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Human Fertility
an international, multidisciplinary journal dedicated to furthering research and promoting good practice
Volume 16, 2013 - Issue 3
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Gene markers of recurrent miscarriage

Endothelial nitric oxide synthase gene variants and haplotypes associated with an increased risk of idiopathic recurrent miscarriage

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Pages 200-206 | Received 02 Sep 2012, Accepted 03 Jan 2013, Published online: 19 Sep 2013

References

  • Baek, K.H., Lee, E.J., & Kim, Y.S. (2007). Recurrent pregnancy loss: the key potential mechanisms. Trends in Molecular Medicine, 13, 310–317.
  • Bashford, M.T., Hefler, L.A., Vertrees, T.W., Roa, B.B., & Gregg, A.R. (2001). Angiotensinogen and endothelial nitric oxide synthase gene polymorphisms among Hispanic patients with preeclampsia. American Journal of Obstetrics and Gynecology, 184, 1345–1351.
  • Buchholz, T., Lohse, P., Kosian, E., & Thaler, C.J. (2004). Vasoconstrictively acting AT1R A1166C and NOS3 4/5 polymorphisms in recurrent spontaneous abortions (RSA). American Journal of Reproductive Immunology, 51, 323–328.
  • Chatterjee, A., Black, S.M., & Catravas, J.D. (2008). Endothelial nitric oxide (NO) and its pathophysiologic regulation. Vascular Pharmacology, 49, 134–140.
  • Ezzidi, I., Mtiraoui, N., Mohamed, M.B., Mahjoub, T., Kacem, M., & Almawi, W.Y. (2008). Association of endothelial nitric oxide synthase Glu298Asp, 4b/a, and −786T> C gene variants with diabetic nephropathy. Journal of Diabetes and its Complications, 22, 331–338.
  • Fan, W., Li, S.W., & Wang, Y. (2007). Association of genetic polymorphisms in endothelial nitric oxide synthase 3 gene with recurrent early spontaneous abortion. Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 24, 23–26.
  • Hefler, L.A., Tempfer, C.B., Bashford, M.T., Unfried, G., Zeillinger, R., Schneeberger, C., et al. (2002). Polymorphisms of the angiotensinogen gene, the endothelial nitric oxide synthase gene, and the interleukin-1b gene promoter in women with idiopathic recurrent miscarriage. Molecular Human Reproduction, 8, 95–100.
  • Hillermann, R., Carelse, K., & Gebhardt, G.S. (2005). The Glu298Asp variant of the endothelial nitric oxide synthase gene is associated with an increased risk for abruptio placentae in pre-eclampsia. Journal of Human Genetics, 50, 415–419.
  • Karaer, A., Karaer, K., Ozaksit, G., Ceylaner, S., & Percin, E.F. (2008). Y chromosome azoospermia factor region microdeletions and recurrent pregnancy loss. American Journal of Obstetrics and Gynecology, 199, 662.e1–e5.
  • Karvela, M., Papadopoulou, S., Tsaliki, E., Konstantakou, E., Hatzaki, A., Florentin-Arar, L., & Lamnissou, K. (2008). Endothelial nitric oxide synthase gene polymorphisms in recurrent spontaneous abortions. Archives of Gynecology and Obstetrics, 278, 349–352.
  • Kumar, S. (2011). Occupational, environmental and lifestyle factors associated with spontaneous abortion. Reproductive Sciences, 18, 915–930.
  • Leeson, C.P., Hingorani, A.D., Mullen, M.J., Jeerooburkhan, N., Kattenhorn, M., Cole, T.J., et al. (2002). Glu298Asp endothelial nitric oxide synthase gene polymorphism interacts with environmental and dietary factors to influence endothelial function. Circulation Research, 90, 1153–1158.
  • Li, R., Lyn, D., Lapu-Bula, R., Oduwole, A., Igho-Pemu, P., Lankford, B., et al. (2004). Relation of endothelial nitric oxide synthase gene to plasma nitric oxide level, endothelial function, and blood pressure in African Americans. American Journal of Hypertension, 17, 560–567.
  • Li, T.C., Makris, M., Tomsu, M., Tuckerman, E., & Laird, S. (2002). Recurrent miscarriage: aetiology, management and prognosis. Human Reproduction Update, 8, 463–481.
  • Makino, A., Nakanishi, T., Sugiura-Ogasawara, M., Ozaki, Y., Suzumori, N., & Suzumori, K. (2004). No association of C677T methylenetetrahydrofolate reductase and an endothelial nitric oxide synthase polymorphism with recurrent pregnancy loss. American Journal of Reproductive Immunology, 52, 60–66.
