Introduction

Recent progress in human genetics and genomics research, highlighted by completion of the nucleotide sequence of the human genome by the Human Genome Project (International Human Genome Sequencing Consortium 2004), has provided substantial benefits to clinical medicine, including facilitation of the characterization of disease pathogenesis at the molecular level and the development of panels of genetic markers for assessment of disease risk. In particular, determination of single nucleotide polymorphisms (SNPs) and haplotype blocks and the specification of tag SNPs in each haplotype block for four ethnic groups by the International HapMap Project (The International HapMap Consortium 2007) have led to increasingly effective approaches to the identification of genetic variation associated with various multifactorial diseases, providing new insight into the pathogenesis of these conditions. Furthermore, technological developments such as cDNA microarrays and SNP chips that provide huge amounts of genetic information have made possible the detection of genetic differences among individuals at the whole-genome level.

Selection of the most appropriate strategies for disease prevention or therapy on the basis of genetic information for a given individual is referred to as personalized or individualized medicine. In conventional medicine, medications are prescribed on the basis of the diagnosis and severity of the disease. However, the efficacy of drugs and the incidence of side effects vary among individuals. The goal of treatment based on genetic or genomic information is to be able to predict therapeutic outcome or side effects in an individual, thereby increasing the effectiveness and safety of therapy. In addition, the clarification of disease etiologies at the molecular level and the identification of genetic variants that confer disease susceptibility are likely to contribute both to disease prevention and to the development of new medicines.

Myocardial infarction (MI) is an important clinical problem because of its large contribution to mortality. In the United States, the total number of individuals affected by coronary heart disease (CHD) was 15.8 million in 2004, with nearly 450,000 patients dying annually from this condition (Rosamond et al. 2007). The annual incidence of MI was 565,000 new attacks and 300,000 recurrent attacks, with an annual mortality of 157,000 (Rosamond et al. 2007). As in the United States, CHD is the most common cause of death in the United Kingdom, where it is responsible for around 101,000 deaths each year (British Heart Foundation; http://www.heartstats.org/homepage.asp). In Japan, the total number of individuals affected by CHD was 910,000 in 2005, and ~50,000 people die annually from MI (Ministry of Health, Labor, and Welfare of Japan).

The main causal and treatable risk factors for MI include hypertension, hypercholesterolemia or dyslipidemia, diabetes mellitus, and smoking. In addition to these risk factors, recent studies have shown the importance of genetic factors and of interactions between multiple genes and environmental factors in this condition (Arnett et al. 2007; Kullo and Ding 2007; Topol et al. 2006). The common forms of CHD and MI are thus thought to be multifactorial and to be determined by many genes, each with a relatively small effect, working alone or in combination with modifier genes or environmental factors (or both). The “common disease, common variants hypothesis” proposes that genetic variants present in many normal individuals contribute to overall CHD risk. In addition, susceptibility to some common diseases may be conferred, in part, by rarer variants (Arnett et al. 2007).

Despite recent advances in therapy, such as drug-eluting stents (Marroquin et al. 2008), for acute coronary syndrome (ACS), CHD remains the leading cause of death in the US and UK and the second leading cause of death in Japan. Disease prevention is an important strategy for reducing the overall burden of CHD and MI, and the identification of biomarkers for disease risk is key both for risk prediction and for potential intervention to reduce the chance of future events.

Linkage analysis of MI, ACS, or CHD

Several genome-wide linkage analyses of families or sib-pairs have identified chromosomal loci linked to or genetic variations that confer susceptibility to MI, ACS, or CHD (Broeckel et al. 2002; Farrall et al. 2006; Francke et al. 2001; Harrap et al. 2002; Hauser et al. 2004; Helgadottir et al. 2004; Pajukanta et al. 2000; The BHF Family Heart Study Research Group 2005; Wang et al. 2003, 2004). The published results of genome-wide linkage analyses for these conditions are summarized in Table 1. Genomic regions identified in the published linkage studies as being correlated with MI or CHD are largely nonoverlapping, suggestive of genetic complexity in which multiple genes are responsible for the development of these conditions, although phenotypic heterogeneity could also have contributed to the nonreplicability of results.

