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. 2024 Sep 30:17:6887-6894.
doi: 10.2147/JIR.S477415. eCollection 2024.

Elevated Serum HMGB1 Levels and Their Association with Recurrence of Acute Ischaemic Stroke

Affiliations

Elevated Serum HMGB1 Levels and Their Association with Recurrence of Acute Ischaemic Stroke

Liping Shen et al. J Inflamm Res. .

Abstract

Purpose: The study aimed to investigate the correlation between baseline serum levels of high mobility group box 1 (HMGB1) and the recurrence of acute ischemic stroke (AIS).

Patients and methods: A total of 544 AIS patients were enrolled and followed up monthly. Serum HMGB1 levels were measured using enzyme-linked immunosorbent assay (ELISA). The primary endpoint was the first recurrence of AIS.

Results: During a median follow-up period of 43 months, 62 of the 544 AIS patients experienced a recurrence. Both HMGB1 levels and national institute of health stroke scale (NIHSS) scores were significantly higher in the recurrence group compared to the no-recurrence group (p<0.05). According to the receiver operating characteristic curve analysis, the combination (0.855, 95% CI: 0.800-0.911) of HMGB1 (0.745, 95% CI: 0.663-0.826) and NIHSS (0.822, 95% CI: 0.758-0.886) had a higher value for predicting AIS recurrence than either of them (p<0.05). Kaplan-Meier analyses demonstrated that the cumulative survival without AIS recurrence was significantly lower in patients in the high HMGB1 level group than in the low HMGB1 level group (p<0.05). The multifactorial Cox analyses indicated that elevated baseline serum HMGB1 levels (HR: 7.489, 95% CI:4.383-12.795) were a highly effective predictor of recurrence in AIS.

Conclusion: Elevated baseline serum HMGB1 levels were found to be a highly effective predictor of recurrence in AIS.

Keywords: acute ischemic stroke; high mobility group box 1; recurrence.

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Conflict of interest statement

The author(s) report no conflicts of interest in this work.

Figures

Figure 1
Figure 1
Flow chart of the study. AIS, acute ischemic stroke.
Figure 2
Figure 2
Receiver operating characteristic curve for predicting AIS recurrence. Receiver operating characteristic curves were used to determine the area under the curve for each variable and z-test comparisons were performed.
Figure 3
Figure 3
Kaplan-Meier curves showing the probability of no recurrence in patients with AIS at different HMGB1 levels. Kaplan-Meier survival curves were used to conduct survival analysis which were then compared using the Log rank test.

References

    1. Collaborators GBDS. Global, regional, and national burden of stroke and its risk factors, 1990-2019: a systematic analysis for the Global Burden of Disease Study 2019. Lancet Neurol. 2021;20(10):795–820. doi:10.1016/S1474-4422(21)00252-0 - DOI - PMC - PubMed
    1. Tu WJ, Zhao Z, Yin P, et al. Estimated Burden of Stroke in China in 2020. JAMA Network Open. 2023;6(3):e231455. doi:10.1001/jamanetworkopen.2023.1455 - DOI - PMC - PubMed
    1. Tu WJ, Wang LD, Special Writing Group of China Stroke Surveillance R. China stroke surveillance report 2021. Mil Med Res. 2023;10(1):33. doi:10.1186/s40779-023-00463-x - DOI - PMC - PubMed
    1. Bejot Y, Daubail B, Giroud M. Epidemiology of stroke and transient ischemic attacks: current knowledge and perspectives. Rev Neurol. 2016;172(1):59–68. doi:10.1016/j.neurol.2015.07.013 - DOI - PubMed
    1. Mohan KM, Crichton SL, Grieve AP, et al. Frequency and predictors for the risk of stroke recurrence up to 10 years after stroke: the South London Stroke Register. J Neurol Neurosurg Psych. 2009;80(9):1012–1018. doi:10.1136/jnnp.2008.170456 - DOI - PubMed

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