CClinicalTrials.gg
CompletedNCT02703766Updated Jan 9, 2019

Weight Gain and Adipose Tissue

An interventional study of overfeeding induced weight gain in Obesity, sponsored by Mayo Clinic. Completed at 2 sites in United States. Open to participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-01-09.

Sponsored by Mayo Clinic · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
14
Allocation
Non-randomized
Ages
18 Years to 40 Years
Sex
All
01

Study summary

This study aims to examine the role of weight gain in adipose tissue immune cell influx and development of obesity related cardiometabolic disorders. Adipose tissue-mediated chronic systemic inflammation is implicated in the development of cardiometabolic disorders in obesity. Therefore, resolution of adipose tissue inflammation may be key to ameliorating obesity-associated dyslipidemia, insulin-resistance, and cardiovascular disease. Proinflammatory cytokines contribute to the initial influx of immune cells into adipose tissue during weight gain. However, mechanisms regulating these cytokines in the adipose tissue milieu and the effects of weight gain on adipose tissue are not completely understood.

The study proposes to investigate the molecular events contributing to increased infiltration of macrophages and T-cells into adipose tissue during weight gain. The central hypothesis is that in lean subjects (with low body fat mass), healthy fat gain which is associated with decreased expression of proinflammatory cytokines. However, in obesity (high body fat mass), adipose tissue is altered, which permits increased expression of inflammatory cytokines and further fat gain results in influx of immune cells. To test the hypothesis, adipose tissue from well characterized lean (control, with low body fat) and obese individuals (with high body fat) at baseline and after a modest 5% weight gain will be used. Adipose tissue samples after subsequent weight loss will also be examined.

For this study, obesity will be defined by body composition rather than body mass index (BMI), as several studies have shown that BMI does not adequately define obesity and several individuals with normal BMI may indeed have high body fat mass. Individuals with body fat content ≤25% for men, \& \<35% for women) will be considered lean and individuals with body fat content >25% for men, ≥35% for women will be considered obese.

02

Conditions studied

  • Obesity

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03

In context

Weight Gain

405 studies on the registry are indexed under Weight Gain; 52 are open to participants now.

This study's enrollment of 14 is below the median of 83 across 324 interventional studies indexed under Weight Gain.

Browse Weight Gain studies →

Lead sponsor

Mayo Clinic is the lead sponsor of 3,218 studies on the registry; 670 are open to participants now.

Of its 445 completed or terminated interventional studies of FDA-regulated products, 313 (70%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Age: 18 to 40 (inclusive) years
  • BMI 18.5 \<30 kg/m2
  • Gender: Both males and females will be allowed to participate in the study
  • Predominantly sedentary
  • Absence of any chronic medical conditions other than seasonal or environmental allergies
  • On no prescription medications other than second generation antihistamines (cetirizine , Fexofenadine, Desloratadine, Loratadine, etc), oral contraceptive pills, or intrauterine devices
  • Not a current smoker or tobacco user
  • Not pregnant or breast feeding and not intending to become pregnant or breast feed
  • Lean (low body fat mass) (body fat content ≤ 25% for men, \< 35% for women) n=7; Obese (high body fat mass) (body fat content >25% for men, ≥ 35% for women) n=7
  • Ability to provide written informed consent

Exclusion criteria

Exclusion Criteria

  • Vulnerable study population will be excluded
  • Presence of chronic diseases such as diabetes, and cardiovascular disease
  • Pregnancy
  • Anemic (hemoglobin \<13.5 g/dL for men and \<12.0 g/dL for women)
  • Postmenopausal
  • Smoking
  • Use of chronic Medications (aspirin, statin, anti-inflammatory drugs)
  • Subjects found to have significant sleep disorders will be excluded
  • Dietary restrictions including lactose intolerance, and vegan diet
  • Eating disorders that may interfere with weight gain and weight loss
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
14 participants (actual)

Study arms

  • Active comparator
    Lean

    Lean individuals are defined as having body fat content less or equal to 25% in men and less than 35% for women. Overfeeding induced weight gain and subsequent weight loss

    Behavioral: overfeeding induced weight gain

  • Experimental
    Obese

    obese individuals are defined as having body fat content more than 25% in men and more than 35% for women. Overfeeding induced weight gain and subsequent weight loss

    Behavioral: overfeeding induced weight gain

Interventions

  • Behavioraloverfeeding induced weight gain
06

What researchers measure

Primary outcomes

  1. Change from baseline in adipose tissue inflammation by 8 week of modest weight gain followed by 8 week of weight loss.

    Adipose tissue inflammation will be measures by RTPCR and Western Blot. These will be presented as ratio to endogenous house keeping gene.

    Time frame: 16-20 weeks

Secondary outcomes

  1. Change from baseline in blood pressure by 8 week of modest weight gain followed by 8 weeks of weight loss.

    Time frame: 16-20 weeks

07

Study locations

2 sites
  • Mayo Clinic in Rochester
    Rochester, Minnesota 55905, United States
  • Mayo Clinic
    Rochester, Minnesota 55905, United States
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 9, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02703766
Lead sponsor
Mayo Clinic
Responsible party
Virend Somers (Professor of Medicine, Mayo Clinic) — Principal investigator
First posted
Mar 9, 2016
Start date
Apr 2016
Primary completion
Mar 2018
Completion
Dec 2018
Last update
Jan 9, 2019

Study contacts

Virend Somers, MD, PhD
principal investigator · Mayo Clinic

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2019. You cannot join it, but the record below documents what was studied.

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