Table 1 Genome-wide linkage analyses of myocardial infarction (MI), acute coronary syndrome (ACS), or coronary heart disease (CHD)
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The deCODE Genetics group (Helgadottir et al. 2004) performed linkage analysis with 1,068 microsatellite markers and found a linkage peak (LOD score of 2.86) at chromosomal region 13q12-q13 for 296 Icelandic families (713 individuals) enrolled on the basis of a history of MI. The researchers then genotyped an additional 120 microsatellite markers in this interval in 802 individuals with MI and 837 controls, and they found that a four-marker SNP haplotype spanning the arachidonate 5-lipoxygenase-activating protein gene (ALOX5AP) was associated with MI (odds ratio, 1.8) and stroke (odds ratio, 1.7). A subsequent study found that ALOX5AP was associated with CHD in British individuals and with stroke in Icelandic and Scottish populations (Helgadottir et al. 2005).

On the basis of the results of the same genome-wide scan, the deCODE Genetics group (Helgadottir et al. 2006) performed fine mapping to determine that a five- to seven-marker SNP haplotype of the leukotriene A4 hydrolase gene (LTA4H) accounted for a linkage peak at 12q22. Of particular interest with this haplotype was its ancestry-specific association with the incidence and risk of MI. In European-Americans, the relative risk for MI was only 1.2, with a population attributable risk of 4.6%, whereas among individuals of African ancestry, the relative risk was 3.5 and the population attributable risk was 14% (Helgadottir et al. 2006). Two different genes (ALOX5AP and LTA4H) in the same inflammation-related pathway of leukotriene B4 production were thus found to be associated with disease in a single genome-wide scan. This pathway had already been implicated in studies of murine experimental atherosclerosis as well as in human epidemiological and pathological studies (Dwyer et al. 2004; Mehrabian et al. 2002; Spanbroek et al. 2003). In addition, a small-molecule inhibitor of ALOX5AP was shown to reduce both leukotriene production and the plasma concentration of C-reactive protein (CRP), an important biomarker for CHD, in a pilot, placebo-controlled, randomized trial with individuals harboring the risk ALOX5AP or LTA4H haplotype (Hakonarson et al. 2005). Of note, LTA4H was the first MI-linked gene to show an ancestry-specific risk (Damani and Topol 2007; Topol et al. 2006).

Association studies of MI or CHD

Various association studies of unrelated individuals have identified genetic variations that confer susceptibility to MI or CHD. The published results for genes associated with these conditions are summarized in Table 2. Numerous candidate genes have been implicated, but those that show reproducible associations between risk alleles and CHD or MI in replication studies are few. The candidate gene approach has been widely applied to analysis of the possible association between genetic variants and disease, with genes selected on the basis of a priori hypotheses regarding their potential etiologic role. It is characterized as a hypothesis-testing approach because of the biological observation supporting a role for the proposed candidate gene. The candidate gene approach is not able, however, to identify disease-associated polymorphisms in unknown genes. The recent development of high-density genotyping arrays has improved the resolution of unbiased genome-wide scans for common variants associated with multifactorial diseases. Currently, the genome-wide association study (GWAS) makes use of high-throughput genotyping technologies that include about 1 million probes for SNPs and 1 million probes for copy number variations to examine their relation to clinical conditions or measurable traits. Since 2005, nearly 100 loci for as many as 40 common diseases or traits have been identified by GWASs, many in genes not previously suspected of having a role in the condition studied, and some in genomic regions containing no known genes. Although GWASs represent a substantial advance in the search for genetic variants that influence disease, they also have important limitations, including the potential for generating false-positive or false-negative results and for biases related to the selection of study participants and genotyping errors (Pearson and Manolio 2008).

Table 2 Genes shown to be related to the prevalence of myocardial infarction or coronary heart disease
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Mendelian randomization

Mendelian randomization analysis is a relatively recent development in genetic epidemiology based on Mendel’s second law, which states that the inheritance of one trait is independent of that of other traits (Davey Smith and Ebrahim 2003; Keavney 2002). It relies on common genetic polymorphisms that are known to influence exposure patterns (such as the propensity to drink alcohol) or to have effects equivalent to those produced by modifiable exposures (such as an increased serum cholesterol concentration). Associations between genetic variants and outcomes are not generally confounded by behavioral or environmental exposures, with the result that observational studies of genetic variants have similar properties to intention-to-treat analyses in randomized controlled trials. The simplest way of appreciating the potential of Mendelian randomization analysis is to consider applications of the underlying principles. The inferences that can be drawn from Mendelian randomization studies depend on the different ways in which genetic variants can serve as a proxy for environmentally modifiable exposures (Davey Smith and Ebrahim 2005).

