Early Neuroinflammatory Changes as a Prognostic Marker in Clinically Isolated Syndromes Patients.
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 发起方
- 入组人数
- 37
- 试验地点
- 5
- 主要终点
- ▪ Change in USPIO enhancing MS lesion
研究概览
简要总结
While significant progress has been made on medical imagery in recent years in the individualization of different lesions in the nervous system for demyelination, axonal loss, atrophy, little progress has been made in the specific recognition the inflammatory process. Yet this point is essential since the currently available treatments have a partial impact mainly on the inflammatory component and that many uncertainties remain about the links between inflammation and tissue destruction affecting myelin and axons. The recent discovery of a macrophage cell marker in the CNS, more specific (USPIO) of inflammation gives us the opportunity to answer important questions which one can sense that this could have a significant impact on therapeutic drug monitoring of these patients. This study will involve 50 patients recruited in five French centers (Marseille, Paris, Reims, Rennes, Toulouse) from the earliest manifestations of the disease with clinical and MRI scheduled for the first 3 years of their disease.
详细描述
Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system affecting 60.000 persons in France and characterized by widespread inflammation, focal demyelination, and a variable degree of axonal loss. In recent years the concept of MS as an inflammatory neurodegenerative disease has been corroborated by neuropathologic and in vivo MR imaging studies. A number of MR studies show that the principal pathological substrate of permanent disability is axonal loss as detected in MR studies as global atrophy, but also regionally in the white or grey matter, and that atrophy already occurs at early stages of the disease. Though MR imaging is a powerful tool for MS in terms of diagnosis, description of the natural history of the disease and treatment monitoring, the major drawback of MRI in MS is the lack of specificity of the MR findings. Furthermore, with the advent of disease modifying drugs, there is a need for robust and specific MR markers to identify e.g. clinically isolated syndrome (CIS) patients at presentation at high risk to develop MS or a more severe disease course. An increasing body of MRI evidence corroborates that CIS show early and dynamic changes detected by MR imaging, such as global or regional brain atrophy, as a sign of progressive axonal loss, but atrophy is already a late stage sign of the disease, when tissue is lost. Considerable efforts are spent today to identify early and prognostic MR markers for high risk CIS patients.
In the current project we endeavour to study CIS patients with inflammatory disease of the central nervous system or early clinical deficit by using cell labelling MR imaging with ultra small superparamagnetic iron oxide particles (USPIO), which specifically label blood-borne macrophages, a key cell population in MS. We hypothesise that number/volume of USPIO (SH U 555 C) enhancement during the first year is a predictive marker for high risk CIS patients at presentation. This hypothesis is in line with recent findings in the animal model of MS, EAE. Secondary measures of this study will include comparison of the USPIO (SH U 555 C) findings with other highly sensitive, but non-specific MR parameters.
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
- 18 Years 至 45 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age between 18 and 45 years
- •Patients with a first episode suggestive of MS (monofocal or multifocal)
- •Presence of a first neurologic event suggestive of MS that lasted for at least 24 hours
- •Patients with a spatial dissemination criteria according to the Mc Donald diagnostic criteria
- •With an Expanded Disability Status Scale (EDSS) score at baseline between 0 and 5
- •USPIO (SH U 555 C) injection has to be performed within 3 months after start of clinical event
- •Patients have to be in-patients for a minimum of 24 hours after the first USPIO (SH U 555 C) injection
- •Patients with positive or negative USPIO-MRI during screening are included
- •Patients must be compliant with study protocol
- •Patients must have given their written consent to participate in this study
排除标准
- •Any CIS patients having received steroid treatment before acquisition of the baseline USPIO MR scan
- •Patients in whom any disease other than MS could explain their signs and symptoms,
- •Patients with complete transverse myelitis or bilateral optic neuritis will be excluded,
- •Patients who had received prior immunosuppressive or immunomodulatory treatment will be excluded.
- •Patients who had received corticoids 30 days before USPIO-RMI
- •Patients which cannot be in-patients for a minimum of 24 hours after the first USPIO (SH U 555 C) injection
- •Female patients without efficient contraception (oral or others) Pregnant or lactating patients
- •Patients with a known allergy to iron particles and/or dextrans
- •Patients having received in the past 5 months iron oxide particles preceding the MRI examination
- •Patients with a past history of bronchial asthma or any other allergic disorder
- •Patients with a past history for a lower threshold of seizures
- •Any patient presenting with a known contra-indication for MR scanning
- •Non-compliant or uncooperative patients with regard to study protocol
- •Patients not having given their written consent to participate in this study
- •Any patient with an accompanying systemic disease, renal disease, cardiac disease or mental disorder
结局指标
主要结局
▪ Change in USPIO enhancing MS lesion
时间窗: Change from baseline in USPIO enhancing MS lesion at 12 months after the first event of the disease
USPIO enhancing MS lesion at baseline and during 12 month after the first event of the disease as a predictor for a higher risk to develop a second clinical event (time to second clinical event) in CIS patients (evidence of USPIO enhancement: yes/no; and number of USPIO lesions).
次要结局
- Relationship of USPIO (SH U 555 C) enhancing MRI lesions with other MR parameters(at 12 months after the first event of the disease)
- Comparison of primary outcome measures with clinical outcomes and role of USPIO(at 12 months after the first event of the disease)
- Change in USPIO and/or Gadolinium enhancing MS lesions (primary outcome measure)(Change from baseline in USPIO and/or Gadolinium enhancing MS lesions at 3 years after the first event of the disease)