In clinical practice, acute optic neuritis (ON) associated with the development of neuromyelitis optica (NMO) after the first attack is often indistinguishable from that associated with multiple sclerosis (MS)1-3; and different therapeutic strategies are required for the two diseases because of their immunopathogenic differences4. Therefore, we aimed to determine the optimal combination of features derived from conventional magnetic resonance imaging (MRI) and diffusion-weighted imaging using readout-segmented echo-planar imaging (RESOLVE-DWI) for the differentiation of the two types of acute ON.
Purpose
In clinical practice, acute optic neuritis (ON) associated with the development of neuromyelitis optica (NMO) after the first attack is often indistinguishable from that associated with multiple sclerosis (MS)1-3; and different therapeutic strategies are required for the two diseases because of their immunopathogenic differences4. Therefore, we aimed to determine the optimal combination of features derived from conventional magnetic resonance imaging (MRI) and diffusion-weighted imaging using readout-segmented echo-planar imaging (RESOLVE-DWI) for the differentiation of the two types of acute ON.Methods
Fifty-four patients with acute ON (NMO-related cases: 26, MS-related cases: 28) were enrolled in this study. Conventional MRI (T1WI, T2WI and contrast-enhanced T1WI) and RESOLVE-DWI images taken within four weeks of their initial attack were included in our evaluation. All the examinations were performed with a 3 T scanner (MAGNETOM Verio, Siemens Healthcare, Erlangen, Germany) using a 32-channel head coil. The features detected by conventional MRI (including laterality, the enhancement pattern, and the extent and position of involvement) and the apparent diffusion coefficient (ADC) measurements were retrospectively compared between the NMO-related and MS-related groups. The parameters for axial/coronal RESOLVE-DWI were as follows: TR, 2700/4000 ms; TE, 68/83 ms; thickness, 2/3 mm; gap, 0.2/0.3 mm; FOV, 210×210/145×145 mm2; acquisition matrix, 192×192/192×192; 9/9 segments; [z1] b value 800/800 s/mm2; NEX, 1/2; and acquisition time, 4/5.5 min. ADC maps were automatically generated on the MR workstation. In order to demonstrate the image quality differences between RESOLVE-DWI and single-shot echo-planar imaging (SS-EPI) DWI, both sequences were performed on several volunteers. The SS-EPI parameters are: TR, 2700/4000 ms; TE, 98/86 ms; thickness, 2/3 mm; gap, 0.2/0.3 mm; FOV, 210×210/150×150 mm2; acquisition matrix, 192×192/192×192; b value, 800/800 s/mm2; NEX, 10/8; and acquisition time, 2.2/3.1 min. An imaging comparison between RESOLVE and SS-EPI is shown in Fig. 1. A multivariate logistic regression analysis was used to identify the most significant variables, [YX2] and receiver operating characteristic curve analyses were performed to determine the ability of a combined diagnostic model based on the qualitative and quantitative characteristics identified in this study to differentiate the two conditions. P values <0.05 were considered statistically significant. [z1]请和技师老师确认,RESOLVE是分几段读出的 [YX2]The variable or imaging features info should be provided1. Toosy AT, Mason DF, Miller DH. Optic neuritis. The Lancet Neurology 2014;13:83-99.
2. Barnett Y, Sutton IJ, Ghadiri M, et al. Conventional and advanced imaging in neuromyelitis optica. AJNR Am J Neuroradiol 2014;35:1458-66.
3. Wingerchuk DM, Lennon VA, Lucchinetti CF, et al. The spectrum of neuromyelitis optica. The Lancet Neurology 2007;6:805-815.
4. Palace J, Leite MI, Nairne A, et al. Interferon Beta treatment in neuromyelitis optica: increase in relapses and aquaporin 4 antibody titers. Arch Neurol 2010;67:1016-7.