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Completed

NCT Number: NCT01413646

Effects of Walnuts on Endothelial Function in Overweight Adults With at Least One Factor of Metabolic Syndrome

The purpose of this study is to examine the effects of walnut consumption on endothelial function and lipid markers in overweight patients with at least one factor of metabolic syndrome as compared to the control group.

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Key information

Age range

25 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Yale-Griffin Prevention Research Center

Derby, Connecticut, 06418, United States

About this study

The prevalence of obesity in both adults and children in the United States has increased significantly over the past 50 years. More than 66% of adults in the US are now overweight or obese and at least 17% of children in the population at large are now considered overweight.Obesity may be a factor predisposing patients to a myriad of comorbidities that increase the associated mortality rate.Several large prospective trials have documented that obesity is an independent risk factor for mortality from cardiovascular disease (CVD). Considering the major metabolic and biochemical changes that occur in obesity, such as atherogenic dyslipidemia, insulin resistance and hyperinsulinemia, endothelial dysfunction, and chronic inflammatory and prothrombotic states, obesity plays a role in the pathogenesis of systemic atherosclerosis and its clinical complications.

Walnuts are rich in alpha-linolenic acid, an essential omega-3 fatty acid, L-arginine and antioxidants. Polyunsaturated fatty acids and antioxidants have anti-oxidative effects and are thought to help preserve the endothelium's capacity to generate nitric oxide (NO), which acts to promote vasodilation, stabilize platelets, and promote the anti-inflammatory abilities of the endothelium. Evidence of this anticipated effect would have implications for strategies to prevent or retard type 2 diabetes mellitus and cardiovascular disease. Endothelial function testing using high frequency ultrasound imaging of the brachial artery to assess endothelium-dependent flow-mediated dilatation (FMD) offers a non-invasive, uniquely valuable means of assessing aggregated influences on cardiac risk by gauging a physiologic response of the vascular endothelium. Proposed, therefore, is a randomized, controlled, cross-over clinical trial, to assess the effects of walnuts on endothelial function in overweight adults with elevated waist circumference and at least one risk factor of metabolic syndrome.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and female age 25-75 years
  • Non-smoker
  • Overweight (BMI ≥ 25) with central adiposity as indicated by waist circumference (102 cm. in men / 88 cm. in women)
  • Meet one risk factor of the metabolic syndrome.
  • blood pressure > 130/85 or taking antihypertensive medication
  • fasting plasma glucose (FPG) >100 mg/dL (6.1 mmol/L)
  • fasting serum triglycerides level (TG) > 150 mg/dL (1.69 mmol/L)
  • fasting high-density lipoprotein (HDL) cholesterol < 40 mg/dL (1.04 mmol/L)in men, and < 50 mg/dL (1.29 mmol/L) in women.

Exclusion criteria

  • Anticipated inability to complete or comply with study protocol
  • Use of lipid-lowering or antihypertensive medications or aspirin unless stable on medication for at least 3 months and willing to refrain from taking medication for 12 hours prior to EF scanning
  • Preexisting cardiovascular disease (including symptomatic coronary artery disease (CAD), myocardial infarction, angina pectoris, anginal equivalent, peripheral vascular disease, congestive heart failure, carotid stenosis)
  • Severe hypertension (systolic blood pressure >180mmHg or diastolic blood pressure >105mmHg), even if well-controlled by medication.
  • Diagnosed diabetes mellitus
  • Regular use of multivitamins, Vitamin C, Vitamin E, fish oil, flax seed oil, omega-3 fatty acids, CoQ10, fiber supplements, garlic pills, arginine, red yeast rice, and any kind of antioxidant and unwillingness to discontinue supplementation for at least 4 weeks prior to study initiation and for study duration
  • Allergic to walnuts or any other nuts
  • Diagnosed eating disorder
  • On any specific diet, weight control diet, vegan diet
  • Any rheumatologic disease requiring regular use of NSAIDs or alternative medications
  • Regular use of fiber supplements
  • Regular use of vasoactive medication (including glucocorticoids, antineoplastic agents, psychoactive agents, or bronchodilators), and anticoagulant drugs (including Coumadin, plavix )
  • Diagnosed sleep apnea
  • Substance abuse (chronic alcoholism, other chemical dependency)
  • Any unstable medical condition that would limit the ability of a subject to participate fully in the trial (e.g., cancer, AIDS, tuberculosis, psychotic disorder)
  • Current or impending pregnancy

Treatment and study plan

Walnut Supplementation

Dietary Supplement

Eight weeks of walnut supplementation

No walnut supplementation

Dietary Supplement

Eight weeks without walnut supplementation

Primary outcomes

  1. Endothelial function

    Time frame: 8 weeks

    Brachial artery flow mediated dilation (FMD)

Secondary outcomes

  1. Weight

    Time frame: 8 weeks

  2. Waist circumference

    Time frame: 8 weeks

  3. Fasting lipid panel

    Time frame: 8 weeks

    Total cholesterol, low density lipoprotein cholesterol, high density lipoprotein cholesterol, triglyceride level, cholesterol / high density lipoprotein cholesterol ratio

  4. Fasting blood glucose

    Time frame: 8 weeks

  5. Fasting insulin

    Time frame: 8 weeks

  6. Blood pressure

    Time frame: 8 weeks

Sponsors and collaborators

Lead sponsor

Griffin Hospital

Other

Collaborators

  • California Walnut Commission

Registry information

Official study title

Effects of Walnuts on Endothelial Function in Overweight Adults With at Least One Factor of Metabolic Syndrome: A Randomized, Controlled, Cross-Over Trial

Acronym: Walnut2

Important dates

Study start
2010
Primary completion
2010
Study completion
2010
First posted
Aug 10, 2011
Registry last updated
Aug 2, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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