Pretražite po imenu i prezimenu autora, mentora, urednika, prevoditelja

Napredna pretraga

Pregled bibliografske jedinice broj: 160043

Ethnic differences in the association of factor V Leiden mutation and the C677T methylenetetrahydrofolate reductase gene polymorphism with preeclampsia


Prasmusinto, D.; Skrablin, S.; Fimmers, R.; van der Ven, K.
Ethnic differences in the association of factor V Leiden mutation and the C677T methylenetetrahydrofolate reductase gene polymorphism with preeclampsia // European journal of obstetrics, gynecology, and reproductive biology, 112 (2004), 2; 162-169 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 160043 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Ethnic differences in the association of factor V Leiden mutation and the C677T methylenetetrahydrofolate reductase gene polymorphism with preeclampsia

Autori
Prasmusinto, D. ; Skrablin, S. ; Fimmers, R. ; van der Ven, K.

Izvornik
European journal of obstetrics, gynecology, and reproductive biology (0301-2115) 112 (2004), 2; 162-169

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
preeclampsia; Leiden mutation

Sažetak
OBJECTIVE: This case-control study evaluates the association of the factor V Leiden mutation with preeclampsia and potential synergistic effects of the MTHFR-677T and factor V Leiden mutations with regard to disease risk in two different ethnic populations. STUDY DESIGN: 198 women and their 143 newborns from Germany/Croatia and Indonesia with normal pregnancy or preeclampsia participated in the study. The factor V Leiden mutation was determined by direct sequencing and the MTHFR genotype by a PCR-based RFLP method. RESULTS: The factor V Leiden mutation is rare in Indonesians. In Germans/Croatians, the frequency of the mutation was significantly increased in mothers with preeclampsia compared to controls. No disease association was found for combined factor V Leiden/MTHFR-677T genotypes on the maternal and fetal level. CONCLUSIONS: Our results underline the need for a clear distinction of ethnicity in association studies of functional gene polymorphisms. They further support the concept of preeclampsia as a complex disease with variable contributions of disease genes in different ethnic groups.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti



POVEZANOST RADA


Projekt / tema
0108261

Citiraj ovu publikaciju

Prasmusinto, D.; Skrablin, S.; Fimmers, R.; van der Ven, K.
Ethnic differences in the association of factor V Leiden mutation and the C677T methylenetetrahydrofolate reductase gene polymorphism with preeclampsia // European journal of obstetrics, gynecology, and reproductive biology, 112 (2004), 2; 162-169 (međunarodna recenzija, članak, znanstveni)
Prasmusinto, D., Skrablin, S., Fimmers, R. & van der Ven, K. (2004) Ethnic differences in the association of factor V Leiden mutation and the C677T methylenetetrahydrofolate reductase gene polymorphism with preeclampsia. European journal of obstetrics, gynecology, and reproductive biology, 112 (2), 162-169.
@article{article, year = {2004}, pages = {162-169}, keywords = {preeclampsia, Leiden mutation}, journal = {European journal of obstetrics, gynecology, and reproductive biology}, volume = {112}, number = {2}, issn = {0301-2115}, title = {Ethnic differences in the association of factor V Leiden mutation and the C677T methylenetetrahydrofolate reductase gene polymorphism with preeclampsia}, keyword = {preeclampsia, Leiden mutation} }

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





Contrast
Increase Font
Decrease Font
Dyslexic Font