MR Unit (IDI), Department of Radiology, and Department of Neurology-Neuroimmunology, CEM-CAT, Hospital Vall d'Hebron, Autonomous University of Barcelona, Barcelona, Spain.
Neuroimaging Research Unit, Department of Neurology, Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy.
Mult Scler. 2014 Oct;20(11):1471-7. doi: 10.1177/1352458514526083. Epub 2014 Feb 27.
Non-enhancing black holes (neBHs) are more common in multiple sclerosis (MS) patients with longer disease durations and progressive disease subtypes.
Our aim was to analyse the added value of neBHs in patients with clinically isolated syndromes (CISs) for predicting conversion to clinically definite MS (CDMS).
Patients were classified based on the presence or absence of neBHs and on the number of Barkhof-Tintoré (B-T) criteria fulfilled. Dissemination in space (DIS) was defined as the presence of at least three of the four B-T criteria. Dissemination in time (DIT)1 was defined by simultaneous presence of enhancing and non-enhancing lesions. DIT2 was defined by simultaneous presence of neBHs and T2 lesions not apparent on T1-weighted images.
Focal T2-hyperintense brain lesions were identified in 87.7% of the 520 CIS patients, and 41.4% of them presented at least one neBH. Patients meeting DIS, DIT1, and DIT2 had a significantly higher rate of conversion to CDMS. After adjusting for DIS, only patients who fulfilled DIT1 preserved a significant increase in CDMS conversion.
Non-enhancing black holes in CIS patients are associated with a higher risk of conversion to CDMS. However, the predictive value of this finding is lost when added to the DIS criteria.
在多发性硬化症(MS)患者中,无强化黑洞(neBHs)在疾病持续时间较长和进展型疾病亚型中更为常见。
我们旨在分析临床孤立综合征(CIS)患者中 neBHs 的附加价值,以预测向临床确诊多发性硬化症(CDMS)的转化。
根据是否存在 neBHs 以及 Barkhof-Tintoré(B-T)标准的满足情况对患者进行分类。空间弥散(DIS)定义为至少满足四个 B-T 标准中的三个。时间弥散 1(DIT1)定义为同时存在强化和非强化病变。时间弥散 2(DIT2)定义为同时存在 neBHs 和 T2 病变,而 T1 加权图像上未见 T2 病变。
520 例 CIS 患者中,87.7%存在局灶性 T2 高信号脑病变,其中 41.4%存在至少一个 neBH。符合 DIS、DIT1 和 DIT2 的患者向 CDMS 的转化率明显更高。在调整 DIS 后,只有满足 DIT1 的患者保留了向 CDMS 转化的显著增加。
CIS 患者中的无强化黑洞与向 CDMS 转化的风险增加相关。然而,当将其添加到 DIS 标准时,这一发现的预测价值就丧失了。