ARG2 single-nucleotide polymorphism rs3742879 affects plasma arginase 2 levels, nitric oxide formation and antihypertensive therapy response in preeclampsia

Detalhes bibliográficos
Autor(a) principal: Luizon, Marcelo R.
Data de Publicação: 2022
Outros Autores: Pinto-Souza, Caroline C. [UNESP], Coeli-Lacchini, Fernanda, Lacchini, Riccardo, Cavalli, Ricardo C., Sandrim, Valeria C. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.2217/pgs-2022-0079
http://hdl.handle.net/11449/241589
Resumo: Aim: This work examined whether ARG1 (rs2781659, rs2781667, rs2246012 and rs17599586) and ARG2 (rs3742879 and rs10483801) single-nucleotide polymorphisms (SNPs) are associated with antihypertensive therapy responsiveness in preeclampsia (PE) and their effects on arginase isoforms and nitrite concentrations in responsive and nonresponsive patients. Methods: SNP genotypes were determined by TaqMan assays. Plasma arginase levels were measured by ELISA and nitrite concentrations were measured using an ozone-based chemiluminescence assay. Results: The G allele for ARG2 rs3742879 (A>G) was less frequent in nonresponsive compared with responsive patients (15.5% vs 24.7%, respectively) and the G carriers of the nonresponsive subgroup had lower arginase 2 (9.2 ± 7.5 ng/ml vs 19.1 ± 17.3 ng/ml) and higher nitrite concentrations (110.2 ± 52.8 nM vs 78.5 ± 37.9 nM) than carriers of the AA genotype (all p < 0.05). Conclusion: ARG2 SNP rs3742879 is associated with diminished arginase 2 levels and increased nitric oxide formation in nonresponsive PE patients.
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spelling ARG2 single-nucleotide polymorphism rs3742879 affects plasma arginase 2 levels, nitric oxide formation and antihypertensive therapy response in preeclampsiaARG2arginase 2genetic polymorphismshypertensionnitric oxidenitritepharmacogeneticspreeclampsiaAim: This work examined whether ARG1 (rs2781659, rs2781667, rs2246012 and rs17599586) and ARG2 (rs3742879 and rs10483801) single-nucleotide polymorphisms (SNPs) are associated with antihypertensive therapy responsiveness in preeclampsia (PE) and their effects on arginase isoforms and nitrite concentrations in responsive and nonresponsive patients. Methods: SNP genotypes were determined by TaqMan assays. Plasma arginase levels were measured by ELISA and nitrite concentrations were measured using an ozone-based chemiluminescence assay. Results: The G allele for ARG2 rs3742879 (A>G) was less frequent in nonresponsive compared with responsive patients (15.5% vs 24.7%, respectively) and the G carriers of the nonresponsive subgroup had lower arginase 2 (9.2 ± 7.5 ng/ml vs 19.1 ± 17.3 ng/ml) and higher nitrite concentrations (110.2 ± 52.8 nM vs 78.5 ± 37.9 nM) than carriers of the AA genotype (all p < 0.05). Conclusion: ARG2 SNP rs3742879 is associated with diminished arginase 2 levels and increased nitric oxide formation in nonresponsive PE patients.Department of Genetics Ecology and Evolution Institute of Biological Sciences Federal University of Minas Gerais (UFMG), MGDepartment of Biophysics and Pharmacology Institute of Biosciences of Botucatu Universidade Estadual Paulista (UNESP), Distrito Rubiao Junior, BotucatuDepartment of Clinical Analyses Toxicology and Food Science School of Pharmaceutical Sciences of Ribeirao Preto University of Sao Paulo (USP), Ribeirao PretoDepartment of Psychiatric Nursing and Human Sciences Ribeirao Preto School of Nursing University of Sao Paulo (USP), Ribeirao PretoDepartment of Gynecology and Obstetrics University of Sao Paulo (USP), Ribeirao PretoDepartment of Biophysics and Pharmacology Institute of Biosciences of Botucatu Universidade Estadual Paulista (UNESP), Distrito Rubiao Junior, BotucatuUniversidade Federal de Minas Gerais (UFMG)Universidade Estadual Paulista (UNESP)Universidade de São Paulo (USP)Luizon, Marcelo R.Pinto-Souza, Caroline C. [UNESP]Coeli-Lacchini, FernandaLacchini, RiccardoCavalli, Ricardo C.Sandrim, Valeria C. [UNESP]2023-03-01T21:11:49Z2023-03-01T21:11:49Z2022-08-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article713-722http://dx.doi.org/10.2217/pgs-2022-0079Pharmacogenomics, v. 23, n. 13, p. 713-722, 2022.1744-80421462-2416http://hdl.handle.net/11449/24158910.2217/pgs-2022-00792-s2.0-85137134448Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPharmacogenomicsinfo:eu-repo/semantics/openAccess2023-03-01T21:11:49Zoai:repositorio.unesp.br:11449/241589Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:07:54.221492Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv ARG2 single-nucleotide polymorphism rs3742879 affects plasma arginase 2 levels, nitric oxide formation and antihypertensive therapy response in preeclampsia
title ARG2 single-nucleotide polymorphism rs3742879 affects plasma arginase 2 levels, nitric oxide formation and antihypertensive therapy response in preeclampsia
spellingShingle ARG2 single-nucleotide polymorphism rs3742879 affects plasma arginase 2 levels, nitric oxide formation and antihypertensive therapy response in preeclampsia
Luizon, Marcelo R.
