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临床试验/NCT04834609
NCT04834609已完成不适用

Identification of Molecular Differences of Adipose-derived Mesenchymal Stem Cells Between Non- Responders and Responders in Treatment of Transsphincteric Perianal Fistulas Using Autologous Fat Graft Injection

University of Aarhus0 个研究点目标入组 27 人开始时间: 2015年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
27
主要终点
Investigation of differentiation potential of AT-MSCs to differentiate into adipocyte

研究概览

简要总结

This study investigated the cellular and molecular characteristics of AT-MSCs obtained from autologous AT therapy in patients with high transphincteric perianal fistulas of crytoglandular origin. Adipose tissue was injected into anal fistulas. Characteristics of adipose tissue mesenchymal stemcells (AT-MSC) was investigated and compared in patients with fistula that healed after the treatment (responders) to patients who failed to heal (non-responders)

详细描述

Injection with allogene or autologous stem cells has been reported to be efficient treatment of perianal fistulas. An alternative to this treatment could be injection with freshly collected autologous adipose tissue. In this study 27 patients with cryptoglandular anal fistulas were treated with freshly collected autologous adipose tissue.A clinical assessment of the patient prior to inclusion was undertaken and a loose seton placed for at least 6 weeks prior to fat injection. An MRI of the pelvis was performed before inclusion. Fistulas with secondary tracts and/or cavities were excluded. The operation was performed in one procedure including liposuction and injection of adipose tissue. A sample of adipose tissue from all 27 patients was analyzed. AT-MSCs were isolated and characterized using cellular and molecular analyses. Clinical and MRI-scanning evaluation of fistula healing and evaluation of ano-rectal function was performed after 6 months. AT-MSCs phenotype was compared between responders and non-responders with respect to fistula healing. The evaluation of the AT-MSCs was performed in a blinded manner.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

盲法说明

Characterisation of adipose tissue (AT-MSCs) was performed blinded to the result of the treatment responder/non-responder

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • high trans-sphincteric fistulas
  • fistula confirmed and classified by an MRI.
  • seton (> 6 weeks) prior to fat injection
  • informed, written consent.

排除标准

  • Anovaginal fistula
  • Active sepsis
  • IBD, immunodeficiency, prior pelvic irradiation and malignancy
  • Insulin dependent diabetes
  • More than 4 prior attempts of fistula closure
  • Tobacco smoking or nicotine substitution 8 weeks prior to fat injection.
  • Pregnancy
  • Psychiatric disorders
  • BMI ≥ 35 or BMI<20
  • Active tuberculosis
  • Patient less than 18 years
  • Unable to undergo MRI

结局指标

主要结局

Investigation of differentiation potential of AT-MSCs to differentiate into adipocyte

时间窗: At start of treatment

Differentiation potential of AT-MSCs: to differentiate into adipocyte measured by Oil-Red O staining and gene expression of adipogenic markers (PPARg and LPL normalized to housekeeping gene beta actin) presented as a Fold change to undifferentiated cells (arbitrary units)

Investigation of differentiation potential of AT-MSCs to differentiate into osteoblast

时间窗: At start of treatment

Differentiation potential of AT-MSCs: to differentiate into osteoblast measured by Alizarin S staining and gene expression of osteogenic markers (BGALP and RUNX2 normalized to housekeeping gene beta actin) presented as a Fold change to undifferentiated cells (arbitrary units)

Investigation of cell proliferation of AT-MSCs

时间窗: At start of treatment

Cell proliferation of AT-MSCs evaluated as number of cells/per day

Measurement of gene expression profile of AT-MSCs

时间窗: At start of treatment

Gene expression of proinflammatory (NFKB, TNFa, IL1B, IL6) and senescence associated molecules(CDKN2A, TP53, TGFB1, VEGFA, IFNG, IL6) of AT-MSCs in relation to the outcome of fistula treatment (i.e. comparison between responders and non-responders). The data are normalized to housekeeping gene beta actin (arbitrary units)

次要结局

  • Evaluation of fistula healing after treatment(6 months after last injection of autologous adipose tissue)
  • Functional gastroenterological outcome after treatment(6 months after last injection of autologous adipose tissue)
  • Functional urological outcome after treatment(6 months after last injection of autologous adipose tissue)
  • Healing of anal fistula after treatment(6 months after last injection of autologous adipose tissue)
  • Defecation disorder evaluation after treatment(6 months after last injection of autologous adipose tissue)

研究者

申办方类型
Other
责任方
Sponsor

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