  • Marroni, A.S., Metzger, I.F., Souza-Costa, D.C., Nagassaki, S., Sandrim, V.C., Correa, R.X., et al. (2005). Consistent interethnic differences in the distribution of clinically relevant endothelial nitric oxide synthase genetic polymorphisms. Nitric Oxide, 12, 177–182.
  • Nakayama, M., Yoshimura, M., Sakamoto, T., Abe, K., Yamamuro, M., Shono, M., et al. (2006). A −786T> C polymorphism in the endothelial nitric oxide synthase gene reduces serum nitrite/nitrate levels from the heart due to an intracoronary injection of acetylcholine. Pharmacogenetics and Genomics, 16, 339–345.
  • Ozturk, E., Balat, O., Pehlivan, S., Ugur, M.G., Ozcan, C., Sever, T., & Kul, S. (2011). Endothelial nitric oxide synthase gene polymorphisms in preeclampsia with or without eclampsia in a Turkish population. Journal of Obstetrics and Gynaecology Research, 37, 1778–1783.
  • Parveen, F., Faridi, R.M., Alam, S., & Agrawal, S. (2011). Genetic analysis of eNOS gene polymorphisms in association with recurrent miscarriage among North Indian women. Reproductive Biomedicine Online, 23, 124–131.
  • Persu, A., Stoenoiu, M.S., Messiaen, T., Davila, S., Robino, C., El-Khattabi, O., et al. (2002). Modifier effect of eNOS in autosomal dominant polycystic kidney disease. Human Molecular Genetics, 11, 229–241.
  • Saidi, S., Mallat, S.G., Almawi, W.Y., & Mahjoub, T. (2010). Endothe lial nitric oxide synthase Glu298Asp, 4b/a, and −786T> C gene polymorphisms and the risk of ischemic stroke. Acta Neurologica Scandinavica, 121, 114–119.
  • Salimi, S., Firoozrai, M., Nourmohammadi, I., Shabani, M., Shafiee, S.M., Mohebbi, A., & Tavilani, H. (2008). Lack of evidence for contribution of intron4a/b polymorphism of endothelial nitric oxide synthase (NOS3) gene to plasma nitric oxide levels. Acta Cardiologica, 63, 229–234.
  • Sandrim, V.C., Palei, A.C., Cavalli, R.C., Araujo, F.M., Ramos, E.S., Duarte, G., & Tanus-Santos, J.E. (2008). ENOS haplotypes associated with gestational hypertension or preeclampsia. Pharmacogenomics, 9, 1467–1473.
  • Shimasaki, Y., Yasue, H., Yoshimura, M., Nakayama, M., Kugiyama, K., Ogawa, H., et al. (1998). Association of the missence Glu298Asp variant of the endothelial nitric oxide gene with myocardial infarction. Journal of the American College of Cardiology, 31, 1506–1510.
  • Shin, S.J, Lee, H.H., Cha, S.H., Kim, J.H., Shim, S.H., Choi, D.H., & Kim, N.K. (2010). Endothelial nitric oxide synthase gene polymorphisms (−786T> C, 4a4b, 894G> T) and haplotypes in Korean patients with recurrent spontaneous abortion. European Journal of Obstetrics, Gynecology and Reproductive Bioogy, 152, 64–67.
  • Su, M.T., Lin, S.H., & Chen, Y.C. (2011). Genetic association studies of angiogenesis- and vasoconstriction-related genes in women with recurrent pregnancy loss: a systematic review and meta-analysis. Human Reproduction Update, 17, 803–812.
  • Suryanarayana, V., Rao, L., Kanakavalli, M., Padmalatha, V., Deenadayal, M., & Singh, L. (2006). Recurrent early pregnancy loss and endothelial nitric oxide synthase gene polymorphisms. Archives of Gynecology and Obstetrics, 274, 119–124.
  • Suzumori, N. & Sugiura-Ogasawara, M. (2010). Genetic factors as a cause of miscarriage. Current Medicinal Chemistry, 17, 3431–3437.
  • Tanus-Santos, J.E., Desai, M., & Flockhart, D.A. (2001). Effects of ethnicity on the distribution of clinically relevant endothelial nitric oxide variants. Pharmacogenetics, 11, 719–725.
  • Yetik-Anacak, G. & Catravas, J.D. (2006). Nitric oxide and the endothelium: history and impact on cardiovascular disease. Vascular Pharmacology, 45, 268–276.
  • Yoshimura, T., Yoshimura, M., Tabata, A., Shimasaki, Y., Nakayama, M., Miyamoto, Y., et al. (2000). Association of the missense Glu298Asp variant of the endothelial nitric oxide synthase gene with severe preeclampsia. Journal of the Society for Gynecologic Investigation, 7, 238–241.
  • Zammiti, W., Mtiraoui, N., & Mahjoub, T. (2008). Lack of consistent association between endothelial nitric oxide synthase gene polymorphisms, homocysteine levels and recurrent pregnancy loss in Tunisian women. American Journal of Reproductive Immunology, 59, 139–145.

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