Figures
Abstract
Background
Vascular fibrinolytic balance is maintained primarily by interplay of tissue plasminogen activator (t-PA) and plasminogen activator inhibitor type 1 (PAI-1). Previous research has shown that polymorphisms in genes from the renin-angiotensin (RA), bradykinin, and fibrinolytic systems affect plasma concentrations of both t-PA and PAI-1 through a set of gene-gene interactions. In the present study, we extend this finding by exploring the effects of polymorphisms in genes from these systems on incident cardiovascular disease, explicitly examining two-way interactions in a large population-based study.
Methodology/Principal Findings
Data from the population-based PREVEND study in Groningen, The Netherlands (n = 8,138) were analyzed. The effects of the polymorphisms and their interactions on cardiovascular events were analyzed via Cox proportional hazards models. There was no association between five of the six polymorphisms singly and risk of cardiovascular disease. There was a significant main effect for the ACE I/D polymorphism for both dominant and additive coding schemes. There were significant interactions between the following polymorphism pairs even after adjustment for known risk factors: ACE I/D & PAI-1 4G/5G (p = 0.012), BDKRB2 C181T & ACE I/D (p = 0.016), BDKRB2 C58T & ACE I/D (p = 0.025), BDKRB2 exon 1 I/D & AT1R A1166C (p = 0.017), and BDKRB2 C58T & AT1R A1166C (p = 0.015).
Conclusions/Significance
This study suggests possible interactions between genes from the RA, bradykinin, and fibrinolytic systems on the risk of cardiovascular disease, extending previous research that has demonstrated that interactions among genes from these systems influence plasma concentrations of both t-PA and PAI-1. Further explorations of these interactions are needed.
Citation: Bentley JP, Asselbergs FW, Coffey CS, Hebert PR, Moore JH, Hillege HL, et al. (2010) Cardiovascular Risk Associated with Interactions among Polymorphisms in Genes from the Renin-Angiotensin, Bradykinin, and Fibrinolytic Systems. PLoS ONE 5(9): e12757. https://doi.org/10.1371/journal.pone.0012757
Editor: Amanda Ewart Toland, Ohio State University Medical Center, United States of America
Received: June 10, 2010; Accepted: August 24, 2010; Published: September 15, 2010
Copyright: © 2010 Bentley et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by National Institutes of Health (NIH) grant HL65234, HL67466, RR018787, LM010098, and by grant E.013 of Netherlands Kidney Foundation. Dr. F.W. Asselbergs is supported by a ZonMW Clinical Fellowship (grant 90700342). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Both tissue plasminogen activator (t-PA) and plasminogen activator inhibitor type 1 (PAI-1) are involved in thrombus formation and degradation. Vascular fibrinolytic balance is determined by the competing effects of t-PA and PAI-1 [1]. Factors that increase PAI-1 levels and decrease t-PA levels may increase the risk of thrombosis as both are risk markers for cardiovascular disease [2], [3]. There is substantial evidence that both the renin-angiotensin (RA) and bradykinin system play a role in the regulation of PAI-1 and t-PA. Previous research has shown that infusion of angiotensin II increases PAI-1 levels in both hypertensive and normotensive patients [4]. In addition, ACE-inhibitors significantly decrease PAI-1 activity in patients with a myocardial infarction [5], in hypertensive subjects [6], and in postmenopausal women [7]. Bradykinin is a potent stimulator of t-PA in the coronary circulation and this effect was augmented by ACE-inhibition [8]. In addition, we previously demonstrated that levels of PAI-1 and t-PA in a population-based sample are partly determined by genetic polymorphisms from the RA and bradykinin systems [9]. Furthermore, we found significant interactions between polymorphisms from the renin-angiotensin (RA), bradykinin, and fibrinolytic systems on the plasma concentrations of t-PA and PAI-1 in two independent studies [10], [11].
