[1] 崔晴梅. 中国人群冠心病环境和遗传综合风险预测模型构建及应用评估研究[D].北京:北京协和医学院,2023. [2] 张闽,彭瑜,吕树铮.脂联素基因多态性与早发冠心病的相关性研究[J].心肺血管病杂志,2015,34(6):429-435. [3] ZHAO Q R,LEI Y Y,Li J,et al.Association between apolipoprotein Epolymorphisms and premature coronary artery disease:A meta-analysis[J].Clin Chem Lab Med,2017,55(2):284-298. [4] 黄健中,吴强,陈冬萍,等.早发冠心病、非早发冠心病与载脂蛋白E基因多态性的相关性[J].岭南急诊医学杂志,2019,24(2):141-143,146. [5] 蒋晓钦. 载脂蛋白基因多态性与早发冠心病的相关性研究[J].国际检验医学杂志,2017,38(11):1547-1548. [6] 于淼,高璐,李潞.早发冠心病患者载脂蛋白E基因多态性及与冠脉病变严重程度的关系[J].航空航天医学杂志,2020,31(7):771-774. [7] 许璐,白春英,陈士萍,等.早发冠心病患者载脂蛋白E基因多态性分析及其与冠状动脉病变严重程度关系研究[J].陕西医学杂志,2022,51(9):1090-1093. [8] ABD EL-AZIZ T A,MOHAMED R H.LDLR,ApoB and ApoE genes polymorphisms and classical risk factors in premature coronary artery disease[J].Gene,2016,590(2):263-269. [9] GOODARZYNEJAD H,BOROUMAND M,BEHMANESH M,et al.The rs5888 single nucleotide polymorphism in scavenger receptor class B type 1(SCARB1)gene and the risk of premature coronary artery disease:A case-control study[J].Lipids Health Dis,2016(15):7. [10] LU Z,LUO Z,JIA A,et al.Associations of the ABCA1 gene polymorphisms with plasma lipid levels:A meta-analysis[J].Medicine(Baltimore),2018,97(50):e13521. [11] 安芳,王秀娟,李学文,等.ABCA1 R219K、-565 C/T基因多态性与早发冠心 [12] ZHANG Y,WANG S,LI Y,et al.Relationship of microRNA 616 gene polymorphism with prognosis of patients with premature coronary artery disease[J].Int J Clin Pharmacol Ther,201 6,54(11):899-903. [13] 杨春强,相彬,路俊生,等.PON1基因多态性与吸烟的交互作用对早发冠心病的影响[J].中国老年学杂志,2019,39(22):5409-5414. [14] DU Y,CHEN K,LIU E,et al.Gender-specific associations of CD36 polymorphisms with the lipid profile and susceptibility to premature multi-vessel coronary artery heart disease in the Northern Han Chinese[J].Gene,2020(753):144806. [15] POSADAS-SÁNCHEZ R,ANGELES-MARTÍNEZ J,PÉREZ-HERNÁNDEZ N,et al.The IL-10-1082(rs1800896)G allele is associated with a decreased risk of developing premature coronary artery disease and some IL-10 polymorphisms were associated with clinical and metabolic parameters.The GEA study[J].Cytokine,2018(106):12-18. [16] VÁZQUEZ-VÁZQUEZ C,POSADAS-SÁNCHEZ R,FRAGOSO J M,et al.IL-12B polymorphisms are associated with the presence of premature coronary artery disease and with cardiovascular risk factors:The genetics of atherosclerotic disease Mexican study[J].DNA Cell Biol,2020,39(7):1347-1355. [17] POSADAS-SÁNCHEZ R,CARDOSO-SALDAÑA G,FRAGOSO J M,et al.Interferon regulatory factor 5(IRF5)gene haplotypes are associated with premature coronary artery disease.association of the IRF5 polymorphisms with cardiometabolic parameters.the genetics of atherosclerotic disease(GEA)Mexican study[J].Biomolecules,2021,11(3):443. [18] 杨勇,孟涛疆,马东星,等.髓样细胞触发受体-1基因rs9471535单核苷酸多态性与男性早发冠心病的相关性[J].武警医学,2019,30(2):97-100,104. [19] 信佳言. 骨保护素水平及149T/C、950T/C基因多态性与早发冠心病的研究[D].