Chronic Consumption of Vinegar on Visceral Adiposity in Overweight Adults (VAnish)

Pennington Biomedical Research Center

Status: Terminated

Conditions: Body Composition

Treatments: Dietary Supplement: Study Beverage Consumption

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT04706520

PBRC-2020-048

Details and patient eligibility

About

To assess, relative to a placebo, the effects of consuming 400 mL/day or 200 mL/day of a vinegar beverage providing either 1,500 mg/day of acetic acid (in two 200 mL doses daily) or 750 mg/day of acetic acid (in one 200 mL dose daily), respectively, for 12 weeks on VAT (MRI). Thus the 2 active comparator arms 400 mL and 200 mL of vinegar will be independently tested compared to placebo.

Full description

It has been reported that increased visceral adipose tissue (VAT) is associated with a range of metabolic abnormalities, including decreased glucose tolerance and insulin sensitivity, as well as adverse lipid profiles, all of which are risk factors for type 2 diabetes and CVD (WHO, 2008). In the European Union, a sustained reduction in abdominal fat, and in particular visceral fat, is considered a beneficial physiological effect for adults with adverse health effects associated with excess abdominal fat, including impaired glucose tolerance, dyslipidemia, and hypertension (EFSA, 2012).

This clinical trial is a randomized, double-blinded, placebo-controlled, parallel, single-center study involving a total of 60 male and female adults (aged 18 to 60 years, inclusive) who are overweight (BMI between 25.0 to ˂30.0 kg/m2) and have abdominal obesity (waist circumference >102 cm for males, >88 cm for females) (ATP III, 2001). Each subject's duration of participation will be a total of ~14 weeks, including a ~2-week screening visit and a ~12-week randomized placebo-controlled double-blinded supplementation period.

On the first day of the ~2-week screening period (~Day -14), subjects will be screened according to the study inclusion and exclusion criteria. Subjects meeting all of the inclusion criteria and none of the exclusion criteria will be invited to return to the clinic for a second screening visit (~Day -7). During this second screening visit, subjects will be instructed on how to use the Fitbit (accelerometer) and on how to properly complete the food intake diary. Subjects will be instructed not to alter their dietary intakes or their physical activity levels during the subsequent week, and to record the information as accurately as possible. Participants will be asked to record at least 3 days of physical activity and dietary measurements that includes at least 1 weekend day. Subjects will then be instructed to return to the clinic ~1 week later for the collection of baseline measures (Day 0).

Following the collection of baseline measures on Day 0, subjects will be randomized to the placebo or one of the vinegar groups. Each group will consist of 20 subjects. Randomization will be adaptive according to sex and age; subjects will be asked to return to the clinic twice, once ~11 weeks after the baseline visit to obtain food intake diary, accelerometer, and stool collection materials, and again, ~12 weeks after the baseline visit (i.e., 12 weeks after the baseline visit). Each subject will be required to make a total of 4 visits to the clinical research site (i.e., Days -14, -7, 0, and 84). The entire duration of the clinical study is expected to be approximately 52 weeks from subject enrollment to study closeout.

Enrollment: 24 patients

Sex: All

Ages: 18 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Males and females between 18 and 60 years of age (inclusive) of any ethnicity, free of medications except for oral contraceptives (see inclusion criterion 8).

2. Subjects are overweight at screening (Visit 1, Day -14), as defined by a BMI of between 25.0 to ˂30.0 kg/m2, inclusive.

3. Subjects have abdominal obesity at screening (Visit 1, Day -14), as defined by a waist circumference of >102 cm for males or >88 cm for females (ATP III, 2001).

4. Physical examination and vital signs are normal, or deemed abnormal but clinically insignificant by the Principle and/or Medical Investigator.

5. Clinical laboratory evaluations (including but not limited to clinical chemistry [fasted at least 8 hours], including creatine phosphokinase (CPK)], amylase, lipid profile, thyroid stimulating hormone (TSH), free thyroxine (T4), cortisol) complete blood count (CBC), are within the reference ranges for the central laboratory, unless deemed not clinically significant by the Investigator.

6. Males who are sterile or agree to use an approved method of contraception, with an approved method of contraception considered a barrier method (diaphragm, cervical cap, or condom) plus a contraceptive jelly (spermicidal foam, gel, film, cream, or suppository). If the female sexual partner of the male is using an approved form of contraception (see inclusion criterion 8), the male is not required to be sterile or, if not sterile, to use an approved form of contraception.

