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临床试验/NCT04078776
NCT04078776已完成不适用

Systemic and White Adipose Tissue Inflammatory Profile in Lean Versus Obese Individuals

Loughborough University1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2019年10月25日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
12
试验地点
1
主要终点
Protein expression (content and phosphorylation) of key markers of metabolic inflammation in white adipose tissue (for example assessment of Nuclear factor kappa B (NFKB) total protein and phosphorylation by western blot analysis)

研究概览

简要总结

This study will compare the systemic and white adipose tissue inflammatory profile of individuals who are classified as lean and obese. Blood and white adipose tissue samples will be collected in the fasted state to assess inflammatory status.

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 18-40 years
  • 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

排除标准

  • Smoker (including vaping)
  • 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

结局指标

主要结局

Protein expression (content and phosphorylation) of key markers of metabolic inflammation in white adipose tissue (for example assessment of Nuclear factor kappa B (NFKB) total protein and phosphorylation by western blot analysis)

时间窗: Cross-sectional (all outcome measures will be collected within a 2 week period)

This will be assessed following the collection of fasted white adipose tissue samples

次要结局

  • Characterisation of immune cell populations (monocyte subsets) from peripheral blood mononuclear cells (measured using flow cytometry analysis)(Cross-sectional (all outcome measures will be collected within a 2 week period))
  • Habitual Dietary Intake(Cross-sectional (all outcome measures will be collected within a 2 week period))
  • Systemic Markers of Inflammation (for example C-reactive protein and interleukin 6 concentrations, determined by spectrophotometric assay/ ELISA)(Cross-sectional (all outcome measures will be collected within a 2 week period))
  • Gene expression of key markers of metabolic inflammation in white adipose tissue(Cross-sectional (all outcome measures will be collected within a 2 week period))
  • Fasting Serum Markers of Insulin Resistance (for example insulin and glucose concentrations, determined using an ELISA/ spectrophotometric assay)(Cross-sectional (all outcome measures will be collected within a 2 week period))
  • Physical Activity(Cross-sectional (all outcome measures will be collected within a 2 week period))
  • Fasting Serum Lipid Profile (for example total cholesterol, HDL cholesterol and triacylglycerol concentrations, measured using a spectrophotometric assay)(Cross-sectional (all outcome measures will be collected within a 2 week period))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr Oonagh Markey

Vice-Chancellor's Research Fellow

Loughborough University

研究点 (1)

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