Frequency of Gene Polymorphisms in Admixed Venezuelan Women with Recurrent Pregnancy Loss: Microsomal Epoxy Hydroxylase (rs1051740) and Enos (rs1799983)

. 2024 Apr 17 ; 46 (4) : 3460-3469. [epub] 20240417

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid38666947

Grantová podpora
PG 09-6599-2006/1 CDCH-UCV

Recurrent pregnancy loss (RPL) affects around 2% of women of reproductive age. Primary RPL is defined by ≥2 pregnancy losses and no normal birth delivery. In secondary RPL, the losses are after a normal pregnancy and delivery. Most cases have no clear aetiology, although primary cases are the most complex. Several gene single nucleotide polymorphisms (SNPs) have been associated with RPL. The frequency of some SNPs is increased in women suffering from RLP from Asian or Caucasian races; however, in admixed populations, the information on possible genetic links is scarce and contradictory. This study aimed to assess the frequency of two SNPs present in two different enzymes involved in medical conditions observed during pregnancy. It is a case-control study. Microsomal epoxy hydrolase (mEPH) is involved in detoxifying xenobiotics, is present in the ovaries, and is hormonally regulated. The endothelial nitric oxide synthase (NOS3) that forms nitric is involved in vascular tone. Two SNPs, rs1051740 (mEPH) and rs1799983 (NOS3), were assessed. The study included 50 controls and 63 primary RPL patients. The frequency of mutated alleles in both SNPs was significantly higher in patients (p < 0.05). Double-mutated homozygotes were encountered only in RPL patients (p < 0.05). Genetic polymorphisms rs1051740 and rs1799983 may be involved in primary RPL in the Venezuelan admix population. Genetic studies could provide crucial information on the aetiology of primary RPL.

Zobrazit více v PubMed

Valko M., Leibfritz D., Moncol J., Cronin M.T., Mazur M., Telser J. Free radicals and antioxidants in normal physiological functions and human disease. Int. J. Biochem. Cell Biol. 2007;39:44–84. doi: 10.1016/j.biocel.2006.07.001. PubMed DOI

Reddy V.P. Oxidative Stress in Health and Disease. Biomedicines. 2023;11:2925. doi: 10.3390/biomedicines11112925. PubMed DOI PMC

Averill-Bates D. Reactive oxygen species and cell signalling. Review. Biochim. Biophys. Acta Mol. Cell Res. 2024;1871:119573. doi: 10.1016/j.bbamcr.2023.119573. PubMed DOI

Pokharel M.D., Garcia-Flores A., Marciano D., Franco M.C., Fineman J.R., Aggarwal S., Wang T., Black S.M. Mitochondrial network dynamics in pulmonary disease: Bridging the gap between inflammation, oxidative stress, and bioenergetics. Redox Biol. 2024;70:103049. doi: 10.1016/j.redox.2024.103049. PubMed DOI PMC

An G., Park J., Song J., Hong T., Song G., Lim W. Relevance of the endoplasmic reticulum-mitochondria axis in cancer diagnosis and therapy. Exp. Mol. Med. 2024;56:40–50. doi: 10.1038/s12276-023-01137-3. PubMed DOI PMC

Dyachenko E.I., Bel’skaya L.V. The Role of Amino Acids in Non-Enzymatic Antioxidant Mechanisms in Cancer: A Review. Metabolites. 2023;14:28. doi: 10.3390/metabo14010028. PubMed DOI PMC

Agarwal A., Aponte-Mellado A., Premkumar B.J., Shaman A., Gupta S. The effects of oxidative stress on female reproduction: A review. Reprod. Biol. Endocrinol. 2012;10:49. doi: 10.1186/1477-7827-10-49. PubMed DOI PMC

Pereira A.C., Martel F. Oxidative stress in pregnancy and fertility pathologies. Cell Biol. Toxicol. 2014;30:301–312. doi: 10.1007/s10565-014-9285-2. PubMed DOI

Grzeszczak K., Łanocha-Arendarczyk N., Malinowski W., Ziętek P., Kosik-Bogacka D. Oxidative Stress in Pregnancy. Biomolecules. 2023;13:1768. doi: 10.3390/biom13121768. PubMed DOI PMC

