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临床试验/NCT07718555
NCT07718555招募中不适用

Host-microbiota Interactions in Auto-inflammatory Diseases

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2026年3月9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
300
试验地点
1
主要终点
Stool and blood Gut-derived metabolites in patients with AID

研究概览

简要总结

Autoinflammatory diseases (AID) are genetic diseases responsible for excessive activation of innate immunity leading to blood inflammation and systemic symptoms. Most patients display digestive involvements that may resemble inflammatory bowel disease. Several studies have found dysbiosis in some AID. Gut microbiota can communicate with the host via gut-derived metabolites (Fatty acids, tryptophan, bile acids) that may have either pro-inflammatory or anti-inflammatory effects. Some metabolites can also activate the Aryl hydrocarbon receptor (AhR) pathway, which enhances gut barrier. Gut barrier dysfunction has already been associated with AID. Therfore, dysbiosis could promote digestive and inflammatory involvements in genetically predisposed patients via perturbations of gut-derived metabolites.

详细描述

Patients will receive oral and written information about the research during a routine consultation.

A 10mL urine tube will be collected for research. A stool collection kit including a self-questionnaire to be filled out on the day of the stool collection will be given to all included patients to be collected on site or at home within three months after inclusion and to be returned to the laboratory by mail using a pre-stamped envelope provided at the time of inclusion and a self-questionnaire to be filled out on the day of the stool collection Blood and urine samples will be brought by an accredited carrier to the laboratory "Microbiota, Intestine and Inflammation"; UMRS-938 Sorbonne University, Hôpital Saint-Antoine where they will be analyzed. Stool samples will be sent by mail for stool samples.

If blood sampling is planned as part of routine care, 3 additional tubes (15mL, one dry tube of 5mL, 2 EDTA tubes of 5mL each) of peripheral blood will be collected.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
12 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with autoinflammatory diseases aged >12 years and followed in the CEREMAIA internal medicine department present for consultation or day hospital for a routine care visit.
  • FMF defined by the Eurofever/PRINTO criteria
  • or CAPS définie by the Eurofever/PRINTO criteria
  • or MKD defined by the Eurofever/PRINTO criteria
  • or - DADA2 defined by the presence of two mutations in the ADA2 gene with pathogenicity of at least ≥ 3
  • or - HA20 defined by the presence of one TNFAIP3 mutation with pathogenicity of at least ≥ 3
  • or - JAAD defined by the presence of one JAK1 mutation with pathogenicity of at least ≥ 3
  • or Juvenile polyarthritis defined by the presence of one LACC1 mutation with pathogenicity of at least ≥ 3
  • or - Unclassified AMI defined by:
  • Fever +/- systemic symptoms Recurrent
  • Biological inflammation (CRP>20mg/l) in crisis or permanent
  • Absence of pathogenic mutation highlighted by current next-generation sequencing techniques in known autoinflammatory disease genes
  • Collection of non-opposition to participation in research and specific consent for the biological collection of the patient or their legal representative in the case of a minor patient
  • Lack of legal protection
  • Patients benefiting from a social security scheme

排除标准

  • Antibiotic therapy within 3 months prior to inclusion. If antibiotic therapy was initiated between inclusion and stool collection (data collected on the self-administered questionnaire accompanying the stool collection), the analysis data performed prior to antibiotic therapy will be retained, and the stool will not be analyzed.
  • Current infection on the day of inclusion
  • No social security
  • Refusal to participate

结局指标

主要结局

Stool and blood Gut-derived metabolites in patients with AID

时间窗: 3 months

Quantification of gut-derived metabolites in stools using mass spectrometry

次要结局

  • Role of AhR on activation of inflammatory pathways(during the inclusion visit, baseline, day 1)
  • Microbiota in AID patients(3 months)
  • Effect of gut-derived metabolites on inflammatory pathways though cytokine production(3 months)
  • Association of microbiota profile with biological control of the disease(3 months)
  • Association of microbiota profile and severity of the disease(3 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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