Cerebrospinal Fluid Human Neutrophil Peptides 1-3: A Potential Prognostic Marker in Intracerebral Hemorrhage.

IF 1.2 4区 生物学 Q4 GENETICS & HEREDITY
Genetic testing and molecular biomarkers Pub Date : 2025-11-01 Epub Date: 2025-11-12 DOI:10.1177/19450265251395955
Zhi He, Jun Xie, Fu-Ling Yan, Lei-Yu Geng, Yue-Xin Zhang, Jing-Jing Liu, Chen Zhang
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引用次数: 0

Abstract

Background: This study aims to investigate whether elevated human neutrophil peptides 1-3 (HNP 1-3) levels in cerebrospinal fluid (CSF) are associated with disease severity and clinical outcomes in patients with intracerebral hemorrhage (ICH). Materials and Methods: HNP 1-3 levels were measured in CSF samples collected within 3 days after hemorrhage onset in ICH patients and control subjects. Results: HNP 1-3 levels were significantly higher in ICH patients with moderate-severe coma and hematoma volume >30 mL group. Univariate and multivariate logistic regression analyses demonstrated that CSF HNP 1-3 levels were associated with unfavorable outcomes. Receiver operating characteristic analysis revealed that CSF HNP 1-3 concentrations >466.95 ng/mL could distinguish ICH patients at risk for an unfavorable prognosis. Conclusions: HNP 1-3 exhibit satisfactory diagnostic efficiency for predicting the prognosis of ICH patients.

脑脊液人中性粒细胞肽1-3:脑出血的潜在预后标志物。
背景:本研究旨在探讨脑脊液(CSF)中人中性粒细胞肽1-3 (HNP 1-3)水平升高是否与脑出血(ICH)患者的疾病严重程度和临床结局相关。材料与方法:测定脑出血患者及对照组脑脊液中HNP 1-3水平。结果:脑出血合并中重度昏迷、血肿容量> ~ 30ml组HNP 1-3水平明显升高。单因素和多因素logistic回归分析表明,脑脊液HNP 1-3水平与不良结果相关。受体工作特征分析显示脑脊液HNP 1-3浓度>466.95 ng/mL可区分脑出血患者预后不良的危险。结论:HNP 1-3在预测脑出血患者预后方面具有满意的诊断效果。
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来源期刊
CiteScore
2.50
自引率
7.10%
发文量
63
审稿时长
1 months
期刊介绍: Genetic Testing and Molecular Biomarkers is the leading peer-reviewed journal covering all aspects of human genetic testing including molecular biomarkers. The Journal provides a forum for the development of new technology; the application of testing to decision making in an increasingly varied set of clinical situations; ethical, legal, social, and economic aspects of genetic testing; and issues concerning effective genetic counseling. This is the definitive resource for researchers, clinicians, and scientists who develop, perform, and interpret genetic tests and their results. Genetic Testing and Molecular Biomarkers coverage includes: -Diagnosis across the life span- Risk assessment- Carrier detection in individuals, couples, and populations- Novel methods and new instrumentation for genetic testing- Results of molecular, biochemical, and cytogenetic testing- Genetic counseling
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