The Effects of Alcohol Consumption on Central Adiposity



Status:Recruiting
Conditions:Obesity Weight Loss, Psychiatric
Therapuetic Areas:Endocrinology, Psychiatry / Psychology
Healthy:No
Age Range:21 - 40
Updated:5/26/2018
Start Date:May 18, 2018
End Date:April 30, 2019
Contact:John W Apolzan, PhD
Email:john.apolzan@pbrc.edu
Phone:2257632827

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The Effects of Alcohol Consumption on Central Adiposity and Testosterone Following Weight Loss in Obese, Pre-menopausal Women

The objective of the proposed study is to enroll women with obesity that will undergo a
controlled, energy restricted feeding intervention to test the effects of chronic ethanol
consumption on adipose distribution and circulating testosterone during weight loss.

Alcohol (i.e. ethanol) is one of the most widely used recreational substances by humans and
is consumed regularly by much of the U.S. population. Despite the high prevalence of alcohol
intake, the metabolic health effects associated with use have not been firmly established.
There is a paucity of data from longitudinal studies in humans that examine the metabolic
response to routine alcohol consumption in a randomized controlled trial (RCT).

This is a novel pilot study to examine, for the first time, the effects of ethanol
consumption on fat distribution and testosterone during weight loss in a RCT. Findings from
this study would provide insight into an interesting and unanswered question -- does routine
alcohol intake exert unfavorable health effects despite the expected beneficial outcomes of
caloric restriction and weight loss? This research may provide new knowledge of the metabolic
outcomes resulting from alcohol intake and pathways that may be involved leading to potential
new therapeutic targets of treatment.

The objective of the proposed study is to enroll women with obesity that will undergo a
controlled, energy restricted feeding intervention to test the effects of chronic ethanol
consumption on adipose distribution and circulating testosterone during weight loss. Women
will be randomized to an ethanol-free control group or an ethanol-consuming group, and all
will consume 30% energy-restricted diets.

Inclusion Criteria:

- − Pre-menopausal women only

- 21-40 years of age

- BMI 30-50 kg/m2 (+/- 0.5 will be accepted)

- Must practice and be willing to continue to practice appropriate birth control
(defined as a method which results in a low failure rate, i.e., less than 1% per
year, when used consistently and correctly, such as double barrier methods [male
condom with spermicide, with or without cervical cap or diaphragm], implants,
intrauterine contraceptive devices, tubal ligation (surgically sterile),
abstinence, or in an established relationship with a vasectomized or same sex
partner) during the entire duration of the study

- Must be willing to adhere to all study procedures, including consumption of all
study foods and beverages and attendance at all study visits

- Must be willing to eat breakfast at PBRC every weekday morning

- Must be willing to consume alcohol

- Must be willing to abstain from alcohol for 8-weeks if randomized to non-alcohol
control group.

- Must be a daily, or almost daily drinker, defined as typically consuming at least
8 drinks per week, but no more than 4 per day

- Must be willing to undergo an overnight alcohol test (at home) of ethanol at the
proposed dose before enrollment in the study

- Must have access to a device that can be used for video monitoring of compliance
(i.e. Skype)

- Must be willing to have your blood stored for future research

Exclusion Criteria:

- − Non-drinkers of alcohol

- Habitual binge drinkers, as defined by the consumption of ≥ 4 standard drinks per
day or ≥ 28 drinks per week.

- Self-reported alcoholics or a history of alcoholism

- Have a 1st degree relative with alcoholism

- Any attendance or inpatient stay for alcohol or drug treatment

- Display any characteristics of current or future substance abuse disorders

- Presence of any psychiatric, behavioral, or medical disorder that, in the opinion
of the PIs, Co-I, or MI, may interfere with study participation, the ability to
adhere to the protocol, or has the potential for increased substance abuse

- Prescription medications that interact with alcohol intake

- Abnormal screening laboratory safety tests

- Smokers

- Diagnosis of Type 1 or 2 diabetes mellitus, cancer, or major organ disease

- Serious digestive disorders

- Conditions that affect metabolism or body weight (i.e. uncontrolled thyroid
conditions, bariatric surgery, pregnancy, breastfeeding)

- Partial and/or full hysterectomy

- Hormonal pharmaceutical contraceptives including oral contraception (birth
control pills), injectables (Depo-Provera), or the patch (Xulane)

- PCOS

- Use of medications that affect body weight or metabolism (i.e. atypical
antipsychotics, weight loss medications).

- Not willing to store biospecimens for future use
We found this trial at
1
site
6400 Perkins Rd
Baton Rouge, Louisiana 70808
(225) 763-2500
Phone: 225-763-2827
Pennington Biomedical Research Center Unlike other medical research facilities where science occurs in separate labs...
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mi
from
Baton Rouge, LA
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