7. Female subjects who are postmenopausal (absence of menses for 1 year or more), women who are surgically sterilized, or women of child-bearing potential (WOCBP) who are nonlactating and have been using an effective form of birth control for a minimum of 6 months prior to screening and agree to continue using the effective form of birth control during the study and for 30 days after the treatment period [effective forms of birth control include oral pills with a concentration of at least 50 μg of the estrogenic component of a biphasic or triphasic pill; transdermal, injectable, or implantable contraceptive; intrauterine device; or double-barrier method (e.g., diaphragm and condom). Abstinence is not considered an acceptable form of birth control.] WOCBP who are using low dose oral birth control must also use a barrier method of contraception for the duration of the study.

8. Subjects who, during the investigative period, are willing to:

   1. Consume the prescribed amount of vinegar beverage;
   2. Wear the accelerometer (Fitbit);
   3. Complete food intake diary as required.
   4. Collect stool sample
   5. Willing to archive blood and stool samples

9. Subjects who are capable of giving informed consent and complying with all study procedures/ requirements.

Exclusion criteria

1. Subjects who, in the past 6 months, have dieted or have used any supplement/medication intended to affect body weight or suppress appetite
2. Subjects with a history of an eating disorder in the last 5 years.
3. Subjects who have had or are planning to have bypass surgery, stomach banding surgery, or any other surgical procedure(s), including those of a cosmetic nature, that attempt to aid/promote weight loss or alter body composition.
4. Subjects with Type I or Type 2 diabetes mellitus.
5. Subjects with endocrine disease (thyroid dysfunction defined by serum levels of T4, TSH or a past diagnosis of Cushing syndrome).
6. Subjects who have a history or presence of significant pulmonary, hepatic, renal, hematological, gastrointestinal, endocrine, immunological (e.g., HIV/AIDS), dermatologic, urological, neurological, psychiatric, or cardiovascular disease or disorder.
7. Subjects with any implanted electric device (such as a cardiac defibrillator) or other medical device that would allow for them to perform an MRI.
8. Women with polycystic ovarian syndrome.
9. Women who began taking oral contraceptives or hormone replacement therapy recently, within the last 6 months.
10. Women who plan to become pregnant during the study or were pregnant or nursing within the past year.
11. Subjects who have recently undergone barium tests/exams (within 7 days), or who have had a nuclear medicine scan or injection with an x-ray dye (within 3 days).
12. Subjects who have a history or presence of alcoholism or drug abuse within the previous 2 years and/or a positive urine drug screen at screening.
13. Subjects who have quit smoking in the last 6 months or who plan on quitting/altering smoking habits during their participation in this clinical trial.
14. Subjects who donated 1 pint or more of blood or blood products within 56 days prior to the study, and/or had a plasma donation within 7 days prior to the study or who plan to donate blood or blood products during their participation in this clinical trial.
15. Subjects with poor peripheral venous access that would preclude blood collection.
16. Subjects who are currently participating or plan to participate in any other investigational trial in which receipt of an investigational product will occur.
17. Subject who resides in the same household as another subject already participating in the study.
18. Subjects who have any condition that would make them, in the opinion of the Investigator, unsuitable for the study.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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24 participants in 3 patient groups, including a placebo group

Group 1: Vinegar

Experimental group

Description:

Participants will consume 400 mL/day vinegar beverage providing 1,500 mg/day acetic acid \[200 mL vinegar beverage, twice per day (prior to breakfast and dinner)\] for 12 weeks.

Treatment:

Dietary Supplement: Study Beverage Consumption

Group 2: Vinegar/Placebo Combination

Experimental group

Description:

Participants will consume 200 mL/day vinegar beverage and 200 mL/day placebo beverage providing 1,200 mg/day lactate \[200 mL placebo beverage 1x/day\] and 750 mg/day acetic acid \[200 mL vinegar beverage 1x/day\] (prior to breakfast and dinner) for 12 weeks.

Treatment:

Dietary Supplement: Study Beverage Consumption

Group 3: Placebo

Placebo Comparator group

Description:

Participants will consume 400 mL/day placebo beverage containing 1,250 mg/day lactate \[200 mL placebo beverage, and 200 mL placebo beverage (prior to breakfast and dinner) for 12 weeks.

Treatment:

Dietary Supplement: Study Beverage Consumption