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NCT Number: NCT07218653

Human Cerebrovascular Blood Flow and Sex Differences in Metabolic Syndrome

This study tests the hypothesis that Metabolic Syndrome (MetSyn) decreases cerebral blood flow (CBF) more in females than males due in part to the sex-specific loss of COX vasodilation. Male and female participants will be enrolled in two groups: Healthy Controls versus participants with MetSyn.

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

University of Wisconsin

Madison, Wisconsin, 53706, United States

About this study

The central hypothesis is that MetSyn decreases CBF more in females than males due in part to the sex-specific loss of COX vasodilation. This hypothesis is based on extensive preliminary data demonstrating MetSyn induces: 1) 3-fold larger reductions in CBF in females that abolish sex differences, 2) region-specific CBF reduction patterns, and 3) a greater loss of COX-mediated vasodilation in females.

This hypothesis is tested via three Specific Aims:

  • Aim 1: Determine the extent of sex differences in MetSyn-driven CBF reductions. The investigators hypothesize females with MetSyn will demonstrate larger decrements in global, grey matter and white matter CBF versus males.
  • Aim 2: Determine the sex-by-region interactions of MetSyn reductions in CBF. The investigators hypothesize females will demonstrate larger regional CBF declines-particularly in regions known to be impacted very early in brain pathologies and/or specifically impaired by insulin resistance.
  • Aim 3: Determine the role of COX signaling in mediating CBF changes in MetSyn. The investigators hypothesize COX vasodilation is reduced more in females than males with MetSyn.

All consented participants will conduct a screening visit with a blood panel to identify control vs MetSyn eligibility.

Once eligible, participants complete three laboratory visits (each lasting about 2 hours):

  • Exercise Visit: VO2 Max, DEXA for adiposity quantification, NIH Toolbox to assess neurocognitive function
  • MRI Visit 1: blinded to either Placebo or Indomethacin
  • MRI Visit 2: blinded to either Placebo or Indomethacin

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

(Healthy Controls):

  • 18-45 years old
  • Normal fasting values for blood glucose (less than 100 g/dl)
  • Normal values for lipids (LDL cholesterol less than 130 mg/dl, triglycerides less than 150 mg/dl) and HDL (men greater than 40, women greater than 50 mg/dl)
  • Women must have a predictable menstrual cycle. Females will be studied on cycle days 1-7 to minimize sex hormone differences and their potential confounding effects on vascular outcomes. Oral contraceptives are allowed, and women will be studied during their placebo phase.

Inclusion criteria

(Participants with Metabolic Syndrome):

  • 18-45 years old
  • Meet at least 3 of the 5 ATP MetSyn criteria. These are:
  • Waist circumference greater than 102 cm (males) or 82 cm (females)
  • Triglycerides greater than 150 mg/dL
  • HDL cholesterol less than 40 mg/dL (males) or 50 mg/dL (females)
  • Blood pressure greater than or equal to 130/85 mmHg
  • Fasting plasma glucose greater than 110 mg/dL

Exclusion criteria

(Healthy Controls):

  • Body Mass Index (BMI) greater than or equal to 25 kg/m2
  • Blood pressure over 130/80 mmHg
  • Meeting any of the 5 MetSyn criteria listed above.

Exclusion criteria

(all participants):

  • Current smoker, defined as more than 5 cigarettes over past 30 days
  • Current diagnosis or history of:
  • peripheral vascular disease
  • hepatic disease
  • renal disease
  • lung disease
  • gastrointestinal disorders/bleeding
  • hematologic disease
  • stroke
  • myocardial infarction
  • coronary heart disease
  • congestive heart failure
  • heart surgery
  • sleep apnea
  • autoimmune diseases
  • HIV
  • traumatic brain injury, concussion, stroke, or seizures
  • Asthma
  • Polycystic ovarian syndrome
  • Type II diabetes
  • Currently pregnant or breastfeeding
  • Current musculoskeletal injury
  • Medication use known to influence cardiovascular function, other than contraceptive hormones. Broadly, the classes of drugs relate to treating blood pressure, diabetes, cholesterol.
  • Claustrophobia
  • Lactose intolerance
  • Magnesium-restricted diet

Treatment and study plan

Indomethacin

Drug

Indomethacin is a nonsteroidal anti-inflammatory. It prevents the production of prostaglandins, endogenous signaling molecules known to cause symptoms from inflammation.

Indomethacin (1.5 mg/kg) will be taken orally prior to one MRI study visit.

Other names: Indo

Placebo

Drug

Participants will be screened for lactose intolerance. Total dosing will be calculated to match the mg needed for the indomethacin study visit.

Other names: Lactose

MRI

Diagnostic Test

CBF testing will be performed on 3T MRI scanners (GE Healthcare)

Other names: Magnetic Resonance Imaging

Primary outcomes

  1. Cerebral Blood Flow

    Time frame: data collected over 2 study visits that must be completed within 6 months

    Data collected via MRI under one of 2 conditions: placebo or indomethacin.

Secondary outcomes

  1. Cardiorespiratory Fitness: VO2 max

    Time frame: data collected at one study visit (must be completed within 6 months)

    Graded exercise test to assess maximal aerobic capacity, reported as VO2 max (milliliters of oxygen consumed per kilogram of body weight per minute)

  2. Body Fat Mass

    Time frame: data collected at one study visit (must be completed within 6 months)

    Dual-energy x-ray absorptiometry (DEXA) to measure fat mass.

  3. Cognitive Testing: Flanker Inhibitory Control and Attention

    Time frame: data collected at one study visit (must be completed within 6 months)

    NIH Toolbox to assess neurocognitive function. The Flanker test is a measure of executive function and is scored using a T-score where 100 is the average, higher scores indicate better performance.

  4. Cognitive Testing: Pattern Comparison Processing Speed Test

    Time frame: data collected at one study visit (must be completed within 6 months)

    NIH Toolbox to assess neurocognitive function. The Pattern Comparison Processing Speed Test measures how many correct responses the participant has within 90 seconds. There is a maximum of 130 items.

  5. Cognitive Testing: List Sorting Working Memory Test

    Time frame: data collected at one study visit (must be completed within 6 months)

    NIH Toolbox to assess neurocognitive function. The List Sorting Working Memory Test is a measure of recall and sorting. Participants scores reflect the number of items recalled and appropriately sorted up to 28 items maximum.

  6. Cognitive Testing: Dimensional Change Card Sort Test

    Time frame: data collected at one study visit (must be completed within 6 months)

    NIH Toolbox to assess neurocognitive function. The Dimensional Change Card Sort Test measures accuracy: the number of accurate responses, up to a maximum of 40.

  7. Cognitive Testing: Picture Vocabulary Test

    Time frame: data collected at one study visit (must be completed within 6 months)

    NIH Toolbox to assess neurocognitive function. The Picture Vocabulary Test has the participant hear a word and then pick from one of four pictures that best represents the word. It is scored using a T-score where 100 is the average, higher scores indicate better performance.

Study contacts

Contact information is provided by the study sponsor or research team.

Shawn Bolin, MS

CONTACT

[email protected]

608-263-6308

Sponsors and collaborators

Lead sponsor

University of Wisconsin, Madison

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

Registry information

Important dates

Study start
2026
Primary completion
2031
Study completion
2031
First posted
Oct 20, 2025
Registry last updated
Jul 27, 2026

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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