Pregled bibliografske jedinice broj: 452090
Functional inference of methylenetetrahydrofolate reductase gene polymorphisms on enzyme stability as a potential risk factor for Down syndrome in Croatia
Functional inference of methylenetetrahydrofolate reductase gene polymorphisms on enzyme stability as a potential risk factor for Down syndrome in Croatia // Disease markers, 28 (2010), 5; 293-298 doi:10.3233/DMA-2010-0704 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 452090 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Functional inference of methylenetetrahydrofolate reductase gene polymorphisms on enzyme stability as a potential risk factor for Down syndrome in Croatia
Autori
Vraneković, Jadranka ; Babić Božović, Ivana ; Starčević Čizmarević, Nada ; Buretić-Tomljanović, Alena ; Ristić, Smiljana ; Petrović, Oleg ; Kapović, Miljenko ; Brajenović- Milić, Bojana
Izvornik
Disease markers (0278-0240) 28
(2010), 5;
293-298
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Down syndrome; enzyme configuration; MTHFR; polymorphisms
Sažetak
Understanding the biochemical structure and function of the methylenetetrahydrofolate reductase gene (MTHFR) provides new evidence in elucidating the risk of having a child with Down syndrome (DS) in association with two common MTHFR polymorphisms, C677T and A1298C. The aim of this study was to evaluate the risk for DS according to the presence of MTHFR C677T and A1298C polymorphisms as well as the stability of the enzyme configuration. This study included mothers from Croatia with a liveborn DS child (n=102) or DS pregnancy (n=9) and mothers with a healthy child (n=141). MTHFR C677T and A1298C polymorphisms were assessed by PCR-RFLP. Allele/genotype frequencies differences were determined using 2 test. Odds ratio and the 95% confidence intervals were calculated to evaluate the effects of different alleles/genotypes. No statistically significant differences were found between the frequencies of allele/genotype or genotype combinations of the MTHFR C677T and A1298C polymorphisms in the case and the control groups. Additionally, the observed frequencies of the stable (677CC/1298AA, 677CC/1298AC, 677CC/1298CC) and unstable (677CT/1298AA, 677CT/1298AC, 677TT/1298AA) enzyme configurations were not significantly different. We found no evidence to support the possibility that MTHFR polymorphisms and the stability of the enzyme configurations were associated with risk of having a child with DS in Croatian population.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
062-0000000-1349 - Prenatalni probir za sindrom Downov (Brajenović-Milić, Bojana, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Rijeka
Profili:
Nada Starčević Čizmarević
(autor)
Bojana Brajenović-Milić
(autor)
Smiljana Ristić
(autor)
Ivana Babić Božović
(autor)
Alena Buretić-Tomljanović
(autor)
Miljenko Kapović
(autor)
Oleg Petrović
(autor)
Jadranka Vraneković
(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