The Influence of Daily Walnut Intake on Vascular Function and Associated Changes in Lipid Mediators and Primary Metabolites.
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- Framingham Reactive Hyperemia Index (fRHI)
研究概览
简要总结
This study seeks to confirm and extend previous finding that four weeks of daily intake of 40 g of walnuts improve microvascular function, increasing the reactive hyperemia index (RHI), effects which were greatest in individuals with the worst initial RHI and correlating to circulating levels of vasoactive plasma epoxides. The current trial will enroll postmenopausal women who are at risk for cardiovascular disease due to their menopausal status and increased central adiposity. The initial trial focused on non-esterified (i.e. plasma) derived oxylipins, but substantial and unique changes were also observed in the esterified lipoprotein pool. The current study will add the esterified lipoprotein pool, important, as the mechanisms by which walnut intake influences endothelial function are currently undefined, but may include lipoprotein induced modulation of vascular hemostasis. As a secondary objective, primary metabolism and urolithin metabotype will be analyzed as a way to capture the influence of potential differences in habitual diet and metabolism on physiologic response. Therefore, this study will combine measures of cardiovascular physiology, metabolomics, and walnut-derived metabolite analyses to assess the 12 week influence of 40 g of daily walnut intake on the health of overweight and obese postmenopausal women.
详细描述
A dietary intervention trial will be conducted to achieve the following objectives and outcomes:
Objective 1: Determine the 12 week change in bioactive lipid mediators, and their relationship to vascular function and platelet reactivity in overweight or obese postmenopausal women with walnut incorporation into their habitual diet.
Objective 2: Assess the contribution of metabolic phenotype on the variance in biomarker response that includes both primary metabolism and urolithin metabotype.
Expected Outcomes: Forty g of daily walnut intake for six- and 12- weeks is predicted to positively impact the production of bioactive lipid mediators known to favorably regulate cardiovascular and inflammatory signaling. AA derived oxylipins produced from COX, LOX, and CYP epoxygenases are known as regulators of inflammation, platelet activation and vascular function. Therefore, understanding how certain foods such as walnuts can change the relative ratio of PUFA substrates (i.e., AA, ALA, LA, EPA and DHA), and their subsequent bioactive species produced through these enzyme pathways is necessary for the refinement of dietary recommendations with regard to specific foods and dietary patterns aimed at reducing the risk of chronic disease. Although a positive outcome is predicted, there may be substantial variability in response. To explore potential genetic and dietary factors that may contribute to the variability in response to the above functional markers, primary metabolism and urolithin metabotype will be assessed.
Objective 3: Assess the influence of 12 weeks of walnut intake on facial wrinkles in postmenopausal women.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Basic Science
- 盲法
- None
入排标准
- 年龄范围
- 45 Years 至 65 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Postmenopausal female: 45-65 years
- •Women: lack of menses for at least two years.
- •Subject is willing and able to comply with the study protocols.
- •Subject is willing to participate in all study procedures
- •BMI 25.0 - 35 kg/m2
排除标准
- •BMI ≥ 35 kg/m2
- •Visit 1 Reactive Hyperemia Index (RHI; EndoPAT 2000) ≥ 2.4
- •Dislike or allergy for walnuts or walnut products
- •Self-reported use of daily anticoagulation agents including aspirin, NSAIDs
- •Vegan, Vegetarians, food faddists or those consuming a non-traditional diet
- •Fruit consumption ≥ 3 cups/day
- •Regular consumption of nuts (2-3 servings/week)
- •Vegetable consumption ≥ 4 cups/day for females
- •Coffee/tea ≥ 3 cups/day
- •Dark chocolate ≥ 3 oz/day
- •Self-reported restriction of physical activity due to a chronic health condition
- •Self-reported chronic/routine high intensity exercise
- •Self-reported diabetes
- •Blood pressure ≥ 140/90 mm Hg
- •Self-reported renal or liver disease
- •Self-reported heart disease, which includes cardiovascular events and stroke
- •Peripheral artery disease, Raynaud's syndrome or disease
- •Inability to properly place or wear the PAT probes or abnormal measurements on pre-screening PAT
- •Abnormal Metabolic or CBC panels (laboratory values outside the reference range) if determined to be clinically significant by the study physician.
- •Self-reported cancer within past 5 years
- •Self-reported malabsorption
- •Currently taking prescription drugs or supplements.
- •Supplement use other than a general formula of vitamins and minerals that meet the RDA
- •Not willing to stop any supplement use, including herbal, plant or botanical, fish oil, oil supplements a month prior to study enrollment.
- •Indications of substance or alcohol abuse within the last 3 years
- •Cannabis use
- •Screening LDL ≥ 190 mg/dl for those who have 0-1 major risk factors apart from LDL cholesterol (i.e. family history of premature coronary artery disease (male first degree relative < 55 years; CHD in female first degree relative < 65 years), cigarette smoker, HDL-C ≤ 40 mg/dL]. (using NCEP calculator http://cvdrisk.nhlbi.nih.gov/calculator.asp)
- •Screening LDL ≥ 160 mg/dl for those who have 2 major risk factors apart from LDL cholesterol [i.e. family history of premature coronary artery disease (male first degree relative < 55 years; CHD in female first degree relative < 65 years), cigarette smoker, HDL-C ≤ 40 mg/dL]. (using NCEP calculator http://cvdrisk.nhlbi.nih.gov/calculator.asp);
- •Screening LDL ≥ 130 mg/dl for those who have 2 major risk factors apart from LDL cholesterol [i.e. family history of premature coronary artery disease (male first degree relative < 55 years; CHD in female first degree relative < 65 years), cigarette smoker, HDL-C ≤ 40 mg/dL], and a Framingham 10-year Risk Score 10-20% (using NCEP calculator http://cvdrisk.nhlbi.nih.gov/calculator.asp).
- •Current enrollee in a clinical research study.
研究组 & 干预措施
Habitual Intake
This will be the comparative arm, of 6 weeks before and after the study participant is on their habitual diet
Walnut Intake
Experimental Arm of 12 weeks of Walnut Intake, with study visits at baseline (prior to walnut intake) and after 6 and 12 weeks of 40g of Walnut Intake.
干预措施: Walnut Intake (Other)
结局指标
主要结局
Framingham Reactive Hyperemia Index (fRHI)
时间窗: 18 weeks
Digital microvascular function as measured by the EndoPAT2000
Reactive Hyperemia Index (RHI)
时间窗: 18 weeks
Digital microvascular function as measured by the EndoPAT2000
次要结局
- Urolithin Metabolites(18 weeks)
- Plasma Oxylipins(18 weeks)
- Esterified Oxylipins(18 weeks)
- Ellagitannin Metabolites(18 weeks)
- Plasma Fatty Acids(18 weeks)
- Esterified Fatty Acids(18 weeks)
- Collagen-Induced Platelet Aggregation(18 weeks)
- ADP-Induced Platelet Aggregation(18 weeks)
- Nitric Oxide metabolites (RNOX)(18 weeks)
- Total Nitrate and Nitrite(18 weeks)