Relationships between TREM-1 gene polymorphism and susceptibility to male premature coronary artery disease
YANG Yong1, MENG Taojing2, MA Dongxin1, LIU Ying1, SHEN Zhiqi1, HUANG Jie1, ZHAO Qing1, WANG Ranran1, and YANG Changchun1
1.Department of Cardiology, the Third Medical Center of PLA General Hospital, Beijing 100039, China;
2.Sanya Rehabilitation Center of PLA Joint Logistics Support Force, Sanya 572000, China
Objective To explore the correlations between gene polymorphisms of triggering receptor expressed on myeloid cells-1 (TREM-1) rs9471535 and susceptibility to male premature coronary artery disease (PCAD).Methods Between August 2015 and January 2017, male inpatients aged 55 or above, treated at the Department of Cardiology of our hospital, and identified by coronary angiography or CTA with CAD (PCAD group) or without CAD (control group), were enrolled into this study. The DNA kit was used to extract DNA from peripheral venous blood, and polymerase chain reaction-ligase detection reaction (PCR-LDR) technology was used to identify the TREM-1 gene polymorphisms. The frequencies of genotypes and alleles of rs9471535 were calculated and binary logistic regression was used to analyze the relationships between rs9471535 polymorphisms and susceptibility to PCAD.Results The percentages of patients with hypertension (57.0%), diabetes (21.5%), hyperlipidemia (59.5%) or with smoking history (74.4%) were significantly higher in the PCAD group than those in the control group (P<0.05). The frequencies of genotypes TT(46.3%), CT (50.4%)and CC (3.3%)of rs9471535 in the PCAD group were significantly different from those of the control group, which were 51.0%, 38.3%,and 10.7% respectively(P=0.017). According to univariate analysis with binary logistic regression, as compared with TT genotype, the distribution of CC genotype was not significantly different between the two groups (P=0.059,OR=0.340,95%CI=0.111-1.041). However, after adjustment of traditional risk factors (age, hypertension, diabetes, hyperlipidemia and smoking), carriers of CC genotype had lower risk of PCAD (P=0.011,OR=0.180,95%CI=0.048-0.679).Conclusions The TREM-1 gene rs9471535 polymorphism may have correlations with the occurrence of male premature CAD. Individuals with CT and TT genotypes may be more vulnerable to premature CAD than those carrying CC genotype that may play a protective role in male PCAD.
杨勇,孟涛疆,马东星,刘英,沈志奇,黄洁,赵清,王冉冉,杨长春. 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.
YANG Yong, MENG Taojing, MA Dongxin, LIU Ying, SHEN Zhiqi, HUANG Jie, ZHAO Qing, WANG Ranran, and YANG Changchun. Relationships between TREM-1 gene polymorphism and susceptibility to male premature coronary artery disease. Med. J. Chin. Peop. Armed Poli. Forc., 2019, 30(2): 97-100.
National Cholesterol Education Program (NCEP) Expert Panel. Third report of the National Cholesterol Education Program (NCEP) Expert Panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel Ⅲ) final report[J]. Circulation, 2002, 106: 3143-3421.
[3]
Wang D,Wang Z,Zhang L,et al. Roles of Cells from the Arterial Vessel Wall in Atherosclerosis[J]. Mediat Inflamm,2017,2017:8135934.
[4]
Knapp S,Gibot S,de Vos A,et al. Cutting edge:expression patterns of surface and soluble triggering receptor expressed on myeloid cells-1 in human endotoxemia[J]. J Immunol,2004,173(12):7131-7134.
[5]
Fortin C F,Lesur O,Fulop T,et al. Effects of TREM-1 activation in human neutrophils:activation of signaling pathways,recruitment into lipid rafts and association with TLR4[J]. Int Immunol,2007,19(1):41-50.
[6]
Pierobon D,Bosco M C,Blengio F,et al. Chronic hypoxia reprograms human immature dendritic cells by inducing a proinflammatory phenotype and TREM-1 expression[J]. Eur J Immunol,2013,43(4):949-966.
[7]
Yuan Z,Mehta H J,Mohammed K,et al. TREM-1 is induced in tumor associated macrophages by cyclo-oxygenase pathway in human non-small cell lung cancer[J]. PLoS One,2014,9(5):e94241.
[8]
Golovkin A S, Ponasenko A V, Khutornaya M V, et al. Association of TLR and TREM-1 gene polymorphisms with risk of coronary artery disease in a Russian population[J]. Gene, 2014, 550(1):101-109.
[9]
Bouchon A, Dietrich J, Colonna M. Cutting edge: inflammatory responses can be triggered by TREM-1, a novel receptor expressed on neutrophils and monocytes [J]. J Immunol, 2000, 164 (10):4991-4995.
[10]
Hosoda H,Tamura H,Nagaoka I. Evaluation of the lipopolysaccharide-induced transcription of the human TREM-1 gene in vitamin D3-matured THP-1 macrophage-like cells[J]. Int J Molecu Med,2015,36(5):1300-1310.
[11]
Zhong J,Huang W,Deng Q,et al. Inhibition of TREM-1 and dectin-1 alleviates the severity of fungal keratitis by modulating innate immune responses[J]. PLoS One,2016,11(3):e0150114.
[12]
Zhao J M,Wang Q. Role of triggering receptor expressed on myeloid cells-1 in the pathogenesis of Kawasaki disease [J]. Zhongguo dang dai er ke za zhi,2016,18(6):522-526.
[13]
Dong L,Zhou Y,Zhu Z Q,et al. Soluble epoxide hydrolase inhibitor suppresses the expression of triggering receptor expressed on myeloid cells-1 byinhibiting NF-k B activation in murine macrophage[J]. Inflammation,2017,40(1):13-20.
[14]
Varanat M,Haase E M,Kay J G,et al. Activation of the TREM-1 pathway in human monocytes by periodontal pathogens and oral commensal bacteria[J]. Mol Oral Microbiol,2017,32(4):275-287.
[15]
Bosco M C,Raggi F,Varesio L. Therapeutic potential of targeting TREM-1 in inflammatory diseases and cancer[J]. Curr Pharm Design,2016,22(41) : 6209-6233.