Neurology, Washington University, St. Louis, MO 63110, USA.
Neurology. 2010 May 25;74(21):1694-701. doi: 10.1212/WNL.0b013e3181e042c4.
Diffusion tensor imaging (DTI) quantifies Brownian motion of water within tissue. Inflammation leads to tissue injury, resulting in increased diffusivity and decreased directionality. We hypothesize that DTI can quantify the damage within acute multiple sclerosis (MS) white matter lesions to predict gadolinium (Gd)-enhancing lesions that will persist 12 months later as T1 hypointensities.
A cohort of 22 individuals underwent 7 brain MRI scans over 15 months. DTI parameters were temporally quantified within regions of Gd enhancement. Comparison to the homologous region in the hemisphere contralateral to the Gd-enhancing lesion was also performed to standardize individual lesion DTI parameters.
After classifying each Gd-enhancing region as to black hole outcome, radial diffusivity, mean diffusivity, and fractional anisotropy, along with their standardized values, were significantly altered for persistent black holes (PBHs), and remained elevated throughout the study. A Gd-enhancing region with a 40% elevation in radial diffusivity had a 5.4-fold (95% confidence interval [CI]: 2.1, 13.8) increased risk of becoming a PBH, with 70% (95% CI: 51%, 85%) sensitivity and 69% (95% CI: 57%, 80%) specificity. A model of radial diffusivity, with volume and length of Gd enhancement, was associated with a risk of becoming a PBH of 5.0 (95% CI: 2.6, 9.9). Altered DTI parameters displayed a dose relationship to duration of black hole persistence.
Elevated radial diffusivity during gadolinium enhancement was associated with increased risk for development of a persistent black hole, a surrogate of severe demyelination and axonal injury. An elevated radial diffusivity within active multiple sclerosis lesions may be indicative of more severe tissue injury.
弥散张量成像(DTI)定量测量组织内水分子的布朗运动。炎症导致组织损伤,从而导致扩散度增加和方向度降低。我们假设 DTI 可以量化急性多发性硬化(MS)白质病变内的损伤,以预测在 12 个月后作为 T1 低信号持续存在的钆增强病变。
一组 22 名个体在 15 个月内接受了 7 次脑部 MRI 扫描。在 Gd 增强区域内对 DTI 参数进行了时间量化。还对 Gd 增强病变对侧半脑的同源区域进行了比较,以标准化个体病变的 DTI 参数。
将每个 Gd 增强区域分类为黑洞结局后,径向扩散系数、平均扩散系数和各向异性分数以及它们的标准化值对于持续黑洞(PBH)发生明显改变,并且在整个研究过程中仍保持升高。径向扩散系数升高 40%的 Gd 增强区域发生 PBH 的风险增加了 5.4 倍(95%置信区间[CI]:2.1,13.8),敏感性为 70%(95%CI:51%,85%),特异性为 69%(95%CI:57%,80%)。径向扩散系数与 Gd 增强体积和长度的模型与发生 PBH 的风险相关,风险比为 5.0(95%CI:2.6,9.9)。改变的 DTI 参数与黑洞持续时间呈剂量关系。
Gd 增强期间的径向扩散系数升高与形成持久性黑洞(脱髓鞘和轴突损伤的替代物)的风险增加相关。活动多发性硬化病变内升高的径向扩散系数可能表明组织损伤更严重。