Serum cold-inducible RNA-binding protein (CIRP) levels as a prognostic indicator in patients with acute ischemic stroke

被引:1
|
作者
Li, Mingming [1 ,2 ,3 ]
Yao, Min [1 ]
Shao, Kangmei [1 ]
Shen, Xueyang [1 ]
Ge, Zhaoming [1 ,2 ,3 ]
Li, Yongnan [4 ]
机构
[1] Lanzhou Univ, Lanzhou Univ, Dept Neurol, Hosp 2, Lanzhou, Peoples R China
[2] Lanzhou Univ, Gansu Prov Neurol Clin Med Res Ctr, Hosp 2, Lanzhou, Peoples R China
[3] Lanzhou Univ, Expert Workstat Academician Wang Longde, Hosp 2, Lanzhou, Peoples R China
[4] Lanzhou Univ, Dept Cardiac Surg, Hosp 2, Lanzhou, Peoples R China
来源
FRONTIERS IN NEUROLOGY | 2023年 / 14卷
关键词
acute ischemic stroke (AIS); biomarker; cold-inducible RNA-binding protein (CIRP); inflammation; prognosis;
D O I
10.3389/fneur.2023.1211108
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Acute ischemic stroke (AIS) is the leading cause of morbidity and mortality among cerebrovascular diseases. While animal studies have suggested a correlation between cold-inducible RNA-binding protein (CIRP) serum levels and the severity and prognosis of cerebral infarction, there has been a lack of research exploring this association in humans with cerebral infarction. Materials and methods: A total of 148 patients diagnosed with AIS within 7 days from symptom onset were included in this study. Comprehensive information regarding the patients' basic demographics, medical history, clinical parameters, the severity of cerebral infarction, and serum CIRP levels was collected. Follow-up data were obtained through telephonic interviews or by reviewing clinical notes for 3 months after the patients were discharged to assess the functional outcomes of treatment. Results: The findings of this study demonstrated a significant increase in serum CIRP levels during the early stages of AIS, followed by a gradual decline after 3 days. Significant differences were observed in the serum CIRP levels between the 1-day group and the 4-7 day group (P < 0.0047), as well as between the 2-3 day group and the 4-7 day group (P < 0.0006). Moreover, a significant positive correlation was observed between the serum CIRP levels and the severity of cerebral infarction. Higher serum CIRP levels were associated with more severe National Institutes of Health Stroke Scale scores (P < 0.05) and larger cerebral infarction volumes (P < 0.05). Furthermore, patients with higher serum CIRP levels exhibited poorer modified Rankin scale scores (P < 0.05). These findings indicate that serum CIRP serves as an essential pro-inflammatory mediator and a valuable biomarker for assessing brain injury in patients with AIS. Conclusion: The findings of this study suggest an elevation in serum CIRP levels among patients with AIS. These levels are positively correlated with the severity of AIS and serve as indicators of a poor prognosis. Therefore, CIRP could serve as a target for early clinical intervention while managing AIS, and further research should explore serum CIRP levels as prognostic indicators in AIS.
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