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Functional polymorphisms of NOS3 and GUCY1A3 affect both nitric oxide formation and association with hypertensive disorders of pregnancy

dc.contributor.authorPereira, Daniela A.
dc.contributor.authorLuizon, Marcelo R. [UNESP]
dc.contributor.authorPalei, Ana C.
dc.contributor.authorTanus-Santos, José E.
dc.contributor.authorCavalli, Ricardo C.
dc.contributor.authorSandrim, Valeria C. [UNESP]
dc.contributor.institutionUniversidade Federal de Minas Gerais (UFMG)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversity of Mississippi Medical Center
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2025-04-29T20:06:07Z
dc.date.issued2024-02-26
dc.description.abstractImpaired nitric oxide (NO) formation may be associated with endothelial dysfunction and increased cardiovascular disease risk in preeclampsia (PE). Functional single-nucleotide polymorphisms (SNPs) of nitric oxide synthase 3 (NOS3) (rs3918226) and guanylate cyclase 1, soluble, alpha 3 (GUCY1A3) (rs7692387) increase susceptibility to the adverse consequences due to inadequate generation of NO by the endothelium. However, no previous study has examined whether these SNPs affect NO formation in healthy pregnancy and in gestational hypertension (GH) and PE. Here, we compared the alleles and genotypes of NOS3 (rs3918226) and GUCY1A3 (rs7692387) SNPs in normotensive pregnant women (NP, n = 153), in GH (n = 96) and PE (n = 163), and examined whether these SNPs affect plasma nitrite concentrations (a marker of NO formation) in these groups. We further examined whether the interaction among SNP genotypes is associated with GH and PE. Genotypes were determined using TaqMan allele discrimination assays, and plasma nitrite concentrations were determined by an ozone-based chemiluminescence assay. Multifactor dimensionality reduction was used to examine the interactions among SNP genotypes. Regarding NOS3 rs3918226, the CT genotype (p = 0.046) and T allele (p = 0.020) were more frequent in NP than in GH, and GH patients carrying the CT+TT genotypes showed lower nitrite concentrations than NP carrying the CT+TT genotypes (p < 0.05). Regarding GUCY1A3 rs7692387, the GA genotype (p = 0.013) and A allele (p = 0.016) were more frequent in PE than in NP, and NP women carrying the GG genotype showed higher nitrite concentrations than GH or PE patients carrying the GG genotype (p < 0.05). However, we found no significant interactions among genotypes for these functional SNPs to be associated with GH or PE. Our novel findings suggest that NOS3 rs3918226 and GUCY1A3 rs7692387 may affect NO formation and association with hypertensive disorders of pregnancy.en
dc.description.affiliationDepartment of Genetics Ecology and Evolution Institute of Biological Sciences Federal University of Minas Gerais, Minas Gerais
dc.description.affiliationDepartment of Biophysics and Pharmacology Institute of Biosciences Universidade Estadual Paulista (UNESP)
dc.description.affiliationDepartment of Surgery University of Mississippi Medical Center
dc.description.affiliationDepartment of Pharmacology Ribeirao Preto Medical School University of Sao Paulo
dc.description.affiliationDepartment of Gynecology and Obstetrics Ribeirao Preto Medical School University of Sao Paulo
dc.description.affiliationUnespDepartment of Biophysics and Pharmacology Institute of Biosciences Universidade Estadual Paulista (UNESP)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipCenter for Information Technology
dc.description.sponsorshipCenter for Scientific Review
dc.description.sponsorshipNational Institutes of Health
dc.description.sponsorshipOffice of Extramural Research, National Institutes of Health
dc.description.sponsorshipOffice of Research Infrastructure Programs, National Institutes of Health
dc.description.sponsorshipIdFAPESP: 2019/07230-8 2021/12010-7
dc.description.sponsorshipIdCNPq: 314486/2023-2 308504/2021-6
dc.description.sponsorshipIdCAPES: Finance Code 001
dc.description.sponsorshipIdCenter for Information Technology: K01HL159032 R01HL148191 U54GM115428
dc.description.sponsorshipIdCenter for Scientific Review: K01HL159032 R01HL148191 U54GM115428
dc.description.sponsorshipIdNational Institutes of Health: K01HL159032 R01HL148191 U54GM115428
dc.description.sponsorshipIdOffice of Extramural Research, National Institutes of Health: K01HL159032 R01HL148191 U54GM115428
dc.description.sponsorshipIdOffice of Research Infrastructure Programs, National Institutes of Health: K01HL159032 R01HL148191 U54GM115428
dc.identifierhttp://dx.doi.org/10.3389/fgene.2024.1293082
dc.identifier.citationFrontiers in Genetics, v. 15.
dc.identifier.doi10.3389/fgene.2024.1293082
dc.identifier.issn1664-8021
dc.identifier.scopus2-s2.0-85187912453
dc.identifier.urihttps://hdl.handle.net/11449/306412
dc.language.isoeng
dc.relation.ispartofFrontiers in Genetics
dc.sourceScopus
dc.subjectgenetic polymorphisms
dc.subjectgestational hypertension
dc.subjectguanylate cyclase 1 soluble alpha 3
dc.subjectnitric oxide
dc.subjectnitric oxide synthase 3
dc.subjectnitrite
dc.subjectpreeclampsia
dc.subjectpregnancy
dc.titleFunctional polymorphisms of NOS3 and GUCY1A3 affect both nitric oxide formation and association with hypertensive disorders of pregnancyen
dc.typeArtigopt
dspace.entity.typePublication

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