Amin Moein, Nakamura Kunio, Daboul Lynn, O'Donnell Carly, Cao Quy, Rodrigues Paulo, Derbyshire John, Azevedo Christina, Bar-Or Amit, Caverzasi Eduardo, Calabresi Peter A, Cree Bruce A C, Freeman Leorah, Henry Roland, Longbrake Erin E, Oh Jiwon, Papinutto Nico, Pelletier Daniel, Prčkovska Vesna, Raza Praneeta C, Ramos Marc, Samudralwar Rohini, Schindler Matthew, Sotirchos Elias S, Sicotte Nancy, Solomon Andrew J, Shinohara Russell, Reich Daniel S, Sati Pascal, Ontaneda Daniel
Mellen Center for Multiple Sclerosis, Cleveland Clinic, Cleveland, United States.
Department of Biomedical Engineering, Lerner Research Institute, Cleveland Clinic, Cleveland, United States.
Mult Scler Relat Disord. 2025 Jan;93:106182. doi: 10.1016/j.msard.2024.106182. Epub 2024 Nov 25.
Diagnosis of multiple sclerosis (MS) frequently relies on MRI dissemination in time (DIT) and space (DIS), as codified in 2017 McDonald criteria (McD 2017). The central vein sign (CVS) is a proposed MS diagnostic biomarker, but its optimal incorporation into McD 2017 has not been extensively studied.
Evaluate the diagnostic performance of several methods incorporating CVS into McD 2017 radiological DIS criteria.
Data were obtained from the CAVS-MS Pilot, a cross-sectional, international multi-center study conducted by the North American Imaging in MS Cooperative (NAIMS) that recruited adults referred for suspicion/diagnosis of demyelinating disease. Diagnostic performance of methods incorporating CVS into McD 2017 radiological DIS were evaluated by comparing sensitivity, specificity, and accuracy.
78 participants (37 MS, 41 others) were included. For MS diagnosis, sensitivity, specificity, and accuracy of DIS based on brain imaging (DIS-B) alone was 92 %, 69 %, and 78 %. Requiring at least one lesion with CVS in any brain location in addition to DIS-B increased specificity (sensitivity 92 %, specificity 81 %, accuracy 86 %). Presence of 2 deep white matter lesions with CVS as an additional topography for DIS-B had higher sensitivity (sensitivity 97 %, specificity 59 %, accuracy 77 %).
Incorporation of CVS in McD 2017 DIS criteria can be used to improve diagnostic accuracy. Validation in additional prospective studies is needed.
多发性硬化症(MS)的诊断通常依赖于2017年麦克唐纳标准(McD 2017)中规定的时间上的弥散(DIT)和空间上的弥散(DIS)。中央静脉征(CVS)是一种提议的MS诊断生物标志物,但其在McD 2017中的最佳纳入方式尚未得到广泛研究。
评估将CVS纳入McD 2017放射学DIS标准的几种方法的诊断性能。
数据来自CAVS-MS试点研究,这是一项由北美MS成像协作组(NAIMS)进行的横断面国际多中心研究,招募了因怀疑/诊断脱髓鞘疾病而转诊的成年人。通过比较敏感性、特异性和准确性,评估将CVS纳入McD 2017放射学DIS的方法的诊断性能。
纳入78名参与者(37名MS患者,41名其他患者)。对于MS诊断,仅基于脑成像(DIS-B)的DIS的敏感性、特异性和准确性分别为92%、69%和78%。除DIS-B外,要求在任何脑区至少有一个具有CVS的病灶可提高特异性(敏感性92%,特异性81%,准确性86%)。将2个具有CVS的深部白质病灶作为DIS-B的额外部位,其敏感性更高(敏感性97%,特异性59%,准确性77%)。
将CVS纳入McD 2017 DIS标准可用于提高诊断准确性。需要在更多前瞻性研究中进行验证。