Published online before print November 25, 2002, doi: 10.1161/01.HYP.0000043680.75107.CF
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
(Hypertension. 2003;41:163.)
© 2003 American Heart Association, Inc.
Scientific Contributions |
Association of Endothelin-1 Gene Variant With Hypertension
From the Department of Geriatric Medicine, School of Medicine, Ehime University, Ehime, Japan.
Correspondence to Dr Jun Nakura, Department of Geriatric Medicine, School of Medicine, Ehime University, Shigenobu-cho, Onsen-gun, Ehime 791-0295, Japan. E-mail nakura{at}m.ehime-u.ac.jp
 |
Abstract |
|---|
 Top Abstract IntroductionMethodsResultsDiscussionReferences |
|---|
Endothelin-1 (ET-1) is a powerful vasoconstrictor peptide produced by endothelial and smooth muscle cells. Many lines of biological evidence suggest that the ET-1 gene is a candidate gene for hypertension. Moreover, recent association studies suggested that a G/T polymorphism with an amino acid substitution (Lys/Asn) at codon 198 in exon 5 of the ET-1 gene interacts with body mass index (BMI) in association with blood pressure. They suggested that T carriers are more sensitive to weight gain than GG homozygotes in association with blood pressure. However, association studies are often irreproducible, and the first study often suggests a stronger genetic effect than is found by subsequent studies. We therefore assessed the interaction in 2 large Japanese populations. The present study showed a nonsignificant but similar trend to the results of previous reports. Moreover, in line with previous reports, this study revealed a significant interaction between the ET-1 K198N (G/T) polymorphism and BMI in association with hypertension in our populations (P=0.027). The interaction was significant, even after adjustment for gender and age (P=0.045) and for all confounding factors (P=0.044). T carriers were more sensitive to weight gain than GG homozygotes in association with hypertension. Considering the combined impact of obesity and hypertension on the development of cardiovascular and cerebrovascular disorders, T allele carriers might represent elective targets for therapy to lower their body weight.
Key Words: endothelin • hypertension, essential • genetics • polymorphism • body mass index
|
Introduction |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Endothelin-1 (ET-1) is a powerful vasoconstrictor peptide produced by vascular endothelial cells.1 Some patients with moderate-to-severe essential hypertension, similar to some experimental rat models with severe blood pressure elevation, exhibit enhanced endothelial expression of the ET-1 gene.2 Plasma ET-1 concentration is elevated in hypertensive patients.3–6 An endothelin-receptor antagonist significantly lowered blood pressure in patients with essential hypertension.7 Given these lines of biological evidence, the ET-1 gene is a candidate responsible for hypertension.
Hypertension is a common, complex phenotype and has been intensively studied to identify susceptibility loci in humans. Nonetheless, there is no known genotypic polymorphism consistently associated with hypertension in humans, thus far. Moreover, albeit that the development of hypertension is considered to be due at least partly to gene-gene and gene-environmental interactions, fewer interaction analyses have been conducted than simple association analyses. In this regard, the ET-1 gene is an attractive candidate because, in addition to its biological function, this gene has been shown to interact with body mass index (BMI) in association with blood pressure in 3 large populations.8,9 However, association studies are often irreproducible, and the first study often suggests a stronger genetic effect than is found by subsequent studies.10 We therefore assessed the interaction in 2 large Japanese populations. The present study showed a significant interaction between the ET-1 K198N (G/T) polymorphism and BMI in the association with hypertension.
|
Methods |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Subjects
The clinical characteristics of the subjects included in the study are shown in Table 1. Population 1 (n=2466) originated from the Ehime region of Japan, and population 2 (n=806) from the Hyogo region of Japan. The initial rate of participation in the present study was 90% and 67% for populations 1 and 2, respectively. All subjects were Japanese urban residents. Subjects in population 1 participated in medical checkups 1 to 11 times (average 6.2 times per person), and the mean values of variables in the personal health records were used in analyses. Subjects in population 2 also underwent a medical checkup, and the values of variables in the personal health records were used in analyses. All subjects gave informed consent, and the study was approved by the ethics committee of Ehime University.
