跳至主要内容
临床试验/NCT02756104
NCT02756104已完成不适用

T Cell Phenotypes in ALS, Influence of Vitamin D

University Hospital, Montpellier1 个研究点 分布在 1 个国家目标入组 97 人开始时间: 2016年6月7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
97
试验地点
1
主要终点
Study of T-cell phenotypes in ALS patients and controls

研究概览

简要总结

ALS is a devastative disorder characterized by motor neuron degeneration. Median survival is 3 years after onset, but may vary from a few months to more than 30 years. Various factors have been suspected to play a role in such a variation, but recently, it has been described that regulatory T-lymphocytes (T regs) may mediate ALS progression and survival. Vitamin D is an hormone know to regulated T reg function in vivo and in vitro. It have recently demonstrated that vitamin D (VD) levels correlated with ALS prognosis. The investigator want to go further in the study of the immune processes that could modulate prognosis in ALS. This could allow proposing VD as a potential treatment of ALS in a future trial. More largely, this could reinforce arguments in favor of an immune intervention to attenuate the severity of this devastating disorder.

详细描述

ALS is a devastative disorder characterized by motor neuron degeneration. Median survival is 3 years after onset, but may vary from a few months to more than 30 years. Various factors have been suspected to play a role in such a variation, but recently, it has been described that regulatory T-lymphocytes (T regs) may mediate ALS progression and survival. Vitamin D is an hormone know to regulated T reg function in vivo and in vitro. It have recently demonstrated that vitamin D (VD) levels correlated with ALS prognosis and patients with a severe VD deficiency had a 6 time more rapid evolution than those with normal VD levels. The investigator want to go further in the study of the immune processes that could modulate prognosis in ALS. We propose 1- to study T cell phenotypes (Treg, CD4 (cluster of differentiation 4) -Th1, -Th17, -Th2, CD8 (cluster of differentiation 8)and NK) in ALS vs controls ; 2- In VD-deficient patients, to analyze the influence of a vitamin D supplementation on T cell phenotypes ; 3- to study the relationships between T cell phenotypes and ALS prognostic factors. The project will include 70 ALS patients and 27 controls in this prospective study. VD-deficient patients will be supplemented, according to national recommendations for 6 months, and the evolution of T cell phenotypes will be followed over 1 year. We hope to demonstrate first that T cell phenotypes in ALS are consistent with a pro inflammatory profile, compared to controls, secondly that VD treatment modulates T cell phenotypes towards a non-inflammatory one and, thirdly, that inflammatory T cell phenotypes correlate with a worse prognosis of the disease. This could allow proposing VD as a potential treatment of ALS in a future trial. More largely, this could reinforce arguments in favor of an immune intervention to attenuate the severity of this devastating disorder.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
30 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Man or woman with sporadic ALS and a possible, probable or definite diagnosis regarding the revised Escorial criteria (Forbes et al., 2001). Patients are followed quarterly according to national recommendations. At the end of the follow up period (1 year for each patient), all patients remaining in the " possible " group of diagnosis will be excluded.
  • Disease onset (date of onset of muscle weakness) < 18 months at the time of inclusion.
  • Age: 30 to 80 years-old, inclusive.
  • Patient treated by riluzole at a steady dosage since at least 3 months.
  • Patient accepting to give informed consent
  • Exclusion criteria will be :
  • A previous treatment with VD in the preceding 2 years, whatever the dose used.
  • Patient with an already known autoimmune disorder
  • Patient with severe ALS involvement suggesting that survival over the 1 year follow up is highly unlikely (ex : tetraplegia, use of non-invasive ventilation for more than 10 hrs/day, ALSFRS-R (ALS Functional Rating Scale) score < à 20).
  • Pregnant or breast-feeding woman.
  • Patient without social security insurance
  • For the Controls:
  • Controls will be spouses of our ALS patients. Such a group has the advantage of similar life style conditions, and frequently similar geographical origin. Controls and ALS patients will match for age and gender. Controls will also fulfill the following inclusion and exclusion criteria
  • Inclusion criteria
  • Subject accepting to give informed consent
  • Exclusion criteria
  • Subject with an already known neurodegenerative disorder
  • Subject with an already known autoimmune disorder
  • Subject who received a treatment with VD in the preceding 2 years, whatever the dose used.
  • Pregnant or breastfeeding woman
  • Subject without social security insurance

排除标准

  • 未提供

结局指标

主要结局

Study of T-cell phenotypes in ALS patients and controls

时间窗: 6 months

Analyses of the expression of T cells phenotypes between volunteers and patients with ALS

次要结局

  • Relationships between expression of T cell phenotypes and ALS criteria(6 months)
  • Relationships between vitamin D blood level and pronostic factors of the ALS(6 months)
  • Influence of vitamin D treatment on T cell phenotypes(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验