Given their role with respect to regulating vascular fibrinolytic balance, it is possible that variations in polymorphisms in genes from these systems may ultimately influence the risk of cardiovascular disease. Some, but not all, studies have shown such associations [12]–[15]. Discrepant results for each individual polymorphism may be the result of interactions with another gene or genes, i.e., each genetic variation may be associated with cardiovascular risk only in the presence of certain other genetic variation. Such gene-gene interactions may occur in the absence of independent main effects. Thus, it is possible that interactions among genes from these three systems might modify the effect of these genes on the risk of cardiovascular disease. Studies often have limited power to explore gene-gene interactions necessitating the use of large datasets. Given this and the biologic plausibility of epistatic effects of polymorphism in genes from the RA, bradykinin, and fibrinolytic systems, the purpose of the present exploratory study was to examine the effects of two-way interactions among these polymorphisms on incident cardiovascular disease in a large, population-based study.
Methods
Study design and participants
Data analyzed in this study were obtained from the Prevention of Renal and Vascular End-stage Disease (PREVEND) study. The PREVEND study is a large observational study currently underway in the city of Groningen, the Netherlands (started in 1997–1998). The PREVEND cohort consists of a random sample of subjects with less than 10 mg/L of urinary albumin and a selected sample of subjects with greater than 10 mg/L of urinary albumin. A total of 8,592 subjects completed the total screening program and were followed over time. Details of the study have been described previously [16]. The original study was approved by a local medical ethics committee and all participants gave written informed consent.
The combined endpoint for the present analysis was incident cardiovascular disease, defined as death from CVD (ICD-10 I00-I02, I05-I15, I20-I28, I30-I52, I60-I89, I95-I99), hospitalization for MI (ICD-10 I21, I22), percutaneous transluminal angioplasty (PCTA), or coronary artery bypass graft (CABG). The first well-defined cardiovascular event of each participant was used for analysis. Event-free survival time for each participant was defined as the period from the date of the outpatient clinic baseline assessment to the date of death, MI, PCTA, or CABG or death from any cause or until December 31, 2005, the latest date on which information regarding specific causes of death follow-up information was available.
Only subjects with a negative history of coronary artery disease (CAD) at baseline were included in the present analysis. Previous documented CAD was defined as history of myocardial infarction, revascularization procedure, or obstructive coronary artery disease prior to inclusion in the PREVEND study. A history of myocardial infarction was based on subjects' medical history, including a structured questionnaire, and information on previous CAD was complemented by review of the medical report. This approach has been used by other published reports from the PREVEND study [17]. Of the 8,592 PREVEND subjects, 453 were excluded for this reason, and one additional subject was excluded due to a missing value on the selection variable (i.e., urinary albumin concentration), leaving an analysis sample of 8,138.
Demographic and clinical information was collected for each participant at baseline. In addition, genotyping was conducted on six polymorphisms as described by Asselbergs et al. [11]. These polymorphisms (with rs numbers), classified by system, can be found in Table 1. Genotype information was unavailable for a number of participants. For example, the largest number of missing cases is for the ACE I/D polymorphism (missing 674 subjects or 8.3% of the analysis sample). About 89% of the subjects had complete data on all six polymorphisms (n = 7,260). To evaluate the potential impact of missing genotype information, six new variables were created to identify cases that had missing data on each of the polymorphisms and another variable to indicate whether a case was missing data on any of the polymorphisms (composite variable). Times to first well-defined cardiovascular event between subjects with missing data and without missing data on each of the six polymorphisms (and the composite variable) were compared using Kaplan-Meier estimates. None of the log-rank tests revealed significantly different survival curves (df = 1, P>0.50 for each of the tests). Based on these findings, for each subsequent analysis, a complete-case approach was utilized (i.e., participants who were missing genotype information were excluded). A similar approach was used by Borggreve et al. [18].
Statistical analysis
SAS 9.1 (SAS Institute, Cary, NC, USA) and STATA SE 9.1 (StataCorp LP, College Station, TX, USA) were used for data analysis. The effects of the polymorphisms on cardiovascular events were analyzed via Cox proportional hazards models. The proportional hazards assumption for the polymorphisms and potential confounders (i.e., demographic and clinical variables) were assessed by graphing log-log survival functions and by evaluation interactions between each variable with time. These examinations suggested that there were no substantial violations of the proportional hazards assumption.