Haram K., Mortensen J.H., Myking O., Magann E.F., Morrison J.C. The Role of Oxidative Stress. Adhesion Molecules and Antioxidants in Preeclampsia. Curr. Hypertens. Rev. 2019;15:105–112. doi: 10.2174/1573402115666190119163942. PubMed DOI

Hussain T., Murtaza G., Metwally E., Kalhoro D.H., Kalhoro M.S., Rahu B.A., Sahito R.G.A., Yin Y., Yang H., Chughtai M.I., et al. The Role of Oxidative Stress and Antioxidant Balance in Pregnancy. Mediat. Inflamm. 2021;2021:9962860. doi: 10.1155/2021/9962860. PubMed DOI PMC

Joó J.G., Sulyok E., Bódis J., Kornya L. Disrupted Balance of the Oxidant-Antioxidant System in the Pathophysiology of Female Reproduction: Oxidative Stress and Adverse Pregnancy Outcomes. Curr. Issues Mol. Biol. 2023;45:8091–8111. doi: 10.3390/cimb45100511. PubMed DOI PMC

Tuuli M.G., Longtine M.S., Nelson D.M. Review: Oxygen and trophoblast biology—A source of controversy. Placenta. 2011;32:S109–S118. doi: 10.1016/j.placenta.2010.12.013. PubMed DOI PMC

Myatt L. Review: Reactive oxygen and nitrogen species and functional adaptation of the placenta. Placenta. 2010;31:S66–S69. doi: 10.1016/j.placenta.2009.12.021. PubMed DOI PMC

Choi S., Kim J.A., Li H.Y., Lee S.J., Seok Y.S., Kim T.H., Han K.H., Park M.H., Cho G.J., Suh S.H. Altered redox state modulates endothelial KCa2.3 and KCa3.1 levels in normal pregnancy and preeclampsia. Antioxid. Redox Signal. 2019;30:505–519. doi: 10.1089/ars.2017.7038. PubMed DOI

Poston L., Igosheva N., Mistry H.D., Seed P.T., Shennan A.H., Rana S., Karumanchi S.A., Chappell L.C. Role of oxidative stress and antioxidant supplementation in pregnancy disorders. Am. J. Clin. Nutr. 2011;94:S1980–S1985. doi: 10.3945/ajcn.110.001156. PubMed DOI

Diniz M.S., Magalhães C.C., Tocantins C., Grilo L.F., Teixeira J., Pereira S.P. Nurturing through Nutrition: Exploring the Role of Antioxidants in Maternal Diet during Pregnancy to Mitigate Developmental Programming of Chronic Diseases. Nutrients. 2023;15:4623. doi: 10.3390/nu15214623. PubMed DOI PMC

Parveen F., Faridi R.M., Das V., Tripathi G., Agrawal S. Genetic association of phase I and phase II detoxification genes with recurrent miscarriages among North Indian women. Mol. Hum. Reprod. 2010;16:207–214. doi: 10.1093/molehr/gap096. PubMed DOI

Shi X., Xie X., Jia Y., Li S. Maternal genetic polymorphisms and unexplained recurrent miscarriage: A systematic review and meta-analysis. Clin. Genet. 2017;91:265–284. doi: 10.1111/cge.12910. PubMed DOI

Hosagrahara V.P., Rettie A.E., Hassett C., Omiecinski C.J. Functional analysis of human microsomal epoxide hydrolase genetic variants. Chem. Biol. Interact. 2004;150:149–159. doi: 10.1016/j.cbi.2004.07.004. PubMed DOI PMC

Gautheron J., Jéru I. The Multifaceted Role of Epoxide Hydrolases in Human Health and Disease. Int. J. Mol. Sci. 2020;22:13. doi: 10.3390/ijms22010013. PubMed DOI PMC

Luo Y., Zhu Y., Basang W., Wang X., Li C., Zhou X. Roles of Nitric Oxide in the Regulation of Reproduction: A Review. Front. Endocrinol. 2021;12:752410. doi: 10.3389/fendo.2021.752410. PubMed DOI PMC

