The Physiological Responses and Adaptation of Brown Adipose Tissue to Chronic Treatment With Beta3-Adrenergic Receptor Agonists
Status and phase
Conditions
Treatments
Details and patient eligibility
About
Background:
Brown adipose tissue (BAT) is a type of fat in the body. It may prevent weight gain, improve insulin sensitivity, and reduce fatty liver. Researchers want to see if BAT helps the body burn energy.
Objective:
To learn more about how BAT works to burn energy.
Eligibility:
People ages 18-40 with a body mass index between 18 and 40
Design:
Participants will be screened with:
Medical history
Physical exam
Blood, urine, and heart tests
Dietitian interview
Participants will have an overnight baseline visit. This includes:
Repeats of screening tests
Exercise test
Scans. For one scan, a radioactive substance is injected into the arm.
FSIVGIT: An IV is inserted into veins in the right and left arms. Glucose and insulin are injected in one arm. Blood glucose and insulin levels are measured from the other.
Metabolic suite: Participants stay 18 19 hours in a room that measures their metabolic rate. Monitors on the body measure heart rate, movement, and temperature.
Optional fat biopsy: A small piece of tissue is removed with a needle.
Participants will take 2-4 pills daily for 4 weeks. All women will take the drug mirabegron. Men will be randomly get either the drug or a placebo.
All participants will have a visit after 2 weeks of the pills. They will repeat the screening tests.
Participants will have an overnight visit 2 weeks later. They will repeat the baseline tests.
Participants will keep food and medication diaries.
Participants will have a follow-up visit 2 weeks after stopping the pills. This includes heart tests.
Full description
Study Description:
This study is intended to address questions about human brown adipose tissue (BAT). Specifically, we plan to visualize BAT activity with acute cold exposure during drug naive and drug experienced visits. Thus, we will be studying changes in BAT activity from a chronic dosage of mirabegron.
Objectives:
Cohort 1: To measure changes in BAT metabolic activity in women seen after four weeks of daily treatment with the beta3-AR agonist mirabegron.
Cohort 2: To measure changes in BAT metabolic activity in men seen after four weeks of daily treatment with 200 mg of the beta3-AR agonist mirabegron compared to placebo
Cohort 3: To compare the changes in insulin sensitivity in each woman after four weeks of daily treatment with 100 mg of the beta3-AR agonist mirabegron with the changes in insulin sensitivity in each woman after four weeks of daily treatment with placebo
Primary Endpoints:
Cohort 1: The change in detectable cold exposure induced BAT metabolic activity in women, as visualized by F-FDG PET/CT.
Cohort 2: The change in detectable cold exposure induced BAT metabolic activity, as visualized by 18F-FDG PET/CT
Cohort 3: The change in glucose infusion rate, as measured by the hyperinsulinemic euglycemic clamp, in women after four weeks of daily treatment with 100 mg of the beta3-AR agonist mirabegron with the change in glucose infusion rate after four weeks of daily treatment with placebo
Secondary Endpoints:
- To identify changes in metabolic health arising from BAT activation and/or prolonged treatment with regular 100 mg (females) or 200mg (men) doses of mirabegron.
- To determine if there is an interaction between (a) BMI and (b) age with respect to the capacity to increase BAT metabolic activity.
- To describe the structural and physiological changes in the adipose tissue depots, including cell lineage, size, and inflammation.
- To assess whether there are improvements in the liver, including reduced stiffness and quantity of hepatic fat.
Enrollment
Sex
Ages
Volunteers
Inclusion and exclusion criteria
- INCLUSION CRITERIA
In order to be eligible to participate in this study, an individual must meet all of the following criteria:
Cohort 1: (complete)
- Female
- Age 18-40 years
- BMI 18.00-40.0 kg/m^2
- Able to understand the research and willing to sign a written informed consent document
Cohort 2: (complete)
- Male
- Age 18-40 years
- BMI 18.00-40.0 kg/m^2
- Able to understand the research and willing to sign a written informed consent document
Cohort 3:
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Female
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Age 18-40 years
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BMI 25.0-50.0 kg/m^2 or BMI > 18.5 kg/m^2 with PCOS diagnosis
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Diagnosis of PCOS based on NIH Criteria; defined by the presence of both clinical and/or biochemical signs of hyperandrogenism and oligo- or chronic anovulation.
