Association of Nitric Oxide Synthase and Matrix Metalloprotease Single Nucleotide Polymorphisms with Preeclampsia and Its Complications

Autor(es):Mostrar menos -

Leonardo, Daniela P. ^[1] ; Albuquerque, Dulcinela M. ^[1] ; Lanaro, Carolina ^[1] ; Baptista, Leticia C. ^[1] ; Cecatti, Jose G. ^[2] ; Surita, Fernanda G. ^[2] ; Parpinelli, Mary A. ^[2] ; Costa, Fernando F. ^[1] ; Franco-Penteado, Carla F. ^[1] ; Fertrin, Kleber Y. ^{[1, 3]} ; Costa, Maria Laura ^[2]

Afiliação do(s) autor(es)

^[1] Univ Campinas UNICAMP, Hematol & Hemotherapy Ctr, Sao Paulo - Brazil

^[2] Univ Campinas UNICAMP, Sch Med, Dept Obstet & Gynaecol, Sao Paulo - Brazil

^[3] Univ Campinas UNICAMP, Sch Med, Dept Clin Pathol, Sao Paulo - Brazil

• Tipo de documento: Artigo Científico
• Fonte: PLoS One; v. 10, n. 8 AUG 28 2015.
• Citações Web of Science: 13

Resumo

Background Preeclampsia is one of the leading causes of maternal and neonatal morbidity and mortality in the world, but its appearance is still unpredictable and its pathophysiology has not been entirely elucidated. Genetic studies have associated single nucleotide polymorphisms in genes encoding nitric oxide synthase and matrix metalloproteases with preeclampsia, but the results are largely inconclusive across different populations. Objectives To investigate the association of single nucleotide polymorphisms (SNPs) in NOS3 (G894T, T-786C, and a variable number of tandem repetitions VNTR in intron 4), MMP2 (C-1306T), and MMP9 (C-1562T) genes with preeclampsia in patients from Southeastern Brazil. Methods This prospective case-control study enrolled 77 women with preeclampsia and 266 control pregnant women. Clinical data were collected to assess risk factors and the presence of severe complications, such as eclampsia and HELLP (hemolysis, elevated liver enzymes, and low platelets) syndrome. Results We found a significant association between the single nucleotide polymorphism NOS3 T-786C and preeclampsia, independently from age, height, weight, or the other SNPs studied, and no association was found with the other polymorphisms. Age and history of preeclampsia were also identified as risk factors. The presence of at least one polymorphic allele for NOS3 T-786C was also associated with the occurrence of eclampsia or HELLP syndrome among preeclamptic women. Conclusions Our data support that the NOS3 T-786C SNP is associated with preeclampsia and the severity of its complications. (AU)

• Processo FAPESP: 08/57441-0 - Alterações clínicas, celulares e moleculares nas hemoglobinopatias e em outras anemias hemolíticas hereditárias
• Beneficiário: Fernando Ferreira Costa
• Linha de fomento: Auxílio à Pesquisa - Temático
• Processo FAPESP: 14/00984-3 - Doenças dos glóbulos vermelhos: fisiopatologia e novas abordagens terapêuticas
• Beneficiário: Fernando Ferreira Costa
• Linha de fomento: Auxílio à Pesquisa - Temático