天津:天津医科大学,2018. [20] PÉREZ-HERNÁNDEZ N,POSADAS-SÁNCHEZ R,VARGAS-ALARCÓN G,et al.Genetic variants and haplotypes in OPG gene are associated with premature coronary artery disease and traditional cardiovascular risk factors in Mexican population:The GEA study[J].DNA Cell Biol,2020,39(11):2085-2094. [21] 路艳,郭纪文,徐晓辉,等.CNP、12/15-LOX基因多态性与早发冠心病关系的研究[J].贵州医药,2020,44(1):17-20. [22] 陈斌,康品方,李妙男,等.MTHFR C677T基因多态性、同型半胱氨酸与早发冠心病的相关性[J].山西医科大学学报,2022,53(8):992-997. [23] SUN J,HAN W,WU S,et al.Associations between hyperhomocysteinemia and the presence and severity of acute coronary syndrome in young adults≤35 years of age[J].BMC Cardiovasc Disord,2021,21(1):47. [24] 涂国胜. 内皮素-1基因Lys198Asn和+138/ex1 ins/delA位点的多态性与江西部分汉族人群早发冠心病患者相关性研究及机制探讨[D].南昌:南昌大学,2020. [25] 杨美艳,韩博,徐勇,等.乙醛脱氢酶2基因型多态性与早发冠心病患者冠状动脉狭窄程度的关系[J].解放军医学院学报,2021,42(1):7-9,16. [26] 许晶晶. 早发冠心病三支病变不同治疗方式的长期预后比较及基因多态性研究[D].北京:北京协和医学院,2017. [27] 乔琳,文星艳,窦克非,等.CDKN2B-AS1基因多态性与女性早发冠心病的相关性研究[J].中国循环杂志,2017,32(12):1154-1157. [28] 贺利平. 微小RNA-1靶基因多态性与蒙古族早发冠心病发生风险的关联研究[J].现代消化及介入诊疗,2019(A02):1736-1737. [29] VARGAS-ALARCÓN G,AVILÉS-JIMÉNEZ F,MEJÍA-SÁNCHEZ F,et al.Helicobacter pylori infection and DNMT3a polymorphism are associated with the presence of premature coronary artery disease and subclinical atherosclerosis.Data from the GEA Mexican Study[J].Microb Pathog, 2022(170):105719. [30] POSADAS-SÁNCHEZ R,LÓPEZ-URIBE ÁR,POSADAS-ROMERO C,et al.Association of the I148M/PNPLA3(rs738409)polymorphism with premature coronary artery disease,fatty liver,and insulin resistance in type 2 diabetic patients and healthy controls.The GEA study[J].Immunobiology,2017,222(10):960-966. [31] VARGAS-ALARCÓN G,GONZÁLEZ-SALAZAR MDC,HERNÁNDEZ-DÍAZ COUDER A,et al.Association of the rs17574 DPP4 polymorphism with premature coronary artery disease in diabetic patients:Results from the cohort of the GEA Mexican study[J].Diagnostics(Basel),2022,12(7):1716. [32] GAMBOA R,HUESCA-GÓMEZ C,LÓPEZ-PÉREZ V,et al.The UCP2 -866G/A,Ala55Val and UCP3-55C/T polymorphisms are associated with premature coronary artery disease and cardiovascular risk factors in Mexican population[J].Genet Mol Biol,2018,41(2):371-378. [33] 黄祥辉,潘伟彪.冠状动脉CTA模拟血流储备分数对于冠心病的诊疗进展[J].现代医院,2022,22(5):803-806. [34] 颜波,郑伟,关祥平,等.早发冠心病急性ST段抬高型心肌梗死患者冠脉病变特点及危险因素分析[J].国际医药卫生导报,2023,29(4):532-536. [35] FERREIRA T D S,FERNANDES J F R,ARAUJO L D S,et al.Serum uric acid levels are associated with cardiometabolic risk factors in healthy young and middle-aged adults[J].Arq Bras Cardiol,2018,111(6):833-840. [36] MENOTTI A,PUDDU P E,KROMHOUT D,et al.Coronary heart disease mortality trends during 50 years as explained by risk factor changes:the European cohorts of the seven countries study[J].Eur J Prev Cardiol,2020,27(9):988-998. [37] 阴赪茜,崔凌宇,郑春梅,等.基因多态性在早发冠心病发病风险中的研究进展[J].中国循证心血管医学杂志,2020,12(5):630-633. |