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The association of APOC4 polymorphisms with premature coronary artery disease in a Chinese Han population
Lipids in Health and Disease volume 14, Article number: 63 (2015)
Hypercholesterolemia arising from abnormal lipid metabolism is one of the critical risk factors for coronary artery disease (CAD), however the roles of genetic variants in lipid metabolism-related genes on premature CAD (≤60 years old) development still require further investigation. We herein genotyped four single nucleotide polymorphisms (SNPs) in lipid metabolism-related genes (rs1132899 and rs5167 in APOC4, rs1801693 and rs7765781 in LPA), aimed to shed light on the influence of these SNPs on individual susceptibility to early-onset CAD.
Genotyping of the four SNPs (rs1132899, rs5167, rs1801693 and rs7765781) was performed in 224 premature CAD cases and 297 control subjects (≤60 years old) using polymerase chain reaction-ligation detection reaction (PCR–LDR) method. The association of these SNPs with premature CAD was performed with SPSS software.
Multivariate logistic regression analysis showed that C allele (OR = 1.50, P = 0.027) and CC genotype (OR = 2.84, P = 0.022) of APOC4 rs1132899 were associated with increased premature CAD risk, while the other three SNPs had no significant effect. Further stratified analysis uncovered a more evident association with the risk of premature CAD among male subjects (C allele, OR = 1.65, and CC genotype, OR = 3.33).
Our data provides the first evidence that APOC4 rs1132899 polymorphism was associated with an increased risk of premature CAD in Chinese subjects, and the association was more significant among male subjects.
Coronary artery disease (CAD) is the predominant cause of death and morbidity worldwide. Previous studies and clinical trials have established numerous environmental factors contributing to the development of CAD , such as obesity, hypercholesterolemia, alcohol intake, smoking, diabetes and hypertension . Among the above risk factors, hypercholesterolemia arising from abnormal lipid metabolism has been considered to be one of the most key risk factors for CAD pathogenesis [3, 4]. Moreover, apart from these modifiable factors, accumulating evidences have demonstrated close associations of genetic variants or polymorphisms in candidate genes with the risk of CAD, especially the early-onset CAD [5–7].
Age is a critical contributing factor for the risk of CAD, age-related functional impairment including weak immune and inflammatory system, and other mechanisms involved in the regulation of the flow in the coronary arteries, exerted crucial effects during CAD development . Thus, in order to exclude the effects of age-related dysfunction of CAD associated mechanisms, the association analysis of these four SNPs in lipids metabolism-related genes with the risk of CAD was performed only among the early-onset CAD subjects. Nonetheless, the definition for early-onset CAD patients discriminating from late-onset CAD is unspecific. In this study, we collected the CAD cases and control subjects younger than 60 years old, according to several previous published studies [9, 10].
Apolipoprotein C-IV (APOC4), a highly conserved lipid-binding protein belonging to the apolipoprotein C family, exerts a critical role in lipid metabolism [11, 12]. The APOC4 gene is located on the chromosome 19q12-13.2, constructs the APOE/C1/C4/C2 gene cluster with apolipoprotein CI (APOC1), apolipoprotein CII (APOC2) and apolipoprotein E (APOE) , which is closely associated with plasma lipid levels, atherosclerotic plaque formation, and thus with the development of coronary artery disease and alzheimer’s disease [14, 15]. APOC4 is predominantly associated with very low-density lipoprotein (VLDL), and plays an important role in triglyceride metabolism . Overexpression of apolipoprotein C-IV in transgenic mice can cause hypertriglyceridemia . Moreover, previous study has revealed a significant association of rs5167 (Leu96Arg) and rs1132899 (Leu36Pro) polymorphisms in APOC4 gene with triglyceride levels in women . In addition, the T allele of APOC4 rs5167 polymorphism conferred modest effects on high density lipoprotein cholesterol (HDL-C) and apoAI levels . Thus it was reasonable to speculate that APOC4 polymorphisms might probably play an important role in CAD pathogenesis through impacting on plasma lipid profile.
