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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Circulating HO-1 levels are not associated with plasma sFLT-1 and GT(n) HMOX1 polymorphism in preeclampsia

Texto completo
Autor(es):
Sandrim, Valeria [1] ; Coeli-Lacchini, Fernanda Borchers [2] ; Tanus-Santos, Jose Eduardo [3] ; Lacchini, Riccardo [4] ; Cavalli, Ricardo Carvalho [5, 6]
Número total de Autores: 5
Afiliação do(s) autor(es):
[1] Univ Estadual Paulista UNESP, Inst Biosci Botucatu, Dept Pharmacol, Dist Rubiao Jr S-N, BR-18618000 Botucatu, SP - Brazil
[2] Univ Sao Paulo, Ribeirao Preto Coll Nursing, Dept Internal Med, Ribeirao Preto - Brazil
[3] Univ Sao Paulo, Ribeirao Preto Coll Nursing, Dept Pharmacol, Ribeirao Preto - Brazil
[4] Univ Sao Paulo, Ribeirao Preto Coll Nursing, Dept Psychiat Nursing & Human Sci, Ribeirao Preto - Brazil
[5] Univ Sao Paulo, Ribeirao Preto Coll Nursing, Fac Med Ribeirao Preto, Dept Gynecol, Ribeirao Preto - Brazil
[6] Univ Sao Paulo, Ribeirao Preto Coll Nursing, Fac Med Ribeirao Preto, Dept Obstet, Ribeirao Preto - Brazil
Número total de Afiliações: 6
Tipo de documento: Artigo Científico
Fonte: HYPERTENSION IN PREGNANCY; v. 38, n. 2, p. 73-77, APR 3 2019.
Citações Web of Science: 0
Resumo

Objectives: We aimed to assess the plasma HO-1 level and its interrelationship with the plasma sFLT-1 level in preeclamptic and healthy pregnant women with different variants of microsatellite polymorphism (GTn) located in the promoter region of the HMOX-1 gene. Methods: HO-1 and sFLT-1 were measured by ELISA. HMOX1 genotyping was performed using fragment analysis. Results: We found similar and higher levels of plasma HO-1 and sFLT-1, respectively, in preeclampsia. Similar genotypes and alleles frequencies were found in both groups and the absence of modulation of HO-1 levels by genotypes were observed. Conclusion: The plasma HO-1 levels are not increased in preeclampsia women and neither related to sFLT-1 levels and GT(n) polymorphism. (AU)

Processo FAPESP: 15/20461-8 - Papel do NRF2 e HO-1 em pré-eclâmpsia: estudo de polimorfismos genéticos, fatores circulantes e ensaios in vitro
Beneficiário:Valeria Cristina Sandrim
Modalidade de apoio: Auxílio à Pesquisa - Regular