Frontiers in Immunology (Dec 2023)

The analysis of serum lipids profile in Guillain-Barre syndrome

  • Lijuan Wang,
  • Lijuan Wang,
  • Lijuan Wang,
  • Yaowei Ding,
  • Yaowei Ding,
  • Yaowei Ding,
  • Jie Liu,
  • Jie Liu,
  • Jie Liu,
  • Guanghui Zheng,
  • Guanghui Zheng,
  • Guanghui Zheng,
  • Siwen Li,
  • Siwen Li,
  • Siwen Li,
  • Wencan Jiang,
  • Wencan Jiang,
  • Wencan Jiang,
  • Kelin Chen,
  • Kelin Chen,
  • Kelin Chen,
  • Xin Luan,
  • Xin Luan,
  • Xin Luan,
  • Yuxin Chen,
  • Yuxin Chen,
  • Yuxin Chen,
  • Siqi Wang,
  • Siqi Wang,
  • Siqi Wang,
  • Guojun Zhang,
  • Guojun Zhang,
  • Guojun Zhang

DOI
https://doi.org/10.3389/fimmu.2023.1301577
Journal volume & issue
Vol. 14

Abstract

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BackgroundGuillain-Barre syndrome (GBS) is an immune-mediated inflammatory peripheral neuropathy. This study aimed to conduct a systematic analysis of the serum lipids profile in GBS.MethodsWe measured the serum lipids profile in 85 GBS patients and compared it with that of 85 healthy controls matched for age and sex. Additionally, we analyzed the correlation between lipids and the severity, subtypes, precursor infections, clinical outcomes, clinical symptoms, immunotherapy, and other laboratory markers of GBS.ResultsCompared to the healthy controls, GBS exhibited significantly elevated levels of Apolipoprotein B (APOB), Apolipoprotein C2 (APOC2), Apolipoprotein C3 (APOC3), Apolipoprotein E (APOE), triglycerides (TG), and residual cholesterol (RC). Conversely, Apolipoprotein A1 (APOA1), Apolipoprotein A2 (APOA2), and high-density lipoprotein (HDL) were substantially lower in GBS. Severe GBS displayed noticeably higher levels of APOC3 and total cholesterol (TC) compared to those with mild disease. Regarding different clinical outcomes, readmitted GBS demonstrated higher RC expression than those who were not readmitted. Moreover, GBS who tested positive for neuro-virus antibody IGG in cerebrospinal fluid (CSF) exhibited heightened expression of APOC3 in comparison to those who tested negative. GBS with cranial nerve damage showed significantly reduced expression of HDL and APOA1 than those without such damage. Additionally, GBS experiencing limb pain demonstrated markedly decreased HDL expression. Patients showed a significant reduction in TC after intravenous immunoglobulin therapy. We observed a significant positive correlation between lipids and inflammatory markers, including TNF-α, IL-1β, erythrocyte sedimentation rate (ESR), white blood cells, monocytes, and neutrophils in GBS. Notably, APOA1 exhibited a negative correlation with ESR. Furthermore, our findings suggest a potential association between lipids and the immune status of GBS.ConclusionThe research demonstrated a strong connection between lipids and the severity, subtypes, clinical outcomes, precursor infections, clinical symptoms, immunotherapy, inflammation, and immune status of GBS. This implies that a low-fat diet or the use of lipid-lowering medications may potentially serve as an approach for managing GBS, offering a fresh viewpoint for clinical treatment of this condition.

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