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Non-lesional cerebellar damage in patients with clinically isolated syndrome: DTI measures predict early conversion into clinically definite multiple sclerosis

机译:临床孤立综合征患者的非损伤性小脑损伤:DTI措施可预测早期转变为临床明确的多发性硬化症

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Background Today, no specific test for the diagnosis of multiple sclerosis (MS) is available due to the lack of characteristic symptoms at beginning. This circumstance also complicates estimation of disease progression. Recent findings provided evidence for early, non-lesional cerebellar damage in patients with (clinically definite) relapsing-remitting MS. Objective To investigate if microstructural cerebellar alterations can also serve as early structural biomarker for disease progression and conversion from clinically isolated syndrome (CIS) to MS. Methods 46 patients diagnosed with CIS and 26 age-matched healthy controls were admitted to high-resolution MRI including diffusion tensor imaging (DTI) to examine atrophy and microstructural integrity of the cerebellum. Microstructural integrity of cerebellar white matter was assessed by fractional anisotropy (FA) as derived from DTI. Results Although all 46 patients of our CIS cohort showed no cerebellar lesions in structural MRI (T1w, T2w, FLAIR), their mean cerebellar FA was already reduced compared to healthy controls. Significant FA reduction at follow-up DTI 6?months after baseline examination was observed. In 16 patients that converted to MS, we found a correlation between initial cerebellar FA and conversion latency ( R ?=?0.71, p ?
机译:背景技术今天,由于开始时缺乏特征性症状,因此尚无用于诊断多发性硬化症(MS)的特定测试。这种情况也使疾病进展的估计复杂化。最新发现为患有(临床上确定的)复发缓解型MS的患者早期,非病变性小脑损伤提供了证据。目的探讨微结构小脑改变是否还可以作为疾病发展和从临床孤立综合征(CIS)转化为MS的早期结构生物标志物。方法46例被诊断为CIS的患者和26例年龄相匹配的健康对照者接受包括弥散张量成像(DTI)在内的高分辨率MRI检查,以检查小脑的萎缩和微结构完整性。小脑白质的微结构完整性通过衍生自DTI的分数各向异性(FA)进行评估。结果尽管我们的CIS队列的所有46例患者在结构MRI(T1w,T2w,FLAIR)中均未显示小脑病变,但与健康对照组相比,他们的平均小脑FA已有所减少。在基线检查后6个月的随访DTI观察到FA显着降低。在16例转化为MS的患者中,我们发现初始小脑FA与转化潜伏期之间存在相关性(R = 0.71,p <0.002)。在FA临界≤0.352的情况下,最初的小脑FA预测在24个月内会转变为复发缓解型MS(FA临界:早期MS患者的平均小脑FA,在另一项研究中确定)。结论DTI似乎反映了MS早期的组织损伤,当时尚无法检测到萎缩和病变。 CIS患者的小脑FA降低可能表明疾病的活动期和不稳定期,从而缩短了向MS的转化时间。强调 ?有说服力的证据表明CIS患者存在隐藏的活动性疾病过程? NAWM中小脑白质FA的广泛改变?小脑FA减少表明向MS转化的时间更短?新的亮点已成为诊断多发性硬化症的时间点。

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