68
Views
8
CrossRef citations to date
0
Altmetric
Original Article

Maternal and fetal angiotensin-converting enzyme gene insertion/deletion polymorphism not associated with pregnancy-induced hypertension in Chinese women

, , , , &
Pages 1119-1123 | Received 05 Aug 2010, Accepted 03 Dec 2010, Published online: 20 Jan 2011

References

  • Xiong X, Mayes D, Demianczuk N, Olson DM, Davidge ST, Newburn-Cook C, Saunders LD. Impact of pregnancy-induced hypertension on fetal growth. Am J Obstet Gynecol 1999;180 (1 Pt 1): 207–213.
  • Xiong X, Buekens P, Pridjian G, Fraser WD. Pregnancy-induced hypertension and perinatal mortality. J Reprod Med 2007;52:402–406.
  • Medica I, Kastrin A, Peterlin B. Genetic polymorphisms in vasoactive genes and preeclampsia: a meta-analysis. Eur J Obstet Gynecol Reprod Biol 2007;131:115–126.
  • Serrano NC. Immunology and genetic of preeclampsia. Clin Dev Immunol 2006;13:197–201.
  • Cross JC. The genetics of pre-eclampsia: a feto-placental or maternal problem? Clin Genet 2003;64:96–103.
  • Shah DM. Preeclampsia: new insights. Curr Opin Nephrol Hypertens 2007;16:213–220.
  • Anton L, Brosnihan KB. Systemic and uteroplacental renin – angiotensin system in normal and pre-eclamptic pregnancies. Ther Adv Cardiovasc Dis 2008;2:349–362.
  • Shah DM. The role of RAS in the pathogenesis of preeclampsia. Curr Hypertens Rep 2006;8:144–152.
  • Lie RT, Rasmussen S, Brunborg H, Gjessing HK, Lie-Nielsen E, Irgens LM. Fetal and maternal contributions to risk of pre-eclampsia: population based study. BMJ 1998;316:1343–1347.
  • Esplin MS, Fausett MB, Fraser A, Kerber R, Mineau G, Carrillo J, Varner MW. Paternal and maternal components of the predisposition to preeclampsia. N Engl J Med 2001;344:867–872.
  • Liang M, Wang X, Li J, Yang F, Fang Z, Wang L, Hu Y, Chen D. Association of combined maternal-fetal TNF-alpha gene G308A genotypes with preterm delivery: a gene-gene interaction study. J Biomed Biotechnol 2010;2010:396184.
  • Ehlers MR, Riordan JF. Angiotensin-converting enzyme: new concepts concerning its biological role. Biochemistry 1989;28:5311–5318.
  • Rigat B, Hubert C, Alhenc-Gelas F, Cambien F, Corvol P, Soubrier F. An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels. J Clin Invest 1990;86:1343–1346.
  • Yue J, Xie X, Feng YJ, Fu Chan Ke XueBeijing: People's Medical Publishing House; 2003.
  • Rigat B, Hubert C, Corvol P, Soubrier F. PCR detection of the insertion/deletion polymorphism of the human angiotensin converting enzyme gene (DCP1) (dipeptidyl carboxypeptidase 1). Nucleic Acids Res 1992;20:1433.
  • Shanmugam V, Sell KW, Saha BK. Mistyping ACE heterozygotes. PCR Methods Appl 1993;3:120–121.
  • Parimi N, Tromp G, Kuivaniemi H, Nien JK, Gomez R, Romero R, Goddard KA. Analytical approaches to detect maternal/fetal genotype incompatibilities that increase risk of pre-eclampsia. BMC Med Genet 2008;9:60.
  • Takimoto E, Ishida J, Sugiyama F, Horiguchi H, Murakami K, Fukamizu A. Hypertension induced in pregnant mice by pla cental renin and maternal angiotensinogen. Science 1996;274:995–998.
  • Morgan L, Foster F, Hayman R, Crawshaw S, Baker PN, Broughton Pipkin F, Kalsheker N. Angiotensin-converting enzyme insertion-deletion polymorphism in normotensive and pre-eclamptic pregnancies. J Hypertens 1999;17:765–768.
  • Uma R, Forsyth SJ, Struthers AD, Fraser CG, Godfrey V, Murphy DJ. Polymorphisms of the angiotensin converting enzyme gene in early-onset and late-onset pre-eclampsia. J Matern Fetal Neonatal Med 2010;23:874–879.
  • Li H, Ma Y, Fu Q, Wang L. Angiotensin-converting enzyme insertion/deletion (ACE I/D) and angiotensin II type 1 receptor (AT1R) gene polymorphism and its association with preeclampsia in Chinese women. Hypertens Pregnancy 2007;26:293–301.
  • Kobashi G, Hata A, Shido K, Ohta K, Yamada H, Kato EH, Minakami H, Tamashiro H, Fujimoto S, Kondo K. Insertion/deletion polymorphism of the angiotensin-converting enzyme gene and preeclampsia in Japanese patients. Semin Thromb Hemost 2005;31:346–350.
  • Kim YJ, Park MH, Park HS, Lee KS, Ha EH, Pang MG. Associations of polymorphisms of the angiotensinogen M235 polymorphism and angiotensin-converting-enzyme intron 16 insertion/deletion polymorphism with preeclampsia in Korean women. Eur J Obstet Gynecol Reprod Biol 2004;116:48–53.
  • Yoo JH. Deletion polymorphism in the gene for angiotensin-converting enzyme is associated with essential hypertension in men born during the Pacific War. Mech Ageing Dev 2005;126:899–905.
  • Tamaki S, Nakamura Y, Tsujita Y, Nozaki A, Amamoto K, Kadowaki T, Kita Y, Okamura T, Iwai N, Kinoshita M, Ueshima H. Polymorphism of the angiotensin converting enzyme gene and blood pressure in a Japanese general population (the Shigaraki Study). Hypertens Res 2002;25:843–848.
  • Huang W, Xie C, Zhou H, Yang T, Sun M. Association of the angiotensin-converting enzyme gene polymorphism with chronic heart failure in Chinese Han patients. Eur J Heart Fail 2004;6:23–27.
  • Berdeli A, Cam FS. Prevalence of the angiotensin I converting enzyme gene insertion/deletion polymorphism in a healthy Turkish population. Biochem Genet 2009;47:412–420.
  • Roberts JM, Cooper DW. Pathogenesis and genetics of pre-eclampsia. Lancet 2001;357:53–56.
  • Dekker GA, Robillard PY, Hulsey TC. Immune maladaptation in the etiology of preeclampsia: a review of corroborative epidemiologic studies. Obstet Gynecol Surv 1998;53:377–382.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.