Lipoprotein (LPA), also refers to as lipoprotein (a), a large glycoprotein attached to the low-density lipoprotein (LDL)-like particles, has been demonstrated to be associated with the risk of coronary artery disease . LPA is highly homologous with plasminogen, can bind to the lysine sites available for plasminogen on the surface of fibrin, and thereby compete with plasminogen to interfere with the fibrinolytic process and inhibit its activation, which increases the formation of thrombosis, and finally promotes the atherogenesis and coronary artery disease pathogenesis [19, 20]. Additionally, the elevated LPA levels and corresponding genotypes were associated with increased risk of aortic valve stenosis (AVS) . Genome-wide association study (GWAS) has revealed that the SLC22A3-LPAL2-LPA gene cluster was a risk locus for coronary artery disease, and the chromosomal region (6p26) where the SLC22A3-LPAL2-LPA gene cluster located is closely associated with the risk of CAD, and the LPA locus on 6q26-27 encoding lipoprotein has the strongest association . Recent studies illustrated that the G allele of rs10455872, and the C allele of rs3798220 in LPA gene significantly elevated the LPA levels in peripheral blood, and the two SNPs in LPA were demonstrated to be the critical risk factors for CAD development, indicating that LPA polymorphisms were associated with CAD risk . We herein focused on two other LPA polymorphisms (rs1801693 and rs7765781) in its exons, in order to investigate into the associations of these two SNPs with premature CAD risk.
Single nucleotide polymorphisms (SNPs) have been established to influence individual susceptibility for diverse human diseases. Accumulating evidences have suggested that SNPs within the lipid metabolism-related genes might potentially contribute to CAD [24–27]. Nonetheless, the genetic causes and underlying molecular mechanisms of these candidate genes for CAD require to be elucidated. Since aging effects, including weak immune system and relative high level exposure to environmental risk factors, rather than direct genetic effects, contribute to the risk of CAD in older subjects. Thus, we herein conducted a case–control study to investigate the association of the four SNPs in the lipid metabolism-related genes (rs5167 and rs1132899 in APOC4, rs1801693 and rs7765781 in LPA) with the risk of premature CAD (≤60 years old). Our data revealed that the C allele of rs1132899 in APOC4 has a significant association with an increased risk of premature CAD in a Chinese population.
Two hundred twenty-four CAD patients and 294 control subjects (age ≤ 60 years old) were consecutively recruited from the First People’s Hospital of Foshan (Foshan, China) and the Affiliated Hospital of Guangdong Medical University (Zhanjiang, China) from March 2011 to February 2013. All the patients were newly diagnosed and previously untreated. Coronary angiography was initially performed to clarify the origin of chest pain or electrocardiographic abnormalities at rest or during exercise test. The diagnosis of CAD was confirmed by coronary angiography performed with the Judkins technique using a quantitative coronary angiographic system. CAD was defined as angiographic evidence of at least one segment of a major epicardial coronary artery with more than 50 % organic stenosis. Two cardiologists who were responsible for the assessment of angiograms both underwent strict training and complied with the same diagnostic criteria. Subjects with a history of hematologic, neoplastic, renal, liver, or thyroid diseases were excluded.
All subjects enrolled in this study were genetically unrelated ethnic Han Chinese. Each subject was interviewed to collect information on demographic data and risk factors related to CAD after obtaining the informed consent. The study was approved by the Medical Ethics Committee of the First People’s Hospital of Foshan and the Affiliated Hospital of Guangdong Medical University.
Biochemical parameters analysis
The blood sample drawn from each subject was centrifuged at 2000 × g for 15 min immediately after collection and stored at −80 °C. The levels of plasma total cholesterol (TC), triglyceride (TG), high density lipoprotein cholesterol (HDL-C), and low density lipoprotein cholesterol (LDL-C) were measured enzymatically using a chemistry analyzer (Olympus, Japan). Glucose was analyzed by the glucose oxidase method with an Abbott V/P Analyzer (Abbott Laboratories, USA).
Genomic DNA was extracted from peripheral whole blood by TIANamp blood DNA extraction kit (TianGen Biotech, Beijing, China) according to the manufacturer’s instructions. All DNA samples were dissolved in water and stored at −20 °C until use.
SNPs genotyping were performed utilizing polymerase chain reaction-ligase detection reaction (PCR-LDR) method (Shanghai Biowing Applied Biotechnology Company), as described in our previous study . The sequence of primers and probes were listed in Additional file 1: Table S1.