In the screening phase of the PREVEND study, subjects with an elevated UAE were over-sampled to acquire sufficient subjects with microalbuminuria (n = 5,661 with UAC ≥10 mg/L and n = 2,477 with UAC <10 mg/L at baseline in the present analysis sample). To overcome this selection bias in the present study, design-based analyses were performed using sampling probability weights. Due to this weighting method, our conclusions can be generalized for the general population [19]. Previously published reports from the PREVEND study have implemented similar design-based analyses [20], [21]. The design-based Cox regression models were built with STATA.
As an initial step, the unadjusted, unmoderated effects of each polymorphism were examined. Prior to this analysis, all genotypes were coded (AA = 0, Aa = 1, aa = 2) to capture additive effects, (AA = 0, Aa or aa = 1) to capture dominant effects, and (AA or Aa = 0, aa = 1) to capture recessive effects (where AA = homozygous wild-type, Aa = heterozygous, and aa = homozygous variant; see Table 1 for the correspondence of AA, Aa, and aa to each genotype for each polymorphism).
The second step was to analyze unadjusted, two-way interaction effects for the 15 possible pairs of polymorphisms. For each pair, nine possible interaction effects were tested (additive by additive, additive by dominant, additive by recessive, dominant by additive, dominant by dominant, dominant by recessive, recessive by additive, recessive by dominant, and recessive by recessive). We used an uncorrected significance level of α = 0.10 as suggestive evidence for interaction and a more conservative significance level of α = 0.025 as strong evidence for interaction. A similar approach was used by Asselbergs et al. [11] who argue that given the exploratory and early-stage nature of their work, they were more concerned with false negatives (type II errors) than false positives (type I errors). A comparable argument can be made for the present hypothesis-generating study. For readers wishing to use more stringent criteria, P values for these tests are reported in supporting information tables S1a-S1f.
The third step of the analysis was to adjust the estimates by including the following demographic and clinical variables collected at baseline: sex, age, body mass index, presence of diabetes, systolic and diastolic blood pressure, HDL cholesterol, total cholesterol, c-reactive protein, current smoking status, and waist-to-hip ratio. Prior to interpretation, for pairs of polymorphisms where there were multiple significant interactions (e.g., additive-additive and dominant-recessive), we selected the model that provided the most parsimonious fit to the data using Akaike's information criterion (AIC) from the covariate-adjusted model.
Finally, because there is some evidence that the prediction of plasma t-PA/PAI-1 levels by these polymorphisms may differ by sex [9] and that the relationship between plasma concentrations of t-PA/PAI-1 and cardiovascular disease-related traits may also differ by sex [22], we evaluated whether the significant interactions differed by sex by fitting three-way interactions (sex x genotype1 x genotype2) in both the unadjusted and adjusted models.
Results
Baseline demographic and clinical characteristics of the sample can be found in Table 1. Groups with small numbers of cases can lead to large parameter estimates and standard errors (i.e., instability of model fitting) in Cox regression. The frequency for the homozygous variant genotype for the BDKRB2 C181T polymorphism (TT) was rare (1.3%). Therefore, neither recessive coding (i.e., TT versus CT + CC) nor additive coding (i.e., CC versus CT versus TT) were used for this polymorphism in any analysis. The symbol “N/A” reflects these models in subsequent tables.
During a median follow-up of 7.52 years (range 1 day to 8.3 years), a total of n = 463 events were detected among the 8,138 subjects in the dataset (5.7%). Table 2 presents results of the analysis of the unadjusted, unmoderated effects of each polymorphism for each coding scheme. Five of the six polymorphisms showed non-significant effects. However, the main effect for the ACE I/D polymorphism was significant at the 0.05 level for the dominant (HR = 0.72, 95% CI: 0.52–0.99, P = 0.042) as well as the additive coding scheme (HR = 0.79, 95% CI: 0.65–0.98, P = 0.029). The findings suggest a smaller hazard associated with the presence of each ACE D allele (i.e., moving from 0 (ACE II genotype) to 1 (ACE ID genotype) to 2 (ACE DD genotype)). This effect is opposite of what one would expect to find based on previous research. The ACE DD genotype has been found to be associated with increased levels of PAI-1 in some [23], but not all [24], studies and also increased levels of angiotensin-converting enzyme (ACE) [25]. High levels of both PAI-I and ACE promote thrombosis.
