Serum Homer1 is a Novel Biomarker for Predicting the Clinical Outcomes of Acute Ischemic Stroke Patients

We aim to explore the relationship between Homer1 and the outcomes of AIS patients at 3 months. This prospective cohort study was conducted from May 2022 to March 2023. In this study, we investigated the association between serum Homer1 levels by enzyme-linked immunosorbent assay at admission and fu...

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Published inJournal of inflammation research Vol. 17; pp. 1337 - 1347
Main Authors Lv, Weihao, Ruan, Zhe, Zhang, Qianqian, Wei, Yaxuan, Wu, Xiuquan, Dou, Ya-Nan, Chao, Wangshu, Fei, Xiaowei, Fei, Zhou
Format Journal Article
LanguageEnglish
Published New Zealand Dove Medical Press 2024
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Summary:We aim to explore the relationship between Homer1 and the outcomes of AIS patients at 3 months. This prospective cohort study was conducted from May 2022 to March 2023. In this study, we investigated the association between serum Homer1 levels by enzyme-linked immunosorbent assay at admission and functional outcomes of patients at 3 months after AIS. Overall, 89 AIS patients (48 good outcomes and 41 poor outcomes) and 83 healthy controls were included. The median serum Homer1 level of patients at admission with poor outcomes was significantly higher than that of patients with good outcomes (39.33 vs 33.15, <0.001). Serum Homer1 levels at admission were positively correlated with the severity of AIS (r = 0.488, <0.001). The optimal cutoff of serum Homer1 level as an indicator for an auxiliary diagnosis of 3 months functional outcomes was 35.07 pg/mL, with a sensitivity of 75.0% and a specificity of 92.7% (AUC 0.837; 95% CI [0.744-0.907]; <0 0.001). The odds ratio of MRS > 2 predicted by the level of serum Homer1 after 3 months was 1.665 (1.306-2.122; <0.001). Serum concentrations of Homer1 have a high predictive value for neurobehavioral outcomes after acute ischemic stroke. Higher serum Homer1 levels (>35.07 pg/mL) were positively associated with poor functional outcomes of patients 3 months post-stroke.
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ISSN:1178-7031
1178-7031
DOI:10.2147/JIR.S453018