All the three SNPs were tested for confirmation with Hardy-Weinberg expectations by a goodness-of-fit χ2 test among the control subjects. Quantitative variables were expressed as mean ± standard deviation (SD), and qualitative variables were expressed as percentages. The differences of the demographic characteristics between the cases and controls were estimated using the χ2 test (for categorical variables) and Student’s t test (for continuous variables).
Multivariate association analyses with CAD risk, genotype frequencies were assessed by means of multivariate methods based on logistic regression analysis, the odds ratios (ORs) and 95 % confidence intervals (CIs) for the effect of SNPs on CAD risk adjusted by age, sex, smoking, drinking, hypertension, diabetes and hyperlipidemia. Association analyses between SNPs and blood lipid profiles were performed by one-way analysis of variance (ANOVA). The statistical analyses were performed using the SPSS software (version 21). A P value of less than 0.05 was used as the criterion of statistical significance.
Characteristics of the study population
The characteristics of CAD cases and control subjects were listed in Table 1. In the lipid profiles comparison, TG and LDL-C were significantly higher in CAD patients than that in controls (P < 0.001, P < 0.001, respectively), whereas serum HDL-C levels were significantly higher among controls (P < 0.001), and no statistically significant difference between cases and controls was observed in TC levels (P = 0.160). Besides, the average fasting plasma glucose (FPG) in CAD cases was significantly higher than in controls (P < 0.001). CAD cases had higher levels of systolic blood pressure, diastolic blood pressure; the prevalence of smokers, alcohol consumers, and individuals with hypertension, diabetes or hyperlipidemia was significantly higher among the CAD patients. In addition, the number of female subjects in CAD cases was much lower than the male subjects. In all, these data demonstrated that male gender, smoking, alcohol intake, hypertension, hyperlipidemia and diabetes mellitus were the critical risk factors for premature CAD development in Chinese population.
Multivariate associations of four SNPs with the risk of premature CAD
Four SNPs (rs5167 and rs1132899 in APOC4, rs1801693 and rs7765781 in LPA) were genotyped in 224 CAD patients and 294 control subjects (≤60 years old). The primary information for rs5167, rs1132899, rs1801693 and rs7765781 polymorphisms was listed in Table 2. Minor allele frequency (MAF) of all three SNPs in our controls was similar to MAF for Chinese in HapMap database (Table 2). All the genotype frequency distributions of the three SNPs in our control subjects followed Hardy-Weinberg equilibrium proportions (all P values ≥ 0.10, Table 2).
The allele and genotype distributions of the four SNPs in the cases and the controls were shown in Table 3. From the allelic association analysis, we found only rs1132899 showed statistical significance, and C allele was associated with a significantly increased risk of CAD (OR = 1.50, 95 % CI = 1.05–2.14, P = 0.027, Table 3). In addition, compared to TT genotype, the CC genotype exhibited an increased risk of CAD as well (OR = 2.84, 95 % CI = 1.17–6.92, P = 0.022, Table 3). These data indicated that APOC4 SNP rs1132899 was associated with premature CAD risk (age ≤ 60 years old), and that individuals carrying C allele might have significantly increased CAD susceptibility. However, we did not find any association between rs5167, rs1801693 and rs7765781 and the risk of CAD (Table 3).
Stratification analyses of APOC4 rs1132899 polymorphism and risk of CAD
We further evaluated the alleles or genotypes of APOC4 rs1132899 and CAD susceptibility after stratifying the subjects by sex, status of smoking or drinking. Stratification analyses by sex revealed that the increased risk of CAD was more evident among male subjects carrying C allele (OR = 1.65, 95 % CI = 1.06–2.58, P = 0.028, Table 4) or the CC genotype (OR = 3.33, 95 % CI =1.14–9.69, P = 0.027, Table 4). In addition, only the CC genotype of rs1132899 polymorphism exhibited an association with enhanced risk of CAD in smokers (OR = 3.59, 95 % CI =1.08–12.0, P = 0.037, Table 4), but not in non-smokers. No more evident association between APOC4 rs1132899 polymorphism and risk of CAD was observed among subgroups by status of drinking (data not shown).
