Long-Term Effects of Walnut Consumption on Brain Function

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age45-75
SponsorMaastricht University Medical Center

About this trial

Rationale: Healthy foods, including mixed nuts, may improve brain function, which is essential for cognitive and metabolic health, and may contribute to improved food intake regulation. It is therefore important to investigate the specific effects of walnuts on cerebral blood flow responses before and after intranasal insulin administration, as well as their associated functional benefits. The investigators hypothesize that long-term walnut consumption improves vascular function and insulin-sensitivity in the brain, thereby enhancing cognitive performance and appetite control in abdominally obese men and women. Objective: The primary objectives are to investigate in abdominally obese adults the effects of 24-week walnut consumption on (regional) vascular function and insulin-sensitivity in the brain, while the investigators will also assess changes in cognitive performance and appetite-related brain reward activity (secondary objectives). Cerebral blood flow responses before (brain vascular function) and after the administration of intranasal insulin spray (brain insulin-sensitivity) will be quantified by the non-invasive gold standard magnetic resonance imaging (MRI)-perfusion method Arterial Spin Labeling (ASL). Study design: This intervention study will have a randomized, controlled parallel design. The total study duration will be 24 weeks. Study population: Fifty-five abdominally obese men and (postmenopausal) women (aged 45-75 years) without a history of cardiovascular diseases or complaints will participate. This study population is expected to have a decreased cerebral blood flow at baseline and are also at increased risk of cognitive impairment, allowing for improvement by the intervention. Intervention: Study participants will receive daily 50 g (about 15% of energy) of raw walnuts (walnut intervention) or no walnuts (control intervention) for 24 weeks. Main study parameters/endpoints: At baseline and after 24 weeks (follow-up), participants will visit the research facilities for assessments. The primary endpoint is the difference in the cerebral blood flow response before and after intranasal insulin administration between the walnut and control intervention. Cognitive performance will be assessed, while the investigators will also focus on appetite-related brain reward activity (secondary outcomes).

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Men and women, aged between 45-75 years

Women postmenopausal: two or more years after last menstruation

Waist circumference of ≥102 cm for men and ≥88 cm for women (abdominal obesity)

Fasting plasma glucose < 7.0 mmol/L

Disqualifiers

Allergy or intolerance to walnuts

Left-handedness (effects on brain function differ between left- and right-handed adults)

Current smoker, or smoking cessation < 12 months

Diabetic patients

Trial design

Design model

Parallel

Treatments tested in this trial

  • Walnuts

    Dietary supplement

    24-week consumption of 50 g/day of walnuts as part of a healthy diet according to the Dutch dietary guidelines

Treatment groups

55 Participants
are divided into 2 treatment groups
Group A: WalnutExperimental treatment 1 intervention
Group B: ControlNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Cerebral blood flow (CBF) prior to and after application of intranasal insulin

CBF will be non-invasively measured using the gold-standard methodology pseudo-continuous arterial spin labeling magnetic resonance imaging (pCASL MRI)

Time frame
From enrollment to the end of treatment at 24 weeks

Secondary outcomes

1

Bloodoxygen level-dependent (BOLD) functional MRI (fMRI) activity to measure appetite-related brain reward activity

BOLD fMRI activity will be measured before and while participants watch food pictures

Time frame
From enrollment to the end of treatment at 24 weeks
2

Cognitive performance

Cognitive performance measurement of the following cognitive domains: memory, executive function and psychomotor speed. Measurements will be performed using the Cambridge Neuropsychological Test Automated Battery (CANTAB).

Time frame
From enrollment to the end of treatment at 24 weeks.

Other outcomes

1

Endothelial function - Flow Mediated Dilation

Changes in diameter during Flow-Mediated Dilation (FMD) of the brachial artery will be assessed using ultrasound.

Time frame
From enrollment to the end of treatment at 24 weeks.
2

Endothelial function - Carotid Artery Reactivity

Changes in diameter during Carotid Artery Reactivity (CAR) in response to a cold stressor will be assessed using ultrasound

Time frame
From enrollment to the end of treatment at 24 weeks.
3

Markers related to arterial stiffness

Pulse Wave Analysis (PWA) of the radial artery and Femoral-to-carotid Pulse Wave Velocity (PWV) in m/s will be measured with a tonometer using Sphygomocor

Time frame
From enrollment to the end of the intervention at 24 weeks.
4

Peripheral insulin sensitivity

7-point oral glucose tolerance test (OGTT) to determine insulin sensitivity based on insulin and glucose concentrations, Matsuda index and 2h glucose tolerance (2h glucose concentrations)

Time frame
From enrollment to the end of the intervention at 24 weeks.

Sponsors and contacts

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Maastricht University Medical Center

Lead sponsor

California Walnut Commission

Collaborator