Kang Hao, Qiu Huaiyu, Hu Xiaofeng, Wei Shihui, Tao Yong
Department of Ophthalmology, Beijing Chaoyang Hospital, Capital Medical University, Beijing, China.
Senior Department of Ophthalmology, The Third Medical Center of PLA General Hospital, Beijing, China.
Front Pain Res (Lausanne). 2022 May 9;3:870211. doi: 10.3389/fpain.2022.870211. eCollection 2022.
The purpose of this study was to investigate pain and radiological features of different types of first-episode demyelinating optic neuritis (ON).
Eighty-three patients presenting with first-episode aquaporin-4 (AQP4) antibody-associated ON (AQP4-ON; = 28), myelin oligodendrocyte glycoprotein (MOG) antibody-associated ON (MOG-ON; = 26) and idiopathic demyelinating optic neuritis (IDON, = 29) were included in this retrospective case-control study. We assessed optic nerve lesions on magnetic resonance imaging (MRI), acute pain associated with onset of optic neuritis and clinical characteristics of those ON patients with different serum autoantibody status.
24 AQP4-ON patients (85.75%), 23 MOG-ON patients (88.5%) and 24 IDON patients (82.8%) suffered from ON-associated pain. MOG-ON had mostly retro-orbital pain; AQP4-ON and IDON had mostly neuropathic pain. In addition, pain was more severe in AQP4ON patients than in other ON patients. In MRI, bilateral involvement was more common in AQP4-ON than IDON (26.9 and 3.7%); radiological optic nerve head swelling was more common in MOG-ON than in AQP4-ON and IDON (68.0 vs. 23.1 vs. 25.9%). MRI lesion in peri-optic nerve sheath was more common in AQP4-ON (53.8 vs. 16.0 vs. 3.7%). In 70 patients with ON-associated pain, gadolinium enhancement of orbital optic nerve was most common in MOG-ON patients (82.4 vs. 55.0 vs. 33.3%, = 0.018), and enhancement of optic chiasma was most common in AQP4-ON patients (40.0 vs. 5.9 vs. 6.7%, = 0.015). Perineural and orbital enhancement was observed only in patients with MOG-ON ( < 0.001). The length of enhancement was longer in AQP4-ON patients than in MOG-ON and IDON patients.
Pain is a common symptom in patients with all types of demyelinating ON. AQP4-ON is frequently associated with severe ON-associated pain and longitudinally extensive optic nerve inflammatory lesions. Intra-orbital and peri-optic inflammation were more frequently observed in patients with MOG-ON, which was closely related to optic disc swelling and retro-orbital pain provoked by eye movements.
本研究旨在调查不同类型的首发脱髓鞘性视神经炎(ON)的疼痛及影像学特征。
本回顾性病例对照研究纳入了83例首发水通道蛋白4(AQP4)抗体相关视神经炎(AQP4-ON;n = 28)、髓鞘少突胶质细胞糖蛋白(MOG)抗体相关视神经炎(MOG-ON;n = 26)和特发性脱髓鞘性视神经炎(IDON,n = 29)的患者。我们评估了磁共振成像(MRI)上的视神经病变、与视神经炎发作相关的急性疼痛以及不同血清自身抗体状态的视神经炎患者的临床特征。
24例AQP4-ON患者(85.75%)、23例MOG-ON患者(88.5%)和24例IDON患者(82.8%)患有与视神经炎相关的疼痛。MOG-ON主要为眶后疼痛;AQP4-ON和IDON主要为神经性疼痛。此外,AQP4-ON患者的疼痛比其他视神经炎患者更严重。在MRI上,AQP4-ON双侧受累比IDON更常见(26.9%和3.7%);放射学上视神经乳头肿胀在MOG-ON中比AQP4-ON和IDON更常见(68.0%对23.1%对25.9%)。视神经周围鞘膜的MRI病变在AQP4-ON中更常见(53.8%对16.0%对3.7%)。在70例与视神经炎相关疼痛的患者中,眼眶视神经钆增强在MOG-ON患者中最常见(82.4%对55.0%对33.3%,P = 0.018),视交叉增强在AQP4-ON患者中最常见(40.0%对5.9%对6.7%,P = 0.015)。仅在MOG-ON患者中观察到神经周围和眼眶增强(P < 0.001)。AQP4-ON患者的增强长度比MOG-ON和IDON患者更长。
疼痛是所有类型脱髓鞘性视神经炎患者的常见症状。AQP4-ON常与严重的视神经炎相关疼痛和纵向广泛的视神经炎性病变相关。MOG-ON患者更常观察到眶内和视神经周围炎症,这与视盘肿胀和眼球运动引起的眶后疼痛密切相关。