Multivariate associations of the APOC4 SNPs with the lipid profile
In order to probe into the potential explanation to the enhanced effects of APOC4 rs1132899 polymorphism on early-onset CAD risk (≤60 years old), we further analyzed the association between APOC4 rs1132899 polymorphism and LDL-C, HDL-C, TC and TG levels. However none of the above lipids profile exhibited significant association with APOC4 rs1132899 polymorphism (data not shown). Nonetheless, CC genotype of rs1132899 conferred about 0.09 mmol/L increase in triglyceride (TG) levels compared to CT/TT genotype (1.95 mmol/L vs 1.86 mmol/L) in male subjects compared to CT/TT genotype, though the difference was non-significant (Table 5). Thus, these results indicated that, in addition to influence the lipid profile, there might be other mechanisms contributing the increased risk of APOC4 rs1132899 polymorphism in premature CAD, which still require further analysis in a larger sample size.
The fundamental pathogenesis of CAD is the dysfunction of lipid metabolism, and thus the disorder of plasma lipid profile, which caused by both individual’s genetic makeup and various environmental factors. Previous studies have demonstrated the effects of APOC4 and LPA in abnormal blood lipids including hypercholesterolemia or hypertriglyceridemia, indicating the potential role of APOC4 and LPA in the CAD development. Nonetheless, the association between SNPs in APOC4 and LPA gene and CAD risk still required to be fully elucidated. The potential risk of CAD in older subjects is more likely due to the aging effects as weak immune system and relative high level exposure to environmental risk factors, rather than direct genetic effects. Thus, in this study, we performed a genetic association analysis on the four SNPs (rs1132899 and rs5167 in APOC4, rs1801693 and rs7765781 in LPA) among early-onset CAD subjects (≤60 years old). Our data revealed that the APOC4 rs1132899 polymorphism was associated with increased risk of both premature CAD, and the association was more remarkable among male subjects. Taken together, our study suggested that APOC4 polymorphisms might play an important role in the early-onset CAD pathogenesis.
The APOE/C1/C4/C2 gene cluster has been established to be a critical region for several human diseases, including CAD, and thus the polymorphisms of the locus have been considered to be closely associated with the risk of CAD. However, the effects of APOC4 rs1132899 and rs5167 polymorphisms on CAD risk are still unknown. Kamboh et al. has reported that the rs1132899 and rs5167 polymorphisms were significantly associated with triglyceride levels in women; moreover, APOC4 rs5167 polymorphism exerted a modest effect on HDL-C levels. Hypertriglyceridemia and hypercholesterolemia are crucial risk factors for atherosclerosis, CAD and other arterial cardiovascular diseases, which indicated the important role of the two APOC4 polymorphisms during CAD development. Our data found that rs1132899 endowed C allele carriers with significant increased CAD risk, which is in consistent with the results from the above association analysis between the two polymorphisms and plasma lipids levels.
Our stratified analyses revealed that the increased risk of APOC4 rs1132899 polymorphism in CAD was more evident among male subjects, whereas no significant association was observed from the female group (Table 4). The potential explanation to the gender variance is as follow: 1. Previous studies have unraveled that the most common risk factor in young men was cigarette smoking, while the major risk factor was hypercholesterolaemia in young women . Our data showed that the rs1132899 polymorphism only exhibited an association with enhanced risk of CAD in smokers, but not in non-smokers, which was consistent with the association in male subjects (Table 5); 2. The stratified analyses showed that the CC genotype of rs1132899 modestly increased the triglyceride (TG) levels compared in male subjects, whereas female subjects carrying CC genotype exhibited mildly decreased TG levels; 3. Sex hormones play an important role in coronary artery disease, a proper ratio of estrogen:testosterone is essential during CAD development s , which might account for the sex variance of rs1132899 polymorphism for the risk of CAD.
Several limitations in this case–control study still need to be addressed. First, the case subjects and controls enrolled from hospitals may not represent the general population. However, the genotype distribution of the controls was in Hardy-Weinberg equilibrium. Second, the moderate sample size limited the statistical power of our study, especially for the case subjects. Finally, further studies in different population could help to further verify the significance of the association between the rs1132899 polymorphism and the risk of early-onset CAD. However, our results provided valuable insights and interesting information and might serve to guide future studies in this area.
In aggregate, our study firstly uncovered that the C allele of APOC4 rs1132899 was associated with an increased risk of early-onset CAD in a Chinese population, and the association is more evident among male subjects, which potentially due to the modestly elevated TG levels. Further studies with larger sample size and in diverse ethnic populations are required to confirm the general validity of our findings.
