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临床试验/NCT03720314
NCT03720314已完成不适用

Microbiota and Metabolite Profiles Linked to Severity in Irritable Bowel Syndrome

Wageningen University1 个研究点 分布在 1 个国家目标入组 121 人开始时间: 2018年9月6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
121
试验地点
1
主要终点
Change in Short chain fatty acid levels

研究概览

简要总结

This study investigates differences in microbiota profiles and metabolite levels between mild and severe IBS patients, compared to matched healthy controls. Two fecal samples, with one month in between, will be analyzed. Secondary parameters such as dietary intake, quality of life and stool pattern will be assessed.

详细描述

Rationale: Irritable Bowel Syndrome (IBS) is a gastro-intestinal disorder that strongly affects Quality of Life and impairs daily functioning. However, the aetiology and pathophysiology has been poorly understood. Studies suggest that intestinal microbiota in IBS is altered, however a general consensus remains elusive. This may be due to the large individual variation in microbiota and IBS symptoms, and the cross-sectional designs. Moreover, other factors like diet, wellbeing and metabolite profiles are often not taken into account. New evidence is suggesting that IBS severity may be an important factor in microbiota composition.

Objective

To determine faecal microbiota composition and metabolite production (such as acetate, propionate and butyrate), and investigate differences between healthy controls and mild or severe patients IBS. Moreover, to investigate whether (clinical) parameters such as symptom severity fluctuated, and if these fluctuations are associated with an alteration in faecal microbiota composition and metabolite production, one month after baseline, compared to healthy controls.

Study design: This study is a repeated cross-sectional study, with two data collection points (baseline, and after one month).

Study population: For this study, 100 IBS patients and 30 healthy controls will be recruited. After the first data collection point (T1), the 30 most mild and 30 most severe IBS patients will be included for data collection at T2 (after one month). All participants will be aged between 18 and 65 years.

Intervention (if applicable): Not applicable. Main study parameters/endpoints: primary endpoint of this study is microbiota composition and metabolite profiles, and the difference between groups and possible change after one month. These are assessed two faecal samples, which are analysed by 16S rRNA gene-based microbiota profiling. Secondary parameters are dietary intake, Quality of Life, depression and anxiety scores, and stool consistency and frequency, which are assessed by validated questionnaires.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

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

  • IBS patients that meet the Rome IV criteria, or healthy subjects with no gastro-intesitnal complaints
  • In close proximity of Wageningen (max. 50 km)
  • Signed informed consent.
  • After baseline measurements, IBS severity will be checked using the IBS-SSS. Participants will be included for follow-up one month later, when they have the most mild symptoms (n=30) or most severe (n=30) symptoms.

排除标准

  • Presence of gastro-intestinal diseases, such as celiac disease, Crohn's disease, or Ulcerative colitis.
  • Have a history of intestinal surgery that might interfere with study outcomes. This does not include an appendectomy or cholecystectomy.
  • Presence of significant systemic diseases, such as diabetes mellitus, cancer, cardiovascular disease or respiratory disease.
  • Female participants: currently pregnant or breast-feeding.
  • Use of antibiotic treatment less than 3 months before start of the study and no use of antibiotics during the study.
  • You are participant in another study during this study.
  • Are an employee or student of the Division of Human Nutrition, Food and Biobased Research or Laboratory of Microbiology, of Wageningen University & Research.
  • Unwilling or unable to fulfil study criteria.
  • If they are not selected in the most mild or most severe group after T1.

结局指标

主要结局

Change in Short chain fatty acid levels

时间窗: baseline, and one month later

Metabolite levels will be measured in fecal samples, using HPLC method

Change in microbiota composition

时间窗: baseline, and one month later

microbiota composition will be measured in fecal samples, using 16S rRNA technique

次要结局

  • Change in Stool pattern(baseline, and one month later)
  • Change in Quality of Life scores(baseline, and one month later)
  • Dietary intake(baseline)
  • Change in Gastro-intestinal complaints(baseline, and one month later)
  • Change in Anxiety and Depression screening scores(baseline, and one month later)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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