Volume 23 Issue 8
Aug.  2025
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SHI Peng, WU Xinyu, HUAI Yushui, SONG Hongwei, NIAN Di. Significance and mechanism of neuroultrasound combined with neuromagnetic resonance imaging in the diagnosis and treatment of Guillain-Barré syndrome[J]. Chinese Journal of General Practice, 2025, 23(8): 1292-1297. doi: 10.16766/j.cnki.issn.1674-4152.004118
Citation: SHI Peng, WU Xinyu, HUAI Yushui, SONG Hongwei, NIAN Di. Significance and mechanism of neuroultrasound combined with neuromagnetic resonance imaging in the diagnosis and treatment of Guillain-Barré syndrome[J]. Chinese Journal of General Practice, 2025, 23(8): 1292-1297. doi: 10.16766/j.cnki.issn.1674-4152.004118

Significance and mechanism of neuroultrasound combined with neuromagnetic resonance imaging in the diagnosis and treatment of Guillain-Barré syndrome

doi: 10.16766/j.cnki.issn.1674-4152.004118
Funds:

 JNFX2024039

 202304295107020075

  • Received Date: 2025-05-14
    Available Online: 2025-10-31
  •   Objective  To explore the significance and mechanism of neuroultrasound and neuromagnetic resonance imaging in the diagnosis of Guillain-Barré syndrome (GBS).  Methods  A total of 43 GBS patients who were first diagnosed at the First Affiliated Hospital of Bengbu Medical University from October 2021 to February 2025 were enrolled, and 24 patients with normal physical examination were enrolled as control group. Based on neurophysiological examinations, the GBS were classified into two subtypes: acute inflammatory demyelinating polyneuropathy (AIDP) and acute motor axonal neuropathy (AMAN). Neuroultrasound and neuromagnetic resonance imaging were performed on all subjects. The cross-sectional area of the cervical nerve roots and peripheral nerves (CSA) was measured by neuroultrasound, and the CSA of the cervical nerve root and lumbar sacral nerve root was measured by neuromagnetic resonance imaging. The degree of neurological impairment in GBS was assessed using the GBS disability scale scores (GDSS), and the correlation between CSA values and the degree of neurological deficit was evaluated. Peripheral venous blood was collected, and the levels of pyroptosis-related inflammatory factors in peripheral blood were measured using ELISA.  Results  Compared with the control group, the nerve roots and peripheral nerves of the limbs in the AIDP group and the AMAN group were thickened, and the CSA value was increased. Among them, nerve ultrasound showed that there were statistically significant differences in C5 and C6 among the three groups (H=20.216, P < 0.001; H=12.452, P=0.002), and the magnetic resonance imaging results showed that compared with the AMAN group and the healthy control group, the CSA values of C4-C8 and L3-S1 in the AIDP group were significantly increased, and the differences were statistically significant (P < 0.01). The CSA value of peripheral nerves was positively correlated with the degree of neurological deficit (P < 0.05). Pyroptotic inflammatory factors were higher than those in the control group, and the difference was statistically significant (P < 0.05).  Conclusion  The elevated CSA values of nerve roots and peripheral nerves, as well as neurological deficits in GBS, may be associated with the inflammatory cascade triggered by pyroptosis pathway activation. The detection of peripheral blood inflammatory cytokines combined with neuroimaging may facilitate early diagnosis of GBS and provide novel insights for its clinical management.

     

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  • [1]
    HE S, LIN Y. Application and value of limbs peripheral nerve ultrasound in Guillain-Barre syndrome[J]. Altern Ther Health M, 2024, 30(10): 416-421.
    [2]
    SHEN D, CHU F, LANG Y, et al. Nuclear factor Kappa B inhibitor suppresses experimental autoimmune neuritis in mice via declining macrophages polarization to M1 type[J]. Clin Exp Immunol, 2021, 206(1): 110-117. doi: 10.1111/cei.13637
    [3]
    DASH S, KAMATH U, PAI A R, et al. Serum inflammatory markers in patients with guillain barre syndrome[J]. Neurol India, 2022, 70(5): 2082-2085. doi: 10.4103/0028-3886.359238
    [4]
    VELTSISTA D, KEFALOPOULOU Z, KINTOS V, et al. Identical late motor responses in early Guillain-Barré syndrome: a-waves and repeater F-waves[J]. J Peripher Nerv Syst, 2023, 28(1): 41-46. doi: 10.1111/jns.12522
    [5]
    FOKKE C, VAN DEN BERG B, DRENTHEN J, et al. Diagnosis of Guillain-Barré syndrome and validation of Brighton criteria[J]. Brain, 2014, 137(1): 33-43. doi: 10.1093/brain/awt285
    [6]
    RATH J, ZULEHNER G, SCHOBER B, et al. Cerebrospinal fluid analysis in Guillain-Barré syndrome: value of albumin quotients[J]. J Neurol, 2021, 268(9): 3294-3300. doi: 10.1007/s00415-021-10479-9
    [7]
    KMEZIC I, GUSTAFSSON R, HANSSON M, et al. Beta-trace protein in chronic inflammatory demyelinating polyradiculoneuropathy and Guillain-Barre syndrome-clinical utilization and a new insight into pathophysiological mechanisms[J]. J Neurol Sci, 2025, 15: 123439. DOI: 10.1016/j.jns.2025.123439.
    [8]
    BOURQUE PR, BREINER A, MOHER D, et al. Adult CSF total protein: higher upper reference limits should be considered worldwide. A web-based survey[J]. J Neurol Sci, 2019, 15(396): 48-51.
    [9]
    GOMEZ Á, DIAZ A, CARRION-PENAGOS J, et al. Clinical and electrophysiological characteristics of Guillain-Barré syndrome in Colombia[J]. Peripher Nerv Syst, 2019, 24(3): 268-271. doi: 10.1111/jns.12340
    [10]
    KENAN G, REGEV T, KUSHNIR M, et al. Reasons for delayed treatment initiation in Guillain-Barre syndrome[J]. J Neurol Sci, 2022, 434: 120179. DOI: 10.1016/j.jns.2022.120179.
    [11]
    GOYAL K, AGGARWAL P, GUPTA M. Ultrasound evaluation of peripheral nerves of the lower limb in diabetic peripheral neuropathy[J]. Eur J Radiol, 2021, 145: 110058. DOI: 10.1016/j.ejrad.2021.110058.
    [12]
    SEEJITH K, SASIDHARANPILLAI S, AJITHKUMAR K, et al. High resolution ultrasound in the assessment of peripheral nerves in leprosy: a comparative cross-sectional study[J]. Indian J Dermatol Ve, 2021, 87(2): 199-206.
    [13]
    崔凯丽, 黄培君, 苏庆杰. 抗CD20单克隆抗体联合FcRn拮抗剂治疗多种神经节苷脂抗体阳性的慢性吉兰-巴雷综合征1例[J]. 河北医学, 2025, 31(1): 174-176.

