跳至主要内容
临床试验/NCT05968378
NCT05968378招募中不适用

Immunometabolic Effects of Time Restricted Eating in Non-alcoholic Fatty Liver Disease

University College Dublin2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
2
主要终点
Change in plasma inflammatory response to a high-fat meal: Tumor necrosis factor alpha (TNF-α)

研究概览

简要总结

This study will assess the impact of 8-hour time restricted eating (8 hours of eating, 16 hours fasting) combined with a Mediterranean diet on metabolism and inflammation in adults with non-alcoholic fatty liver disease (NAFLD).

详细描述

Non-alcoholic fatty liver disease (NAFLD), defined as the accumulation of fat in the liver that is not related to alcohol intake, is the number 1 global cause of chronic liver disease. Excessive consumption of energy, saturated fat, and simple sugars is a key contributor to hepatic lipid accumulation and obesity-induced metabolic inflammation, reflecting cross-talk between immune and metabolic pathways. Moreover, dietary factors including saturated fatty acids, cholesterol, and their derivatives, as well as gut-derived metabolites, can prime innate immune cells to induce an exaggerated pro-inflammatory response upon re-exposure to such stimuli and may contribute to chronic low grade inflammation.

Dietary strategies focusing on replacing inflammatory dietary triggers with monounsaturated fats, fiber and complex carbohydrates have been shown to improve metabolic dysfunction, but how this relates to a rewiring of the innate immune system is less clear. Time-restricted eating (TRE) is another dietary strategy which has been shown to elicit beneficial effects that reduce the risk of chronic metabolic disease and consolidates eating to a 6-10 hour period daily. Early TRE (eTRE), wherein eating occurs from morning to early afternoon, is associated with greater cardiometabolic health benefits than eating late in the evening. This includes improved insulin sensitivity, glucose tolerance and lipid metabolism, and reduced inflammatory markers.

This study will determine the impact of an 8-week intervention of 8-hour eTRE combined with an anti-inflammatory Mediterranean diet on the metabolic and immune phenotype of individuals with NAFLD, a population at high risk of progressive cardiometabolic decline and chronic inflammation. By focusing on improving both nutrient quality and nutrient timing, a greater understanding of the interaction between systemic metabolism and immune cell rewiring will be gained.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Males and females
  • Age 18-65 years, from all ethnic groups, capable of providing informed consent to participate
  • Obesity (body mass index >30kg/m^2) and of stable body weight (±3% for ≥3 months)
  • Fasting blood glucose <7.0 mmol/L and HbA1c <6.5%.
  • Liver fat >10% (CAP score >238 dB/m) and no fibrosis (liver stiffness score 2-7 kPa) as assessed by liver elastography (FibroScan)

排除标准

  • Impaired renal function
  • Abnormal hematocrit
  • History of cardiovascular events
  • Uncontrolled hypertension
  • Type 2 diabetes
  • Medications or supplements known to affect glucose or lipid metabolism
  • Active inflammatory, autoimmune, infectious, gastrointestinal, or malignant disease
  • Uncontrolled neurological or psychiatric disease
  • Iron deficiency anemia, (hemoglobin < 12g/dl men, < 11g/dl women)
  • Fatty acid supplements and consumers of high doses of anti- antioxidant vitamins (A, C, E, b-carotene)

结局指标

主要结局

Change in plasma inflammatory response to a high-fat meal: Tumor necrosis factor alpha (TNF-α)

时间窗: To be assessed at baseline and post 8-week intervention

Postprandial changes in (TNF-α) (pg/mL) will be measured in response to a high-fat meal

Change in plasma inflammatory response to a high-fat meal: C-reactive protein (CRP)

时间窗: To be assessed at baseline and post 8-week intervention

Postprandial changes in CRP (mg/L) will be measured in response to a high-fat meal

Change in plasma inflammatory response to a high-fat meal: Interleukin-6 (IL-6)

时间窗: To be assessed at baseline and post 8-week intervention

Postprandial changes in IL-6 (pg/mL) will be measured in response to a high-fat meal

Change in plasma inflammatory response to a high-fat meal: Interleukin-1-beta (IL-1β)

时间窗: To be assessed at baseline and post 8-week intervention

Postprandial changes in IL-1β (pg/mL) will be measured in response to a high-fat meal

次要结局

  • Change in metabolic response to a high-fat meal: Glucose(To be assessed at baseline and post 8-week intervention)
  • Change in metabolic response to a high-fat meal: Insulin(To be assessed at baseline and post 8-week intervention)
  • Change in metabolic response to a high-fat meal: Glucagon(To be assessed at baseline and post 8-week intervention)
  • Change in metabolic response to a high-fat meal: Non-esterified fatty acids (NEFA)(To be assessed at baseline and post 8-week intervention)
  • Waist and hip circumferences(To be assessed at baseline and post 8-week intervention)
  • Adipose tissue insulin resistance(To be assessed at baseline and post 8-week intervention)
  • HDL Proteome(To be assessed at baseline and post 8-week intervention)
  • Gut microbiome composition and function(To be assessed at baseline and post 8-week intervention)
  • Mediterranean diet adherence(To be assessed at baseline and post 8-week intervention)
  • Innate immune training(To be assessed at baseline and post 8-week intervention)
  • Body weight(To be assessed at baseline and post 8-week intervention)
  • Change in metabolic response to a high-fat meal: Triglycerides(To be assessed at baseline and post 8-week intervention)
  • Innate immune function(To be assessed at baseline and post 8-week intervention)
  • Change in liver stiffness measurement(To be assessed at baseline and post 8-week intervention)
  • Body fat percentage(To be assessed at baseline and post 8-week intervention)
  • Dietary intake(To be assessed at baseline and post 8-week intervention)
  • Insulin resistance(To be assessed at baseline and post 8-week intervention)
  • Change in intrahepatic triglyceride content(To be assessed at baseline and post 8-week intervention)
  • Body mass index (BMI)(To be assessed at baseline and post 8-week intervention)
  • Physical activity level (PAL)(To be assessed at baseline and post 8-week intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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