1 Division of Receptor Biology, Advanced Medical Research Center, Nihon University School of Medicine

2 Department of Biotechnology and Applied Chemistry, Toyo University Graduate School of Engineering

3 Fifth-year Medical Student, Nihon University School of Medicine

4 Department of Obstetrics and Gynecology, Nihon University School of Medicine

5 Department of Neurology, Division of Neurology, Department of Medicine, Nihon University School of Medicine

6 Department of Neurology, Graduate School of Medicine, Nihon University

7 Division of Nephrology and Endocrinology, Department of Medicine Nihon University School of Medicine, Tokyo, Japan

Corresponding Author: Tomohiro Nakayama MD, Division of Receptor Biology, Advanced Medical Research Center, Nihon University School of Medicine, Ooyaguchi-kamimachi, 30-1 Itabashi-ku, Tokyo 173-8610, Japan. Tel: +81 3-3972-8111(ext.2753)

Running title: tissue plasminogen activator gene and essential hypertension

	ABSTRACT
	INTRODUCTION
	METHODS
	RESULTS
	DISCUSSION
	ACKNOWLEDGEMENT
	REFERENCES

	ABSTRACT

	INTRODUCTION

 Essential hypertension (EH) is caused by both genetic and environmental factors. It is generally presumed that EH is a multifactorial inheritance disorder involving several susceptibility genes. Thus, it is important to identify susceptibility genes of EH. However, although there have been studies of relationships between several candidate genes and EH, the major susceptibility genes of EH have not been identified[1]. It was previously predicted that EH is related to disorders in the coagulation-fibrinolytic balance [2,3]. The blood coagulation and fibrinolysis system is regulated by the interaction of many factors. Tissue plasminogen activator (t-PA), which converts plasminogen to plasmin, plays an important role in plasma circulation [4], and increased levels of t-PA antigen may predict risk of cardiovascular diseases such as myocardial infarction (MI) and thrombotic stroke [5,6]. It has been reported that release of t-PA appears to be associated with activity of the endogenous kininogen/kinin system, which is related to EH [7]. Thus, the available evidence suggests that the t-PA gene is associated with EH. However, the relationship between EH and the t-PA gene has not been examined using an association study. The human t-PA gene has been mapped to chromosome 8p12-p11.2. It consists of 14 exons and 13 introns, and spans approximately 32 kb [8]. The present haplotype-based case-control study is the first to investigate whether single nucleotide polymorphisms (SNPs) in the human t-PA gene are associated with EH.

	METHODS

Subjects

The EH subjects were 276 Japanese patients (mean age, 60.0±5.6 years years) with EH diagnosed according to World Health Organization criteria, which included a sitting systolic blood pressure (SBP) of >160 mmHg and/or diastolic blood pressure (DBP) of >100 mmHg on 3 different occasions during the 2 months following the first medical examination. None of the EH subjects was using antihypertensive medication. Patients diagnosed with secondary hypertension were excluded. The controls were 283 Japanese normotensive (NT) healthy individuals (mean age, 77.9±4.6 years). None of the control subjects had a family history of hypertension, and all had a SBP of <130 mmHg and a DBP of <85 mmHg. A family history of hypertension was defined as prior diagnosis of hypertension in a grandparent, uncle, aunt, parent or sibling. Both groups were recruited from the northern area of Tokyo, Japan. Informed consent was obtained from each subject according to a protocol approved by the Human Studies Committee of Nihon University [9].

Biochemical analysis

Plasma concentrations of total cholesterol and high-density lipoprotein (HDL)-cholesterol and serum concentrations of creatinine and uric acid were measured using the methods of the Clinical Laboratory Department of Nihon University Hospital [10].

Genotyping

Based on information from the National Center for Biotechnology Information (NCBI) SNP database or the Applied Biosystems (Foster City, CA) - Celera Discovery System (CDS) database (http://www.appliedbiosystems.com), we chose SNPs that had a minor allele frequency of >20%. For the genetic association analysis, we selected the following 3 SNPs in the human t-PA gene: rs7007329 (G/C), located at nucleotide (nt) -4360 upstream of the transcription initiation site; rs8178750 (T/C), nt +20324 in intron 6; rs4471024 (G/A), nt +624 downstream of the terminal codon (Figure 1). Genotypes were determined using Assays-on-Demand kits (Applied Biosystems) and TaqMan PCR , as described previously [11].