|
Diagnostic Categories
Each subject was assigned to one of the blood pressure diagnostic categories defined by the following criteria. Hypertensive subjects were those who had a previous diagnosis of hypertension and were being treated with antihypertensive medications (7.6%) or whose systolic/diastolic blood pressure was 
140/90 mm Hg. Normotensive subjects were those who had never been treated with medication for hypertension and whose systolic/diastolic blood pressure was <140/90 mm Hg. Blood pressure was measured with a mercury sphygmomanometer fewer than 3 times per year in a sitting position in clinics. Obesity was defined as BMI 25 kg/m2 (Japan Society for the Study of Obesity). Hypertriglyceremia was defined as triglyceride (TG) 150 mg/dL (Japan Atherosclerosis Society).
DNA Analysis
The TaqMan chemical method was used to detect the ET-1 K198N (G/T) polymorphism. The forward primer was 5'-GGT CGG AGA CCA TGA GAA ACA-3', the reverse primer was 5'-TGT GGG TCA CAT AAC GCT CTC T-3', the T allele–specific probe was 5'-Fam-AAG GCA ATC CCT C-Tamura-3', and the G allele–specific probe was 5'-Tet-AAG GCA AGC CCT C-Tamura-3'. The person who assessed the genotype was blinded to the clinical data of the subjects from whom the samples originated. We validated the TaqMan chemical method with more standard polymerase chain reaction (PCR)/single-strand conformation polymorphism and PCR/sequencing methods in selected 57 subjects.
Statistical Methods
Analysis of variance was used to assess differences in means and variances of continuous variables. Comparisons of categorical variables were performed using the 
2 test. General linear models were used to assess whether the ET-1 K198N (G/T) polymorphism made a statistically significant contribution to prediction of blood pressure, with consideration of interactions between the polymorphism and BMI in regression models. Logistic regression models were used to assess whether the ET-1 K198N (G/T) polymorphism made a statistically significant contribution to prediction of hypertension, with consideration of interactions between the polymorphism and BMI in regression models. Logarithmically transformed plasma TG values were used in the analyses. Probability values less than 0.05 were considered statistically significant. Statistical analysis was performed with SPSS statistical software (SPSS Inc).
|
Results |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Frequencies of Alleles and Genotypes
Table 1 presents the clinical characteristics of the participants as a function of the 3 genotypes. The relative frequencies of the GG, GT, and TT genotypes were 53%, 38%, and 8%, respectively. The allele frequencies were 72% and 28% for the G and T alleles, respectively. These results are consistent with the Hardy-Weinberg equilibrium. The frequencies of the genotypes and the alleles in Japanese were similar to, but significantly different from, those in Caucasians.
Interaction of ET-1 G/T Polymorphism With BMI in the Association With Blood Pressure and Hypertension Status
Because the Etude Cas-Temoin de l’Infarctus Myocarde (ECTIM) study8 has shown a strong interaction of the ET-1 K198N (G/T) polymorphism with BMI in association with blood pressure, we analyzed the interaction in our 2 populations. This analysis showed that the interaction between the polymorphism and BMI was not significant (Table 2, Figure 1). In relation to the interaction, the ECTIM study also showed that both systolic and diastolic blood pressure in T allele carriers were significantly higher than those in GG homozygotes in obese subjects but nonsignificantly lower in lean subjects. Similar analyses in our populations showed that both systolic and diastolic blood pressures in T allele carriers were nonsignificantly higher than those in GG homozygotes in obese subjects and nonsignificantly lower in lean subjects (Table 3). These results were similar when subjects on current antihypertensive treatment were excluded.
