Effect of Equol Supplementation on Arterial Stiffness and Cognition in Healthy Volunteers (ACE)

Akira Sekikawa

Status and phase

Active, not recruiting

Phase 2

Conditions

Cognitive Decline

White Matter Lesions

Arterial Stiffness

Treatments

Drug: S-equol

Drug: Placebo

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT05741060

STUDY22010165

R01AG074971 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The ACE Trial, funded by the National Institute on Ageing/National Institutes of Health (NIH), is a multicenter clinical trial. The ACE Trial will determine if taking the dietary supplement Equol could slow the progression of stiffening of the arteries, small blood vessel disease in the brain and memory decline. Equol is a soy-based supplement that has plant estrogen-like compounds in it.

Equol is a metabolite of soy isoflavone. Our studies in Japan and other studies suggest that Equol may slow mechanisms related to memory decline. No previous studies in the United States have tested the effect of Equol on these mechanisms or memory decline. Supplementation of Equol in the ACE Trial is approved by the Food and Drug Administration (FDA).

Researchers at the University of Pittsburgh, Pittsburgh, Pennsylvania, Wake Forest University, Winston-Salem, North Carolina, and Emory University, Atlanta, Georgia, are recruiting participants.

The ACE Trial will ask participants to complete 7 clinic visits over a two-year period. The participants are asked to take Equol tablets daily for 24 months. Clinic procedures include Pulse Wave Velocity (to measure arterial stiffness), Magnetic Resonance Imaging (MRI) of the brain and tests of awareness and thinking.

Full description

The ACE trial is an early-stage multi-center randomized controlled trial (RCT) designed to test the effect of a 24-month intervention of 10 mg/day equol supplementation on arterial stiffness, white matter lesions (WMLs) in the brain and cognitive decline among 400 individuals aged 65 and 85 without dementia. Recent studies in Japan reported that a diet high in soy and soy isoflavones is inversely associated with incident cognitive impairment and dementia. The Women's Isoflavone Soy Health (WISH) in the US, an RCT of soy isoflavones, however, showed no significant effect on cognition. We posit that the discrepant result is due to the difference in equol-producing capability. Equol, a metabolite of soy isoflavone daidzein transformed by the gut microbiome, is the most bioactive among all soy isoflavones and their metabolites. 50-70% of Japanese convert daidzein to equol in contrast to 20-30% of Americans. Arterial stiffness, a significant predictor of cognitive decline, is significantly improved in a short-duration RCT of 10 mg/day equol supplementation in middle-aged subjects. WMLs are a risk factor for age-related cognitive decline and dementia. We reported a longitudinal association of equol-producing status with WML% (WML volume normalized to total brain volume) in cognitively normal elderly in Japan. The subgroup analysis of WISH showed that equol producers had better cognition than the control group, suggesting that equol may slow cognitive decline. No previous study has tested the effect of equol supplementation on arterial stiffness, WMLs or cognitive decline in older adults.

Enrollment

369 patients

Sex

All

Ages

65 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Men and women age between 65 and 85 at entry of European Americans or African Americans

Inclusion criteria via screening visit:

Individuals who are able to provide informed consent
Individuals who are willing to be randomized to the intervention or placebo group

Exclusion criteria

Exclusion criteria via initial screening by phone

Individuals who are regularly taking isoflavone supplements or eat soy product ≥ 2 times a week (by specific questionnaire)
Individuals who do not agree to maintain isoflavone supplements or soy product intake described above during the study period.
Individuals who have allergy or intolerance to soy isoflavones.
Individuals whose score for the Telephone Interview for Cognitive Status is 22 and below.
Individuals with stroke, neurological disorders, bipolar disease whether or not under medical treatment, cancer treatment in the past 6 months, head trauma or other condition which is not appropriate for the study (e.g., contraindication to magnetic resonance imaging (MRI)).
Individuals with untreated depression
Individuals with atrial fibrillation
Individuals with heart failure
Individuals with heart attack or coronary intervention in the past 6 months
Individuals with carotid endarterectomy or peripheral artery disease
Individuals currently undergoing treatment for pulmonary embolism or deep vein thrombosis
Individuals with aortic (abdominal, thoracic) aneurysm
Individuals with inflammatory bowel diseases
Individuals currently undergoing hemodialysis
Women with a past or family history of breast cancer.*1
Women on estrogen replacement therapy
Individuals unable to lay supine for 30-60 minutes
Individuals with weight ≥300 lbs
Individuals who are planning to move out of the area in the next 2 years
Individuals who participated in another clinical trial in the past 3 months

Exclusion criteria via screening visit

Individuals with Quick Dementia Rating System (QDRS) score ≥ 6.0
Individuals who are regularly taking isoflavone supplements or eat soy product ≥ 2 times a week (by specific questionnaire)
Individuals who do not agree to maintain isoflavone supplements or soy product intake described above during the study period.
Individuals who have allergy or intolerance to soy isoflavones.
Blood pressure (BP) - systolic BP ≥ 180 mmHg or diastolic BP ≥ 110 mmHg
Heart rate ≥110 or ≤40
Hemoglobin <10 g/dL
HbA1c ≥ 7.5%
Blood creatinine > 2.0 mg/dL
Liver function tests > 2 X upper limit of normal
Abnormal thyroid function (Thyroid Stimulating Hormone)
Vitamin B12 levels ≤ 210 pg/mL
Hematocrit <30%
White blood cell count <3,000 or >15,000
Platelet count <100,000 or >600,000
Urinary protein ≥ + by dipstick
Any condition or therapy which, in the opinion of the investigator, might pose a risk to the participant or make participation in the study not in the participant's best interest

In addition, individuals with the following condition will be excluded because these conditions do not allow subjects to undergo examinations the investigators proposed in the project:

Those who are contraindicated for 3 Tesla (3T) structural brain magnetic resonance imaging (MRI) such as pacemakers.
Atrial fibrillation because pulse wave velocity is not accurately measured.
Hearing impairment which interferes with cognitive testing
Vision impairment which interferes with cognitive testing

Exclusion criteria at structural brain MRI Any other conditions which, in the opinion of the investigator, might pose a risk to the participant or make participation in the study not in the participant's best interest

*1 Few studies have investigated the association of equol, a metabolite of soy isoflavone daidzein, with breast cancer. These studies reported no significant association of serum or urine equol with the risk of breast cancer. Dietary intake of soy and soy isoflavones is generally considered to have benefits for menopausal symptoms, cardiovascular health, bone health, and cancers of the breast and prostate. Observational studies show that soy consumption is associated with a reduced risk of many cancers including breast cancer. Moreover, a prospective cohort study of 6,000+ North American women with breast cancer showed that dietary intake of soy and isoflavones was associated with reduced all-cause mortality. However, there is little evidence to support that the use of supplements containing soy isoflavones or soy protein powder to reduce cancer risk. A recent large prospective cohort study in France reported that supplementation of soy isoflavones increased the risk of estrogen receptor-negative breast cancer, especially among women who had a history of breast cancer in first-degree relatives.

Exclusion criteria at the baseline visit

The investigators recruit subjects without dementia. Thus, at the initial screening by phone, the investigators exclude individuals whose score for the Telephone Interview for Cognitive Status is 22 and below. Then, at the screening visit, investigators will exclude individuals with a Quick Dementia Rating System score ≥ 6.0.