Anterograde and trans-synaptic neurodegeneration in aquaporin-4-antibody neuromyelitis optica spectrum disorder patients with a history of transverse myelitis

水通道蛋白4抗体阳性视神经脊髓炎谱系障碍患者(有横贯性脊髓炎病史)的前向性和跨突触神经退行性变

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Abstract

Neuromyelitis optica spectrum disorder associated with aquaporin-4-antibodies (AQP4-NMOSD) is an autoimmune disease of the CNS with a high risk of visual, motor and sensory disability secondary to optic neuritis (ON) and transverse myelitis (TM) attacks. The degree of recovery is difficult to predict and may be affected by the extent of ensuing neurodegeneration. While neurodegeneration in AQP4-NMOSD is reported in the visual system after ON, its occurrence in patients with TM remains largely unknown. The aim of this study was to use advanced MRI to cross-sectionally examine the sensory and motor pathways in 18 AQP4-NMOSD patients with a history of TM and 20 healthy controls. The results showed that AQP4-NMOSD patients had decreased cross-sectional area (mean 63.62 versus 70.75, P = 0.016) and reduced fractional anisotropy (mean 0.60 versus 0.65, P = 0.014) in the cervical spinal cord, and changes in the sensory, but not motor, cerebral pathway as evidenced by higher isotropic volume fraction in the ventral posterolateral (VPL) nuclei (mean 0.06 versus 0.05, P = 0.03), reduced neurite density in the right superior thalamic radiation and lower T1 relaxation rates in the primary somatosensory cortex (mean 0.72 versus 0.74, P = 0.04) when compared with healthy controls. Neurite density in the VPL nuclei significantly correlated with the Expanded Disability Status Scale (r = -0.469, P < 0.05). In conclusion, AQP4-NMOSD patients who had TM display features of anterograde and trans-synaptic neurodegeneration in the sensory pathway, which correlate with clinical outcomes. Further studies will clarify the temporal dynamics of such changes and their potential utility as clinical trial outcomes.

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