小儿髓鞘少突胶质细胞糖蛋白抗体相关疾病的血液参数

IF 2.3 3区 医学 Q3 CLINICAL NEUROLOGY
Alina Peternell , Christian Lechner , Markus Breu , Martin Preisel , Mareike Schimmel , Astrid Eisenkölbl , Joachim Zobel , Eva-Maria Wendel , Markus Reindl , Kevin Rostásy , Matthias Baumann
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引用次数: 0

摘要

背景和目的髓鞘少突胶质细胞糖蛋白抗体相关性疾病(MOGAD)患者临床表现为急性播散性脑脊髓炎(ADEM)、视神经炎(ON)、横贯性脊髓炎(TM)或水光素-4-IgG(AQP4-IgG)阴性神经脊髓炎视谱系障碍(NMOSD)样表型。我们旨在分析和比较MOGAD、AQP4-IgG阳性NMOSD(因此是NMOSD)、多发性硬化症(MS)和健康对照组(HC)患儿的血液参数。方法我们评估了这四组之间以及组内临床发作、急性治疗和缓解期间全血细胞计数(CBC)、中性粒细胞与淋巴细胞比值(NLR)、血小板与淋巴细胞比值(PLR)、单核细胞与淋巴细胞比值(MLR)和 C 反应蛋白(CRP)的差异:66 名患者患有 MOGAD(202 个时间点),11 名患者患有 NMOSD(76 个时间点),58 名患者患有 MS(219 个时间点),39 名患者患有 HC(53 个时间点)。在临床发作时,与缓解期相比(p <0.001),以及与所有其他组别相比(p <0.001),MOGAD 的白细胞计数升高。MOGAD和NMOSD的NLR较高,而NMOSD的PLR较高,然而,经多重检验校正后,这些结果并不显著。在 NMOSD 和 MS 中,糖皮质激素导致白细胞计数和 NLR 增加,而在 MOGAD 中,这些数值在急性治疗期间保持稳定。在缓解期,MOGAD 的 NLR 恢复正常,而 NMOSD 的 NLR 则居高不下。讨论一些血液参数,主要是白细胞计数和差值计数,可以帮助临床医生评估疾病的活动性,区分复发和假性复发,甚至区分不同的疾病实体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Blood parameters in pediatric myelin oligodendrocyte glycoprotein antibody-associated disorders

Background and objectives

Patients with myelin oligodendrocyte glycoprotein antibody-associated disorders (MOGAD) clinically present e.g. with acute disseminated encephalomyelitis (ADEM), optic neuritis (ON), transverse myelitis (TM) or aquaporin-4-IgG (AQP4-IgG) negative neuromyelitis optica spectrum disorders (NMOSD)-like phenotypes. We aimed to analyze and compare blood parameters in children with MOGAD, AQP4-IgG-positive NMOSD (hence NMOSD), multiple sclerosis (MS) and healthy controls (HC).

Methods

We evaluated differences in complete blood counts (CBC), neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), monocyte-to-lymphocyte ratio (MLR) and C-reactive protein (CRP) between these four groups and within the groups between clinical attack, acute treatment and remission.

Results

Our cohort consisted of 174 children and adolescents with a total of 550 timepoints: 66 patients had MOGAD (202 timepoints), 11 NMOSD (76 timepoints), 58 MS (219 timepoints) and 39 were HC (53 timepoints). At clinical attack, leukocyte counts were elevated in MOGAD compared to remission (p < 0.001) and compared to all other groups (p < 0.001). NLR was high in MOGAD and NMOSD, and PLR was high in NMOSD, however, after correction for multiple testing these findings did not remain significant. While glucocorticoids caused an increase of leukocyte counts and NLR in NMOSD and MS, these values remained stable during acute treatment in MOGAD. In remission, NLR normalized in MOGAD, while it stayed high in NMOSD. PLR increased in NMOSD and was significantly higher compared to all other groups.

Discussion

Some blood parameters, mainly leukocyte and differential counts, might help clinicians to evaluate disease activity, differentiate relapses from pseudo-relapses and even distinguish between different disease entities.

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来源期刊
CiteScore
6.30
自引率
3.20%
发文量
115
审稿时长
81 days
期刊介绍: The European Journal of Paediatric Neurology is the Official Journal of the European Paediatric Neurology Society, successor to the long-established European Federation of Child Neurology Societies. Under the guidance of a prestigious International editorial board, this multi-disciplinary journal publishes exciting clinical and experimental research in this rapidly expanding field. High quality papers written by leading experts encompass all the major diseases including epilepsy, movement disorders, neuromuscular disorders, neurodegenerative disorders and intellectual disability. Other exciting highlights include articles on brain imaging and neonatal neurology, and the publication of regularly updated tables relating to the main groups of disorders.
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