Pregled bibliografske jedinice broj: 1156180
VDR gene polymorphisms and DNA methylation in idiopathic spontaneous preterm birth
VDR gene polymorphisms and DNA methylation in idiopathic spontaneous preterm birth // The 8th World Congress on Controversies in Preconception, Preimplantation and Prenatal Genetic Diagnosis
online conference, 2021. str. 1-1 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1156180 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
VDR gene polymorphisms and DNA methylation in
idiopathic spontaneous preterm birth
Autori
Mladenić, Tea ; Dević Pavlić, Sanja ; Barišić, Anita ; Vraneković, Jadranka ; Stanković, Aleksandra ; Peterlin, Ana ; Peterlin, Borut ; Ostojić, Saša ; Pereza, Nina
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Skup
The 8th World Congress on Controversies in Preconception, Preimplantation and Prenatal Genetic Diagnosis
Mjesto i datum
Online conference, 06.11.2021
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
DNA methylation ; preterm birth ; vitamin D
Sažetak
Introduction: The deficiency of vitamin D has been associated with premature birth. The effects of vitamin D are mediated by its receptor (VDR), which is encoded by the VDR gene. Both VDR gene polymorphisms and DNA methylation play important roles during normal and pathological pregnancy. The aim of this study was to evaluate whether maternal VDR gene polymorphisms and long interspersed nucleotide elements 1 (LINE-1) DNA methylation, alone or in combination, are a risk factor for idiopathic spontaneous preterm birth (ISPTB) in Croatian and Slovenian women. Material and methods: This case-control study included 50 women who delivered spontaneously early preterm (23-336/7 weeks of gestation) and 50 control women who delivered at term. The FokI (rs2228570), ApaI (rs7975232), Bsml (rs1544410), TaqI (rs 731236), and Cdx2 (rs11568820) single nucleotide polymorphisms (SNPs) in the VDR gene were identified using the combination of polymerase chain reaction and restriction fragment length polymorphism. Quantification of LINE-1 DNA methylation was determined using the MethyLight method. Results: There was no significant difference observed in genotype and allele frequencies of VDR gene polymorphism between women with ISPTB and control women (P > 0.050). Moreover, no significant differences were found in inheritance models between groups of subjects. The values of LINE-1 DNA methylation in patients with ISPTB did not significantly differ compared to the control group (P = 0.767). Additionally, no association was observed in DNA methylation between any of the analyzed genotypes of VDR gene polymorphisms (P > 0.050). Conclusion: The results of our study indicate that VDR gene polymorphisms are not associated with the occurrence of ISPTB. In addition, based on the LINE-1 quantification, DNA methylation is not associated with ISPTB nor with VDR gene polymorphisms. Considering the number of patients enrolled, further research is needed to detect and clarify the role of DNA methylation and VDR gene polymorphisms in ISPTB.
Izvorni jezik
Engleski
POVEZANOST RADA
Profili:
Tea Mladenić (autor)
Saša Ostojić (autor)
Anita Barišić (autor)
Sanja Dević Pavlić (autor)
Nina Pereza (autor)
Jadranka Vraneković (autor)