Li Q., Chen S., Dong X., Fu S., Zhang T., Zheng W., Tian Y., Huang D. The Progress of Research on Genetic Factors of Recurrent Pregnancy Loss. Genet. Res. 2023;2023:9164374. doi: 10.1155/2023/9164374. PubMed DOI PMC

Cao Y., Zhang Z., Xu J., Wang J., Yuan W., Shen Y., Du J. Genetic association studies of endothelial nitric oxide synthase gene polymorphisms in women with unexplained recurrent pregnancy loss: A systematic and meta-analysis. Mol. Biol. Rep. 2014;41:3981–3989. doi: 10.1007/s11033-014-3266-7. PubMed DOI

Pereza N., Peterlin B., Volk M., Kapović M., Ostojić S. A critical update on endothelial nitric oxide synthase gene variations in women with idiopathic recurrent spontaneous abortion: Genetic association study, systematic review and meta-analyses. Mol. Hum. Reprod. 2015;21:466–478. doi: 10.1093/molehr/gav008. PubMed DOI

Azani A., Hosseinzadeh A., Azadkhah R., Zonouzi A.A.P., Zonouzi A.P., Aftabi Y., Khani H., Heidary L., Danaii S., Bargahi N., et al. Association of endothelial nitric oxide synthase gene variants (-786 T>C. intron 4 b/a VNTR and 894 G>T) with idiopathic recurrent pregnancy loss: A case-control study with haplotype and in silico analysis. Eur. J. Obstet. Gynecol. Reprod. Biol. 2017;215:93–100. doi: 10.1016/j.ejogrb.2017.05.024. PubMed DOI

Zhao X., Li Q., Yu F., Lin L., Yin W., Li J., Feng X. Gene polymorphism associated with endothelial nitric oxide synthase (4VNTR, G894T, C786T) and unexplained recurrent spontaneous abortion risk: A meta-analysis. Medicine. 2019;98:e14175. doi: 10.1097/MD.0000000000014175. PubMed DOI PMC

Golestanpour H., Bahrami R., Dastgheib S.A., Tabatabaei R.S., Javaheri A., Karimi-Zarchi M., Mirjalili S.R., Neamatzadeh H. A meta-analysis for association of eNOS VNTR 4b/a,  - 786 T > C and + 894G > T polymorphisms with risk of recurrent pregnancy loss. Arch. Gynecol. Obstet. 2021;304:1135–1151. doi: 10.1007/s00404-021-06172-x. PubMed DOI

Conesa A., Fernández-Mestre M., Padrón D., Toro F., Silva N., Tassinari P., Blanca I., Martin M.P., Carrington M., Layrisse Z. Distribution of killer cell immunoglobulin-like receptor genes in the mestizo population from Venezuela. Tissue Antigens. 2010;75:724–729. doi: 10.1111/j.1399-0039.2010.01446.x. PubMed DOI PMC

Del Pilar Fortes M., Gill G., Paredes M.E., Gamez L.E., Palacios M., Blanca I., Tassinari P. Allele and haplotype frequencies at human leukocyte antigen class I and II genes in Venezuela’s population. Ann. Biol. Clin. 2012;70:175–181. PubMed

Alemán I., Ramírez A.M., Hung A., Ramírez C. Endothelial and inducible nitric oxide synthase expression in Venezuelan patients with pre-eclampsia. Investig. Clin. 2008;49:321–330. PubMed

Hao F., Tang L.C., Sun J.X., Li W.X., Zhao Y., Xu X.H., Jin L.P. Decreased nitric oxide content mediated by asymmetrical dimethylarginine and protein l-arginine methyltransferase 3 in macrophages induces trophoblast apoptosis: A potential cause of recurrent miscarriage. Hum. Reprod. 2021;36:3049–3061. doi: 10.1093/humrep/deab225. PubMed DOI

