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临床试验/NCT02539355
NCT02539355已完成不适用

Diet and Metabolic Inflammation

Fred Hutchinson Cancer Center2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2015年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
16
试验地点
2
主要终点
Change in adipose tissue macrophage cell surface expression of metabolic activation marker ABCA1 as measured by relative mean fluorescence intensity (rMFI)

研究概览

简要总结

Obesity is a risk factor for several common cancers, including those of the breast, colon, liver, and pancreas. Proposed molecular links between obesity and these types of cancer include systemic inflammation, hyperinsulinemia, and changes in the serum concentrations of sex steroid hormones and adipokines. All of these are strongly linked to low-grade chronic inflammatory processes in expanded adipose tissue. The objective of this proposal is to test the hypothesis that adipose tissue inflammation can be reduced by the foods we eat.

详细描述

Overweight or obese individuals with evidence of insulin resistance will be enrolled, until 16 have completed all study procedures. Enrolled subjects will be randomized to follow one of two healthy diets for 12 weeks to determine how each diet affects inflammation in the body and sugar and insulin levels in the blood.

We will address the following specific aims:

Primary specific aim: To investigate whether the consumption of either diet reduces the metabolic activation of adipose tissue macrophages (ATM) as assessed by quantifying the ATM cell surface expression (relative mean fluorescence intensity, rMFI) of the metabolic activation markers, CD36 and ABCA1.

Secondary specific aim 1: To compare how each of the study diets affects endpoints downstream of metabolic activation of ATM, specifically (a) adipose tissue expression of the key pro-inflammatory cytokines tumor necrosis factor α (TNFα) and interleukins (IL)-1 beta and 6; (b) adipose tissue expression of the key anti-inflammatory adipokine, adiponectin; (c) systemic insulin sensitivity, as assessed by the Matsuda-DeFronzo Insulin Sensitivity Index (ISI), based on a 3-hour frequently sampled oral glucose tolerance test (FS-OGTT); and oral glucose tolerance, as assessed by measuring the total area-under-the-curve glucose in the FS-OGTT.

Secondary specific aim 2: To compare the impact of each of the study diets on low-grade chronic systemic inflammation, as assessed by measuring the concentrations of high sensitivity C-reactive protein (hsCRP), IL-6, and total adiponectin in fasting plasma.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Body Mass Index (BMI) ≥ 28 kg/m2
  • Homeostasis model assessment insulin resistance (HOMA-IR) index > 2.0
  • Body weight within 10% of weight 3 months before starting the study
  • Able to come to the FHCRC Prevention Center for one 1-hour pre-study visit and two clinic visits of ~4.5 hours duration each
  • Able and willing to attend bi-weekly dietary group counseling sessions at FHCRC during the 12-week intervention period
  • Willingness and ability to follow the dietary regimen
  • Able to complete repeated 3-day food records before and during the dietary intervention.
  • Willingness to maintain usual lifestyle habits (other than diet) throughout the study (e.g., physical activity habits)
  • Ability to understand, speak, and write in English
  • Ability to provide informed written consent

排除标准

  • Any previous or current use of antidiabetic medications or insulin
  • Presence or history of major chronic inflammatory or autoimmune disease (e.g., lupus, rheumatoid arthritis, Hashimoto's thyroiditis, inflammatory bowel disease, celiac disease, multiple sclerosis), malabsorption syndromes, or diseases of the liver, thyroid, or kidneys (stage IV or later chronic kidney disease)
  • Food allergies or intolerances against major study foods
  • Intake of drugs likely to interfere with study endpoints, including corticosteroids and anabolic steroids, hormone replacement therapy, NSAIDS (more than 3 times per week and/ or more than 600 mg per day), warfarin (within 3 months of starting the study), antibiotics or probiotics (within 2 weeks of starting the study)
  • Presence or recent history of anemia (within 3 months of starting the study)
  • Participation in another study that includes an intervention of any kind or a blood draw >300 mL over 3 months
  • Alcohol intake > 2 drinks per day
  • Use of tobacco products, eCigarettes, or recreational drugs on more than 2 days per month
  • Current or recent (within 12 months of starting the study) pregnancy or breastfeeding

结局指标

主要结局

Change in adipose tissue macrophage cell surface expression of metabolic activation marker ABCA1 as measured by relative mean fluorescence intensity (rMFI)

时间窗: Change between beginning (day 1) and end (week 12) of the study diet period.

As measured by relative mean fluorescence intensity (rMFI) on abdominal subcutaneous adipose tissue macrophages

Change in adipose tissue macrophage cell surface expression of metabolic activation marker CD36 as measured by relative mean fluorescence intensity

时间窗: Change between beginning (day 1) and end (week 12) of the study diet period.

As measured by relative mean fluorescence intensity (rMFI) on abdominal subcutaneous adipose tissue macrophages

次要结局

  • Change in adipose tissue expression of the key pro-inflammatory cytokine, tumor necrosis factor α (TNFα) assessed by qPCR(Change between beginning (day 1) and end (week 12) of the study diet period.)
  • Change in oral glucose tolerance assessed by measuring total area under the curve glucose in the FS-OGTT(Change between beginning (day 1) and end (week 12) of the study diet period.)
  • Change in fasting plasma total adiponectin assessed by ELISA(Change between beginning (day 1) and end (week 12) of the study diet period.)
  • Change in adipose tissue expression of the key pro-inflammatory cytokine, interleukin-6 (IL-6) assessed by qPCR(Change between beginning (day 1) and end (week 12) of the study diet period.)
  • Change in adipose tissue expression of the key pro-inflammatory cytokine, interleukin-1 beta (IL-1beta) assessed by qPCR(Change between beginning (day 1) and end (week 12) of the study diet period.)
  • Change in adipose tissue expression of the key anti-inflammatory adipokine, adiponectin assessed by qPCR(Change between beginning (day 1) and end (week 12) of the study diet period.)
  • Change in systemic insulin sensitivity assessed by the Matsuda-DeFronzo Insulin Sensitivity Index(Change between beginning (day 1) and end (week 12) of the study diet period.)
  • Change in fasting plasma C-reactive protein assessed by immunonephelometry(Change between beginning (day 1) and end (week 12) of the study diet period.)
  • Change in fasting plasma IL-6 assessed by high-sensitivity ELISA(Change between beginning (day 1) and end (week 12) of the study diet period.)

研究者

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

Mario Kratz

Associate Member

Fred Hutchinson Cancer Center

研究点 (2)

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