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Completed

NCT Number: NCT05408338

Acute Effects of Added Sugar Intake on Cerebrovascular Function and Brain Integrity

This study will focus on acute effects of added sugars on brain health in a specific age group (30-64 years old). We will provide participants two meals (one meal containing 16 g of added sugars and the other containing 61 g of added sugars) and examine blood vessel function and brain structure using a MRI.

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Key information

Age range

30 year–64 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Delaware

Newark, Delaware, 19713, United States

About this study

Cardiometabolic risk factors are strongly influenced by lifestyle-related environmental factors including the consumption of an unhealthy Western diet (WD). Added sugars (i.e., caloric sweeteners added to food during processing or preparation) have become a major component of the WD that are especially high in added fructose. Americans currently consume more calories from added sugars than is recommended by the American Heart Association (AHA), leading to an increased risk of cardiovascular disease (CVD), which in turn shares common risk factors with age-related memory loss and dementia. Whereas glucose is used as an immediate energy source or stored as glycogen, fructose is associated with the delayed production of triglycerides (TGs) and uric acid. Previous studies have shown that a single high-sugar meal can increase TGs in the blood 150-180 minutes after meal consumption. Increased blood TGs promote release of harmful substances that contribute to the reduction in blood vessel function and may also impact brain blood vessel function; however, these effects are not well established in humans. Our preliminary data has shown a positive association between high added sugars and plasma TG and uric acid concentration, which has been associated with reduced blood vessel function. However, the direct effects of acute added sugar intake on brain blood vessel function is currently unknown. We have also observed that high blood TGs are associated with reduced microstructural integrity of the hippocampus, a brain structure important for memory and other thinking abilities. Therefore, the purpose of this study is to establish a causal link between high added sugar consumption and reduced brain blood vessel function and microstructural integrity. We propose to examine the acute effects of high TGs and uric acid from a single high-sugar meal on brain blood vessel function and brain integrity. To test this hypothesis, we will conduct a randomized-controlled crossover trial of a high-sugar meal vs. a low-sugar meal. This project has the potential to identify future risk of dementia and other memory-related brain diseases caused from repetitive acute insults from high added sugar consumption and will help us inform the public to make better dietary choices.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Ability to provide informed consent;
  • Men and women within the ages of 30-64 years;
  • Habitual added sugar intake of <150 kcal/day for men and <100kcal/day for women;
  • No allergies/intolerance to ingredients in the study meal (e.g., nuts, gluten)

Exclusion criteria

  • Blood chemistries indicative of abnormal liver enzymes and renal function;
  • Abnormal blood chemistry marker that is +/-2.5x the upper or lower limit;
  • Chronic clinical diseases (e.g., coronary artery, peripheral artery, or cerebrovascular diseases, diabetes (type 1 and type 2), stages 5-6 chronic kidney disease, chronic obstructive pulmonary disease);
  • Major psychiatric disorder (e.g. schizophrenia, bipolar disorder, major depression within past two years);
  • Neurological or autoimmune conditions affecting cognition (e.g. Parkinson's disease, epilepsy, multiple sclerosis, head trauma with loss of consciousness greater than 30 min, large vessel infarct);
  • Current medication use likely to affect central nervous system functions (e.g. long active benzodiazepines) and lipid-lowering medications (e.g., statins)
  • Conditions which would contra-indicate MRI: implant of pacemakers or pacemaker wires; artificial heart valve; brain aneurysm surgery; middle ear implant; non-removable hearing aid or jewelry; braces; cataract surgery or lens implant; implanted mechanical or electrical device; foreign metallic objects in the body such as bullets, BBs, shrapnel, or metalwork fragments, claustrophobia;
  • Current smoking;
  • Pregnancy or breastfeeding

Treatment and study plan

Low Added Sugar Meal

Other

Consumption of a single 1,250 kcal meal containing 16 g of added sugars (5% of total energy)

High Added Sugar Meal

Other

Consumption of a single 1,250 kcal meal containing 61 g of added sugars (20% of total energy)

Primary outcomes

  1. Change from baseline in cerebrovascular reactivity at 3 hours post-consumption of each meal

    Time frame: Over 2 weeks, at baseline and 3 hours post-consumption of each meal (low and high added sugar), separated by a 1-week washout

    % change in total cerebral perfusion measured using pseudo-continuous arterial spin labeling in response to 3-minutes of hypercapnia (+9 mmHg increase in PETCO2)

  2. Change from baseline in hippocampal stiffness after 3 hours post-consumption of each meal

    Time frame: Over 2 weeks, at baseline and 3 hours post-consumption of each meal (low and high added sugar), separated by a 1-week washout

    Magnetic Resonance Elastography (MRE) of the brain to assess hippocampal viscoelastic properties while the head will be vibrated using the Resoundant acoustic driver system

  3. Change from baseline in hippocampal damping ratio at 3 hours post-consumption of each meal

    Time frame: Over 2 weeks, at baseline and 3 hours post-consumption of each meal (low and high added sugar), separated by a 1-week washout

    Magnetic Resonance Elastography (MRE) of the brain to assess hippocampal viscoelastic properties while the head will be vibrated using the Resoundant acoustic driver system

  4. Change from baseline in uric acid at 3 hours post-consumption of each meal

    Time frame: Over 2 weeks, at baseline and 3 hours post-consumption of each meal (low and high added sugar), separated by a 1-week washout

    Blood biomarker of uric acid (e.g. serum uric acid)

  5. Change from baseline in triglycerides at 3 hours post-consumption of each meal

    Time frame: Over 2 weeks, at baseline and 3 hours post-consumption of each meal (low and high added sugar), separated by a 1-week washout

    Blood biomarker of triglycerides (e.g. serum triglycerides)

  6. Change from baseline in oxidative stress at 3 hours post-consumption of each meal

    Time frame: Over 2 weeks, at baseline and 3 hours post-consumption of each meal (low and high added sugar), separated by a 1-week washout

    Blood biomarker of oxidative stress (e.g. superoxide)

Secondary outcomes

  1. Change from baseline in hippocampal cerebrovascular reactivity at 3 hours post-consumption of each meal

    Time frame: Over 2 weeks, at baseline and 3 hours post-consumption of each meal (low and high added sugar), separated by a 1-week washout

    % change in total cerebral perfusion measured using pseudo-continuous arterial spin labeling in response to 3-minutes of hypercapnia (+9 mmHg increase in PETCO2)

  2. Changes from baseline in resting cerebral blood flow at 3 hours post-consumption of each meal

    Time frame: Over 2 weeks, at baseline and 3 hours post-consumption of each meal (low and high added sugar), separated by a 1-week washout

    Total cerebral perfusion measured using pseudo-continuous arterial spin labeling

  3. Change from baseline in other lipid profile at 3 hours post-consumption of each meal

    Time frame: Over 2 weeks, at baseline and 3 hours post-consumption of each meal (low and high added sugar), separated by a 1-week washout

    Blood biomarkers of lipid profile (e.g. cholesterol, HDL, LDL, and VLDL)

  4. Change from baseline in blood pressure at 3 hours post-consumption of each meal

    Time frame: Over 2 weeks, at baseline and 3 hours post-consumption of each meal (low and high added sugar), separated by a 1-week washout

    Blood pressure measures at baseline and every half hour until post-consumption of meal

Sponsors and collaborators

Lead sponsor

University of Delaware

Other

Registry information

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Jun 7, 2022
Registry last updated
May 10, 2023

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

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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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