Systemic and White Adipose Tissue Inflammatory Profile in Lean Versus Obese Individuals
NCT ID: NCT04078776
Last Updated: 2022-05-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
12 participants
OBSERVATIONAL
2019-10-25
2020-08-01
Brief Summary
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There is evidence to suggest that markers of inflammation in the blood and white adipose tissue increase with increasing levels of obesity. However, the white adipose tissue total protein content and phosphorylation of proteins involved in inflammatory pathways has not previously been compared between lean and obese individuals.
The investigators hypothesise that obese individuals will have increased levels of inflammation in the blood and white adipose tissue, compared to their lean counterparts.
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Lean Individuals
waist circumference ≤94 cm (men) and 80 cm (women) and BMI ≥ 21.0 kg/m2
No intervention
There is no intervention in this study
Obese Individuals
waist circumference ≥102cm (men) and 88 cm (women) and BMI ≥ 30.0kg/m2
No intervention
There is no intervention in this study
Interventions
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No intervention
There is no intervention in this study
Eligibility Criteria
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Inclusion Criteria
* Waist circumference/BMI criteria:
* Lean participants: waist circumference ≤94 cm (men) and 80 cm (women) and BMI ≥ 21.0 kg/m2 or
* Obese participants: waist circumference ≥102 cm (men) and 88 cm (women) and BMI ≥ 30.0kg/m2
* Recreationally active (\> 3 x 30 min moderate exercise per week)
* Blood pressure systolic blood pressure \<160 mmHg and diastolic blood pressure \<100 mmHg
Exclusion Criteria
* Cardiometabolic or inflammatory disease (e.g. heart disease, high blood pressure, type 2 diabetes)
* Taking medication or nutritional supplements (e.g. fish oil/prebiotics) known to interfere with study outcomes (including inflammation, immune function or lipid/carbohydrate metabolism) or prescribed antibiotics within the last 3 months
* Unstable weight history (≥ 3kg loss or gain in previous 3 months)
* An allergy to lidocaine (determined by the Schools standard health questionnaire)
* Parallel participation in another intervention study
* Women who are pregnant or lactating
* Any other unusual medical history or diet and lifestyle habits or practices that would preclude volunteers from participating in a metabolic study
* Alcohol consumption \>28 units per week for a man or \>21 units per week for a woman
18 Years
40 Years
ALL
Yes
Sponsors
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Loughborough University
OTHER
Responsible Party
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Dr Oonagh Markey
Vice-Chancellor's Research Fellow
Principal Investigators
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Oonagh Markey, BSc, PhD
Role: PRINCIPAL_INVESTIGATOR
Vice-Chancellor's Research Fellow, Loughborough University
Locations
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Loughborough University
Loughborough, , United Kingdom
Countries
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Other Identifiers
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R19-P144
Identifier Type: -
Identifier Source: org_study_id
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