Deciphering a Novel and Unique Brown Adipose Tissue Depot in Women

NCT ID: NCT06426082

Last Updated: 2024-05-23

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-11-01
• Study Completion Date: 2026-08-31

Brief Summary

Type of Study: Clinical Trial

Goal: The goal of this clinical trial is to investigate specific brown and beige fat cells in the dorsocervical area of young, lean adult women.

Participant Population/Health Conditions: The study will involve 40 young, lean adult women.

Main Questions: The main questions this study aims to answer are:

• Are there active brown or beige adipocytes in the subcutaneous fat of the dorsocervical area (i.e., iBAT)?
• What is the secretory function of these adipocytes?
• How do traditional interventions like cold exposure, as well as new approaches like Beta-2 agonist stimulation and exercise, affect the thermogenesis of these fat cells at the cellular and molecular levels?

Participants Will:

Be randomized into one of four groups: thermoneutral exposure, cold exposure, aerobic exercise, or Beta-2 agonist treatment.

Follow their assigned regimen for 4 weeks. Provide tissue samples from the dorsocervical area and abdomen before and after the 4-week intervention.

Undergo analysis of these samples using advanced techniques to understand the presence and activity of brown and beige fat cells.

Comparison Group: Researchers will compare the effects of different interventions (thermoneutral exposure, cold exposure, aerobic exercise, Beta-2 agonist treatment) on the presence and thermogenesis of brown and beige fat cells in the dorsocervical area.

Detailed Description

Cardiometabolic diseases affect almost 50% of the population in the Western World. While lifestyle plus pharmacological interventions may provide short-term benefits, more research is needed to understand the long-term effectiveness and underlying molecular mechanisms. Brown adipose tissue (BAT) is a thermogenic tissue that combusts large amounts of glucose and lipids to generate heat and secretes signalling molecules known as 'batokines' that can influence cardiometabolic health. Previous research has shown that BAT is active in adults, primarily in the supraclavicular region, as demonstrated by the uptake of 18F-Fluorodeoxyglucose. Recently, it has been demonstrated that a rare subpopulation of brown adipocytes increases their abundance at higher temperatures and can regulate the thermogenesis of neighbouring adipocytes. Thus, it is plausible that classical (e.g., cold exposure) and novel interventions (i.e., Beta-2 stimulation and exercise) that can activate BAT, would induce a remodelling in the brown/beige subpopulation adipocytes that govern whole tissue thermogenesis. These unstudied changes in human BAT physiology could potentially explain how BAT activation could enhance cardiometabolic health. However, despite over a decade of research, our understanding of the role of BAT in human physiology in humans is limited. This lack of knowledge may be mainly explained because i) obtaining biological samples of human BAT is very difficult and ii) the seasonal variation strongly influences the current gold standard (PET-CT scan). Given the pilot data found in this proposal, young, lean adult women may have a novel and undescribed thermogenic active BAT depot at the dorsocervical area (i.e., interscapular BAT=iBAT).

Based on that, the main hypothesis is that there are brown and/or beige adipocytes present within the subcutaneous adipose tissue of the dorsocervical area (i.e., iBAT) that have a unique composition of adipocyte subpopulations and specific secretory functions. Additionally, the specific subpopulations of brown and/or beige adipocytes related to thermogenesis in iBAT can be increased through exposure to cold temperatures, Beta-2 agonist stimulation, and exercise in young, lean women.

Thus, the main objective of this study is to investigate whether the subcutaneous fat in the dorsocervical area contains active brown and/or beige adipocytes (i.e., iBAT), understand its secretory function, and study the impact of traditional (e.g. cold exposure) and new interventions (e.g. Beta-2 agonist and exercise) on iBAT thermogenesis at the cellular and molecular levels.

Thus, the DEBATE project will carry out a randomized controlled trial where 40 young, lean adult women will be randomized into a thermoneutral exposure group (2 hours/day at 32ºC; 5 days/week) or a cold exposure group (2 hours/day at 18ºC; 5 days/week) or an aerobic exercise group (5 days/week at 65% heart rate reserve for 60 minutes) or a Beta-2 agonist group (salbutamol 12 mg/day. 7 days week). Before and after the 4-week intervention, iBAT tissue samples from the dorsocervical area and subcutaneous white adipose tissue (scWAT) from the abdomen will be collected. In these biological samples, the investigators will apply a set of cutting-edge omics (e.g., single nucleus RNA-seq) that will allow us to investigate whether iBAT is present and metabolically active in adults. The investigators will also conduct a set of in vitro experiments to discover the secretory function of this novel depot.

