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糖化血红蛋白A1c与载脂蛋白A-1比值评估急性冠状动脉综合征患者预后的临床研究 被引量:2

Value of glycosylated hemoglobin A1c and apolipoprotein A-1 ratio on predicting outcome of patients with acute coronary syndrome
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摘要 目的探讨糖化血红蛋白A1c(HbA1c)与载脂蛋白A-1(ApoA-1)比值(HbA1c/ApoA-1)对急性冠状动脉综合征(ACS)患者随访期间主要不良心血管事件(MACEs)的预测价值。方法本研究为回顾性队列研究,连续入选2017年3月至2019年3月于北京医院住院并接受冠状动脉造影的ACS患者,收集性别、年龄、既往史、Gensini评分、HbA1c和ApoA-1等基线资料。依据随访期间有无MACEs发生分为MACEs组和无MACEs组,分析2组间HbA1c/ApoA-1的差异。按HbA1c/ApoA-1水平的三分位数将患者分为高、中、低HbA1c/ApoA-1组,使用Cox比例风险模型评估3组间MACEs、全因死亡率等终点事件的差异。使用Kaplan-Meier生存分析比较各HbA1c/ApoA-l组间无MACEs生存率差异。使用Spearman秩相关分析评价HbA1c/ApoA-1与Gensini评分的相关性。结果共纳入ACS患者366例,59例发生MACEs,10例发生全因死亡。所有患者平均年龄为(65.9±10.3)岁,随访(22.3±4.4)个月,校正年龄、收缩压、糖尿病病史、冠状动脉病变严重程度后,高HbA1c/ApoA-1组患者MACEs发生率是低HbA1c/ApoA-1组患者的2.45倍(95%CI:1.16~5.18,P=0.019),但2组全因死亡率差异无统计学意义(P=1.000)。Kaplan-Meier生存分析显示高HbA1c/ApoA-l组MACEs风险最高,低HbA1c/ApoA-l组风险最低,差异有统计学意义(P<0.01)。Spearman秩相关分析结果显示,HbA1c/ApoA-1比值高低与ACS患者Gensini评分呈正相关(r=0.274,P<0.01)。结论HbA1c/ApoA-1是ACS患者MACEs的独立危险因素。高HbA1c/ApoA-1患者冠状动脉病变程度更重。HbA1c/ApoA-1水平可能作为评估ACS患者心血管风险的潜在指标,用于早期识别高危人群,预测MACEs的发生。 Objective To investigate the predictive value of glycosylated hemoglobin A1c/apolipoprotein A-1(HbA1c/ApoA-1)ratio for major adverse cardiovascular events(MACEs)in patients with acute coronary syndrome(ACS).Methods The present study is a retrospective cohort study.ACS patients who were hospitalized and underwent coronary angiography at Beijing Hospital from March 2017 to March 2019 were enrolled.Baseline information such as sex,age,previous history,Gensini score,HbA1c and ApoA-1 were analyzed.Patients were divided into two groups according to presence or absence of MACEs and the difference on HbA1c/ApoA-1 ratio was compared between the two groups.According to the tertiles of HbA1c/ApoA-1 levels,patients were divided into high(5.87-16.12),medium(4.50-5.83)and low(2.11-4.48)HbA1c/ApoA-1 groups.Cox proportional risk model was used to evaluate the differences in MACEs and all-cause mortality among the three groups.Kaplan-Meier survival analysis was used to compare the differences of MACEs between the various HbA1c/ApoA-1 groups.Results A total of 366 ACS patients were included in this study.The mean age of the patients was(65.9±10.3)years.There were 59 MACEs and 10 all-cause deaths during the mean of(22.3±4.4)months follow-up.After adjusting for age,systolic blood pressure,history of diabetes and Gensini score,the incidence of MACEs was 2.45 times higher in the high HbA1c/ApoA-1 group than in the low HbA1c/ApoA-1 group(95%CI 1.16-5.18,P=0.019).There was no significant difference in all-cause mortality between the high and low HbA1c/ApoA-1 groups(P=1.000).Kaplan-Meier survival analysis showed that patients in the high HbA1c/ApoA-1 group had the highest risk of MACEs,while patients in the low HbA1c/ApoA-1 group had the lowest risk of MACEs(P<0.01).Spearman rank correlation analysis showed that HbA1/ApoA-1 ratio was positively correlated with Gensini score in ACS patients(r=0.274,P<0.01).Conclusion High HbA1c/ApoA-1 ratio was an independent risk factor for MACEs in ACS patients.Patients with high HbA1c/ApoA-1 ratio had more severe coronary artery disease lesions.HbA1c/ApoA-1 ratio may be used as a potential risk stratification biomarker for ACS patients,it might be useful for the early identification of high-risk population and for predicting the incidence of MACEs among ACS patients.