Coronary artery disease
Single nucleotide polymorphism
Polymerase chain reaction-ligase detection reaction
Low density lipoprotein cholesterol
High density lipoprotein cholesterol
Prins BP, Lagou V, Asselbergs FW, Snieder H, Fu J. Genetics of coronary artery disease: genome-wide association studies and beyond. Atherosclerosis. 2012;225:1–10.
Zhang XH, Lu ZL, Liu L. Coronary heart disease in China. Heart. 2008;94:1126–31.
Austin MA, Hutter CM, Zimmern RL, Humphries SE. Familial hypercholesterolemia and coronary heart disease: a HuGE association review. Am J Epidemiol. 2004;160:421–9.
Steinberg D. Thematic review series: the pathogenesis of atherosclerosis. An interpretive history of the cholesterol controversy: part II: the early evidence linking hypercholesterolemia to coronary disease in humans. J Lipid Res. 2005;46:179–90.
Niemiec P, Nowak T, Iwanicki T, Krauze J, Gorczynska-Kosiorz S, Grzeszczak W, et al. The -930A > G polymorphism of the CYBA gene is associated with premature coronary artery disease. A case–control study and gene-risk factors interactions. Mol Biol Rep. 2014;41:3287–94.
Alfakih K, Lawrance RA, Maqbool A, Walters K, Ball SG, Balmforth AJ, et al. The clinical significance of a common, functional, X-linked angiotensin II type 2-receptor gene polymorphism (−1332 G/A) in a cohort of 509 families with premature coronary artery disease. Eur Heart J. 2005;26:584–9.
Ghaderian SM, Akbarzadeh Najar R, Tabatabaei Panah AS. Genetic polymorphisms and plasma levels of matrix metalloproteinases and their relationships with developing acute myocardial infarction. Coron Artery Dis. 2010;21:330–5.
Shah M, Sikkel MB. Coronary artery disease and age: beyond atherosclerosis. J Physiol. 2013;591:5807–8.
Wang TJ, Nam BH, D’Agostino RB, Wolf PA, Lloyd-Jones DM, MacRae CA, et al. Carotid intima-media thickness is associated with premature parental coronary heart disease: the Framingham Heart Study. Circulation. 2003;108:572–6.
Thompson SR, McCaskie PA, Beilby JP, Hung J, Jennens M, Chapman C, et al. IL18 haplotypes are associated with serum IL-18 concentrations in a population-based study and a cohort of individuals with premature coronary heart disease. Clin Chem. 2007;53:2078–85.
Zhang LH, Kotite L, Havel RJ. Identification, characterization, cloning, and expression of apolipoprotein C-IV, a novel sialoglycoprotein of rabbit plasma lipoproteins. J Biol Chem. 1996;271:1776–83.
Kotite L, Zhang LH, Yu Z, Burlingame AL, Havel RJ. Human apoC-IV: isolation, characterization, and immunochemical quantification in plasma and plasma lipoproteins. J Lipid Res. 2003;44:1387–94.
Allan CM, Walker D, Segrest JP, Taylor JM. Identification and characterization of a new human gene (APOC4) in the apolipoprotein E, C-I, and C-II gene locus. Genomics. 1995;28:291–300.
Cervantes S, Samaranch L, Vidal-Taboada JM, Lamet I, Bullido MJ, Frank-Garcia A, et al. Genetic variation in APOE cluster region and Alzheimer’s disease risk. Neurobiol Aging. 2011;32:2107. e7–17.
Ken-Dror G, Talmud PJ, Humphries SE, Drenos F. APOE/C1/C4/C2 gene cluster genotypes, haplotypes and lipid levels in prospective coronary heart disease risk among UK healthy men. Mol Med. 2010;16:389–99.
Allan CM, Taylor JM. Expression of a novel human apolipoprotein (apoC-IV) causes hypertriglyceridemia in transgenic mice. J Lipid Res. 1996;37:1510–8.
Kamboh MI, Aston CE, Hamman RF. DNA sequence variation in human apolipoprotein C4 gene and its effect on plasma lipid profile. Atherosclerosis. 2000;152:193–201.
Erqou S, Kaptoge S, Perry PL, Di Angelantonio E, Thompson A, White IR, et al. Lipoprotein(a) concentration and the risk of coronary heart disease, stroke, and nonvascular mortality. JAMA. 2009;302:412–23.