We found evidence for RAS-fibrinolytic and bradykinin-RAS interaction effects on incident CVD (P values for the statistical tests for unadjusted two-way interactions among the polymorphisms are provided supporting information tables S1a-S1f. Significant results with strong or suggestive evidence for interaction are in bold). A total of 6 gene-gene interactions were detected out of 15 possible pairs of polymorphisms. Of the 9 possible interactions for the combination of ACE I/D and PAI-1 4G/5G, 8 were significant (the ACE I/D x PAI-1 4G/5G (recessive-dominant) was the only non-significant interaction for this pair).
A summary of the 16 gene-gene interactions with strong or suggestive evidence can be found in Table 3 along with the covariate-adjusted results. The model with the lowest AIC among covariate-adjusted models within each pair of polymorphisms is noted. For one of the interactions (i.e., AT1R A1166C x PAI-1 4G/5G), it appears that adjusting for known risk factors attenuates the suggestive significance observed in the unadjusted analysis (unadjusted P = 0.026, adjusted P = 0.151). Hence, this interaction is not further explored. Statistical significance was maintained for the other five interactions following adjustment for potential confounders.
The subgroup effects of the five remaining gene-gene interactions are further explored in Table 4. The BDKRB2 C58T x ACE I/D interaction shows non-significant subgroup effects in the unadjusted model and one significant subgroup effect only after adjustment for covariates. Given these findings and the exploratory nature of this study, we do not provide further interpretations of this interaction. For the four remaining interactions, the interaction appears to be due to significant effects of one genetic variation only at certain levels of other genetic variation (Table 4). Each of these interactions is further described below.
Among those with at least one PAI-1 5G allele, there is a significantly lower hazard of cardiovascular disease associated with the presence of each ACE D allele (For PAI-1 4G5G: adjusted HR = 0.74, 95% CI: 0.60–0.92; For PAI-1 5G5G: adjusted HR = 0.49, 95% CI: 0.32–0.75). For those with the PAI-1 4G4G genotype, the effect of the ACE I/D polymorphism was in the opposite direction, but not statistically significant (adjusted HR = 1.13, 95% CI: 0.79–1.62).
Among those with at least one ACE I allele, individuals with the BDKRB2 C181T TT or BDKRB2 C181T CT genotypes had a significantly higher hazard of cardiovascular disease as compared to those who carried the BDKRB2 C181T CC genotype (adjusted HR = 1.77, 95% CI: 1.20–2.61). For those with the ACE DD genotype, the effect of the BDKRB2 C181T polymorphism was in the opposite direction, but was not statistically significant in the adjusted model (although it was statistically significant in the model unadjusted for covariates) (adjusted HR = 0.52, 95% CI: 0.21–1.31).
For those with the AT1R A1166C AA genotype, individuals with the BDKRB2 exon 1 I/D +9/+9 genotype had a significantly lower hazard of cardiovascular disease as compared to those who carried either the BDKRB2 exon 1 I/D −9/+9 or −9/−9 genotypes (adjusted HR = 0.45, 95% CI: 0.24–0.82). Among those with at least one AT1R A1166C C allele, the effect of the BDKRB2 exon 1 I/D polymorphism was in the opposite direction, but was not statistically significant (adjusted HR = 1.08, 95% CI: 0.66–1.76).
For those with the AT1R A1166C AA genotype, individuals with the BDKRB2 C58T TT or BDKRB2 C58T CT genotypes had a significantly higher hazard of cardiovascular disease as compared to those who carried the BDKRB2 C58T CC genotype (adjusted HR = 1.67, 95% CI: 1.04–2.70). Among those with at least one AT1R A1166C C allele, the effects of the BDKRB2 C58T polymorphism were in the opposite direction, but not statistically significant.
