跳至主要内容
临床试验/NCT06563921
NCT06563921尚未招募不适用

PRObiotic Mixed With Exercise THErapy USe in MAFLD (PROMETHEUS in MAFLD)

Nicolaus Copernicus University0 个研究点目标入组 180 人开始时间: 2026年4月10日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
180
主要终点
Change in liver fat measured using MRI

研究概览

简要总结

This project aims to evaluate the roles of the autonomic nervous system (ANS) and gut microbiota as correlates of clinical improvement in metabolic dysfunction-associated fatty liver disease (MAFLD) and non-alcoholic fatty liver disease (NAFLD) in response to a therapeutic regimen comprising resistance exercise and probiotic supplementation. The primary objective is to investigate the effects of these non-pharmacological interventions on MAFLD/NAFLD and to identify patient phenotypes based on baseline ANS profiles and gut microbiota composition that predict clinical responses.

详细描述

The human microbiome, understood here as the collective community of microorganisms, their genetic material, and metabolic products that colonize the body from birth, is particularly concentrated in the gut. The gut microbiome, dominated primarily by anaerobic bacteria, encompasses thousands of species and millions of genes distributed among the major phyla: Firmicutes, Bacteroidetes, Actinobacteria, Proteobacteria, and Verrucomicrobia. Recent research has increasingly focused on the gut microbiome due to its dysbiosis being linked to numerous diseases that may be modifiable through diet, supplementation, or physical activity. Dysbiosis of the gut microbiome has also been implicated in MAFLD and NAFLD, which are the most prevalent liver diseases globally, affecting approximately 35% of the adult population, with this prevalence expected to rise. The gut-liver axis has been extensively studied in relation to MAFLD/NAFLD due to the bidirectional interactions between the gut microbiota and hepatic function. The portal vein, which supplies approximately 70% of the liver's blood flow, facilitates this interaction by connecting the intestines to the liver. Patients with NAFLD/MAFLD typically exhibit increased intestinal permeability compared to healthy individuals, thereby increasing the liver's exposure to gut-derived bacteria, endotoxins, bacterial products, and inflammatory mediators.

Probiotics, defined as live microorganisms that confer health benefits to the host, have been shown in previous studies to enhance the integrity of the intestinal barrier, regulate the gut microbiota, reduce intestinal permeability, and mitigate immune and metabolic disturbances. These effects are particularly relevant in patients with NAFLD/MAFLD, where probiotics have been observed to reduce hepatic steatosis and inflammation-related damage.

Physical exercise, particularly structured programs, has been demonstrated to significantly improve liver function in patients with NAFLD/MAFLD and positively modulate the gut microbiota. Exercise may attenuate the production of reactive oxygen species (ROS) and other oxidative agents in NAFLD by regulating antioxidant enzymes and anti-inflammatory mediators. Additionally, exercise interventions in these patients have been shown to improve blood lipid profiles, including triglycerides, cholesterol, AST, and ALT levels, offering substantial clinical benefits. Although the existing literature predominantly emphasizes aerobic training, this study seeks to compare the effects of resistance training and probiotic supplementation in patients with NAFLD/MAFLD and to assess potential changes in clinical outcomes. Furthermore, the study will explore the influence of baseline ANS and gut microbiota profiles on the patients' responses to these non-pharmacological therapies.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Study population: Patients diagnosed with non-alcoholic or metabolically mediated fatty liver disease (NAFLD/MAFLD), including the inflammatory form (NASH), confirmed by imaging (ultrasound, MRI-PDFF) or histopathological (liver biopsy) methods.
  • Inclusion criteria:
  • Diagnosis of NAFLD/MAFLD or NASH (imaging or histological confirmation of fatty liver disease, e.g., ultrasound, MRI-PDFF, biopsy)
  • Age 18-60 years
  • Ability to understand the study procedures and provide informed consent.
  • Stable clinical condition for at least 3 months prior to study initiation.

