648
Views
12
CrossRef citations to date
0
Altmetric
State of the Art Review

Association between Endothelial Nitric Oxide Synthase Glu298Asp Gene Polymorphism and Diabetic Nephropathy Susceptibility

, &
Pages 173-178 | Received 12 Jul 2012, Accepted 23 Sep 2012, Published online: 01 Nov 2012

REFERENCES

  • Lee AS, Lee YJ, Lee SM, . An aqueous extract of Portulaca oleracea ameliorates diabetic nephropathy through suppression of renal fibrosis and inflammation in diabetic db/db mice. Am J Chin Med. 2012;40:495–510.
  • Palmer ND, Freedman BI. Insights into the genetic architecture of diabetic nephropathy. Curr Diab Rep. 2012;12:423–431.
  • Yu ZY, Chen LS, Zhang LC, Zhou TB. Meta-analysis of the relationship between ACE I/D gene polymorphism and end-stage renal disease in patients with diabetic nephropathy. Nephrology (Carlton). 2012;17:480–487.
  • Reis KA, Ebinc FA, Koc E, . Association of the angiotensinogen M235T and APO E gene polymorphisms in Turkish type 2 diabetic patients with and without nephropathy. Ren Fail. 2011;33:469–474.
  • Datta SK, Kumar V, Pathak R, . Association of glutathione S-transferase M1 and T1 gene polymorphism with oxidative stress in diabetic and nondiabetic chronic kidney disease. Ren Fail. 2010;32:1189–1195.
  • Larsen T, Mose FH, Bech JN, Pedersen EB. Effect of nitric oxide inhibition on blood pressure and renal sodium handling: A dose– response study in healthy man. Clin Exp Hypertens. 2012. doi:10.3109/10641963.2012.681727.
  • Schwartz IF, Grupper A, Soetendorp H, . Attenuated glomerular arginine transport prevents hyperfiltration and induces HIF-1alpha in the pregnant uremic rat. Am J Physiol Renal Physiol. 2012;303:F396–F404.
  • Tsai KD, Chang WW, Lin CC, . Differential effects of LY294002 and wortmannin on inducible nitric oxide synthase expression in glomerular mesangial cells. Int Immunopharmacol. 2012;12:471–480.
  • Zhou TB, Qin YH, Su LN, . Insertion/deletion (I/D) polymorphism of angiotensin-converting enzyme gene in steroid-resistant nephrotic syndrome for children: A genetic association study and meta-analysis. Ren Fail. 2011;33:741–748.
  • Zhou TB, Qin YH, Su LN, . The association between angiotensin-converting enzyme insertion/deletion gene variant and risk of focal segmental glomerulosclerosis: A systematic review and meta-analysis. J Renin Angiotensin Aldosterone Syst. 2011;12:624–633.
  • Zhou TB, Ou C, Qin YH, . Association of angiotensin converting enzyme insertion/deletion gene polymorphism with idiopathic nephrotic syndrome susceptibility in children: A meta-analysis. J Renin Angiotensin Aldosterone Syst. 2011;12:601–610.
  • Zhou TB, Qin YH, Su LN, Lei FY, Huang WF, Zhao YJ. ACE I/D gene polymorphism can’t predict the steroid responsiveness in Asian children with idiopathic nephrotic syndrome: A meta-analysis. PLoS One. 2011;6:e19599.
  • Zhou TB, Liu YG, Lin N, . Relationship between angiotensin-converting enzyme insertion/deletion gene polymorphism and systemic Lupus Erythematosus/Lupus Nephritis: A systematic review and metaanalysis. J Rheumatol. 2012;39:686–693.
  • Noiri E, Satoh H, Taguchi J, . Association of eNOS Glu298Asp polymorphism with end-stage renal disease. Hypertension. 2002;40:535–540.
  • Nagase S, Suzuki H, Wang Y, . Association of ecNOS gene polymorphisms with end stage renal diseases. Mol Cell Biochem. 2003;244:113–118.
  • Shin SY, Baek SH, Chang KY, . Relations between eNOS Glu298Asp polymorphism and progression of diabetic nephropathy. Diabetes Res Clin Pract. 2004;65:257–265.
  • Thaha M, Pranawa, Yogiantoro M, . Association of endothelial nitric oxide synthase Glu298Asp polymorphism with end-stage renal disease. Clin Nephrol. 2008;70:144–154.
  • El-Din BS, Hamdy SM. Impact of nitric oxide synthase Glu298Asp polymorphism on the development of end-stage renal disease in type 2 diabetic Egyptian patients. Ren Fail. 2011;33:878–884.
  • Santos KG, Crispim D, Canani LH, Ferrugem PT, Gross JL, Roisenberg I. Association of eNOS gene polymorphisms with renal disease in Caucasians with type 2 diabetes. Diabetes Res Clin Pract. 2011;91:353–362.
  • Fu Z, Li C, Xiao Z, Wang Z. The relationship between chromosome 7q35 region gene mutation and diabetic nephropathy. Chin J Nephrol. 2006;22:59.
  • Li X, Yu M, Wu X, Shui H, Xiao J. Assodatiml of endothelial nitric oxide synthase gene Glu298Asp polymorphism with diabetic kidney disease. J Clin Nephrol. 2011;11:351–353.
  • Su MT, Lin SH, Chen YC. Genetic association studies of angiogenesis- and vasoconstriction-related genes in women with recurrent pregnancy loss: A systematic review and meta-analysis. Hum Reprod Update. 2011;17:803–812.
  • Casas JP, Bautista LE, Humphries SE, Hingorani AD. Endothelial nitric oxide synthase genotype and ischemic heart disease: Meta-analysis of 26 studies involving 23028 subjects. Circulation. 2004;109:1359–1365.
  • Shaik AP, Sultana A, Bammidi VK, Sampathirao K, Jamil K. A meta-analysis of eNOS and ACE gene polymorphisms and risk of pre-eclampsia in women. J Obstet Gynaecol. 2011;31:603–607.
  • Yu CK, Casas JP, Savvidou MD, Sahemey MK, Nicolaides KH, Hingorani AD. Endothelial nitric oxide synthase gene polymorphism (Glu298Asp) and development of pre-eclampsia: A case– control study and a meta-analysis. BMC Pregnancy Childbirth. 2006;6:7.
  • Shoukry A, Shalaby SM, Abdelazim S, . Endothelial nitric oxide synthase gene polymorphisms and the risk of diabetic nephropathy in type 2 diabetes mellitus. Genet Test Mol Biomarkers. 2012;16:574–579.

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.