To assess whether the four significant gene-gene interactions varied by sex, three-way interaction terms were added to each model (sex x genotype1 x genotype2), along with the appropriate lower order effects (i.e., the main effects plus the following two-way interactions: genotype1 x genotype2, sex x genotype1, and sex x genotype2). For three of the four interactions, none of the three-way interactions were statistically significant at the 0.10 level of significance in the unadjusted or adjusted models. However, for the ACE I/D x PAI-1 4G/5G (additive-additive) interaction, the three-way interaction was significant in the unadjusted (P = 0.028) and the adjusted models (P = 0.028). Thus, sex may play a role in the ACE I/D x PAI-1 4G/5G interaction. Preliminary examination of the results suggests that the findings described earlier for the ACE I/D x PAI-1 4G/5G interaction may be stronger for females than for males. There was strong evidence of an ACE I/D x PAI-1 4G/5G interaction effect for females (adjusted P = 0.001), while the evidence was less convincing for males (adjusted P>0.10) (data not shown). Subsequent research is necessary to validate this finding.
Discussion
Vascular fibrinolytic balance is maintained primarily by an interplay of t-PA and PAI-1 [1] and polymorphisms in genes from the RA, bradykinin, and fibrinolytic systems may affect plasma concentrations of both t-PA and PAI-1 through a set of gene-gene interactions [10], [11], suggesting a potential involvement of these systems in determining the risk of cardiovascular disease. The present study suggests possible interactions between the ACE I/D and PAI-1 4G/5G polymorphisms, the BDKRB2 C181T and ACE I/D polymorphisms, the BDKRB2 exon 1 I/D and AT1R A1166C polymorphisms, and the BDKRB2 C58T and AT1R A1166C polymorphisms on the risk of cardiovascular disease. The interaction between the ACE I/D and PAI-1 4G/5G polymorphisms appears to be robust to the choice of genotype coding scheme. Interestingly, several of these interactions were noted in a study of the epistatic effects of these polymorphisms on plasma t-PA and PAI-1 levels [11]. Specifically, 5 out of the 6 interactions noted in the present study were also found by Asselbergs et al. [11] to be significant in the prediction of t-PA or PAI-1 in either males or females – the exception is the BDKRB2 C181T x ACE I/D interaction).
The association between ACE I/D and risk of cardiovascular disease appears to be limited to those who carry the PAI-1 5G allele and suggests a protective effect of the ACE D allele. While an unexpected finding, a protective effect of ACE DD in the presence of the PAI-1 5G allele is consistent with the multifactor dimensionality reduction analysis findings of Coffey et al. [26]. In addition, other studies showed also a protective effect of the D allele on the occurrence of thrombosis [27], [28]. Interestingly, both studies found that the effect was more pronounced in men suggesting a gender interaction. Moreover, the absolute PAI-levels were lower in the ACE DD group in the presence of PAI-1 5G5G, which would be expected considering the observed protective effect in the present study (data not shown). Although not significant in the present study, there was a suggestion of increased risk of the ACE D allele among those with the PAI-1 4G4G genotype in the present study. This is consistent with previous basic science and human clinical studies. Both the ACE DD genotype and the PAI-1 4G allele are associated with increased PAI-1 levels [23], [29], [30], which promotes thrombosis and is a known risk factor for myocardial infarction.
The other three interactions involve the bradykinin and RA systems. Bradykinin plays an important role in determining t-PA levels. In addition to its role in the inflammatory process, bradykinin is a potent endothelial cell stimulant that has been shown to induce the acute release of t-PA from the endothelium through a B2 receptor mechanism [31]. In addition, ACE-inhibition augments the effects of bradykinin on the B2 receptor, which leads to t-PA release from the endothelium [32], providing a mechanistic explanation for the interaction between the bradykinin and RA systems. Moreover, genetic polymorphisms of the RAS and bradykinin genes showed epistatic effects on both PAI-1 as t-PA levels among females and males, similar to the results in the current study.
