Cerebrospinal fluid YKL-40 level evolution is associated with autoimmune encephalitis remission

IF 4.6 2区 医学 Q2 IMMUNOLOGY
Guillaume Dorcet, Marie Benaiteau, Jérémie Pariente, Fabienne Ory-Magne, Emmanuel Cheuret, Marie Rafiq, Wesley Brooks, Bénédicte Puissant-Lubrano, Fran?oise Fortenfant, Yves Renaudineau, Chloé Bost
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引用次数: 0

Abstract

Objective

Because of its heterogeneity in clinical presentation and course, predicting autoimmune encephalitis (AIE) evolution remains challenging. Hence, our aim was to explore the correlation of several biomarkers with the clinical course of disease.

Methods

Thirty-seven cases of AIE were selected retrospectively and divided into active (N = 9), improved (N = 12) and remission (N = 16) AIE according to their disease evolution. Nine proteins were tested in both serum and cerebrospinal fluid (CSF) at diagnosis (T0) and during the follow-up (T1), in particular activated MMP-9 (MMP-9A) and YKL-40 (or chitinase 3-like 1).

Results

From diagnosis to revaluation, AIE remission was associated with decreased YKL-40 and MMP-9A levels in the CSF, and with decreased NfL and NfH levels in the serum. The changes in YKL-40 concentrations in the CSF were associated with (1) still active AIE when increasing >10% (P-value = 0.0093); (2) partial improvement or remission when the changes were between +9% and −20% (P-value = 0.0173); and remission with a reduction > −20% (P-value = 0.0072; overall difference between the three groups: P-value = 0.0088). At T1, the CSF YKL-40 levels were significantly decreased between active and improved as well as improved and remission AIE groups but with no calculable threshold because of patient heterogeneity.

Conclusion

The concentration of YKL-40, a cytokine-like proinflammatory protein produced by glial cells, is correlated in the CSF with the clinical course of AIE. Its introduction as a biomarker may assist in following disease activity and in evaluating therapeutic response.

Abstract Image

脑脊液YKL-40水平进化与自身免疫性脑炎缓解相关
目的由于自身免疫性脑炎(AIE)在临床表现和病程上的异质性,预测其发展仍具有挑战性。因此,我们的目的是探索几种生物标志物与疾病临床病程的相关性。方法回顾性分析37例AIE患者,根据病情进展分为活动性AIE(9例)、改善性AIE(12例)和缓解性AIE(16例)。在诊断(T0)和随访(T1)期间,在血清和脑脊液(CSF)中检测了9种蛋白质,特别是活化的MMP-9 (MMP-9A)和YKL-40(或几次质酶3-样1)。结果从诊断到重新评估,AIE缓解与脑脊液中YKL-40和MMP-9A水平降低以及血清中NfL和NfH水平降低有关。脑脊液中YKL-40浓度的变化与(1)当AIE升高>10%时仍有活性(p值= 0.0093);(2)变化在+9% ~ - 20%之间部分改善或缓解(p值= 0.0173);缓解,减少> - 20% (p值= 0.0072;三组间总差异:p值= 0.0088)。在T1时,脑脊液YKL-40水平在AIE活动组和改善组以及改善组和缓解组之间显著降低,但由于患者异质性,没有可计算的阈值。结论脑脊液中胶质细胞产生的细胞因子样促炎蛋白YKL-40的浓度与AIE的临床病程相关。其作为生物标志物的引入可能有助于跟踪疾病活动和评估治疗反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical & Translational Immunology
Clinical & Translational Immunology Medicine-Immunology and Allergy
CiteScore
12.00
自引率
1.70%
发文量
77
审稿时长
13 weeks
期刊介绍: Clinical & Translational Immunology is an open access, fully peer-reviewed journal devoted to publishing cutting-edge advances in biomedical research for scientists and physicians. The Journal covers fields including cancer biology, cardiovascular research, gene therapy, immunology, vaccine development and disease pathogenesis and therapy at the earliest phases of investigation.
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