The relations of polymorphisms of the CRP gene (CRP) to circulating CRP concentrations and the prevalence of CHD or MI have been examined by Mendelian randomization analysis. Pooled data from 4,659 Caucasian men in six studies revealed that individuals homozygous for the T allele of the 1444C→T polymorphism of CRP had a higher circulating CRP concentration than carriers of the C allele. However, men with the TT genotype were not at increased risk of nonfatal MI (Casas et al. 2006). This unbiased and nonconfounded estimate of the effect of CRP genotype on coronary events was smaller than estimates provided by previous studies. In two independent prospective cohort studies of 32,826 women and 18,225 men in the US, the minor alleles of 1919A→T and 4741G→C polymorphisms of CRP were associated with higher plasma CRP levels, and those of 2667G→C and 3872C→T polymorphisms of CRP were associated with lower plasma CRP levels. Two of the five common haplotypes of CRP were associated with lower CRP levels. However, neither the individual SNPs nor the common haplotypes were associated with risk of CHD in the direction that would be predicted by their association with CRP levels (Pai et al. 2008). These data suggest that the underlying inflammatory processes that predict coronary events cannot be captured solely by variation in CRP. The CRP CHD Genetics Collaboration is a consortium of investigators generating and pooling analyses of data on genetic determinants of circulating CRP levels and CHD. These data should help to clarify the likelihood and magnitude of any causal association between circulating CRP concentration and CHD. The collaboration is likely to advance understanding of the relevance of low-grade inflammation to CHD and indicate whether or not CRP itself should be prioritized as a therapeutic target for long-term prevention strategies (CRP CHD Genetics Collaboration 2008).

Candidate gene association studies for MI or CHD

Association studies based on the candidate gene approach have revealed many polymorphisms to be associated with the prevalence of MI or CHD (Table 2). In this section, we discuss the association of polymorphisms in MTHFR, LPL, and APOE with MI or CHD.

MTHFR

Homocysteine is a sulfur-containing amino acid that plays a pivotal role in methionine metabolism. 5,10-Methylenetetrahydrofolate reductase (MTHFR) catalyzes the reduction of 5,10-methylenetetrahydrofolate to 5-methylenetetrahydrofolate, a reaction that provides a substrate for the methylation of homocysteine to methionine catalyzed by methionine synthase. Individuals with the 677C→T (Ala222Val) substitution of MTHFR manifest reduced MTHFR activity and higher plasma homocysteine levels compared with those without it (Deloughery et al. 1996; Ma et al. 1996; Schwartz et al. 1997). Association of the 677C→T (Ala222Val) polymorphism of MTHFR with CHD or MI has been described by several groups, with the TT genotype being a risk factor for these conditions (Gallagher et al. 1996; Kluijtmans et al. 1996; Mager et al. 1999; Morita et al. 1997; Yamada et al. 2006). Other studies, however, did not support such an association (Folsom et al. 1998; Schwartz et al. 1997). These apparently contradictory results are attributable, at least in part, to differences in intake of folate and other B vitamins (Verhoef et al. 1998). A meta-analysis of the association of the 677C→T (Ala222Val) polymorphism of MTHFR with the risk of CHD in 11,162 cases and 12,758 controls from 40 studies revealed that individuals with the TT genotype had an odds ratio of 1.16 for CHD compared with those with the CC genotype (Klerk et al. 2002). These observations suggest that impaired folate metabolism, resulting in high homocysteine concentrations, is an important determinant of CHD. Another meta-analysis of the association of the 677C→T (Ala222Val) polymorphism of MTHFR with CHD in 26,000 cases and 31,183 controls from 80 studies yielded an overall odds ratio of 1.14 for the TT genotype versus the CC genotype; odds ratios for Europe, Australia, and North America were about 1.0, whereas those for the Middle East and Asia were 2.61 and 1.23, respectively (Lewis et al. 2005). These results indicate that the 677C→T (Ala222Val) polymorphism of MTHFR is associated with CHD in the Middle East and Asia, but not in Europe, North America, or Australia, with this geographic variability possibly reflecting higher folate intake in the latter regions (Lewis et al. 2005).