Controlling for traditional risk factors of cardiovascular disease did not lead to substantive changes in the results with respect to statistical significance. However, this does not allow us to totally rule out chance as a potential explanation of the findings. Although there are plausible biologic mechanisms to support interactions among genes from the RA, bradykinin, and fibrinolytic systems, this study used an exploratory analysis plan searching for all possible two-way interactions between six genes. Furthermore, for each possible pair of polymorphisms, we tested nine different interactions based on different genotype coding schemes. Multiple tests increase the possibility of chance associations, especially when conducting a non-replicated study. Given that these tests are correlated in the present study, it is difficult to calculate how many interactions are expected by chance. However, by making some simplifying assumptions, and noting that a total of 105 interactions were tested (nine possible interaction effects were tested for the 15 possible pairs of polymorphisms minus 30 interactions since only dominant coding was used for the BDKRB2 C181T polymorphism), one can estimate that under the null hypothesis, one would expect 2.6 and 10.5 interactions to be nominally significant at α = 0.025 and α = 0.10, respectively, by chance alone (as described earlier, these are the two uncorrected significance levels used in the present study). We found a total of 16 significant gene-gene interactions (P<0.10), most of which remained significant after adjusting for known risk factors. The findings of significant interactions between genes from the RA, bradykinin, and fibrinolytic systems on the risk of cardiovascular disease warrant further exploration, including attempting to replicate these results in other populations with other study designs.
It is important to recognize that cardiovascular disease is a relatively infrequent event in this cohort due to the young age (mean 48.6 years at baseline) and gender composition (51% female). The onset of symptoms is age related and additional cardiovascular events are expected to be observed in the PREVEND cohort as more time passes. In addition, the penetrance of the alleles may also be age related. Future analyses should examine whether these potential interactions remain as additional events become available and the population grows older.
Furthermore, because this study was limited to the investigation of potential two-way interactions, future studies should consider higher-order interactions using a multifactor dimensionality reduction (MDR) type analysis [33], [34]. Such analyses have revealed the presence of gene-gene interactions in the absence of statistically significant independent main effects and also may assist in confirming the findings of the current exploratory study. Future research should also explore the role of sex in moderating these interactions. Finally, although this study was intended to evaluate possible underlying mechanisms and not to suggest the use of these gene polymorphisms as diagnostic tools, it may be of some interest to explore whether the significant gene-gene interactions found in the present study can improve the predictive ability of known models [35], [36].
In summary, this study suggests possible interplay between genes from the RA, bradykinin, and fibrinolytic systems on the risk of cardiovascular disease, extending previous research that has demonstrated that interactions among genes from these systems influence plasma concentrations of both t-PA and PAI-1.
Supporting Information
Table S1.
Table S1a - S1f. P values for the unadjusted first-order gene-gene interactions are reported in supporting information tables S1a-S1f.
https://doi.org/10.1371/journal.pone.0012757.s001
(0.09 MB DOC)
Acknowledgments
A portion of this work was described in a paper submitted by Dr. John P. Bentley in partial fulfillment of the requirements for the M.S. degree in Biostatistics at the University of Alabama at Birmingham. We would like to thank Dr. Charles Katholi and Dr. David Redden, both of the University of Alabama at Birmingham, for providing comments on an earlier version of the manuscript.
Author Contributions
Conceived and designed the experiments: JPB FWA CSC JHM HLH WHvG. Performed the experiments: FWA HLH. Analyzed the data: JPB FWA CSC. Contributed reagents/materials/analysis tools: JHM WHvG. Wrote the paper: JPB FWA CSC JHM HLH WHvG.
References
- 1. Saksela O, Rifkin DB (1988) Cell-associated plasminogen activation: Regulation and physiological functions. Annu Rev Cell Biol 4: 93–126.
- 2. Thögersen AM, Jansson JH, Boman K, Nilsson TK, Weinehall L, et al. (1998) High plasminogen activator inhibitor and tissue plasminogen activator levels in plasma precede a first acute myocardial infarction in both men and women: Evidence for the fibrinolytic system as an independent primary risk factor. Circulation 98: 2241–2247.
- 3. Wiman B, Andersson T, Hallqvist J, Reuterwall C, Ahlbom A, et al. (2000) Plasma levels of tissue plasminogen activator/plasminogen activator inhibitor-1 complex and von Willebrand factor are significant risk markers for recurrent myocardial infarction in the Stockholm Heart Epidemiology Program (SHEEP) study. Arterioscler Thromb Vasc Biol 20: 2019–2023.
- 4. Ridker PM, Gaboury CL, Conlin PR, Seely EW, Williams GH, et al. (1993) Stimulation of plasminogen activator inhibitor in vivo by infusion of angiotensin II. Evidence of a potential interaction between the renin-angiotensin system and fibrinolytic function. Circulation 87: 1969–1973.
