Skip to main content
Log in

E-selectin gene polymorphism (A561C) and essential hypertension

Meta-analysis in the Chinese population

E-Selectin-Genpolymorphismus (A561C) und essenzielle Hypertonie

Eine Metaanalyse chinesischer Kollektive

  • Review article
  • Published:
Herz Aims and scope Submit manuscript

Abstract

Background

The A561C polymorphism of the E-selectin gene (SELE) has been reported to be associated with essential hypertension (EH) in several studies; however, results among these studies were inconsistent. Here, we conducted a meta-analysis to explore the association of the A561C polymorphism with EH.

Methods

Publications were retrieved through searching PubMed, Web of Science, the China National Knowledge Infrastructure (CNKI), China Biological Medicine, and the Wanfang database. Odds ratios (OR) and 95 % confidence intervals (CI) were calculated to estimate the strength of association of A561C with EH. Subgroup analysis was also performed to assess ethnic discrepancies. A total of seven studies comprising 2,127 EH patients and 2,078 controls were analyzed.

Results

In the dominant model analysis, we found significant associations between the A561C polymorphism and EH in all subjects (CC+AC vs. AA, OR = 1.96, 95 %CI 1.57–2.44, P heterogeneity = 0.381), in a Han Chinese subgroup (CC+AC vs. AA, OR = 2.38, 95 %CI 1.73–3.29, P heterogeneity = 0.269), and in non-Han Chinese minorities (CC+AC vs. AA, OR = 1.62, 95 %CI 1.19–2.21, P heterogeneity = 0.84).

Conclusion

The findings suggest that C allele carriers of the SELE gene polymorphism (A561C) might be predisposed to EH in the Chinese population. Further investigations in other ethnic populations should be conducted to verify these findings.

Zusammenfassung

Hintergrund

Zwar wurde in verschiedenen Studien eine Assoziation zwischen A561C-Polymorphismus des E-selectin -Gens (SELE) und essenzieller Hypertonie (EH) postuliert, doch die Ergebnisse zwischen diesen Studien waren nicht konsistent.

Methoden

Wir führten eine Metaanalyse zur Assoziation zwischen dem A561C-Polymorphismus und EH durch. Entsprechende Publikationen wurden PubMed, Web of Science, China National Knowledge Infrastructure (CNKI), China Biological Medicine und der Wanfang Datenbank entnommen. Berechnet wurden Odds Ratios (OR) und 95%-Konfidenzintervalle (KI), um die Stärke des Zusammenhangs von A561C mit EH abzuschätzen. Zur Ermittlung ethnisch bedingter Diskrepanzen wurde eine Subgruppenanalyse durchgeführt. Analysiert wurden 7 Studien mit insgesamt 2127 Patienten mit EH und 2078 Kontrollen.

Ergebnisse

In der Analyse des Hauptmodells fanden sich signifikante Assoziationen zwischen dem A561C-Polymorphismus und einer EH bei allen Probanden (CC+AC vs. AA, OR = 1,96, 95 %-KI: 1,57–2,44, P heterogeneity = 0,381), in einer han-chinesischen Subgruppe (CC+AC vs. AA, OR = 2,38, 95 %-KI: 1,73–3,29, P heterogeneity = 0,269) und bei nicht-han-chinesischen Minderheiten (CC+AC vs. AA, OR = 1,62, 95 %-KI: 1,19–2,21, P heterogeneity = 0,84).

Schlussfolgerung

Dies weist darauf hin, dass das C-Allel des SELE -Genpolymorphismus (A561C) in der chinesischen Bevölkerung für eine EH disponieren könnte. Um diese Ergebnisse zu verifizieren, sollten weitere Studien mit anderen ethnischen Kollektiven durchgeführt werden.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. O’Shaughnessy KM (2001) The genetics of essential hypertension. Br J Clin Pharmacol 51(1):5–11

    Google Scholar 

  2. Dominiczak AF, Negrin DC, Clark JS et al (2000) Genes and hypertension: from gene mapping in experimental models to vascular gene transfer strategies. Hypertension 35(1 Pt 2):164–172

    Article  CAS  PubMed  Google Scholar 

  3. Abu-Amero KK, Al-Boudari OM, Mohamed GH, Dzimiri N (2006) E-selectin S128R polymorphism and severe coronary artery disease in Arabs. BMC Med Genet 7:52

    Article  PubMed Central  PubMed  Google Scholar 

  4. Roldan V, Marin F, Lip GY, Blann AD (2003) Soluble E-selectin in cardiovascular disease and its risk factors. A review of the literature. Thromb Haemost 90(6):1007–1020

    CAS  PubMed  Google Scholar 

  5. Blann AD, Lip GY (2003) Effects of C-reactive protein on the release of von Willebrand factor, E-selectin, thrombomodulin and intercellular adhesion molecule-1 from human umbilical vein endothelial cells. Blood Coagul Fibrinolysis 14(4):335–340