排除标准

  • Lack of fluency in English or Polish
  • Significant (structural) limitation of upper and/or lower limb mobility
  • Pregnancy or breastfeeding
  • Inability to understand instructions
  • Shift work
  • Participation in any study or research project within the last 3 months
  • Participation in an interventional drug study within the last 3 months
  • Participants with hepatic steatosis and regular alcohol consumption > 30 g/day
  • Individuals with any concomitant liver disease (viral hepatitis, drug-induced liver injury, metabolic/genetic diseases (e.g., Wilson's disease))
  • Anticoagulant/antiplatelet therapy, antithrombotic therapy, immunosuppressive medications, prolonged immunosuppression (e.g., recent cytotoxic chemotherapy, HIV infection with CD4 count < 240), antibiotics, corticosteroids, valproic acid, amiodarone, tamoxifen within 3 months prior to study enrollment
  • Use of medications such as steroids, methotrexate, metformin
  • Use of agents such as vitamin E, omega-3 fatty acids, or medications with evidence of an effect on NAFLD (pioglitazone, GLP-1 analogues, dipeptidyl peptidase IV inhibitors, ursodeoxycholic acid)
  • Active or previous history of invasive cancer (excluding curatively treated carcinoma in situ [e.g., cervical] or benign skin cancer), unless complete remission has been achieved
  • Regular use of probiotic or prebiotic supplements within 3 months prior to study enrollment
  • Known allergy to probiotics
  • History of using an alternative diet within 3 months prior to study enrollment or changing diet during study entry
  • Previous surgery (bariatric surgery, gastric or intestinal resection)
  • Parenteral nutrition (TPN) within the last 6 months
  • Insulin therapy
  • Uncontrolled diabetes
  • Cardiovascular disease (e.g., uncontrolled blood pressure, coronary artery disease, NYHA class III-IV heart failure, severe arrhythmias, orthostatic intolerance)
  • Nervous system disorders
  • Cognitive impairment and dementia
  • Osteoporosis/osteopenia
  • Active thyroid disease
  • Cushing's syndrome
  • Any implanted battery-powered device (e.g., AICD, pacemaker, cardiac rhythm recorder, cochlear implant)

研究组 & 干预措施

Experimental: probiotics supplementation + physical exercise program

Experimental

Behavioral: physical exercise program in the form of a resistance/hypertrophy-oriented resistance program Dietary Supplement: probiotics supplementation

干预措施: physical exercise programme (Behavioral)

Active Comparator: placebo + resistance/hypertrophy-oriented resistance program plus placebo

Active Comparator

placebo + resistance/hypertrophy-oriented resistance program

干预措施: physical exercise programme (Behavioral)

Experimental: probiotics supplementation + physical exercise program

Experimental

Behavioral: physical exercise program in the form of a resistance/hypertrophy-oriented resistance program Dietary Supplement: probiotics supplementation

干预措施: probiotics supplementation (Dietary Supplement)

Active Comparator: placebo + resistance/hypertrophy-oriented resistance program plus placebo

Active Comparator

placebo + resistance/hypertrophy-oriented resistance program

干预措施: Placebo (Dietary Supplement)

probiotics supplementation

Experimental

Dietary Supplement: probiotics supplementation

干预措施: probiotics supplementation (Dietary Supplement)

placebo

Placebo Comparator

placebo

干预措施: Placebo (Dietary Supplement)

结局指标

主要结局

Change in liver fat measured using MRI

时间窗: 12 weeks

Changes in liver fibrosis (FIB-4 score)

时间窗: 12 weeks

次要结局

  • HDL(12 weeks)
  • changes in free-fat mass in kilograms measured using bioelectrical impedance method(12 weeks)
  • changes in weight in kilograms using scale(12 weeks)
  • changes in body fat mass in kilograms measured using bioelectrical impedance method(12 weeks)
  • LDL(12 weeks)
  • ALT(12 weeks)
  • changes in visceral fat level measured using bioelectrical impedance method(12 weeks)
  • AST(12 weeks)
  • HDL cholesterol concentration measured in mg/dL (or mmol/L) using a standardized direct enzymatic assay from fasting venous blood samples(12 weeks)
  • LDL cholesterol concentration measured in mg/dL (or mmol/L) using a standardized direct enzymatic assay from fasting venous blood samples(12 weeks)
  • Aspartate aminotransferase (AST) activity measured in U/L using a standardized spectrophotometric enzymatic assay from serum samples(12 weeks)
  • Alanine aminotransferase (ALT) activity measured in U/L using a standardized spectrophotometric enzymatic assay from serum samples(12 weeks)

研究者

发起方
Nicolaus Copernicus University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Prof. Paweł Zalewski, PhD

Prof.

Nicolaus Copernicus University

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