LPL

Lipoprotein lipase (LPL) is the rate-limiting enzyme in lipolysis of triglyceride-rich lipoproteins in the circulation. It is synthesized in parenchymal cells of adipose tissue as well as in skeletal and cardiac muscle, and it is then transferred to heparan sulfate-binding sites of the vascular endothelium (Kastelein et al. 2000). The hydrolytic function of LPL is important for the processing of triglyceride-rich chylomicrons and very low density lipoproteins to remnant particles as well as for the transfer of phospholipids and apolipoproteins to high density lipoproteins (HDLs). LPL also plays an important role in the receptor-mediated removal of lipoproteins from the circulation (Groenemeijer et al. 1997). LPL is polymorphic, with amino acid substitutions of the encoded protein affecting triglyceride and HDL-cholesterol levels, which are implicated in atherosclerosis risk (Wittrup et al. 1999). The 1595C→G (Ser447Stop) substitution of LPL results in carboxyl-terminal truncation of LPL by two amino acids. This change is thought to increase the binding affinity of the protein for receptors or to facilitate or otherwise affect its formation of dimers (Wittrup et al. 1999). The G (Stop) allele of the 1595C→G (Ser447Stop) polymorphism has also been shown to be related to decreased plasma triglyceride or increased HDL-cholesterol levels, or both (Groenemeijer et al. 1997; Jemaa et al. 1995; Kuivenhoven et al. 1997; Wittrup et al. 1999). In addition, the G (Stop) allele of this polymorphism was found to be associated with a reduced risk of CHD or MI (Wittrup et al. 1999; Yamada et al. 2006; Yang et al. 2004). Evidence suggests that the catalytic activity and stability of the truncated variant of LPL may be largely normal, but that it may be present at higher concentrations in the circulation, resulting in a higher level of LPL activity (Groenemeijer et al. 1997; Henderson et al. 1999; Humphries et al. 1998; Zhang et al. 1996).

APOE

Apolipoprotein E (ApoE) plays an important role in lipid transport and metabolism. Three common alleles (ε2, ε3, and ε4) of APOE encode the three major isoforms (E2, E3, and E4) of ApoE, which differ at amino acid positions 112 and 158. Allelic variation of APOE accounts for interindividual variability in total cholesterol and low density lipoprotein (LDL)–cholesterol concentrations, with studies in human populations demonstrating associations of the ε4 and ε2 alleles with increased and decreased LDL-cholesterol levels, respectively (Ehnholm et al. 1986; Sing and Davignon 1985; Xhignesse et al. 1991). The various ApoE isoforms interact differently with specific lipoprotein receptors, ultimately affecting circulating levels of cholesterol (Eichner et al. 2002). ApoE from very low density lipoprotein, chylomicrons, and chylomicron remnants binds to specific receptors on cells in the liver. Carriers of the ε2 allele of APOE are less efficient than carriers of the ε3 or ε4 alleles at synthesizing very low density lipoprotein and chylomicrons and at transferring them from plasma to the liver as a result of the binding properties of the ApoE2 isoform. Thus, compared with carriers of the ε3 or ε4 alleles, carriers of the ε2 allele are slower to clear dietary fat from their blood (Weintraub et al. 1987). The difference in uptake of postprandial lipoprotein particles results in differences in regulation of hepatic LDL receptors, which in turn contribute to genotypic differences in total and LDL-cholesterol levels (Davignon et al. 1988; Hallman et al. 1991; Schaefer et al. 1994).

The relation of APOE polymorphisms to CHD or MI has been extensively investigated in the last 2 decades. In many studies, the ε4 allele has been associated with CAD or MI (Lahoz et al. 2001; van Bokxmeer and Mamotte 1992; Wilson et al. 1994). A meta-analysis of 15,492 subjects with CHD and 32,965 controls pooled from 48 studies revealed that, compared with individuals with the ε3/ε3 genotype, carriers of the ε4 allele had a higher risk for CHD (odds ratio, 1.42), whereas the ε2 allele was not associated with CHD risk (Song et al. 2004). The ε4 allele of APOE is thus an important risk factor for CHD.

The -219G→T SNP of APOE has been associated with MI for men in France and Northern Ireland, with the T allele representing a risk factor for this condition (Lambert et al. 2000). Consistent with its location in the promoter region of APOE, the -219G→T SNP was shown to be associated with the plasma concentration of ApoE, with the T allele conferring a reduced ApoE concentration (Lambert et al. 2000). The deleterious influence of the T allele on MI therefore cannot be explained by its effect on the circulating level of ApoE. The T allele of this SNP was also shown to be a risk factor for CHD in low-risk Japanese men (Hirashiki et al. 2003).

Genome-wide association studies of MI or CHD

GWASs have identified susceptibility genes for various multifactorial diseases, including CHD and MI (Table 3).