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Women of childbearing potential must agree to use a highly effective method of birth control, confirmed by the Investigator, for at least 3 months prior to the first study visit and continuing throughout the study duration.
a. Highly effective methods of birth control include:
i. Combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation: oral, intravaginal, or transdermal
ii. Progestogen-only hormonal contraception associated with inhibition of ovulation: oral, injectable, or implantable
iii. Intrauterine device
iv. Intrauterine hormone-releasing system
v. Bilateral tubal occlusion
vi. Sexual abstinence, i.e., refraining from heterosexual intercourse (the reliability of sexual abstinence needs to be evaluated in relation to the duration of the clinical study and the preferred and usual lifestyle of the participant)
vii. Vasectomized sexual partner (provided that partner is the sole sexual partner of the study participant and that the vasectomized partner has received medical assessment of the surgical success)
b. Women not of childbearing potential are defined as women who are either permanently sterilized (hysterectomy, bilateral oophorectomy, or bilateral salpingectomy) or who are postmenopausal. Women will be considered postmenopausal if they have been amenorrhoeic for >=12 months prior to the planned date of enrollment without an alternative medical cause.
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Insulin resistance defined by either
- HOMA-IR score > 5.9 OR
- HOMA-IR score > 2.8 and <5.9, with HDL <51 mg/dL OR
- Fasting Insulin > 10.6 microU/mL
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Able to understand the research and willing to sign a written informed consent document
EXCLUSION CRITERIA
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Hypersensitivity and associated allergic reactions to mirabegron (or similar drug substances or components)
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Abnormal bladder function, diagnosis of bladder outlet obstruction, urinary incontinence, urgency, and urinary frequency or use of antimuscarinic medication to treat overactive bladder (OAB)
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Type 1 or Type 2 Diabetes mellitus, fasting serum glucose >125 mg/dL, and/or an HbA1c test >6.5%
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Hypertension, defined as blood pressure (Bullet)140/90 mmHg, based on WHO guidelines (https://www.who.int/news-room/fact-sheets/detail/hypertension)
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Hypo- or hyper-thyroid disease (TSH >5.0, <0.4 miU/L) that is controlled for less than one year
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Anemia, defined by hemoglobin < 11.3 g/dL (females) or < 13.8 g/dL (males); sickle cell anemia or other blood disorders; and/or wound healing problems
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Cardiovascular disease, cardiac arrhythmias, orthostasis, unstable vasomotor system, or renal impairment
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A clinically significant abnormal ECG and/or QTc interval above normal
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Elevated liver enzymes with probable or diagnosed liver disease (other than fatty liver disease)
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Psychological conditions such as claustrophobia, untreated clinical depression or anxiety, untreated bipolar disorders, or forms of mental incapacity that would be incompatible with safe and successful participation in this study
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Recent history in last 4 weeks of any local or systemic infectious disease with fever or requiring antibiotics
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Self-reported intolerance of cold that would prevent the individual from spending several hours in a chilled room with a cooling vest
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Current use of any drugs known to:
- have major drug-drug interactions with mirabegron
- Prolong QT interval
- Alter glucose metabolism or cause insulin resistance (in last six months)
- Treat diabetes mellitus
- Treat hypertension
- Be drugs of abuse
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Self-reported weight loss or weight gain > 5% in the preceding 6 months.
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Pregnancy, childbirth within the last year, or breastfeeding in the past 12 months
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Individuals who spend >70% of daily hours outdoors since the exposure to varied environmental temperatures will potentially impact the ability to influence and measure BAT activity.
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Addiction to alcohol or substances of abuse within the last 5 years
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Self-reported current alcohol consumption of more than 2 servings of alcohol per day
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Self-reported current use of nicotine and/or tobacco products
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Has participated in a clinical trial with an investigational or marketed drug within 2 months
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Have had previous radiation exposure (X-rays, PET scans, etc.) within the last year or anticipate radiation exposure in the upcoming year - clinical and/or research - that would exceed research limits
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Donated blood within last 2 months
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Unwilling or unable to eat metabolic meals, as determined by dietitian consult.
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Any other circumstances or criteria that would preclude safe participation in the study in the clinical judgment of the investigator
Trial design
Primary purpose
Allocation
Interventional model
Masking
100 participants in 5 patient groups, including a placebo group
Trial contacts and locations
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Central trial contact
Ashley M Schmitz, C.R.N.P.; Aaron M Cypess, M.D.
Data sourced from clinicaltrials.gov
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