- 5. Vaughan DE, Rouleau JL, Ridker PM, Arnold JM, Menapace FJ, et al. (1997) Effects of ramipril on plasma fibrinolytic balance in patients with acute anterior myocardial infarction. HEART Study Investigators. Circulation 96: 442–447.
- 6. Brown NJ, Agirbasli M, Vaughan DE (1999) Comparative effect of angiotensin-converting enzyme inhibition and angiotensin II type 1 receptor antagonism on plasma fibrinolytic balance in humans. Hypertension 34: 285–290.
- 7. Brown NJ, Abbas A, Byrne D, Schoenhard JA, Vaughan DE (2002) Comparative effects of estrogen and angiotensin-converting enzyme inhibition on plasminogen activator inhibitor-1 in healthy postmenopausal women. Circulation 105: 304–309.
- 8. Minai K, Matsumoto T, Horie H, Ohira N, Takashima H, et al. (2001) Bradykinin stimulates the release of tissue plasminogen activator in human coronary circulation: Effects of angiotensin-converting enzyme inhibitors. J Am Coll Cardiol 37: 1565–1570.
- 9. Asselbergs FW, Williams SM, Hebert PR, Coffey CS, Hillege HL, et al. (2006) The gender-specific role of polymorphisms from the fibrinolytic, renin-angiotensin, and bradykinin systems in determining plasma t-PA and PAI-1 levels. Thromb Haemost 96: 471–477.
- 10. Moore JH, Smolkin ME, Lamb JM, Brown NJ, Vaughan DE (2002) The relationship between plasma t-PA and PAI-1 levels is dependent on epistatic effects of the ACE I/D and PAI-1 4G/5G polymorphisms. Clin Genet 62: 53–59.
- 11. Asselbergs FW, Williams SM, Hebert PR, Coffey CS, Hillege HL, et al. (2007) Epistatic effects of polymorphisms in genes from the renin-angiotensin, bradykinin, and fibrinolytic systems on plasma t-PA and PAI-1 levels. Genomics 89: 362–369.
- 12. Cambien F, Poirier O, Lecerf L, Evans A, Cambou JP, et al. (1992) Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction. Nature 359: 641–644.
- 13. Ruiz J, Blanché H, Cohen N, Velho G, Cambien F, et al. (1994) Insertion/deletion polymorphism of the angiotensin-converting enzyme gene is strongly associated with coronary heart disease in non-insulin-dependent diabetes mellitus. Proc Natl Acad Sci U S A 91: 3662–3665.
- 14. Eriksson P, Kallin B, van't Hooft FM, Båvenholm P, Hamsten A (1995) Allele-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associated with myocardial infarction. Proc Natl Acad Sci U S A 92: 1851–1855.
- 15. Margaglione M, Cappucci G, Colaizzo D, Giuliani N, Vecchione G, et al. (1998) The PAI-1 gene locus 4G/5G polymorphism is associated with a family history of coronary artery disease. Arterioscler Thromb Vasc Biol 18: 152–156.
- 16. Pinto-Sietsma SJ, Janssen WM, Hillege HL, Navis G, De Zeeuw D, et al. (2000) Urinary albumin excretion is associated with renal functional abnormalities in a nondiabetic population. J Am Soc Nephrol 11: 1882–1888.
- 17. Geluk CA, Post WJ, Hillege HL, Tio RA, Tijssen JG, et al. (2008) C-reactive protein and angiographic characteristics of stable and unstable coronary artery disease: Data from the prospective PREVEND cohort. Atherosclerosis 196: 372–382.
- 18. Borggreve SE, Hillege HL, Wolffenbuttel BH, de Jong PE, Zuurman MW, et al. (2006) An increased coronary risk is paradoxically associated with common cholesteryl ester transfer protein gene variations that relate to high high-density lipoprotein cholesterol: A population-based study. J Clin Endocrinol Metab 91: 3382–3388.
- 19.
Skinner CJ, Holt D, Smith TMF (1989) Analysis of complex surveys. Chichester: John Wiley and Sons.
- 20. Verhave JC, Hillege HL, Burgerhof JG, Janssen WM, Gansevoort RT, et al. (2004) Sodium intake affects urinary albumin excretion especially in overweight subjects. J Intern Med 256: 324–330.
