No association between endothelin-1 gene polymorphisms and preeclampsia in Korean population
Journal of Genetic Medicine
; : 34-40, 2008.
Artículo
en Inglés
| WPRIM (Pacífico Occidental)
| ID: wpr-62803
Biblioteca responsable:
WPRO
ABSTRACT
PURPOSE:
Preeclampsia is a major cause of maternal and perinatal mortality and morbidity and is considered to be a multifactorial disorder involving a genetic predisposition and environmental factors. Endothelin-1 (ET-1) is a potent vasoconstrictor peptide, and alterations in the ET-1 system are thought to play a role in triggering the vasoconstriction seen with preeclampsia. The aim of this study was to examine the frequency of the 4 common single-nucleotide polymorphisms (SNPs) (c.1370T>G, c.137_139delinsA, c.3539+2T>C, and c.5665G>T) of the ET-1 gene in normotensive and preeclamptic pregnancies and to investigate whether these SNPs are associated with preeclampsia in pregnant Korean women.METHODS:
We analyzed blood samples from 206 preeclamptic and 216 normotensive pregnancies using a commercially available SNapShot kit and an ABI Prism 3100 Genetic analyzer.RESULTS:
There were no significant differences in genotype or allele frequencies of the 4 SNPs in the ET-1 gene between preeclamptic and normotensive pregnancies. The respective frequencies of the 3 haplotypes (TDTG, GDCT, and TICT; >10% haplotype frequency) were 61%, 13% and 13%, respectively, in preeclampsic pregnancies and 62%, 14% and 12%, respectively, in normotensive pregnancies. The frequencies of these haplotypes were similar for both groups. Using multiple logistic regression analysis, we did not observe an increase in the risk of preeclampsia for the 4 SNPs of the ET-1 gene under either a recessive or dominant model.CONCLUSION:
This study suggests that the 4 SNPs of the ET-1 gene are not associated with an increased risk for preeclampsia in pregnant Korean women.
Texto completo:
Disponible
Base de datos:
WPRIM (Pacífico Occidental)
Asunto principal:
Preeclampsia
/
Vasoconstricción
/
Haplotipos
/
Modelos Logísticos
/
Endotelina-1
/
Predisposición Genética a la Enfermedad
/
Polimorfismo de Nucleótido Simple
/
Mortalidad Perinatal
/
Frecuencia de los Genes
/
Genotipo
Tipo de estudio:
Factores de riesgo
Límite:
Femenino
/
Humanos
/
Embarazo
Idioma:
Inglés
Revista:
Journal of Genetic Medicine
Año:
2008
Tipo del documento:
Artículo