ARG2
arginase 2
genetic polymorphisms
hypertension
nitric oxide
nitrite
pharmacogenetics
preeclampsia
title_short ARG2 single-nucleotide polymorphism rs3742879 affects plasma arginase 2 levels, nitric oxide formation and antihypertensive therapy response in preeclampsia
title_full ARG2 single-nucleotide polymorphism rs3742879 affects plasma arginase 2 levels, nitric oxide formation and antihypertensive therapy response in preeclampsia
title_fullStr ARG2 single-nucleotide polymorphism rs3742879 affects plasma arginase 2 levels, nitric oxide formation and antihypertensive therapy response in preeclampsia
title_full_unstemmed ARG2 single-nucleotide polymorphism rs3742879 affects plasma arginase 2 levels, nitric oxide formation and antihypertensive therapy response in preeclampsia
title_sort ARG2 single-nucleotide polymorphism rs3742879 affects plasma arginase 2 levels, nitric oxide formation and antihypertensive therapy response in preeclampsia
author Luizon, Marcelo R.
author_facet Luizon, Marcelo R.
Pinto-Souza, Caroline C. [UNESP]
Coeli-Lacchini, Fernanda
Lacchini, Riccardo
Cavalli, Ricardo C.
Sandrim, Valeria C. [UNESP]
author_role author
author2 Pinto-Souza, Caroline C. [UNESP]
Coeli-Lacchini, Fernanda
Lacchini, Riccardo
Cavalli, Ricardo C.
Sandrim, Valeria C. [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de Minas Gerais (UFMG)
Universidade Estadual Paulista (UNESP)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Luizon, Marcelo R.
Pinto-Souza, Caroline C. [UNESP]
Coeli-Lacchini, Fernanda
Lacchini, Riccardo
Cavalli, Ricardo C.
Sandrim, Valeria C. [UNESP]
dc.subject.por.fl_str_mv ARG2
arginase 2
genetic polymorphisms
hypertension
nitric oxide
nitrite
pharmacogenetics
preeclampsia
topic ARG2
arginase 2
genetic polymorphisms
hypertension
nitric oxide
nitrite
pharmacogenetics
preeclampsia
description Aim: This work examined whether ARG1 (rs2781659, rs2781667, rs2246012 and rs17599586) and ARG2 (rs3742879 and rs10483801) single-nucleotide polymorphisms (SNPs) are associated with antihypertensive therapy responsiveness in preeclampsia (PE) and their effects on arginase isoforms and nitrite concentrations in responsive and nonresponsive patients. Methods: SNP genotypes were determined by TaqMan assays. Plasma arginase levels were measured by ELISA and nitrite concentrations were measured using an ozone-based chemiluminescence assay. Results: The G allele for ARG2 rs3742879 (A>G) was less frequent in nonresponsive compared with responsive patients (15.5% vs 24.7%, respectively) and the G carriers of the nonresponsive subgroup had lower arginase 2 (9.2 ± 7.5 ng/ml vs 19.1 ± 17.3 ng/ml) and higher nitrite concentrations (110.2 ± 52.8 nM vs 78.5 ± 37.9 nM) than carriers of the AA genotype (all p < 0.05). Conclusion: ARG2 SNP rs3742879 is associated with diminished arginase 2 levels and increased nitric oxide formation in nonresponsive PE patients.
publishDate 2022
dc.date.none.fl_str_mv 2022-08-01
2023-03-01T21:11:49Z
2023-03-01T21:11:49Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.2217/pgs-2022-0079
Pharmacogenomics, v. 23, n. 13, p. 713-722, 2022.
1744-8042
1462-2416
http://hdl.handle.net/11449/241589
10.2217/pgs-2022-0079
2-s2.0-85137134448
url http://dx.doi.org/10.2217/pgs-2022-0079
http://hdl.handle.net/11449/241589
identifier_str_mv Pharmacogenomics, v. 23, n. 13, p. 713-722, 2022.
1744-8042
1462-2416
10.2217/pgs-2022-0079
2-s2.0-85137134448
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Pharmacogenomics
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 713-722
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1808128320195264512