Mariotto Sara, Carta Sara, Dinoto Alessandro, Lippi Giuseppe, Salvagno Gian Luca, Masin Laura, Alberti Daniela, Marignier Romain, Ferrari Sergio
Neurology Unit, Department of Neurosciences, Biomedicine, and Movement Sciences, University of Verona, Verona, Italy.
Section of Clinical Biochemistry, University of Verona, Verona, Italy.
Eur J Neurol. 2022 Jun;29(6):1855-1858. doi: 10.1111/ene.15304. Epub 2022 Mar 14.
Anti-myelin oligodendrocyte glycoprotein antibodies (MOG-Abs) distinguish a group of inflammatory disorders which can be preceded by specific or non-specific infections. A few single cases have been reported in association with SARS-CoV-2 infection, but a specific study on the correlation between COVID-19 and myelin oligodendrocyte glycoprotein (MOG)-associated disorder (MOGAD) has not yet been performed. The aim of this study was to determine the impact of the pandemic on this condition.
We analysed SARS-CoV-2 serology in patients newly diagnosed with MOGAD (1 August 2020 to 31 May 2021). MOG-Ab-seronegative age- and time-matched subjects were used as controls. SARS-CoV-2 immunoglobulin G (IgG) levels were analysed using an anti-SARS-CoV-2 US Food and Drug Administration-approved ELISA assay and confirmed with a trimeric anti-SARS-CoV-2 S1/S2 IgG immunochemiluminescent test, concomitantly assaying the anti-receptor binding domain (RBD) of spike protein IgG and anti-RBD total Ig. We actually compared the number of cases referred in each of the last 3 years.
Presence of SARS-CoV-2 IgG antibodies was more common (12/30, 40%) in MOGAD patients than in controls (6/30, 20%), although the difference was not significant (p = 0.16; odds ratio 2.67, 95% confidence interval 0.85-9.17). The most common clinical presentations of MOGAD SARS-CoV-2-seropositive patients included optic neuritis (n = 6) and myelitis (n = 3). The number of diagnosed cases increased over the last 3 years, in particular, when including cases referred to us before the COVID-19 pandemic, in the initial phase of the first wave and in the late phase of the second wave (n = 9, rate 10.6% in 2019; n = 13, rate 12.3% in 2020; n = 15, rate 14.7% in 2021).
Our findings provide preliminary data on SARS-CoV-2 as a potential trigger of MOGAD.
抗髓鞘少突胶质细胞糖蛋白抗体(MOG-Abs)可区分出一组炎症性疾病,这些疾病可能由特定或非特定感染引发。此前已有少数与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染相关的单病例报告,但尚未对2019冠状病毒病(COVID-19)与髓鞘少突胶质细胞糖蛋白(MOG)相关疾病(MOGAD)之间的相关性进行专门研究。本研究旨在确定这一疫情对该疾病的影响。
我们分析了2020年8月1日至2021年5月31日新诊断为MOGAD患者的SARS-CoV-2血清学情况。将MOG-Ab血清阴性、年龄和时间匹配的受试者作为对照。使用美国食品药品监督管理局批准的抗SARS-CoV-2酶联免疫吸附测定(ELISA)检测法分析SARS-CoV-2免疫球蛋白G(IgG)水平,并用三聚体抗SARS-CoV-2 S1/S2 IgG免疫化学发光试验进行确认,同时检测刺突蛋白IgG的抗受体结合域(RBD)和抗RBD总Ig。我们实际比较了过去三年中每年转诊病例的数量。
MOGAD患者中SARS-CoV-2 IgG抗体的存在比对照组更常见(12/30,40%),而对照组为(6/30,20%),尽管差异不显著(p = 0.16;优势比2.67,95%置信区间0.85 - 9.17)。SARS-CoV-2血清阳性的MOGAD患者最常见的临床表现包括视神经炎(n = 6)和脊髓炎(n = 3)。在过去三年中,确诊病例数量有所增加,特别是当包括在COVID-19大流行之前、第一波初期和第二波后期转诊给我们的病例时(2019年n = 9,发病率10.6%;2020年n = 13,发病率12.3%;2021年n = 15,发病率14.7%)。
我们的研究结果提供了关于SARS-CoV-2作为MOGAD潜在触发因素的初步数据。