    CUI K L, HUANG P J, SU Q J. One case of chronic Guillain-Barre syndrome positive for multiple ganglioside antibodies was treated with anti-CD20 monoclonal antibody combined with FcRn antagonist[J]. Hebei Medicine, 2025, 31(1): 174-176.
    [14]
    ALANAZY M H, BAKRY S S, ALQAHTANIl A, et al. Clinical features and outcome of Guillain-Barre syndrome in Saudi Arabia: a multicenter, retrospective study[J]. BMC Neurol, 2021, 21(1): 275-283. doi: 10.1186/s12883-021-02314-5
    [15]
    LI X Y, YU M, ZHOU X L, et al. A method of ultrasound diagnosis for unilateral peripheral entrapment neuropathy based on multilevel side-to-side image contrast[J]. Math Biosci Eng, 2019, 16(4): 2250-2265. doi: 10.3934/mbe.2019111
    [16]
    GRIMM A, DECARD B F, SCHRAMM A, et al. Ultrasound and electrophysiologic findings in patients with Guillain-Barré syndrome at disease onset and over a period of six months[J]. Clin Neyrophysiol, 2016, 127(2): 1657-1663. doi: 10.1016/j.clinph.2015.06.032
    [17]
    ALTHUBAITIl F, GUIOMARD C, RIVIER F, et al. Prognostic value of contrast-enhanced MRI in Guillain-Barré syndrome in children[J]. Arch Pediatrie, 2022, 29 (3): 230-235. doi: 10.1016/j.arcped.2022.01.004
    [18]
    LI X, YANG L, WANG G, et al. Extensive cytokine biomarker analysis of Guillain-Barré Syndrome[J]. Sci Rep, 2023, 13(1): 8354-8366. doi: 10.1038/s41598-023-35610-w
    [19]
    漆星月, 赵旭东, 李雷. 炎症负荷指数与吉兰-巴雷综合征严重程度的相关性分析[J]. 中华全科医学, 2024, 22(9): 1487-1490. doi: 10.16766/j.cnki.issn.1674-4152.003665

    QI X Y, ZHAO X D, LI L. Correlation analysis between the inflammatory burden index and the severity of Guillain-Barre syndrome[J]. Chinese Journal of General Practice, 2024, 22(9): 1487-1490. doi: 10.16766/j.cnki.issn.1674-4152.003665
    [20]
    HIGASHIKUNI Y, LIU W, NUMATA G, et al. NLRP3 infammasome activation through heart-brain interaction initiates cardiac infammation and hypertrophy during pressure overload[J]. Circulation, 2023, 147(4): 338-355. doi: 10.1161/CIRCULATIONAHA.122.060860
    [21]
    DE CARVALHO RIBEIRO M, IRACHETA-VALLVE A, BABUTA M, et al. Alcohol-induced extracellular ASC specks perpetuate liver inflammation and damage in alcohol-associated hepatitis even after alcohol cessation[J]. Hepatology, 2023, 78(1): 225-242. doi: 10.1097/HEP.0000000000000298
    [22]
    WU X, GONG L, XIE L, et al. NLRP3 defciency protects against intermittent hypoxia-induced neuroinfammation and mitochondrial ROS by promoting the PINK1-Parkin pathway of mitophagy in a murine model of sleep apnea[J]. Front Immunol, 2021, 12: 628168. DOI: 10.3389/fimmu.2021.628168.
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