Department of Pediatric Neurology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Department of Pediatric Neurology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Pediatr Neurol. 2022 Sep;134:7-10. doi: 10.1016/j.pediatrneurol.2022.06.004. Epub 2022 Jun 10.
The pathogenesis of multiple sclerosis (MS) involves immune-mediated mechanisms, and disease-modifying therapies (DMTs) administered in MS have immunomodulatory effects. The concern about MS patients' susceptibility to coronavirus disease 2019 (COVID-19) has prompted several studies based on clinical observations and questionnaires. Information about COVID-19 in pediatric-onset multiple sclerosis (POMS) is scarce. The objective of this study was to collect information on the experience of POMS patients with COVID-19 during the pandemic.
This cross-sectional study was conducted with POMS patients diagnosed at Hacettepe University Pediatric Neurology Department and under 23 years of age between October 1 and December 31, 2021. Those who experienced COVID-19 or had a history of contact and were found seropositive for COVID-19 were evaluated for the severity of COVID-19, disability, treatment status, and comorbidities.
Among the 101 POMS patients, 13 reported having had COVID-19 and five were exposed and seropositive but clinically asymptomatic. Of these 18 patients, 14 were ≤18 years of age at the time of the study. All 13 patients (72%) reported mild symptoms without hospitalization or respiratory support. Four of 18 had a neurological disability (Expanded Disability Status Scale [EDSS] scores ranging between 1 and 7.5), while the remaining had a score of 0. The outcome of COVID-19 was not affected by DMTs, neurological disabilities, and comorbidities.
In this single-center POMS series, the small subgroup of patients who had contacted the SARS-CoV-2 virus or developed COVID-19 had reported no or mild symptoms. This may be partly related to the infrequent use of rituximab in this group. Our results corroborate those in adult-onset MS where no increased risk is reported for patients whose EDSS scores are <6 and who are not on B cell-depleting DMTs. Although less frequently than in adult MS, immunosuppressive DMTs may be needed in POMS; therefore, the importance of appropriate vaccination is to be underlined.
多发性硬化症(MS)的发病机制涉及免疫介导机制,MS 中使用的疾病修正疗法(DMT)具有免疫调节作用。对 MS 患者易感染 2019 年冠状病毒病(COVID-19)的担忧促使了几项基于临床观察和问卷调查的研究。关于儿科发病多发性硬化症(POMS)的 COVID-19 信息很少。本研究的目的是收集 POMS 患者在大流行期间感染 COVID-19 的经验信息。
这是一项横断面研究,纳入了 2021 年 10 月 1 日至 12 月 31 日期间在哈塞特佩大学儿科神经病学系诊断为 POMS 且年龄在 23 岁以下的患者。评估了 COVID-19 严重程度、残疾、治疗状况和合并症的患者为经历过 COVID-19 或有接触史且 COVID-19 血清阳性的患者。
在 101 名 POMS 患者中,13 名报告患有 COVID-19,5 名有接触史且血清阳性但无临床症状。这 18 名患者中,14 名在研究时年龄≤18 岁。所有 13 名患者(72%)报告有轻微症状,无需住院或呼吸支持。18 名患者中有 4 名有神经残疾(扩展残疾状态量表[EDSS]评分在 1 至 7.5 之间),其余患者的评分为 0。COVID-19 的结局不受 DMT、神经残疾和合并症的影响。
在本单中心 POMS 系列中,接触 SARS-CoV-2 病毒或发生 COVID-19 的小亚组患者报告无或轻微症状。这可能部分与该组中很少使用利妥昔单抗有关。我们的结果与成人发病 MS 相符,在 EDSS 评分<6 且未使用 B 细胞耗竭 DMT 的患者中,报告 COVID-19 风险无增加。虽然不如成人 MS 常见,但 POMS 可能需要使用免疫抑制性 DMT;因此,强调适当接种疫苗的重要性。