作者 王一佳 牟洪娜 杨睿悦 张闻多 王欣越 王思明 季福绥 董军 于雪 Wang Yijia;Mu Hongna;Yang Ruiyue;Zhang Wenduo;Wang Xinyue;Wang Siming;Ji Fusui;Dong Jun;Yu Xue(Department of Cardiology,Beijing Hospital,National Center of Gerontology,Institute of Geriatric Medicine,Chinese Academy of Medical Sciences,Beijing 100730,China;Chinese Academy of Medical Sciences,Graduate School of Peking Union Medical College,Beijing 100730,China;The Key Laboratory of Geriatrics,Beijing Institute of Geriatrics,Beijing Hospital,National Center of Gerontology,National Health Commission,Institute of Geriatric Medicine,Chinese Academy of Medical Sciences,Beijing 100730,China)
出处 《中华心血管病杂志》 CAS CSCD 北大核心 2023年第1期38-44,共7页 Chinese Journal of Cardiology
基金 北京市自然科学基金(7214250) 国家自然科学基金(81672075)。
关键词 急性冠状动脉综合征 糖化血红蛋白A1c/载脂蛋白A-1 主要不良心血管事件 全因死亡率 Acute coronary syndrome Glycosylated hemoglobin A1c/apolipoprotein A-1 Major adverse cardiovascular events All-cause mortality rate
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  • 1路雅茹,秦勤,赵炳让.血脂及载脂蛋白水平与冠心病严重程度的关系[J].中国分子心脏病学杂志,2002,2(4):30-32. 被引量:5
  • 2Lewis GF, Rader DJ. New insights into the regulation of HDL metabolism and reverse cholesterol transport[J]. Circ Res,2005, 96(12) : 1221 - 1232.
  • 3Martinez LO, Jacquet S, Terce F, et al. New insight on the molecular mechanisms of high-density lipoprotein cellular interactions[ J]. Cell Mol Life Sci, 2004, 61 (18) :2343 - 2360.
  • 4Kuchler M, Silver L. Antidyslipidemic action of fenofibrate in dyslipidemic-diabetic hamster model [ J ]. Biochem Biophys Res Commun, 2003, 305(2) :215 -222.
  • 5Wang PR, Guo Q, Ippolito M, et al. High fat fed hamster, a unique animal model for treatment of diabetic dyslipidemia with peroxisome proliferator activated receptor alpha selective agonists[J]. Eur J Pharmacol, 2001,427(3) :285 - 293.
  • 6Contreras JA, Castro M, Bocos C, et al. Combination of an enzymatic method and HPLC for the quantitation of cholesterol in cultured cells[J]. J Lipid Res, 1992, 33(6) :931 - 936.
  • 7Bauer BE,Wolfger H, Kuchler K. Inventory and function of yeast ABC proteins: about sex, stress, pleiotropic drug and heavy metal resistance[J]. J Biochim Biophys Acta, 1999, 1461:217 - 236.
  • 8Wang N, Silver DL, Costet P, et al. Specific binding of ApeA- I, enhancedcholesterol efflux, and altered plasmamembrane morphology in cellsexpressing ABC1 [ J ]. J Biol Chem, 2000, 275(42): 33053 - 33058.
  • 9Alenezi MY, Marcil M, Blank D, et al. Is the decreased high-density lipoprotein cholesterol in the metabolic syndrome due to cellular lipid efflux defect [J]. J Clin Endocrinol Metab, 2004, 89(2):761 -764.
  • 10Ansell B J, Navab M, Hama S, et al. Inflammatory/anti-inflammatory properties of high-density lipoprotein distinguish patients from coronary subjects better than high-density lipoprotein cholesterol levels and are favorably affected by simvastatin treatment [J]. Circulation, 2003, 108 : 2751 - 2756.

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