- 21. Mahmoodi BK, Gansevoort RT, Veeger NJ, Matthews AG, Navis G, et al. (2009) Microalbuminuria and risk of venous thromboembolism. JAMA 301: 1790–1797.
- 22. Asselbergs FW, Williams SM, Hebert PR, Coffey CS, Hillege HL, et al. (2007) Gender-specific correlations of plasminogen inhibitor-1 and tissue plasminogen activator levels with cardiovascular disease-related traits. J Thromb Haemost 5: 313–320.
- 23. Kim DK, Kim JW, Kim S, Gwon HC, Ryu JC, et al. (1997) Polymorphism of angiotensin converting enzyme gene is associated with circulating levels of plasminogen activator inhibitor-1. Arterioscler Thromb Vasc Biol 17: 3242–3247.
- 24. Pankow JS, Arnett DK, Borecki IB, Hunt SC, Eckfeldt JH, et al. (2000) Lack of association between the angiotensin-converting enzyme insertion/deletion polymorphism and plasminogen activator inhibitor-1 antigen levels in the National Heart, Lung, and Blood Institute Family Heart Study. Blood Coagul Fibrinolysis 11: 551–558.
- 25. Rigat B, Hubert C, Alhenc-Gelas F, Cambien F, Corvol P, et al. (1990) An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels. J Clin Invest 86: 1343–1346.
- 26. Coffey CS, Hebert PR, Ritchie MD, Krumholz HM, Gaziano JM, et al. (2004) An application of conditional logistic regression and multifactor dimensionality reduction for detecting gene-gene interactions on risk of myocardial infarction: The importance of model validation. BMC Bioinformatics 5: 49–58.
- 27. González Ordóñez AJ, Fernández Carreira JM, Medina Rodríguez JM, Martín Sánchez L, Alvarez Díaz R, et al. (2000) Risk of venous thromboembolism associated with the insertion/deletion polymorphism in the angiotensin-converting enzyme gene. Blood Coagul Fibrinolysis 11: 485–490.
- 28. Wells PS, Rodger MA, Forgie MA, Langlois NJ, Armstrong L, et al. (2003) The ACE D/D genotype is protective against the development of idiopathic deep vein thrombosis and pulmonary embolism. Thromb Haemost 90: 829–834.
- 29. Dawson S, Hamsten A, Wiman B, Henney A, Humphries S (1991) Genetic variation at the plasminogen activator inhibitor-1 locus is associated with altered levels of plasma plasminogen activator inhibitor-1 activity. Arterioscler Thromb 11: 183–190.
- 30. Dawson SJ, Wiman B, Hamsten A, Green F, Humphries S, et al. (1993) The two allele sequences of a common polymorphism in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene respond differently to interleukin-1 in HepG2 cells. J Biol Chem 268: 10739–10745.
- 31. Brown NJ, Gainer JV, Murphey LJ, Vaughan DE (2000) Bradykinin stimulates tissue plasminogen activator release from human forearm vasculature through B(2) receptor-dependent, NO synthase-independent, and cyclooxygenase-independent pathway. Circulation 102: 2190–2196.
- 32. Labinjoh C, Newby DE, Pellegrini MP, Johnston NR, Boon NA, et al. (2001) Potentiation of bradykinin-induced tissue plasminogen activator release by angiotensin-converting enzyme inhibition. J Am Coll Cardiol 38: 1402–1408.
- 33. Ritchie MD, Hahn LW, Roodi N, Bailey LR, Dupont WD, et al. (2001) Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer. Am J Hum Genet 69: 138–147.
- 34. Hahn LW, Ritchie MD, Moore JH (2003) Multifactor dimensionality reduction software for detecting gene-gene and gene-environment interactions. Bioinformatics 19: 376–382.
- 35. Gerds TA, Schumacher M (2007) Efron-type measures of prediction error for survival analysis. Biometrics 63: 1283–1287.
- 36. Pencina MJ, D'Agostino RB Sr, D'Agostino RB Jr, Vasan RS (2008) Evaluating the added predictive ability of a new marker: From area under the ROC curve to reclassification and beyond. Stat Med 27: 157–172.