Table 3 Genome-wide association studies of myocardial infarction (MI) or coronary heart disease (CHD)
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LTA

Screening of 65,671 SNPs revealed that two polymorphisms of the lymphotoxin-α gene (LTA) were associated with susceptibility to MI in a study with 1,133 MI patients and 1,878 controls (Ozaki et al. 2002). Functional analysis in vitro indicated that the G allele of one of these two polymorphisms, 252A→G in intron 1 (rs909253), was associated with an increase in the transcriptional activity of LTA and that the A (Asn) allele of the second SNP, 804C→A (Thr26Asn) in exon 3 (rs1041981), was associated with increased expression of the genes for vascular cell adhesion molecule 1 and selectin E. Ozaki et al. (2002) thus suggested that variants of LTA are risk factors for MI and that they influence the vascular inflammation that underlies this condition. These researchers subsequently showed that the 3279C→T polymorphism in intron 1 of the lectin, galactoside-binding, soluble, two gene (LGALS2) was associated with the prevalence of MI (Ozaki et al. 2004). LGALS2 plays a role in the secretion of LTA from smooth muscle cells and macrophages, and the identified polymorphism affects the transcriptional activity of LGALS2. These results suggested that an LGALS2–LTA axis is important in the pathophysiology of coronary atherosclerosis and thrombosis.

The relation of seven SNPs (rs2071590, rs1800683, rs909253, rs746868, rs2857713, rs3093543, and rs1041981) distributed throughout LTA and of their corresponding haplotypes to risk of MI was examined in the International Study of Infarct Survival (ISIS) case–control study involving 6,928 cases of nonfatal MI and 2,712 unrelated controls (Clarke et al. 2006). The seven SNPs were in strong linkage disequilibrium with each other and formed six common haplotypes. None of the SNPs or haplotypes was associated with risk of MI. A meta-analysis of rs909253 or rs1041981 in six previously published studies and the ISIS study (Clarke et al. 2006) found no association with CHD risk in a recessive model (odds raio, 1.07) and only a moderate association in a dominant model (odds raio, 1.09). Overall, these studies suggest that these common polymorphisms of LTA are not associated with susceptibility to CHD or MI. Given that the effect of LTA variants on the development of MI might differ among ethnic groups or among individuals exposed to different environmental factors such as smoking, further investigation is warranted with large independent subject panels of different ethnic groups.

Chromosome 9p21.3

In 2007, independent GWASs based on the use of SNP chips identified four SNPs on chromosome 9p21.3 that were associated with CHD or MI in several white cohorts (Helgadottir et al. 2007; McPherson et al. 2007; Samani et al. 2007; Wellcome Trust Case Control Consortium 2007). McPherson et al. (2007) identified two susceptibility SNPs (rs10757274 and rs2383206) that were located within 20 kbp of each other on chromosome 9p21.3 and were associated with CHD in a Canadian population and five other white cohorts. Helgadottir et al. (2007) described an association between MI and two SNPs (rs2383207 and rs10757278) located in the same 9p21.3 region in an Icelandic population, and they replicated the finding in four white cohorts. The same genetic locus was also identified by a GWAS performed with 1,926 CHD cases and 3,000 controls from a British population (Wellcome Trust Case Control Consortium 2007), and the finding was replicated in a German population (Samani et al. 2007). Association of SNPs on chromosome 9p21.3 was also replicated for MI in an Italian population (Shen et al. 2008b) and for CHD in a Korean population (Shen et al. 2008a). Interestingly, the independent population-based case–control studies also identified several SNPs at 9p21.3 that were significantly associated with type 2 diabetes mellitus in white populations in England (Zeggini et al. 2007), Finland (Scott et al. 2007), and Sweden (Saxena et al. 2007). In addition to MI, SNP rs10757278 at this locus was found to be associated with abdominal aortic aneurysm and intracranial aneurysm (Helgadottir et al. 2008). Schunkert et al. (2008) genotyped a SNP (rs1333049) representing the 9p21.3 locus in seven case–control studies including a total of 4,645 subjects with MI or CHD and 5,177 controls. The risk allele (C) of this SNP was uniformly associated with MI or CHD in each study, with pooled analysis revealing the odds ratio per copy of the risk allele to be 1.29. Meta-analysis of rs1333049 in 12,004 cases and 28,949 controls provided further evidence for association of this SNP with MI or CHD, yielding an odds ratio of 1.24 per risk allele.

