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Neutrophil-to-lymphocyte ratio is a risk indicator of Guillain-Barré syndrome and is associated with severity and short-term prognosis

INTRODUCTION: Guillain-Barré syndrome (GBS) is an autoimmune disorder targeting the peripheral nervous system. The neutrophil-to-lymphocyte ratio (NLR), a simple indicator of immune function, is potentially related to its incidence and severity; however, this should be confirmed. We aimed to evaluat...

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Detalles Bibliográficos
Autores principales: Sun, Shujun, Wen, Yiyong, Li, Shu, Huang, Zhihua, Zhu, Jianming, Li, Yandeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036506/
https://www.ncbi.nlm.nih.gov/pubmed/36967912
http://dx.doi.org/10.1016/j.heliyon.2023.e14321
Descripción
Sumario:INTRODUCTION: Guillain-Barré syndrome (GBS) is an autoimmune disorder targeting the peripheral nervous system. The neutrophil-to-lymphocyte ratio (NLR), a simple indicator of immune function, is potentially related to its incidence and severity; however, this should be confirmed. We aimed to evaluate the role of NLR in the diagnosis, severity, and prognosis of GBS. METHODS: Data of GBS patients and controls visiting our hospital from January 2010 to December 2020 were retrospectively analyzed (Clinical trial registration: ChiCTR2100053540). Risk factors were determined through logistic regression. Smoothing curves, receiver-operating characteristic curves, and forest plots were drawn. RESULTS: We included 136 GBS patients and 211 controls. NLR, as a continuous variable, was associated with GBS risk (OR, 2.32; 95% CI, 1.68–3.21; p < 0.001), severe functional disability (OR, 1.23; 95% CI, 1.06–1.43; p = 0.006), severe weakness (OR, 1.19; 95% CI, 1.06–1.35, p = 0.004), and short-term prognosis (OR, 1.21; 95% CI, 1.08–1.36; p = 0.001). NLR was more strongly associated with GBS risk in older (≥60 years) (OR, 7.17; 95% CI, 2.38–21.61) or male (OR, 2.88; 95% CI, 1.78–4.64) patients than in younger (<60 years) (OR, 1.88; 95% CI, 1.37–2.57) or female (OR, 1.85; 95% CI, 1.24–2.77) patients. NLR was significantly associated with severe functional disability in faster disease progression (OR, 1.53; 95% CI, 1.03–12.29) and male patients (OR, 1.41; 95% CI, 1.03–1.92) versus in slower disease progression (OR, 1.12; 95% CI, 0.77–1.64) and female patients (OR, 1.12; 95% CI, 0.77–1.64). CONCLUSIONS: NLR may be an independent GBS risk factor and predictor of severe functional disability, severe weakness, and short-term prognosis.