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Impact of Cashew Nuts in the Human Diet: Measured Energy Value and Effects on Cardiovascular Disease Risk Factors

Not Applicable
Completed
Conditions
Healthy Volunteers
Interventions
Other: Base Diet
Other: Base Diet with Cashew Nuts
Registration Number
NCT02628171
Lead Sponsor
USDA Beltsville Human Nutrition Research Center
Brief Summary

This study evaluates the effect of cashew nut consumption on traditional and emerging markers of cardiovascular disease (CVD) risk and determines the usable energy content of a serving of cashew nuts for accurate food labelling.

Detailed Description

The cardioprotective effects of nuts have been well documented in the scientific literature; however, most of the research has been done with almonds, walnuts, and pistachios, while studies with cashew nuts are lacking. In addition to the cardiovascular literature, our recent studies measuring the metabolizable energy of nuts have demonstrated that the measured energy value of almonds, pistachios, and walnuts is lower than that predicted using the Atwater factors. However, the measured energy value of cashew nuts is unknown. There are two distinct aims of this study - determining the effects of cashew nut consumption on risk factors of CVD, and determining the energy value of cashew nuts in the human diet. The cardiovascular effects of cashew nuts will be determined by measuring both traditional and emerging risk factors. The metabolizable energy value of cashew nuts will be calculated based on the chemical composition and energy content of the consumed diet and excreta. This will provide a better estimate of the energy value than simply calculating energy value based on Atwater factors.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
42
Inclusion Criteria
  • BMI between 20 and 38 kg/m2
  • Fasting glucose ≤ 126 mg/dL
  • Blood pressure ≤ 160/100 mm Hg
Exclusion Criteria
  • Presence of kidney disease, liver disease, gout, hyperthyroidism, untreated or unstable hypothyroidism, certain cancers, gastrointestinal disease, pancreatic disease, other metabolic diseases, or malabsorption syndromes
  • Use of cholesterol lowering medication
  • Use of medication to treat hypertension for less than 6 months
  • Active cardiovascular disease (such as a heart attack or procedure within the past six months or participation in a cardiac rehabilitation program within the last six months, stroke, or history/treatment for transient ischemic attacks in the past six months, or documented history of pulmonary embolus in the past six months)
  • Women who have given birth during the previous 12 months
  • Pregnant women or women who plan to become pregnant or become pregnant during the study
  • Lactating women
  • Type 2 diabetes
  • Use of prescription or over-the-counter antiobesity medications or supplements (e.g., phenylpropanolamine, ephedrine, caffeine, during and for at least 6 months prior to the start of the study) or history of a surgical intervention for obesity
  • Smokers or other tobacco users (during 6 months prior to the start of the study)
  • History of eating disorders or other dietary patterns which are not consistent with the dietary intervention (e.g., vegetarians, very low fat diets, high protein diets)
  • Known (self-reported) allergy or adverse reaction to cashew nuts or other nuts
  • Unable or unwilling to give informed consent or communicate with study staff
  • Self-report of alcohol or substance abuse within the past 12 months and/or current acute treatment or rehabilitation program for these problems (long-term participation in Alcoholics Anonymous is not an exclusion)
  • Other medical, psychiatric, or behavioral factors that in the judgment of the Principal Investigator may interfere with study participation or the ability to follow the intervention protocol

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
ControlBase DietParticipants will receive a controlled diet (base diet), typical of an American diet, with 0 g/day of cashew nuts (control).
CashewBase Diet with Cashew NutsParticipants will receive a controlled diet, typical of an American diet, with 42 g/day of cashew nuts (base diet with cashew nuts).
Primary Outcome Measures
NameTimeMethod
Metabolizable energy will be measured based on energy content of the consumed diet and excretaSecond week of diet period 2 (week 8)

The measured metabolizable energy value of cashew nuts will be calculated based on the energy content of the consumed diet and excreta.

Change in lipid/lipoprotein profile will be measured in bloodWeek 0, end of diet period 1 (week 4), beginning of diet period 2 (week 6), end of diet period 2 (week 10)

The following will be measured in the blood on 2 consecutive days at the beginning and end of each 4-week diet period: lipids and lipoproteins, apolipoproteins, lipoprotein particle number/size, and proprotein convertase subtilisin/kexin type 9 (PCSK9).

Secondary Outcome Measures
NameTimeMethod
Change in systemic inflammation will be measured in bloodWeek 0, end of diet period 1 (week 4), beginning of diet period 2 (week 6), end of diet period 2 (week 10)

Markers of systemic inflammation will be measured, such as IL-6, TNF-alpha, serum amyloid A, and CRP.

Pulse Wave will be measured using Sphygmocor EXCELWeek 0, end of diet period 1 (week 4), beginning of diet period 2 (week 6), end of diet period 2 (week 10)

Pulse wave analysis and pulse wave velocity will be conducted.

Digestibility (%) will be calculated as (intake - excreted)/intakeSecond week of diet period 1 (week 2), second week of diet period 2 (week 8)

Fat, protein, and fiber digestibility will be calculated (%) and the effect of cashew nuts on nutrient digestibility (%) will be assessed.

Markers of vascular health will be measured in bloodWeek 0, end of diet period 1 (week 4), beginning of diet period 2 (week 6), end of diet period 2 (week 10)

Adhesion molecules and endothelin-1 will be measured in the blood.

Change in hemostasis will be measured in bloodWeek 0, end of diet period 1 (week 4), beginning of diet period 2 (week 6), end of diet period 2 (week 10)

Fibrinogen and factor VII will be measured in the blood.

Trial Locations

Locations (1)

USDA Beltsville Human Nutrition Research Center

🇺🇸

Beltsville, Maryland, United States

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