    Article  CAS  PubMed  Google Scholar 

  6. Wenzel K, Hanke R, Speer A (1994) Polymorphism in the human E-selectin gene detected by PCR-SSCP. Hum Genet 94(4):452–453

    Article  CAS  PubMed  Google Scholar 

  7. DerSimonian R, Laird N (1986) Meta-analysis in clinical trials. Control Clin Trials 7(3):177–188

    Article  CAS  PubMed  Google Scholar 

  8. Mantel N, Haenszel W (1959) Statistical aspects of the analysis of data from retrospective studies of disease. J Natl Cancer Inst 22(4):719–748

    CAS  PubMed  Google Scholar 

  9. Pereira TV, Rudnicki M, Cheung BM et al (2007) Three endothelial nitric oxide (NOS3) gene polymorphisms in hypertensive and normotensive individuals: meta-analysis of 53 studies reveals evidence of publication bias. J Hypertens 25(9):1763–1774

    Article  CAS  PubMed  Google Scholar 

  10. Chen Y, Pei J (2009) An assessment of a TNF polymorphic marker for the risk of HCV infection: meta-analysis and a new clinical study design. Infect Genet Evol 9(6):1356–1363

    Article  CAS  PubMed  Google Scholar 

  11. Gu W, Liu Y, Wang Z et al (2012) Association between the angiotensinogen gene T174M polymorphism and hypertension risk in the Chinese population: a meta-analysis. Hypertens Res 35(1):70–76

    Article  PubMed  Google Scholar 

  12. Begg CB, Mazumdar M (1994) Operating characteristics of a rank correlation test for publication bias. Biometrics 50(4):1088–1101

    Article  CAS  PubMed  Google Scholar 

  13. Egger M, Davey Smith G, Schneider M, Minder C (1997) Bias in meta-analysis detected by a simple, graphical test. BMJ 315(7109):629–634

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  14. Li Y WY, Zhang PA, Li XY (2003) E-selectin gene A561C polymorphism in the elderly with hypertension. Chin J Geriatr Cardiovasc Cerebrovasc Dis 5(6):384

    Google Scholar 

  15. Chen HL, Hua Q, Liu RK, Yang Z (2005) The effect of E-selectin A561C (S128R) polymorphism on ambulatory blood pressure monitoring. J Cardiovas Pulm Dis 24(4):5

    CAS  Google Scholar 

  16. Chen HL, Hua Q, Liu RK, Yang Z (2005) Effect of E-selectin A561C (S128R) polymorphism on blood pressure, cardiac structure and cardiac function in patients with essential hypertension. Chin J Med Imaging Technol 21(3)

  17. Chen HL, Hua Q, Liu RK, Yang Z (2005) Effect of E-selectin A561C (S128R) polymorphism on blood pressure. Chin J Cardiol 33(7)

  18. Liu ZC ZY, Wang XK, Yang CM (2006) Relationship between E-selectin gene A561C polymorphism and essential hypertension. Acta Acad Med Mil Tert 28(23)

  19. Song Y LX, Wang DW, Dong DD (2007) Association of E-selectin +G98T,+A561C gene polymorphisms and left ventricle reconstitution in patients with essential hypertension. J Fourth Mil Med Univ 28(22)

  20. Li MN WZ, Zhang Q, Li L (2009) Association between E selectin gene polymorphism and essential hypertension in Han minority. Chin J Birth Health Hered 17(2)

  21. Zheng WW GQ, Zhang LC, Cai WJ (2009) Correlation of E-selectin gene polymorphisms in Xinjiang Kazak people with essential hypertension. China Pract Med 4(10)

  22. Wang Z, Liu Y, Liu J et al (2010) E-selectin gene polymorphisms are associated with essential hypertension: a case-control pilot study in a Chinese population. BMC Med Genet11:127

    Google Scholar 

  23. Wang Z CS, Wang L, Lu GL (2010) Relationship between E-selectin gene polymorphism and essential hypertension in Uygur and Han in Xinjiang. J Clin Res 27(6)

  24. Faruque MU, Chen G, Doumatey A et al (2011) Association of ATP1B1, RGS5 and SELE polymorphisms with hypertension and blood pressure in African-Americans. J Hypertens 29(10):1906–1912

    Article  CAS  PubMed  Google Scholar 

  25. Wang Z, Xu Y, Chen S et al (2012) A common missense single nucleotide polymorphism in the E-selectin gene is significantly associated with essential hypertension in the Han population but only weakly associated in the Uygur population. Hypertens Res 35(4):413–417

    Article  PubMed  Google Scholar 

  26. Faruque MU, Chen G, Doumatey A et al (2011) Association of ATP1B1, RGS5 and SELE polymorphisms with hypertension and blood pressure in African-Americans. J Hypertens 29(10):1906-1912

