跳至主要内容
临床试验/NCT04924712
NCT04924712招募中不适用

Controlled Multicenter Epidemiological Study of Peripheral Leukocyte Populations and Microbiota in Patients With Idiopathic Nephrotic Syndrome (INS)

Nantes University Hospital4 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2022年1月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
30
试验地点
4
主要终点
Sequencing and analysis of intestinal microbiota

研究概览

简要总结

Idiopathic nephrotic syndrome (NIS) is a clinical entity defined by the association of selective albuminuria, hypoalbuminemia, and nonspecific glomerular lesions (lesions minimal glomerular (LGM) or segmental and focal hyalinosis (HSF). The complication of this kidney disease is the progression towards chronic renal failure and in case of kidney transplantation, its immediate recurrence on the graft . The origin of this syndrome is unknown but a number of clinical observations tend to show an involvement of immune system. A link has been highlighted between atopy, diet and nephrotic flare-ups. The speed of recurrence of this initial disease on the graft and the observation of remissions obtained after treatment by plasma exchange or immunoadsorptions support the presence of a pathogenic plasma factor. Anti-CD20 treatments depleting B lymphocytes has made it possible to favorably treat a number of patients. Dysfunction of regulatory T cells has also been shown in SNI patients. This modification seems linked to allergies and could be due to an aberrant microbiota. The hypothesis of causality between dysbiosis, alteration lymphocyte and triggering of an SNI was mentioned recently. Two studies have shown intestinal dysbiosis in pediatric SNI/LGM, with reduction of T circulating regulators

研究设计

研究类型
Observational
观察模型
Cohort
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

  • Patient treated in participating centers
  • In nephrotic attack, defined biologically by:
  • Proteinuria > 3g 24h or A proteinuria/creatinuria ratio > 3 or Defined at the discretion of the clinician
  • Non inclusion Criteria :
  • Patient with a history of NIS flare-ups resistant to corticosteroid therapy
  • Patient treated with immunosuppressant
  • Patient treated with corticosteroids > 10 mg/d
  • Weight <50 kg
  • Pregnant woman
  • Patient under guardianship / curatorship

排除标准

  • 未提供

研究组 & 干预措施

Patient with nephrotic syndrome idiopathic

nephrotic INS patients in primary visit: harvesting of 27.5 ml supplementary blood, 40 mlurine and feces at inclusion visit and at 3 months. No intervention, no treatment administration other than usual/routine INS treatment.

干预措施: Measurement of blood immune populations and microbiota distribution. (Other)

Patient with nephrotic syndrome no idiopathic, IgA or GEM type or other glomerulopathy

At least 10 NS no idipathic patients: harvesting of 27.5 ml supplementary blood, 40 ml urine and feces at inclusion visit and at 3 months. No intervention, no treatment administration other than usual/routine care treatment.

干预措施: Measurement of blood immune populations and microbiota distribution. (Other)

结局指标

主要结局

Sequencing and analysis of intestinal microbiota

时间窗: 3 months

The microbiota will be analyzed using DNA extracted from fecal samples.

Sequencing and analysis of blood peripheral immune populations and intestinal and urinary microbiota

时间窗: 3 months

For the analysis of peripheral populations, blood cells will be collected by density gradient (Ficoll) and frozen in 20% DMSO. They will then be marked and identified by flow cytometry.

Sequencing and analysis of urinary microbiota

时间窗: 3 months

The microbiota will be analyzed using DNA extracted from urine samples.

次要结局

  • Compare blood peripheral immune populations in patients with SNI to that of type SN patients.(3 months)
  • Compare intestinal microbiota in patients with SNI to that of type SN patients.(3 months)
  • Compare urine microbiota in patients with SNI to that of type SN patients.(3 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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