The prospective Northwick Park Heart Study II analyzed complete trait and genotype information available for 2,057 men (183 CHD events over 10.8 years). For a panel of selected genotypes for UCP2, APOE, LPL, APOA4, IL6, and PECAM1, CHD risk estimates incorporating conventional risk factors (age, triglyceride and cholesterol levels, systolic blood pressure, and smoking) and genetic risk interactions were more effective than those based on conventional risk factors alone (Humphries et al. 2007). In a study of the same cohort involving 2,742 men (270 CHD events over 15 years), although rs10757274 at 9p21.3 was associated with CHD, it did not add substantially to the usefulness of the Framingham risk score based on conventional risk factors alone for predicting future CHD events. However, it did improve reclassification of CHD risk and thus may be of clinical utility (Talmud et al. 2008).

Although this broad replication of the association with chromosome 9p21.3 provides important new information on the molecular genetics of CHD and MI, the underlying mechanism is as yet elusive. The region is defined by two flanking recombination hot spots and contains the coding sequences of genes for two cyclin-dependent kinase inhibitors, CDKN2A and CDKN2B. These genes play an important role in regulation of the cell cycle and belong to a family of genes that have been implicated in the pathogenesis of atherosclerosis as a result of their contribution to inhibition of cell growth by transforming growth factor-β1. However, the SNPs associated most strongly with MI or CHD lie considerably upstream of these genes, with the nearest being located 10 kbp upstream of CDKN2B. Although an effect mediated through one or both of these genes is possible, other explanations for the association of the 9p21.3 region with MI or CHD need to be considered (Schunkert et al. 2008).

The high-risk CHD haplotype at 9p21.3 [T (rs10116277)–T (rs6475606)–G (rs10738607)–T (rs10757272)–G (rs10757274)–G (4977574)–G (2891168)–G (1333042)–G (2383206)–G (2383207)–C (1333045)–G (10757278)–C (1333048)–C (1333049)] was recently shown to overlap with exons 13 to 19 of ANRIL (Broadbent et al. 2008) (Fig. 1), a newly annotated gene for a large antisense noncoding RNA that was identified by deletion analysis of an extended French family with hereditary melanoma–neural system tumors (Pasmant et al. 2007). Reverse transcription and polymerase chain reaction analysis showed that ANRIL is expressed in atheromatous human vessels (specimens of abdominal aortic aneurysm or carotid endarterectomy), which manifest a cell type profile similar to that of atherosclerotic coronary arteries. ANRIL was found to be expressed in vascular endothelial cells, monocyte-derived macrophages, and coronary smooth muscle cells (Broadbent et al. 2008), all of which contribute to atherosclerosis. Little is known of the function of ANRIL, as is typical of most genes for noncoding RNAs, which in general are thought to participate in transcriptional control (Mattick and Makunin 2006). A survey of the dbSNP database revealed no SNPs that map within the exons of ANRIL that colocalize with the risk haplotype. However, multiple SNPs coupled to the high-risk haplotype map to intronic or downstream sequences of this gene; these variants are plausible candidates for determinants of the level of ANRIL expression. The targets of ANRIL action remain to be discovered, as do any interactions with neighboring genes (Broadbent et al. 2008). Clarification of the functional relevance of SNPs at 9p21.3 to CHD and MI may provide insight into the pathogenesis of these conditions as well as into the role of genetic factors in their development.

Fig. 1
figure 1

Genomic region at chromosome 9p21.3

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Conclusion

There has been a growing effort to find genetic variants that confer risk for CHD and MI as a means to understand the underlying biological events of these conditions. Such studies may ultimately lead to the personalized prevention of MI (Yamada 2006). It may thus become possible to predict the future risk for MI in each individual on the basis of conventional laboratory examinations and genetic analyses. It should also be possible to assess how the risk level of an individual will decrease if treatable risk factors, including hypertension, diabetes mellitus, hypercholesterolemia or dyslipidemia, and smoking, are ameliorated or eliminated. Furthermore, it may be possible to prevent an individual from undergoing MI by medical intervention based on his or her genotype for specific polymorphisms. In the future, we may have the ability to use specific therapeutic agents individualized on the basis of certain genetic susceptibility factors, thereby increasing the efficacy and limiting the toxicity of treatment (Damani and Topol 2007). Identification of disease susceptibility genes will thus contribute to the prevention, early diagnosis, and treatment of CHD and MI.