Serum neurofilament light chain predicts disease severity in axonal variants of acute immune neuropathies: A retrospective monocentric cohort study

被引:1
作者
Afzali, Ali Maisam [1 ,2 ]
Vosko, Milan [1 ]
Reinhardt, Nya [1 ]
Zinevych, Iaroslav [1 ]
Gmeiner, Vincent [1 ]
Korn, Thomas [1 ,2 ,3 ]
Gasperi, Christiane [1 ]
Berthele, Achim [1 ]
Feneberg, Emily [1 ]
Hemmer, Bernhard [1 ,3 ]
机构
[1] Tech Univ Munich, Sch Med & Hlth, Dept Neurol, Ismaninger Str 22, D-81675 Munich, Germany
[2] Tech Univ Munich, Inst Expt Neuroimmunol, Sch Med & Hlth, Munich, Germany
[3] Munich Cluster Syst Neurol, Munich, Germany
关键词
acute axonal immune neuropathy; GBS; immune neuropathies; NfL; GUILLAIN-BARRE-SYNDROME; DIAGNOSIS;
D O I
10.1111/ene.16539
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and purpose: The purpose was to explore the prognostic utility of neurofilament light chain (NfL) in patients with immune-mediated polyradiculoneuropathies (IMPs). Methods: This retrospective monocentric study analysed serum and cerebrospinal fluid samples from patients diagnosed with IMP collected prior to treatment initiation. NfL concentrations were correlated with clinical outcomes, including F score and hospitalization duration. Results: Amongst 115 IMP patients tested, baseline cerebrospinal fluid and serum NfL (sNfL) concentrations were higher in acute inflammatory axonal polyradiculoneuropathy (AIAP) than other IMP variants. In the AIAP cohort, a positive correlation was observed between baseline sNfL concentrations, F score and hospitalization duration. Multivariate linear regression analysis further supported the predictive relationship between elevated baseline sNfL concentrations and clinical outcomes. Using receiver operating characteristic analysis, a cut-off value for sNfL of 351 pg/mL was found to predict an F score >3 in AIAP with a sensitivity of 40% and specificity of 81.8%. AIAP patients with sNfL concentrations above this threshold required longer hospitalization (extended by 15 days). Discussion: Our findings highlight the potential of baseline sNfL as an effective marker for distinguishing between IMP variants and predicting the prognosis of AIAP. Further validation may facilitate translation of sNfL into clinical practice, potentially identifying high-risk patients for tailored treatment approaches.
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