    Article  CAS  PubMed  Google Scholar 

  27. Conen D, Cheng S, Steiner LL et al (2009) Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women’s Genome Health Study. J Hypertens 27(3):476

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  28. Wang J, Pan H-F, Hu Y-T et al (2010) Polymorphism of IL-8 in 251 allele and gastric cancer susceptibility: a meta-analysis. Dig Dis Sci 55(7):1818–1823

    Article  CAS  PubMed  Google Scholar 

  29. Khazen D, Jendoubi-Ayed S, Aleya WB et al (2009) Polymorphism in ICAM-1, PECAM-1, E-selectin, and L-selectin genes in Tunisian patients with inflammatory bowel disease. Eur J Gastroenterol Hepatol 21(2):167–175

    Article  CAS  PubMed  Google Scholar 

  30. Bird MI, Foster MR, Priest R, Malhotra R (1997) Selectins: physiological and pathophysiological roles. Biochem Soc Trans 25(4):1199–1206

    CAS  PubMed  Google Scholar 

  31. Kansas GS (1996) Selectins and their ligands: current concepts and controversies. Blood 88(9):3259–3287

    CAS  PubMed  Google Scholar 

  32. Forlow SB, White EJ, Barlow SC et al (2000) Severe inflammatory defect and reduced viability in CD18 and E-selectin double-mutant mice. J Clin Invest 106(12):1457–1466

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  33. Varpula M, Pulkki K, Karlsson S et al (2007) Predictive value of N-terminal pro-brain natriuretic peptide in severe sepsis and septic shock. Crit Care Med 35(5):1277–1283

    Article  CAS  PubMed  Google Scholar 

  34. Amer MS, Elawam AE, Khater MS et al (2011) Association of high-sensitivity C-reactive protein with carotid artery intima-media thickness in hypertensive older adults. J Am Soc Hypertens 5(5):395–400

    Article  CAS  PubMed  Google Scholar 

  35. Blake GJ, Rifai N, Buring JE, Ridker PM (2003) Blood pressure, C-reactive protein, and risk of future cardiovascular events. Circulation 108(24):2993–2999

    Article  CAS  PubMed  Google Scholar 

  36. Chang YP, Liu X, Kim JD et al (2007) Multiple genes for essential-hypertension susceptibility on chromosome 1q. Am J Hum Genet 80(2):253–264

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  37. Sass C, Pallaud C, Zannad F, Visvikis S (2000) Relationship between E-selectin L/F554 polymorphism and blood pressure in the Stanislas cohort. Hum Genet 107(1):58–61

    Article  CAS  PubMed  Google Scholar 

  38. Wenzel K, Ernst M, Rohde K et al (1996) DNA polymorphisms in adhesion molecule genes—a new risk factor for early atherosclerosis. Hum Genet 97(1):15–20

    Article  CAS  PubMed  Google Scholar 

  39. Bannan S, Mansfield MW, Grant PJ (1998) Soluble vascular cell adhesion molecule-1 and E-selectin levels in relation to vascular risk factors and to E-selectin genotype in the first degree relatives of NIDDM patients and in NIDDM patients. Diabetologia 41(4):460–466

    Article  CAS  PubMed  Google Scholar 

  40. Mlekusch W, Exner M, Schillinger M et al (2004) E-Selectin and restenosis after femoropopliteal angioplasty: prognostic impact of the Ser128Arg genotype and plasma levels. Thromb Haemost 91(1):171–179

    CAS  PubMed  Google Scholar 

  41. Hoffmann SC, Stanley EM, Darrin Cox E et al (2001) Association of cytokine polymorphic inheritance and in vitro cytokine production in anti-CD3/CD28-stimulated peripheral blood lymphocytes. Transplantation 72(8):1444–1450

    Article  CAS  PubMed  Google Scholar 

  42. Colhoun HM, McKeigue PM, Davey Smith G (2003) Problems of reporting genetic associations with complex outcomes. Lancet 361(9360):865–872

    Article  PubMed  Google Scholar 

Download references

Compliance with ethical guidelines

Conflict of interest. H. Wu, A. Tan, H. Yang, Y. Gao, H. Li, S. Lu, Y. Hu, X. Tang, and H, Zhang state that there are no conflicts of interest.

Acknowledgments

This work was supported by the National Natural Science Foundation of China (81060029, 81260130), the Guangxi Natural Science Foundation Program (2012GXNSFDA053016), and the Guangxi Foundation for Science Research and Technology Development (GuiKeGong1140003A-21).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to H. Zhang.

Additional information

Y. Ouyang, H. Wu, and A.Tan contributed equally to this study.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Ouyang, Y., Wu, H., Tan, A. et al. E-selectin gene polymorphism (A561C) and essential hypertension. Herz 40 (Suppl 2), 197–202 (2015). https://doi.org/10.1007/s00059-014-4122-1

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00059-014-4122-1

Keywords

Schlüsselwörter

Navigation