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Clinical Trials/NCT02322073
NCT02322073RecruitingNot Applicable

Inflammation and Obesity-associated Disease

Göteborg University1 site in 1 country80 target enrollmentStarted: December 1, 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
80
Locations
1
Primary Endpoint
Inflammatory status

Study Overview

Brief Summary

Visceral obesity and adipose inflammation is considered a driving force of obesity-related systemic disease, e.g. cardiometabolic disease, liver cirrhosis and chronic kidney disease (CKD). Inflammatory resolution is actively regulated by specialized pro-resolving mediators (SPMs), including the endogenous eicosanoid LXA4. Impairment of SPMs may underlie development of obesity-related pathology.We hypothesize that obese patients who develop obesity-related disease do so because they suffer from impaired endogenous production of pro-resolving lipids. This will result in aggravated adipose inflammation and fibrosis, which contribute to the systemic pathologies. We thus wish to investigate adipose inflammation and the pro-resolving lipid profile of obese subjects with and without obesity associated metabolic disease. We also aim to investigate whether LXA4, LXB4 and other anti-inflammatory agents (such as AICAR) can alter the phenotype of human adipose macrophages in ex vivo tissue culture. We also investigate basic pathways in inflammatory regulation and obesity related cardiometabolic disease.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Obese BMI 35-55 kg/m2
  • Lean BMI 18.5-24.9

Exclusion Criteria

  • Medical treatment with NSAIDs, corticosteroid treatment, immune-suppressants.
  • Other: smoking, alcohol abuse.

Outcomes

Primary Outcomes

Inflammatory status

Time Frame: One year

inflammatory status vs cardiometabolic disease and tissue fibrosis

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Göteborg University
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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