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评估中国获得性脱髓鞘疾病儿童及青少年的临床特征与眼部表现

Evaluating the Clinical Characteristics and Ophthalmic Manifestations in Children and Adolescents with Acquired Demyelinating Disorders in China.

作者信息

Li Si-Yuan, Peng Chun-Xia, Zuo Hua-Xin, Lin Qi, Yu Ji-Feng, Liu Wen, Li Li, Shi Wei

机构信息

Department of Ophthalmology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.

出版信息

Br J Hosp Med (Lond). 2025 Mar 26;86(3):1-12. doi: 10.12968/hmed.2024.0555. Epub 2025 Mar 18.

Abstract

Pediatric acquired demyelinating disorders (ADS) include various monophasic and recurrent inflammatory conditions of the central nervous system (CNS). Optic neuritis (ON) is a demyelinating disease primarily affecting the optic nerve axons due to autoimmune inflammation. To investigate the clinical characteristics, ophthalmic manifestations, laboratory test results, and prognostic indicators of Chinese children and adolescents with ADS. The clinical data of 57 patients with ADS treated in the Beijing Children's Hospital from March 2021 to December 2023, were retrospectively collected and analyzed. The primary outcomes include best-corrected visual acuity (BCVA) at onset, peripapillary retinal nerve fiber layers (RNFL) thickness, serum myelin oligodendrocyte glycoprotein (MOG) antibody level, aquaporin-4 (AQP4) antibody level, and final BCVA after hormone therapy. The analyses included 57 children and adolescents in the study, including 38 optic neuritis (ON), 12 neuromyelitis optica spectrum disorder (NMOSD), 5 acute disseminated encephalomyelitis (ADEM), and 2 multiple sclerosis (MS) patients. The median age of patients facing the initial attack of ON was 9 years (3-15 years), with 23 children and adolescents (40.4%) aged eight years or younger, and 37 patients (64.9%) were bilaterally affected. Half of the children and adolescents (15/30) were MOG-Ab seropositive, and 19.4% (6/31) were AQP4-Ab seropositive. Children and adolescents with NMOSD were more likely to have severe visual impairment at acute onset ( < 0.05), with 84.2% of them having low vision acuity (BCVA worse than 0.1), as compared with 64.9% in the ON group. The RNFL thickness of affected eye was thinner than unaffected eyes (median 72.0 μm vs. median 102.0 μm, < 0.05). Patients with NMOSD exhibited lower RNFL thickness across all measured sectors compared to those with ON. Significant differences were noted in the average RNFL and in each specific region of the retina, including the temporal RNFL, nasal RNFL, nasal superior RNFL, nasal inferior RNFL, temporal superior RNFL, and temporal inferior RNFL (all < 0.05). After the treatment with intravenous methylprednisolone, both patients with ON (52 eyes; 86.7%) or NMOSD (20 eyes; 90.9%) group had functional visual recovery (BCVA better or equal 0.4). This study shows that Chinese children and adolescents with ADS present distinctive clinical features, including earlier onset and more bilateral involvement. Furthermore, NMOSD patients experience more severe visual acuity impairment and thinner peripapillary RNFL. All children and adolescents of ON or NMOSD respond well to methylprednisolone treatment.

摘要

儿童获得性脱髓鞘疾病(ADS)包括中枢神经系统(CNS)的各种单相和复发性炎症性疾病。视神经炎(ON)是一种脱髓鞘疾病,主要由于自身免疫性炎症影响视神经轴突。为了研究中国儿童和青少年ADS的临床特征、眼部表现、实验室检查结果和预后指标。回顾性收集并分析了2021年3月至2023年12月在北京儿童医院接受治疗的57例ADS患者的临床资料。主要观察指标包括发病时的最佳矫正视力(BCVA)、视乳头周围视网膜神经纤维层(RNFL)厚度、血清髓鞘少突胶质细胞糖蛋白(MOG)抗体水平、水通道蛋白4(AQP4)抗体水平以及激素治疗后的最终BCVA。该分析纳入了57名儿童和青少年,其中包括38例视神经炎(ON)、12例视神经脊髓炎谱系障碍(NMOSD)、5例急性播散性脑脊髓炎(ADEM)和2例多发性硬化症(MS)患者。ON初次发作患者的中位年龄为9岁(3 - 15岁),其中23名儿童和青少年(40.4%)年龄在8岁及以下,37例患者(64.9%)为双侧受累。一半的儿童和青少年(15/30)MOG - Ab血清学阳性,19.4%(6/31)为AQP4 - Ab血清学阳性。NMOSD的儿童和青少年在急性发作时更易出现严重视力损害(<0.05),其中8�.2%视力低下(BCVA低于0.1),而ON组为64.9%。患眼的RNFL厚度比未患眼薄(中位数72.0μm对中位数102.0μm,<0.05)。与ON患者相比,NMOSD患者在所有测量区域的RNFL厚度均较低。在平均RNFL以及视网膜的每个特定区域,包括颞侧RNFL、鼻侧RNFL、鼻上侧RNFL、鼻下侧RNFL、颞上侧RNFL和颞下侧RNFL,均存在显著差异(均<0.05)。静脉注射甲基强的松龙治疗后,ON组(52只眼;86.7%)和NMOSD组(20只眼;90.9%)的患者视力均有功能性恢复(BCVA改善或等于0.4)。本研究表明,中国儿童和青少年ADS具有独特的临床特征,包括发病较早和双侧受累更多。此外,NMOSD患者视力损害更严重,视乳头周围RNFL更薄。所有ON或NMOSD的儿童和青少年对甲基强的松龙治疗反应良好。

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