Conditions

Cardiometabolic Diseases

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: SINGLE

Study Groups

Thermoneutral condition

n=10; receiving a thermoneutral exposure 2 hours/day at 32ºC; 5 days/week; Total 4 weeks

Group Type: PLACEBO_COMPARATOR

Thermoneutral condition

Intervention Type: BEHAVIORAL

Participants will be exposed 2 hours/day at 32ºC for 5 days/week

Cold condition

n=10; receiving 2 hours/day at 18ºC; 5 days/week; Total 4 weeks

Group Type: EXPERIMENTAL

Cold condition

Intervention Type: BEHAVIORAL

Participants will be exposed 2 hours/day at 18ºC for 5 days/week

Salbutamol

n=10; salbutamol 12 mg/day. 7 days week. Total 4 weeks

Group Type: EXPERIMENTAL

Salbutamol

Intervention Type: DRUG

Participants will take salbutamol 12 mg/day. 7 days week

Aerobic exercise

n=10; receiving 5 days/week at 65% heart rate reserve for 60 minutes each training session. Total 4 weeks

Group Type: EXPERIMENTAL

Aerobic exercise condition

Intervention Type: BEHAVIORAL

Participants will perform aerobic exercise training 5 days/week at 65% heart rate reserve for 60 minutes each training session

Interventions

Thermoneutral condition

Participants will be exposed 2 hours/day at 32ºC for 5 days/week

Intervention Type: BEHAVIORAL

Cold condition

Participants will be exposed 2 hours/day at 18ºC for 5 days/week

Intervention Type: BEHAVIORAL

Aerobic exercise condition

Participants will perform aerobic exercise training 5 days/week at 65% heart rate reserve for 60 minutes each training session

Intervention Type: BEHAVIORAL

Salbutamol

Participants will take salbutamol 12 mg/day. 7 days week

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• 18-22 years of age women.
• BMI between ≥18 and <25 kg/m2
• Are willing to be randomized to either of these 4 groups.
• Must be sedentary (i.e., do not perform exercise or go to the gym).
• Participants should have regular menstrual cycles.
• Must be willing to adhere to all study procedures, including attendance at all study visits.
• Must be willing to have biological samples stored for future research.
• Must accept the use of the Period Calendar and Google Fit Apps on their mobile phones.

Exclusion Criteria

• Diabetes mellitus (determined based on fasting glucose levels defined by ADA criteria).
• Any other active endocrine disease (thyroid disease, any signs of Cushing's syndrome, adrenal disease and lipid-associated disorders such as familial hypercholesterolemia).
• Any cardiac disease (i.e., ischemic cardiac disease, arrhythmias, severe heart failure).
• Use of medication known to influence glucose and/or lipid metabolism or brown fat activity (e.g., beta-blockers, antidepressants, corticosteroids).
• Use of medication shown to increase risk of hypokalemia after salbutamol administration (e.g., xanthine derivatives, steroids and diuretics).
• Clinically relevant abnormalities in clinical chemistry or electrocardiogram (ECG) at screening (to be judged by the study physician).
• A first-degree family member with sudden cardiac death.
• Any chronic renal or hepatic disease.
• Any other contra-indications for the use of salbutamol or propranolol.
• Abuse of alcohol or other substances.
• Smoking.
• Current participation in another research projects that may influence the current research project.
• Use of beta-adrenergic receptor agonists (e.g., asthma).
• Polycystic ovary syndrome.
• Diagnosed psychotic conditions.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 22 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Leiden University Medical Center

OTHER

Sponsor Role: collaborator

ETH Zurich (Switzerland)

OTHER

Sponsor Role: collaborator

Universidad de Almeria

OTHER

Sponsor Role: lead

Responsible Party

Borja Martínez Tellez

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Universidad de Almería

Almería, , Spain

Countries

Spain

Central Contacts

Borja Martinez Tellez, PhD

Role: CONTACT

borjammt@ual.es

+34 950215334 ext. +34

References

Martinez-Tellez B, Sanchez-Delgado G, Alcantara JMA, Acosta FM, Amaro-Gahete FJ, Osuna-Prieto FJ, Perez-Bey A, Jimenez-Pavon D, Llamas-Elvira JM, Gil A, Aguilera CM, Rensen PCN, Ruiz JR. Evidence of high 18 F-fluorodeoxyglucose uptake in the subcutaneous adipose tissue of the dorsocervical area in young adults. Exp Physiol. 2019 Feb;104(2):168-173. doi: 10.1113/EP087428. Epub 2018 Dec 18.

Reference Type: BACKGROUND

PMID: 30468689 (View on PubMed)

Other Identifiers

PID2022-141442OA-I00

Identifier Type: -

Identifier Source: org_study_id