 

View larger version : [in a new window] Figure 1: Organization of the human t-PA gene and location of the SNPs used for the association analysis. Closed black boxes indicate exons, and lines indicate introns.

Haplotype-based case-control analysis

We performed haplotype-based case-control analysis of 4 combinations of the 3 SNPs. The frequency of each haplotype was estimated using the expectation/maximization (EM) algorithm [12,13]. Haplotype and linkage disequilibrium (LD) analyses were performed using the software SNPAlyze version 3.2 (DYNACOM Co., Ltd. Yokohama, Japan), which is available from the website http://www.dynacom.co.jp/products/package/snpalyze/index.html.

Statistical analysis

Data are shown as mean ± SD. Differences in clinical data between the EH and NT groups were assessed using analysis of variance (ANOVA) followed by a Fisher's protected least significant difference (PLSD) test. Hardy-Weinberg equilibrium was assessed using chi-square analysis. If expected values were small (<2.0), the genotypes with the small expected values were combined [14]. The overall distribution of SNP alleles was analyzed using 2 ×2 contingency tables, and differences in distribution of the SNP genotypes between the EH patients and NT controls were assessed using a 2-sided Fisher exact test and multiple logistic regression analysis. Statistical significance was established at p < 0.05. The threshold value of the frequencies of the haplotypes included in the analysis was set to 1%. All haplotypes below the threshold value were excluded from the analysis. Overall distribution of haplotypes was analyzed using 2 ×m contingency tables, with a p value of <0.05 considered to indicate statistical significance. The p value of each haplotype was determined using chi-square analysis, the permutation method, and SNPAlyze version 3.2 [14]. Pair-wise linkage disequilibrium (LD) patterns for the t-PA gene were evaluated using |D´| and r2.

RESULTS

Table 1 shows clinical characteristics of the subjects. There were significant differences in body mass index (BMI), SBP and DBP between EH and NT subjects. Among male subjects, there were significant differences in pulse rate, total cholesterol, smoking habit, uric acid and alcohol consumption between EH and NT subjects. There were no significant differences in creatinine or HDL-cholesterol between EH and NT subjects.

Table 2 shows the distributions of genotype and allelic frequencies for the 3 SNPs in EH patients and NT subjects. There were no significant differences in genotype or allelic distributions of any of the SNPs between the two groups, for total subjects, male subjects or female subjects.

There were no significant differences in haplotype distributions between EH patients and NT subjects (Table 3).

Table 4 shows pair-wise linkage disequilibrium (LD) patterns for the t-PA gene. All SNPs were located in 1 haplotype block.

DISCUSSIONS

In the present study, using haplotype-based case-control analysis and 3 SNPs, we did not find an association between EH and the human t-PA gene.
There have been several previous studies of relationships between the fibrinolytic system and EH. The fibrinolytic system consists of many factors, including t-PA and plasminogen activator inhibitor 1 (PAI-1). A study by Keskin et al. suggests that indicators of fibrinolytic activity such as plasma levels of PAI-1 and beta thromboglobulin (BTG) are associated with EH, but they did not find a relationship between EH and plasma levels of t-PA [15]. In addition, the function of t-PA is modulated by interaction with other factors such as PAI-1. Jastrzebska et al. studied relationships between t-PA levels and PAI-1 gene polymorphisms in EH and NT subjects. Their comparison of the 4G allele of an insertion/deletion polymorphism in PAI-1 gene carriers (4G/4G homozygotes) revealed that EH patients had significantly higher levels of fibrinogen (p=0.045), PAI-1 (p=0.009), and t-PA (p=0.007) than NT controls [16]. Their data indicate that the t-PA gene is associated with atherothrombotic disease, but not EH.
In a previous association study using an Alu-repeat polymorphism in the t-PA gene, there were no significant differences between EH and NT subjects [17]. The present strategy of haplotype-based case-control analysis is a more effective method of identifying susceptibility genes than case-control analysis using 1 plolymorphism [18,19]. Our previous LD analysis showed that the |D´| and r2 values of the 3 present SNPs were suitable for haplotype-based case-control analysis [20,21]. Moreover, those 3 SNPs are very useful as genetic markers because they have high minor allele frequencies (> 20%).
In conclusion, the present results do not indicate an association between the t-PA gene and EH.

	ACKNOWLEDGEMENT

We would like to thank Ms. K. Sugama for her excellent technical assistance. This work was supported by a grant from the TORAY Co., Ltd.

	REFERENCES

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