|
|
|
However, blood pressure readings before the start of antihypertensive treatment were not available for 248 hypertensive subjects, and the inclusion or exclusion of subjects with antihypertensive treatment could influence the distribution of blood pressure. In addition, blood pressure is unstable even in the resting condition. Therefore, considering that logistic regression analyses may be more suitable than linear regression analyses and t statistics, we analyzed the possible interaction between the ET-1 K198N (G/T) polymorphism and BMI in association with hypertension status in our populations. These analyses showed a significant interaction in population 1 (P=0.035; OR=1.070, 95% CI=1.005 to 1.134, where OR indicates odds ratio and 95% CI indicates 95% confidence interval) (Figure 2a). A similar but nonsignificant interaction was shown in population 2 (P=0.55; OR=1.038, 95% CI=0.918 to 1.174) (Figure 2b). Analysis combining populations 1 and 2 yielded a probability value of 0.027 for the interaction between the polymorphism and BMI in association with hypertension (Figure 2c). The interaction was significant even after adjustment for gender and age (P=0.045) and for all confounding factors (P=0.044).
|
|
Discussion |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Association studies are often irreproducible.10 Replication studies in large populations are indispensable to establishing an association.11 The ECTIM study showed a strong interaction between the ET-1 K198N (G/T) polymorphism and BMI in association with both systolic and diastolic resting blood pressure levels.8 That is, the study has shown that T carriers are more sensitive to weight gain than GG homozygotes in association with blood pressure. Moreover, the study has shown that, in obese subjects, both systolic and diastolic resting blood pressure levels are significantly higher in T carriers than GG homozygotes.
However, other studies have shown similar but not the same results. The Glasgow Heart Scan study showed a similar strong interaction between the polymorphism and BMI in association with the maximum blood pressure achieved during a treadmill exercise test, but not with the resting blood pressure.8
The Ohasama study did not assess the interaction, but has shown a significant association, that is, in obese subjects, casual diastolic blood pressure level is significantly higher in T carriers than in GG homozygotes.9 The study has also shown a similar trend in the relation of the polymorphism with casual systolic blood pressure in obese subjects.
Finally, the present study showed a similar trend that T carriers are more sensitive to weight gain than GG homozygotes in association with blood pressure. This study also showed a similar trend that, in obese subjects, both systolic and diastolic resting blood pressure were higher in T carriers than in GG homozygotes. Thus, the trends were all similar to those in previous reports. Moreover, in line with previous reports, the present study revealed a significant interaction between the ET-1 K198N (G/T) polymorphism and BMI in the association with hypertension in population 1, and a similar trend was shown in population 2.
Taken together, all of the studies have shown a similar trend, that is, that T allele carriers are more sensitive to weight gain than GG homozygotes in association with blood pressure and with hypertension (chance occurrence <0.063), providing evidence in favor of interaction between the polymorphism and BMI in association with hypertension. Consequently, the ET-1 gene may be a promising candidate responsible for hypertension. However, the first study often suggests a stronger genetic effect than is found by subsequent studies, as in the case of the ET-1 polymorphism.10 Therefore, further studies in large populations and a systematic meta-analytical approach are needed to accurately assess the genetic effect of the ET-1 gene. Moreover, haplotype studies, as well as examinations of variants in linkage disequilibrium with the polymorphism, are also needed.
To establish an association, it is also important that reported associations make biological sense and that associated alleles affect the gene product in a physiologically meaningful way.11 In this context, plasma ET-1 levels were shown to be significantly higher in obese normotensives than in lean normotensives, suggesting an influence of obesity on plasma ET-1 level.12,13 Indeed, weight loss significantly decreased the plasma ET-1 level in both obese normotensives and obese hypertensives.12,14 Thus, the interaction between the ET-1 polymorphism and BMI may make biological sense. However, thus far, there is no evidence showing that the ET-1 K198N (G/T) polymorphism affects the gene product in a physiologically meaningful way, although the polymorphism changes the corresponding amino acid (Lys/Asn). Therefore, it is required to investigate a possible biological change of the gene product by the K198N (G/T) polymorphism or another variant in linkage disequilibrium with it.
