or 5.7-6.4
- •LDL cholesterol > 115mg/dL
- •Serum levels of biochemical and hematological parameters and fat-soluble vitamins within reference ranges.
排除标准
- •Subjects on cholesterol-lowering pharmacological treatment
- •Alcohol consumption above 30 g/day
- •Pregnant or lactating women
- •Any infection, serious illness or co-morbidity that may affect the bioavailability of PS (e.g., malabsorption, celiac disease, allergies or food intolerances)
- •Diseases of the gastrointestinal tract
- •Antibiotic, hormonal or anabolic treatment
- •Participants consuming foods enriched with PS or food supplements that contain PS
- •Participants who follow specialist weight loss diets, vegans or vegetarians
结局指标
主要结局
Changes in plasmatic LDL-c
时间窗: 0, 8, 14 and 22 weeks
LDL-c, calculated by the Friedewald's formula, with repeated measures (at the beginning and at the end of each period the intervention)
次要结局
- Changes in oxidized glutathione (GSSG)(0, 8, 14 and 22 weeks)
- Changes in plasmatic total cholesterol(0, 8, 14 and 22 weeks)
- Changes in plasmatic HDL-c(0, 8, 14 and 22 weeks)
- Changes in plasmatic Apo A(0, 8, 14 and 22 weeks)
- Changes in feces levels of the sterols and metabolites profile(0, 8, 14 and 22 weeks)
- Changes in serum interleukin 1β (IL-1β)(0, 8, 14 and 22 weeks)
- Changes in serum interleukin 8 (IL-8)(0, 8, 14 and 22 weeks)
- Changes in plasmatic 8-isoprostane(0, 8, 14 and 22 weeks)
- Changes in plasmatic triglycerides(0, 8, 14 and 22 weeks)
- Changes in plasmatic High-sensitivity C-reactive protein (hsCRP)(0, 8, 14 and 22 weeks)
- Changes in plasmatic Homeostatic Model Assessment for Insulin Resistance (HOMA-IR)(0, 8, 14 and 22 weeks)
- Changes in serum E-Selectin(0, 8, 14 and 22 weeks)
- Changes in serum endothelin (ET-1)(0, 8, 14 and 22 weeks)
- Changes in plasmatic fibrinogen(0, 8, 14 and 22 weeks)
- Changes in serum levels of the sterols and metabolites profile(0, 8, 14 and 22 weeks)
- Changes in serum interleukin 10 (IL-10)(0, 8, 14 and 22 weeks)
- Changes in plasmatic LDL-cholesterol oxidation(0, 8, 14 and 22 weeks)
- Changes in Bioelectrical impedance analysis (BIA)(0, 8, 14 and 22 weeks)
- Evaluation of the Mediterranean diet adherence to measure quality of life(0, 8, 14 and 22 weeks)
- Changes in plasmatic non-HDL cholesterol(0, 8, 14 and 22 weeks)
- Changes in plasmatic Apo B(0, 8, 14 and 22 weeks)
- Changes in plasmatic insulin(0, 8, 14 and 22 weeks)
- Changes in serum tumor necrosis factor alpha (TNFα)(0, 8, 14 and 22 weeks)
- Changes in serum plasminogen activator inhibitor-1(PAI-1)(0, 8, 14 and 22 weeks)
- Changes in the composition of microbiota in feces(0, 8, 14 and 22 weeks)
- Changes in plasmatic glucose(0, 8, 14 and 22 weeks)
- Changes in serum interleukin 12p70 (IL-12p70)(0, 8, 14 and 22 weeks)
- Changes in serum interleukin 6 (IL-6)(0, 8, 14 and 22 weeks)
- Changes in serum vascular cell adhesion molecule-1 (VCAM-1)(0, 8, 14 and 22 weeks)
- Changes in plasmatic malondialdehyde (MDA)(0, 8, 14 and 22 weeks)
- Changes in reduced glutathiones (GSH)(0, 8, 14 and 22 weeks)
- Changes in feces of short-chain fatty acids (SCFAs)(0, 8, 14 and 22 weeks)
- Changes in body weight (WT)(0, 8, 14 and 22 weeks)
- Changes in body height (HT)(0, 8, 14 and 22 weeks)
- Assessment of dietary intake(0, 8, 14 and 22 weeks)
- Changes in plasmatic levels of cholesterol oxidation products (COPs)(0, 8, 14 and 22 weeks)
- Changes in body circumferences(0, 8, 14 and 22 weeks)
- Evaluation of the physical activity to measure quality of life(0, 8, 14 and 22 weeks)
研究者
Guadalupe García Llatas
Principal investigator
University of Valencia