Angles-Cano E, Hervio L, Rouy D, Fournier C, Chapman JM, Laplaud M, et al. Effects of lipoprotein(a) on the binding of plasminogen to fibrin and its activation by fibrin-bound tissue-type plasminogen activator. Chem Phys Lipids. 1994;67–68:369–80.
Simon DI, Fless GM, Scanu AM, Loscalzo J. Tissue-type plasminogen activator binds to and is inhibited by surface-bound lipoprotein(a) and low-density lipoprotein. Biochemistry. 1991;30:6671–7.
Arsenault BJ, Dube MP, Brodeur MR, de Oliveira Moraes AB, Lavoie V, Kernaleguen AE, et al. Evaluation of links between high-density lipoprotein genetics, functionality, and aortic valve stenosis risk in humans. Arterioscler Thromb Vasc Biol. 2014;34:457–62.
Tregouet DA, Konig IR, Erdmann J, Munteanu A, Braund PS, Hall AS, et al. Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. Nat Genet. 2009;41:283–5.
Clarke R, Peden JF, Hopewell JC, Kyriakou T, Goel A, Heath SC, et al. Genetic variants associated with Lp(a) lipoprotein level and coronary disease. N Engl J Med. 2009;361:2518–28.
Abd El-Aziz TA, Mohamed RH, Hagrass HA. Increased risk of premature coronary artery disease in Egyptians with ABCA1 (R219K), CETP (TaqIB), and LCAT (4886C/T) genes polymorphism. J Clin Lipidol. 2014;8:381–9.
Wu Z, Lou Y, Qiu X, Liu Y, Lu L, Chen Q, et al. Association of Cholesteryl Ester Transfer Protein (CETP) gene polymorphism, high density lipoprotein cholesterol and risk of coronary artery disease: a meta-analysis using a Mendelian randomization approach. BMC Med Genet. 2014;15:118.
Lambert JC, Brousseau T, Defosse V, Evans A, Arveiler D, Ruidavets JB, et al. Independent association of an APOE gene promoter polymorphism with increased risk of myocardial infarction and decreased APOE plasma concentrations-the ECTIM study. Hum Mol Genet. 2000;9:57–61.
Sediri Y, Kallel A, Feki M, Mourali S, Elasmi M, Abdessalem S, et al. Association of a DNA polymorphism of the apolipoprotein AI-CIII-AIV gene cluster with myocardial infarction in a Tunisian population. Eur J Intern Med. 2011;22:407–11.
Xiong XD, Luo XP, Cheng J, Liu X, Li EM, Zeng LQ. A genetic variant in pre-miR-27a is associated with a reduced cervical cancer risk in southern Chinese women. Gynecol Oncol. 2014;132:450–4.
Yasar AS, Turhan H, Basar N, Metin F, Erbay AR, Ilkay E, et al. Comparison of major coronary risk factors in female and male patients with premature coronary artery disease. Acta Cardiol. 2008;63:19–25.
Yang C, Wang X, Geng C, Ding H. Prevention of coronary artery disease in men: male hormone, female hormone, or both? Med Hypotheses. 2010;75:671–3.
We thanks to the First People’s Hospital of Foshan and the Affiliated Hospital of Guangdong Medical University, Guangdong Province, China, for their kind assistance in collecting the samples and data. This work was supported by grants from the National Natural Science Foundation of China (81000143, 81370456), the Natural Science Foundation of Guangdong Province (2014A030311015, S2012010008219, 2014A030310027), the Science and Technology Planning Project of Dongguan City (2013108101057), Scientific Research Foundation of Guangdong Medical University (B2013002).
The authors declare that they have no competing interests.
SX and JC carried out the molecular genetic studies and the statistical analysis, and SX drafted the manuscript. Y-nC and N-hL carried out the genotyping. M-yC, S-sT, HH, BZ, J-mC, X-lY and CC helped to collect study subjects. SX and X-dX participated in the design of the study. XL and X-dX helped to revise the manuscript. All authors read and approved the final Manuscript.
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Xu, S., Cheng, J., Li, N. et al. The association of APOC4 polymorphisms with premature coronary artery disease in a Chinese Han population. Lipids Health Dis 14, 63 (2015). https://doi.org/10.1186/s12944-015-0065-7
- Single nucleotide polymorphism
- Premature coronary artery disease