In conclusion, the present study revealed a significant interaction between the ET-1 K198N (G/T) polymorphism and BMI in association with hypertension in large Japanese populations. This result is in line with biological evidence on ET-1 and with the results of 3 previous association studies. Considering the combined impact of obesity and hypertension on the development of cardiovascular and cerebrovascular disease, T allele carriers might represent elective targets for therapy to lower their body weight.
Perspectives
Thus far, the interaction between the ET-1 K198N (G/T) polymorphism and BMI in association with blood pressure and hypertension was assessed in 5 large populations including ours. Although these populations were studied in different design and differed in characteristics including BMI and race, all of the results showed a similar trend, suggesting the presence of the interaction. Consequently, together with several lines of biological evidence, the ET-1 gene may be a promising candidate gene for hypertension. Meanwhile, this study may have a broad implication, the importance of categorical analyses of blood pressure. The present study showed a significant interaction between the ET-1 K198N (G/T) polymorphism and BMI in association with hypertension, but a nonsignificant trend in association with blood pressure. This is possibly due to the unstable nature of blood pressure and to the presence of treated hypertensive subjects. Thus, in some populations, blood pressure may have much information content but less correct information than categorical hypertension status.
|
Acknowledgments |
|---|
This work was supported by a grant-in-aid for Scientific Research on Priority Areas (C) "Medical Genome Science" from the Ministry of Education, Culture, Sports, Science and Technology of Japan and a grant-in-aid for Research on the Human Genome, Tissue Engineering Food Biotechnology from the Ministry of Health Labor and Welfare.
Received June 27, 2002; first decision September 11, 2002; accepted October 16, 2002.
|
References |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
- Yanagisawa M, Kurihara H, Kimura S, Tomobe Y, Kobayashi M, Mitsui Y, Yazaki Y, Goto K, Masaki T. A novel potent vasoconstrictor peptide produced by vascular endothelial cells. Nature. 1988; 332: 411–415.[CrossRef][Medline] [Order article via Infotrieve]
- Schiffrin EL, Deng LY, Sventek P, Day R. Enhanced expression of endothelin-1 gene in resistance arteries in severe human essential hypertension. J Hypertens. 1997; 15: 57–63.[CrossRef][Medline] [Order article via Infotrieve]
- Shichiri M, Hirata Y, Ando K, Emori T, Ohta K, Kimoto S, Ogura M, Inoue A, Marumo F. Plasma endothelin levels in hypertension and chronic renal failure. Hypertension. 1990; 15: 493–496.
[Abstract/Free Full Text] - Schiffrin EL, Thibault G. Plasma endothelin in human essential hypertension. Am J Hypertens. 1991; 4(pt 1): 303–308.[Medline] [Order article via Infotrieve]
- Lemne CE, Lundeberg T, Theodorsson E, de Faire U. Increased basal concentrations of plasma endothelin in borderline hypertension. J Hypertens. 1994; 12: 1069–1074.[Medline] [Order article via Infotrieve]
- Ergul S, Parish DC, Puett D, Ergul A. Racial differences in plasma endothelin-1 concentrations in individuals with essential hypertension. Hypertension. 1996; 28: 652–655.
[Abstract/Free Full Text] - Krum H, Viskoper RJ, Lacourciere Y, Budde M, Charlon V. The effect of an endothelin-receptor antagonist, bosentan, on blood pressure in patients with essential hypertension. Bosentan Hypertension Investigators. N Engl J Med. 1998; 338: 784–790.
[Abstract/Free Full Text] - Tiret L, Poirier O, Hallet V, McDonagh TA, Morrison C, McMurray JJ, Dargie HJ, Arveiler D, Ruidavets JB, Luc G, Evans A, Cambien F. The Lys198Asn polymorphism in the endothelin-1 gene is associated with blood pressure in overweight people. Hypertension. 1999; 33: 1169–1174.
