Correlation analysis of serum SERPINA3, CLEC2 and hs-CRP/ALB with major adverse cardiovascular events (MACE) after percutaneous coronary intervention (PCI) in STEMI.

IF 1.9 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yuncong Ma, Suxia Fang, Shasha Liu, Zhencong Jiang
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引用次数: 0

Abstract

Background: To examine the main adverse cardiovascular events that occur in individuals who have had an acute ST-segment elevation myocardial infarction (STEMI) after receiving percutaneous coronary intervention (PCI), such as serum C-type lectin domain family member 2 (CLEC2), serine protease inhibitor family member A3 (SERPINA3), and high-sensitivity C-reactive protein/albumin (hs-CRP/ALB) levels.

Methods: The STEMI group included 132 patients who were observed for 1 year after hospitalisation between January 2023 and September 2024. The patients were divided into two groups: the MACE group and the non-MACE group, based on whether MACE came after PCI. Additionally, the control group consisted of 68 healthy individuals who were physically examined at the hospital during the same time period. Using an enzyme-linked immunosorbent test, the levels of serum CLEC2, SERPINA3, hs-CRP and ALB were measured in each research participant, and the hs-CRP to ALB ratio was computed. After PCI, multivariate logistic regression was used to examine variables associated with MACEs in STEMI patients. Receiver operating characteristic (ROC) curves were used to analyse the predictive value of single and combined detection of serum CLEC2, SERPINA3, and hs-CRP/ALB for MACEs in STEMI patients after PCI.

Results: The incidence of MACE after PCI in 132 STEMI patients was 31.06% (41/132). The levels of serum CLEC2, SERPINA3 and hs-CRP/ALB in the STEMI group were significantly greater than those in the control group (P< 0.05). Independent risk factors for MACEs following PCI in STEMI patients included age >62 years, Killip grade > grade III, cardiac troponin I level >1.7 ng/mL, CLEC2 level >155 pg/mL, SERPINA3 level >350 ng/L, and hs-CRP/ALB >0.50 (P< 0.05), while left ventricular ejection fraction >50% was an independent protective factor. The area under the ROC curve (0.856) of the combined detection of serum CLEC2, SERPINA3, and hs-CRP/ALB for the prediction of MACEs in STEMI patients after PCI was greater than that of the individual detection of each index.

Conclusions: Serum CLEC2 levels >155 pg/mL, SERPINA3 levels >350 ng/L, and hs-CRP/ALB>0.50 are closely related to the occurrence of MACEs in STEMI patients after PCI and can be used as auxiliary predictive indicators for the occurrence of MACEs in STEMI patients after PCI.

STEMI患者经皮冠状动脉介入治疗(PCI)后血清SERPINA3、CLEC2、hs-CRP/ALB与主要不良心血管事件(MACE)的相关性分析
背景:研究急性st段抬高型心肌梗死(STEMI)患者接受经皮冠状动脉介入治疗(PCI)后发生的主要心血管不良事件,如血清c型凝集素结构域家族成员2 (CLEC2)、丝氨酸蛋白酶抑制剂家族成员A3 (SERPINA3)和高敏c反应蛋白/白蛋白(hs-CRP/ALB)水平。方法:STEMI组纳入132例患者,于2023年1月至2024年9月住院观察1年。根据PCI术后是否发生MACE,将患者分为MACE组和非MACE组。此外,对照组由68名健康个体组成,他们在同一时期在医院接受了身体检查。采用酶联免疫吸附试验,测定每位研究对象血清CLEC2、SERPINA3、hs-CRP和ALB水平,计算hs-CRP与ALB比值。PCI术后,多因素logistic回归分析与STEMI患者mes相关的变量。采用受试者工作特征(ROC)曲线分析单纯及联合检测血清cle2、SERPINA3、hs-CRP/ALB对STEMI患者PCI术后mace的预测价值。结果:132例STEMI患者PCI术后MACE发生率为31.06%(41/132)。STEMI组患者血清CLEC2、SERPINA3、hs-CRP/ALB水平均显著高于对照组(p < 0.05)。STEMI患者PCI术后mace的独立危险因素为年龄62岁、Killip分级为三级、心肌肌钙蛋白I水平为1.7 ng/mL、CLEC2水平为155 pg/mL、SERPINA3水平为350 ng/L、hs-CRP/ALB水平为0.50 (P< 0.05),而左心室射血分数为50%是独立的保护因素。联合检测血清CLEC2、SERPINA3、hs-CRP/ALB预测STEMI患者PCI术后mace的ROC曲线下面积(0.856)大于单项检测。结论:血清CLEC2水平>;155 pg/mL、SERPINA3水平>;350 ng/L、hs-CRP/ALB>;0.50与STEMI患者PCI后mace发生密切相关,可作为STEMI患者PCI后mace发生的辅助预测指标。
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来源期刊
Journal of Medical Biochemistry
Journal of Medical Biochemistry BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
3.00
自引率
12.00%
发文量
60
审稿时长
>12 weeks
期刊介绍: The JOURNAL OF MEDICAL BIOCHEMISTRY (J MED BIOCHEM) is the official journal of the Society of Medical Biochemists of Serbia with international peer-review. Papers are independently reviewed by at least two reviewers selected by the Editors as Blind Peer Reviews. The Journal of Medical Biochemistry is published quarterly. The Journal publishes original scientific and specialized articles on all aspects of clinical and medical biochemistry, molecular medicine, clinical hematology and coagulation, clinical immunology and autoimmunity, clinical microbiology, virology, clinical genomics and molecular biology, genetic epidemiology, drug measurement, evaluation of diagnostic markers, new reagents and laboratory equipment, reference materials and methods, reference values, laboratory organization, automation, quality control, clinical metrology, all related scientific disciplines where chemistry, biochemistry, molecular biology and immunochemistry deal with the study of normal and pathologic processes in human beings.
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