Pregled bibliografske jedinice broj: 1077811
Vitamin D receptor polymorphisms in spontaneous preterm birth: a case-control study
Vitamin D receptor polymorphisms in spontaneous preterm birth: a case-control study // Croatian medical journal, 61 (2020), 338-345 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1077811 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Vitamin D receptor polymorphisms in spontaneous
preterm birth: a case-control study
Autori
Gašparović Krpina, Milena ; Barišić, Anita ; Peterlin, Ana ; Tul, Nataša ; Ostojić, Saša ; Peterlin, Borut ; Pereza, Nina
Izvornik
Croatian medical journal (0353-9504) 61
(2020);
338-345
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
pregnancy ; premature birth ; single nucleotide polymorphism ; vitamin D receptor
Sažetak
Aim To evaluate the association between the FokI (rs2228570), ApaI (rs7975232), Bsml (rs1544410), TaqI (rs731236), and Cdx2 (rs11568820) single nucleotide polymorphisms (SNPs) in the vitamin D receptor (VDR) gene and spontaneous preterm birth (SPTB), as well as their effect on clinical characteristics of women with SPTB and their newborns. Methods This case-control study enrolled women who gave birth at the Department of Obstetrics and Gynecology, University Medical Center Ljubljana between 2010 to 2019. Cases were 118 women with spontaneous initiation of PTB after natural conception and 119 controls with a term singleton delivery after an uncomplicated pregnancy. The molecular analysis of VDR SNPs employed polymerase chain reaction and restriction fragment length polymorphism. Results Patients and controls did not significantly differ in the distribution of genotype or allele SNP frequencies. However, the FokI polymorphism had a significant effect on newborn birth weight in women with SPTB but not in controls (F=5.17, P=0.007, one-way ANOVA with post-hoc Scheffe test), with newborns of FokI TT carriers having the lowest birth weight (P=0.011). No other VDR SNP was associated with any other clinical characteristic of women with SPTB and their newborns. Conclusion The TT genotype of the VDR FokI polymorphism is associated with newborn birth weight in women of European origin with SPTB.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Rijeka,
Klinički bolnički centar Rijeka
Profili:
Saša Ostojić (autor)
Anita Barišić (autor)
Nina Pereza (autor)
Milena Gašparović Krpina (autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE