Contribution of rs1799998 polymorphism in CYP11B2 gene in susceptibility to preeclampsia

Abstract Objectives: the present study aimed to evaluate the association between the rs1799998 polymorphism of the CYP11B2 gene and the susceptibility to preeclampsia (PE) in a Brazilian population. Methods: the study group comprised 61 women who were diagnosed with PE. The control group included 11...

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Main Authors: Kaio Raffael Valotta Bezerra (Author), Sarah Cristina Sato Vaz Tanaka (Author), Vanessa Resende Souza Silva (Author), Marina Carvalho Paschoinni (Author), Roseane Lopes da Silva Grecco (Author), Fernanda Caroline Soardi (Author), Marly Aparecida Spadotto Balarin (Author)
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Published: Instituto Materno Infantil de Pernambuco.
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042 |a dc 
100 1 0 |a Kaio Raffael Valotta Bezerra  |e author 
700 1 0 |a Sarah Cristina Sato Vaz Tanaka  |e author 
700 1 0 |a Vanessa Resende Souza Silva  |e author 
700 1 0 |a Marina Carvalho Paschoinni  |e author 
700 1 0 |a Roseane Lopes da Silva Grecco  |e author 
700 1 0 |a Fernanda Caroline Soardi  |e author 
700 1 0 |a Marly Aparecida Spadotto Balarin  |e author 
245 0 0 |a Contribution of rs1799998 polymorphism in CYP11B2 gene in susceptibility to preeclampsia 
260 |b Instituto Materno Infantil de Pernambuco. 
500 |a 1806-9304 
500 |a 10.1590/1806-93042020000200008 
520 |a Abstract Objectives: the present study aimed to evaluate the association between the rs1799998 polymorphism of the CYP11B2 gene and the susceptibility to preeclampsia (PE) in a Brazilian population. Methods: the study group comprised 61 women who were diagnosed with PE. The control group included 116 women who did not show changes in their blood pressure levels during their pregnancies. The rs1799998 polymorphism of the CYP11B2 gene was amplified by allele-specific polymerase chain reaction (PCR). A multiple logistic regression analysis was performed using the SNPStat program to evaluate the risk of the CYP11B2 gene rs1799998 polymorphism contributing to PE. Results: the PE group had the following genotypes: 1.64% CC, 91.80% CT, and 6.56% TT. In the control group, the observed genotypic frequencies were: 11% CC, 73% CT, and 16% TT. The genotypic frequency distribution did not fit the Hardy Weinberg Equilibrium (HWE) in either study group. The multiple logistic regression analysis showed a statistically significant difference for the rs1799998 polymorphism in the recessive model. Conclusion: the results suggest an association between the recessive model of C/C genotype of the rs1799998 polymorphism of the CYP11B2 gene and susceptibility to PE. 
546 |a EN 
546 |a PT 
690 |a Genetic Polymorphism 
690 |a Preeclampsia 
690 |a Cytochrome P-450 
690 |a Gynecology and obstetrics 
690 |a RG1-991 
655 7 |a article  |2 local 
786 0 |n Revista Brasileira de Saúde Materno Infantil 
787 0 |n http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1519-38292020000200467&tlng=pt 
787 0 |n http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1519-38292020000200467&tlng=en 
787 0 |n http://www.scielo.br/pdf/rbsmi/v20n2/pt_1519-3829-rbsmi-20-02-0467.pdf 
787 0 |n http://www.scielo.br/pdf/rbsmi/v20n2/1519-3829-rbsmi-20-02-0467.pdf 
787 0 |n https://doaj.org/toc/1806-9304 
856 4 1 |u https://doaj.org/article/ae9bf0d51a784bb2a5df7b90ffd4fc17  |z Connect to this object online.