| Literature DB >> 34046868 |
Tamara Sljivancanin Jakovljevic1, Olivera Kontic-Vucinic2,3, Nadja Nikolic4, Jelena Carkic4, Jelena Stamenkovic2,3, Ivan Soldatovic5, Jelena Milasin4.
Abstract
The aim of the present study was to analyze the distribution of genotypes and haplotypes of functional eNOS gene polymorphisms in the promoter (-786 T/C), intron 4 (VNTR4b/a) and exon 7 (894 G/T), in Serbian population of pregnant women, and establish a possible association between these polymorphisms and preeclampsia development. DNA was isolated from venous blood samples of 50 heathy pregnant women and 50 preeclampsia patients. Polymerase Chain Reaction/Restriction Fragment Length Polymorphism (PCR/RFLP) technique, with appropriate sets of primers and specific restriction enzymes, was used to determine polymorphisms in eNOS gene. Statistical analysis was done using the SPSS and HAPLOVIEW software packages. eNOS -786 T/C polymorphism was significantly associated with preeclampsia (P = 0.006). Homozygotes for the VNTR polymorphism had also an elevated risk of developing preeclampsia (OR=7.68, 95%CI (0.89-65.98)), especially the mild (OR=9.33, 95%CI (0.98-88.57)) and late form (OR=8.52, 95%CI (0.90-80.58)). The 894 G/T polymorphism was not associated with preeclampsia. "G-C-b" and "T-4a-T" haplotypes were more frequent in preeclampsia, though without reaching statistical significance. -786 T/C and VNTR 4b/a eNOS gene polymorphisms were associated with preeclampsia risk in Serbian patients.Entities:
Keywords: Endothelial nitric oxide synthase; Gene polymorphisms; Haplotypes; Preeclampsia
Mesh:
Substances:
Year: 2021 PMID: 34046868 DOI: 10.1007/s43032-021-00632-0
Source DB: PubMed Journal: Reprod Sci ISSN: 1933-7191 Impact factor: 3.060