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血清 NfL 和 EGFR/NfL 比值 mRNA 作为髓鞘少突胶质细胞糖蛋白 IgG 相关疾病表型和疾病严重程度的生物标志物。

Serum NfL and EGFR/NfL ratio mRNAs as biomarkers for phenotype and disease severity of myelin oligodendrocyte glycoprotein IgG-associated disease.

机构信息

Second Department of Neurology, Hebei Children's Hospital, Shijiazhuang, China.

Department of Science and Education, Hebei Children's Hospital, Shijiazhuang, China.

出版信息

Front Immunol. 2024 May 14;15:1388734. doi: 10.3389/fimmu.2024.1388734. eCollection 2024.

Abstract

BACKGROUND AND PURPOSE

Myelin oligodendrocyte glycoprotein (MOG) IgG is frequently elevated in pediatric patients with acquired demyelinating syndrome (ADS). However, no specific biomarkers exist for phenotype classification, symptom severity, prognosis, and treatment guidance of MOG-IgG-associated disease (MOGAD). This study evaluated neurofilament light chain (NfL) and endothelial growth factor receptor (EGFR) mRNA expression levels in serum and cerebrospinal fluid (CSF) as potential biomarkers for MOGAD in Chinese children.

METHODS

This was a cross-sectional and single-center study. We enrolled 22 consecutive pediatric patients hospitalized with MOGAD and 20 control pediatric patients hospitalized for noninflammatory neurological diseases in Hebei Children's Hospital. Serum and CSF were collected from MOGAD patients within 3 days before immunotherapy. The mRNA levels of NfL and EGFR in serum and CSF were measured by real-time polymerase chain reaction (qPCR), and the EGFR/NfL ratio mRNA was calculated. These measurement values were then compared between disease groups and among MOGAD phenotypes. In addition, the correlations between the mRNAs of three markers (NfL, EGFR, EGFR/NfL ratio), extended disability status scale (EDSS) scores, and clinical phenotypes were analyzed.

RESULTS

Serum and CSF NfL mRNA levels were significantly higher of acute-stage MOGAD patients than those of control patients ( 0.05 and 0.01, respectively), while the mRNA levels of serum EGFR and EGFR/NfL ratio were significantly lower of MOGAD patients than those of controls ( 0.05, 0.0001). Serum NfL mRNA was significantly correlated with mRNA of serum EGFR ( =0.480, < 0.05). Serum and CSF NfL mRNA levels in MOGAD patients with the ADEM-like phenotype were also significantly higher than those in control patients ( < 0.01, < 0.01) and optic neuritis (ON) phenotype ( < 0.05, < 0.05). Both mRNAs of NfL in CSF and EGFR/NfL ratio in serum were correlated with EDSS scores ( < 0.05, = 0.424; < 0.05, = -0.521).

CONCLUSION

The mRNA levels of elevated NfL in serum and CSF as well as lower EGFR and EGFR/NfL ratio in serum could help distinguish acute-phase MOGAD. Higher mRNA levels of NfL in serum and CSF of MOGAD patients help distinguish ADEM-like phenotype. In addition, serum EGFR/NfL mRNA ratio is indicative of disease severity in pediatric patients with MOGAD. Further investigations are warranted to elucidate the pathological mechanisms underlying these associations.

摘要

背景与目的

髓鞘少突胶质细胞糖蛋白(MOG)IgG 在患有获得性脱髓鞘综合征(ADS)的儿科患者中经常升高。然而,目前尚无针对 MOG-IgG 相关疾病(MOGAD)的表型分类、症状严重程度、预后和治疗指导的特异性生物标志物。本研究评估了神经丝轻链(NfL)和内皮生长因子受体(EGFR)mRNA 在血清和脑脊液(CSF)中的表达水平,作为中国儿童 MOGAD 的潜在生物标志物。

方法

这是一项横断面和单中心研究。我们纳入了 22 例连续住院的 MOGAD 儿科患者和 20 例因非炎症性神经系统疾病住院的河北儿童医院儿科对照患者。在免疫治疗前 3 天内从 MOGAD 患者中采集血清和 CSF。通过实时聚合酶链反应(qPCR)测量血清和 CSF 中 NfL 和 EGFR 的 mRNA 水平,并计算 EGFR/NfL 比值 mRNA。然后比较疾病组之间和 MOGAD 表型之间的这些测量值。此外,分析了三个标志物(NfL、EGFR、EGFR/NfL 比值)的 mRNAs 与扩展残疾状况量表(EDSS)评分和临床表型之间的相关性。

结果

急性 MOGAD 患者的血清和 CSF NfL mRNA 水平明显高于对照组(分别为 0.05 和 0.01),而 MOGAD 患者的血清 EGFR 和 EGFR/NfL 比值 mRNA 水平明显低于对照组(分别为 0.05,0.0001)。血清 NfL mRNA 与血清 EGFR mRNA 显著相关(=0.480,<0.05)。MOGAD 患者的血清和 CSF NfL mRNA 水平也明显高于对照组(分别为<0.01,<0.01)和视神经炎(ON)表型(分别为<0.05,<0.05)。CSF 中 NfL 的两种 mRNAs 和血清中 EGFR/NfL 比值与 EDSS 评分相关(<0.05,=0.424;<0.05,= -0.521)。

结论

血清和 CSF 中升高的 NfL mRNA 水平以及血清中降低的 EGFR 和 EGFR/NfL 比值有助于区分急性 MOGAD。MOGAD 患者血清和 CSF 中 NfL mRNA 水平升高有助于区分 ADEM 样表型。此外,血清 EGFR/NfL mRNA 比值可反映儿科 MOGAD 患者的疾病严重程度。需要进一步研究以阐明这些关联的病理机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4986/11130348/f4b235234d9e/fimmu-15-1388734-g001.jpg

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