Cleveland Clinic Foundation, Cleveland, OH, United States.
Cedars Sinai, Los Angeles, CA, United States; NINDS, NIH, Bethesda, MD, United States.
Neuroimage Clin. 2021;32:102834. doi: 10.1016/j.nicl.2021.102834. Epub 2021 Sep 23.
The specificity and implementation of current MRI-based diagnostic criteria for multiple sclerosis (MS) are imperfect. Approximately 1 in 5 of individuals diagnosed with MS are eventually determined not to have the disease, with overreliance on MRI findings a major cause of MS misdiagnosis. The central vein sign (CVS), a proposed MRI biomarker for MS lesions, has been extensively studied in numerous cross sectional studies and may increase diagnostic specificity for MS. CVS has desirable analytical, measurement, and scalability properties. "Central Vein Sign: A Diagnostic Biomarker in Multiple Sclerosis (CAVS-MS)" is an NIH-supported, 2-year, prospective, international, multicenter study conducted by the North American Imaging in MS Cooperative (NAIMS) to evaluate CVS as a diagnostic biomarker for immediate translation into clinical care. Study objectives include determining the concordance of CVS and McDonald Criteria to diagnose MS, the sensitivity of CVS to detect MS in those with typical presentations, and the specificity of CVS among those with atypical presentations. The study will recruit a total of 400 participants (200 with typical and 200 with atypical presentations) across 11 sites. T2*-weighted, high-isotropic-resolution, segmented echo-planar MRI will be acquired at baseline and 24 months on 3-tesla scanners, and FLAIR* images (combination of FLAIR and T2*) will be generated for evaluating CVS. Data will be processed on a cloud-based platform that contains clinical and CVS rating modules. Imaging quality control will be conducted by automated methods and neuroradiologist review. CVS will be determined by Select6* and Select3* lesion methods following published criteria at each site and by central readers, including neurologists and neuroradiologists. Automated CVS detection and algorithms for incorporation of CVS into McDonald Criteria will be tested. Diagnosis will be adjudicated by three neurologists who served on the 2017 International Panel on the Diagnosis of MS. The CAVS-MS study aims to definitively establish CVS as a diagnostic biomarker that can be applied broadly to individuals presenting for evaluation of the diagnosis of MS.
目前基于磁共振成像(MRI)的多发性硬化症(MS)诊断标准的特异性和实施情况并不完美。大约每 5 名被诊断为 MS 的患者中,最终有 1 名被确定没有该疾病,而过度依赖 MRI 结果是 MS 误诊的主要原因。中央静脉征(CVS)是一种用于 MS 病变的 MRI 生物标志物,已在许多横断面研究中进行了广泛研究,可能会提高 MS 的诊断特异性。CVS 具有理想的分析、测量和可扩展性属性。“中央静脉征:多发性硬化症的诊断生物标志物(CAVS-MS)”是一项由美国国立卫生研究院(NIH)支持的、为期 2 年的前瞻性、国际、多中心研究,由北美多发性硬化症成像合作组织(NAIMS)进行,旨在评估 CVS 作为一种诊断生物标志物,以便立即转化为临床护理。研究目标包括确定 CVS 与 McDonald 标准诊断 MS 的一致性、CVS 诊断具有典型表现的 MS 的敏感性以及 CVS 在具有非典型表现的患者中的特异性。该研究将在 11 个地点共招募 400 名参与者(200 名具有典型表现,200 名具有非典型表现)。在 3T 扫描仪上采集基线和 24 个月的 T2*-加权、高各向同性分辨率、分段回波平面 MRI,以及生成 FLAIR图像(FLAIR 和 T2的组合)以评估 CVS。数据将在一个包含临床和 CVS 评分模块的基于云的平台上进行处理。成像质量控制将通过自动方法和神经放射学家审查进行。CVS 将根据在每个站点和由神经科医生和神经放射科医生等中央读者遵循的已发表标准,通过 Select6和 Select3病变方法来确定。将测试自动 CVS 检测和将 CVS 纳入 McDonald 标准的算法。诊断将由三位参加 2017 年 MS 国际诊断小组的神经科医生进行裁决。CAVS-MS 研究旨在明确确立 CVS 作为一种诊断生物标志物,可广泛应用于因 MS 诊断评估而就诊的个体。