[Abstract/Free Full Text] - Asai T, Ohkubo T, Katsuya T, Higaki J, Fu Y, Fukuda M, Hozawa A, Matsubara M, Kitaoka H, Tsuji I, Araki T, Satoh H, Hisamichi S, Imai Y, Ogihara T. Endothelin-1 gene variant associates with blood pressure in obese Japanese subjects: the Ohasama Study. Hypertension. 2001; 38: 1321–1324.
[Abstract/Free Full Text] - Ioannidis JP, Ntzani EE, Trikalinos TA, Contopoulos-Ioannidis DG. Replication validity of genetic association studies. Nat Genet. 2001; 29: 306–309.[CrossRef][Medline] [Order article via Infotrieve]
- Freely associating. Nat Genet. 1999; 22: 1–2.Editorial.[CrossRef][Medline] [Order article via Infotrieve]
- Ferri C, Bellini C, Desideri G, Di Francesco L, Baldoncini R, Santucci A, De Mattia G. Plasma endothelin-1 levels in obese hypertensive and normotensive men. Diabetes. 1995; 44: 431–436.[Abstract]
- Parrinello G, Scaglione R, Pinto A, Corrao S, Cecala M, Di Silvestre G, Amato P, Licata A, Licata G. Central obesity and hypertension: the role of plasma endothelin. Am J Hypertens. 1996; 9(pt 1): 1186–1191.[CrossRef][Medline] [Order article via Infotrieve]
- Wolpert HA, Steen SN, Istfan NW, Simonson DC. Insulin modulates circulating endothelin-1 levels in humans. Metabolism. 1993; 42: 1027–1030.[CrossRef][Medline] [Order article via Infotrieve]
This article has been cited by other articles:
 |
|
 |
|
  T. Rankinen, T. Church, T. Rice, N. Markward, A. S. Leon, D. C. Rao, J. S. Skinner, S. N. Blair, and C. Bouchard Effect of Endothelin 1 Genotype on Blood Pressure Is Dependent on Physical Activity or Fitness Levels Hypertension, December 1, 2007; 50(6): 1120 - 1125. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 D. K. Arnett, A. E. Baird, R. A. Barkley, C. T. Basson, E. Boerwinkle, S. K. Ganesh, D. M. Herrington, Y. Hong, C. Jaquish, D. A. McDermott, et al. Relevance of Genetics and Genomics for Prevention and Treatment of Cardiovascular Disease: A Scientific Statement From the American Heart Association Council on Epidemiology and Prevention, the Stroke Council, and the Functional Genomics and Translational Biology Interdisciplinary Working Group Circulation, June 5, 2007; 115(22): 2878 - 2901. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 E. Thomson, P. Kumarathasan, P. Goegan, R. A. Aubin, and R. Vincent Differential Regulation of the Lung Endothelin System by Urban Particulate Matter and Ozone Toxicol. Sci., November 1, 2005; 88(1): 103 - 113. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
Y. Dong, X. Wang, H. Zhu, F. A. Treiber, and H. Snieder Endothelin-1 Gene and Progression of Blood Pressure and Left Ventricular Mass: Longitudinal Findings in Youth Hypertension, December 1, 2004; 44(6): 884 - 890. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 K. Diefenbach, F. A. Nahad, C. Meisel, I. Fietze, I. Cascorbi, K. Stangl, O. Landt, R. Kerb, U. Brinkmann, and I. Roots Identification of Twelve Polymorphisms in the Endothelin-1 Gene by Use of Fluorescently Labeled Oligonucleotides and PCR with Restriction Fragment Polymorphism Analysis Clin. Chem., February 1, 2004; 50(2): 448 - 451. [Full Text] [PDF]
|
|
|
|
|
|
C. Cardillo, U. Campia, M. Iantorno, and J. A. Panza Enhanced Vascular Activity of Endogenous Endothelin-1 in Obese Hypertensive Patients Hypertension, January 1, 2004; 43(1): 36 - 40. [Abstract] [Full Text] [PDF]
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||