血清SFRP5、ApoA-I、HDL3-C水平与急性心肌梗死PCI术后支架内再狭窄的关系及联合预测值

Li-Qiang Cui, Xue-Dong Wang
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引用次数: 0

摘要

本研究旨在探讨急性心肌梗死(AMI)患者经皮冠状动脉介入治疗(PCI)后血清分泌卷曲相关蛋白5 (SFRP5)、载脂蛋白A-I (ApoA-I)、高密度脂蛋白3-胆固醇(HDL3-C)与支架内再狭窄(ISR)的关系及其综合预测价值。回顾性分析2020年7月至2023年7月我院行PCI治疗的128例AMI患者的临床资料。随访12个月,根据冠脉造影结果将患者分为ISR组(24例)和非ISR组(104例)。24例ISR患者分为III级(管腔狭窄面积50% ~ 70%,15例)和IV级(管腔狭窄面积76% ~ 100%,9例)。比较两组一般资料。术后第2天分析两组患者血清SFRP5、ApoA-I、HDL3-C水平。比较不同狭窄程度患者的SFRP5、ApoA-I、HDL3-C水平。采用双变量相关Kendall tau-b (K)分析PCI术后血清SFRP5、ApoA-I、HDL3-C水平与ISR的相关性,采用Logistic回归分析PCI术后ISR的影响因素。绘制受试者工作特征(ROC)曲线,分析SFRP5、ApoA-I、HDL3-C在PCI术后ISR中的预测价值。ISR组糖尿病和吸烟史患者比例高于非ISR组。ISR组支架长度(29.52±5.47 mm)和hs-CRP水平(3.38±0.51 mg/L)均高于非ISR组(23.56±5.37 mm和2.78±0.52 mg/L) (p < 1, p < 0.70),具有一定的预测价值,且两者综合价值更高。综上所述,糖尿病和高hs-CRP水平是PCI术后AMI患者发生ISR的危险因素。高水平的SFRP5、ApoA-I、HDL3-C是PCI术后ISR的保护因素,其联合检测对PCI术后ISR有一定的预测价值。为临床及时采取干预措施,减少AMI患者PCI术后ISR的发生提供指导策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Relationship Between Serum SFRP5, ApoA-I, HDL3-C Level and In-Stent Restenosis After PCI in Acute Myocardial Infarction and the Combined Predictive Value.

This study aims to investigate the relationship between serum secreted frizzled-related protein 5 (SFRP5), apolipoprotein A-I (ApoA-I), high-density lipoprotein 3-cholesterol (HDL3-C) and in-stent restenosis (ISR) after percutaneous coronary intervention (PCI) in acute myocardial infarction (AMI) and their combined predictive value. The clinical data of 128 AMI patients who underwent PCI in our hospital from July 2020 to July 2023 were retrospectively analyzed. After 12 months of follow-up, the patients were divided into the ISR group (24 cases) and the non-ISR group (104 cases) according to the results of coronary angiography. The 24 patients with ISR were divided into Grade III (lumen stenosis area of 50%-70%, 15 cases) and Grade IV (lumen stenosis area of 76%-100%, 9 cases). The general data of the two groups were compared. The serum levels of SFRP5, ApoA-I, and HDL3-C in the two groups were analyzed on the second day after the operation. The levels of SFRP5, ApoA-I, and HDL3-C in patients with different degrees of stenosis were compared. The correlation between serum SFRP5, ApoA-I, HDL3-C levels and ISR after PCI was analyzed by bivariate correlation Kendall tau-b (K). Logistic regression was used to analyze the influencing factors of ISR after PCI. The receiver operating characteristic (ROC) curve was drawn to analyze the predictive value of SFRP5, ApoA-I, and HDL3-C in ISR after PCI. The proportion of patients with diabetes and a smoking history in the ISR group was higher than that in the non-ISR group. The stent length (29.52 ± 5.47 mm) and hs-CRP level (3.38 ± 0.51 mg/L) in the ISR group were higher than those in the non-ISR group (23.56 ± 5.37 mm and 2.78 ± 0.52 mg/L) (p < 0.05). SFRP5 (15.33 ± 2.60 ng/mL), ApoA-I (1.22 ± 0.37 g/L) and HDL3-C (0.31 ± 0.07 mmol/L) in the ISR group were higher than those in the non-ISR group (19.79 ± 3.09 ng/mL, 1.77 ± 0.41 g/L, and 0.46 ± 0.11 mmol/L) (p < 0.001). The levels of SFRP5 (17.57 ± 2.57 ng/mL), ApoA-I (1.56 ± 0.34 g/L) and HDL3-C (0.36 ± 0.07 mmol/L) in the Grade III group were higher than those in the Grade IV group (13.15 ± 2.35 ng/mL, 0.98 ± 0.20 g/L, and 0.25 ± 0.05 mmol/L) (p < 0.05). The results of bivariate correlation Kendall tau-b (K) analysis showed that the levels of serum SFRP5, ApoA-I, and HDL3-C were negatively correlated with ISR (r < 0, p < 0.05). Logistic regression analysis showed that diabetes and hs-CRP were risk factors for ISR after PCI (OR > 1, p < 0.05). SFRP5, ApoA-I, and HDL3-C were protective factors for ISR after PCI (OR < 1, p < 0.05). The ROC curve showed that the AUC of SFRP5, ApoA-I, and HDL3-C levels alone and in combination to predict ISR in AMI patients after PCI was > 0.70, which had certain predictive value, and the combined value was higher. In conclusion, diabetes and high levels of hs-CRP were risk factors for ISR in patients with AMI after PCI. High levels of SFRP5, ApoA-I, and HDL3-C were protective factors for ISR after PCI, and their combined detection had certain value in predicting ISR after PCI. This would provide guidance strategy for clinical timely intervention measures to reduce the occurrence of ISR in AMI patients after PCI.

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