Zhu X.Z., Deng Z.M., Dai F.F., Liu H., Cheng Y.X. The impact of early pregnancy metabolic disorders on pregnancy outcome and the specific mechanism. Eur. J. Med. Res. 2023;28:197. doi: 10.1186/s40001-023-01161-z. PubMed DOI PMC

Garmendia J.V., Gutiérrez Y., Blanca I., Bianco N.E., De Sanctis J.B. Nitric oxide in different types of hypertension during pregnancy. Clin. Sci. 1997;93:413–421. doi: 10.1042/cs0930413. PubMed DOI

Cheng S.L., Yu C.J., Chen C.J., Yang P.C. Genetic polymorphism of epoxide hydrolase and glutathione S-transferase in COPD. Eur. Respir. J. 2004;23:818–824. doi: 10.1183/09031936.04.00104904. PubMed DOI

Leeson C.P., Hingorani A.D., Mullen M.J., Jeerooburkhan N., Kattenhorn M., Cole T.J., Muller D.P., Lucas A., Humphries S.E., Deanfield J.E. Glu298Asp endothelial nitric oxide synthase gene polymorphism interacts with environmental and dietary factors to influence endothelial function. Circ. Res. 2002;90:1153–1158. doi: 10.1161/01.RES.0000020562.07492.D4. PubMed DOI

Václaviková R., Hughes D.J., Souček P. Microsomal epoxide Hydrolase 1 (EPHX1): Gene. structure. Function. and role in human disease. Gene. 2015;571:1–8. doi: 10.1016/j.gene.2015.07.071. PubMed DOI PMC

Jiang H., Quilley J., Doumad A.B., Zhu A.G., Falck J.R., Hammock B.D., Stier C.T., Jr., Carroll M.A. Increases in plasma trans-EETs and blood pressure reduction in spontaneously hypertensive rats. Am. J. Physiol. Heart Circ. Physiol. 2011;300:H1990–H1996. doi: 10.1152/ajpheart.01267.2010. PubMed DOI PMC

Dalle Vedove F., Fava C., Jiang H., Zanconato G., Quilley J., Brunelli M., Guglielmi V., Vattemi G., Minuz P. Increased epoxyeicosatrienoic acids and reduced soluble epoxide hydrolase expression in the preeclamptic placenta. J. Hypertens. 2016;34:1364–1370. doi: 10.1097/HJH.0000000000000942. PubMed DOI PMC

Sari I., Pinarbasi H., Pinarbasi E., Yildiz C. Association between soluble epoxy hydrolase gene and preeclampsia. Hypertens. Pregnancy. 2017;36:315–325. doi: 10.1080/10641955.2017.1388390. PubMed DOI

Sarı İ., Ökten H., Aktan Ç., Cihan E. Association of the sEH gene promoter polymorphisms and haplotypes with preeclampsia. J. Med. Biochem. 2020;39:428–435. doi: 10.5937/jomb0-27745. PubMed DOI PMC

Morisseau C. The Role of Hydrolases in Biology and Xenobiotics Metabolism. Int. J. Mol. Sci. 2022;23:4870. doi: 10.3390/ijms23094870. PubMed DOI PMC

Hattori N., Fujiwara H., Maeda M., Fujii S., Ueda M. Epoxide hydrolase affects estrogen production in the human ovary. Endocrinology. 2000;141:3353–3365. doi: 10.1210/endo.141.9.7682. PubMed DOI

Popp S.L., Abele I.S., Buck M.B., Stope M.B., Blok L.J., Hanifi-Moghaddam P., Burger C.W., Fritz P., Knabbe C. Microsomal epoxide hydrolase expression in the endometrial uterine corpus is regulated by progesterone during the menstrual cycle. J. Mol. Histol. 2010;41:111–119. doi: 10.1007/s10735-010-9266-6. PubMed DOI

Lorenzi D., Fernández C., Bilinski M., Fabbro M., Galain M., Menazzi S., Miguens M., Perassi P.N., Fulco M.F., Kopelman S., et al. First custom next-generation sequencing infertility panel in Latin America: Design and first results. JBRA Assist. Reprod. 2020;24:104–114. doi: 10.5935/1518-0557.20190065. PubMed DOI PMC

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...