Obesity, Iron Regulation and Colorectal Cancer Risk
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 17
- 试验地点
- 2
- 主要终点
- Change in colonic inflammation
研究概览
简要总结
Obesity is an independent risk factor for colorectal cancer (CRC) although the underlying mechanisms have not been elucidated. Dietary nutrients play a key role in both the prevention and promotion of CRC. While iron is an essential nutrient, excess iron is associated with carcinogenesis. Unlike the systemic compartment, the intestinal lumen lacks an efficient system to regulate iron. In conditions when dietary iron malabsorption and intestinal inflammation co-exist, greater luminal iron is associated with increased intestinal inflammation and a shift in the gut microbiota to more pro-inflammatory strains. However, treatments designed to reduce luminal, including diet restriction and chelation, are associated with lower intestinal inflammation and the colonization of protective gut microbes. Obesity is associated with inflammation-induced, hepcidin-mediated, iron metabolism dysfunction characterized by iron deficiency and dietary iron malabsorption. Obesity is also linked to intestinal inflammation. Currently, there is a fundamental gap in understanding how altered iron metabolism impacts CRC risk in obesity.
The investigator's objective is to conduct a crossover controlled feeding trial of: 1) a "Typical American" diet with "high" heme/non-heme iron", 2) a "Typical American" diet with "low" iron, and 3) a Mediterranean diet with "high" non heme iron and examine effects on colonic and systemic inflammation and the gut microbiome.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Crossover
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 55 Years 至 70 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Self-identify as Hispanic, African American, or Caucasian.
- •Meet body mass index (BMI > = 30.0 kg/m2) and C-reactive protein (CRP) criteria (> 2.0 mg/dl)
- •Post-menopausal (no menstruation in the past 12 months)
- •Weight stable (< 3% weight change in the past 3 months)
- •Non-smoker
- •No major medical problems
- •Have a working phone
- •No known allergies, intolerance, medical, secular or religious dietary restrictions
排除标准
- •Chronic constipation (less than three stools per week for several months)
- •History or intestinal cancer, inflammatory bowel disease, celiac disease, or malabsorptive bariatric surgery
- •Previous intestinal surgery
- •H pylori infection or taking H2 blockers (e.g., Zantac, Pepcid) /antacids (e.g., Rolaids) more than 3 times per week
- •Significant blood loss or blood donation in past 3 months
- •Active gastrointestinal bleed
- •Any surgery in the past 3 months
- •Hemochromatosis
- •Sickle cell disease
- •Hereditary polyposis
- •Rheumatoid arthritis
- •Type I or Type II diabetes
- •Antibiotic use in the past 2 months
- •Excessive alcohol consumption [> 2 standard alcoholic drinks (12 ounces of beer, 5 ounces of wine, 1 shot of hard liquor) per day]
- •Aspirin use >81 mg/day OR >325 mg/every other day
- •Regularly taking probiotics, fiber supplements, Orlistat (over the counter brand name: Alli), or steroids (inhaled or oral)
研究组 & 干预措施
Plant-based high non-heme iron diet
干预措施: Plant-based high non-heme iron diet (Other)
High heme iron diet
干预措施: High heme iron diet (Other)
Low iron diet
干预措施: Low iron diet (Other)
结局指标
主要结局
Change in colonic inflammation
时间窗: Baseline and post-diet (day 22) for each of the three 3-week diets
Fecal calprotectin, a proxy for colon tissue inflammation, will be measured from stool an calprotectin immunoassay
次要结局
- Change in systemic inflammation(Baseline and post-diet (day 22) for each of the three 3-week diets)
- Change in stool microbial community profile at the phylum and genus level(Baseline and post-diet (day 22) for each of the three 3-week diets)
- Change in serum hepcidin(Baseline and post-diet (day 22) for each of the three 3-week diets)
研究者
Lisa Tussing-Humphreys
Associate Professor
University of Illinois at Chicago