Premium
ORIGINAL ARTICLE: Transforming Growth Factor‐Beta1 Gene Polymorphisms in Korean Patients with Pre‐eclampsia
Author(s) -
Kim Shin Young,
Lim Ji Hyae,
Park So Yeon,
Yang Jae Hyug,
Kim Moon Young,
Kim Min Hyoung,
Ryu Hyun Mee
Publication year - 2010
Publication title -
american journal of reproductive immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 97
eISSN - 1600-0897
pISSN - 1046-7408
DOI - 10.1111/j.1600-0897.2009.00795.x
Subject(s) - genotype , polymorphism (computer science) , allele , medicine , biology , intrauterine growth restriction , transforming growth factor , preeclampsia , allele frequency , genotype frequency , population , eclampsia , single nucleotide polymorphism , endocrinology , gene , genetics , pregnancy , fetus , environmental health
Citation Kim SY, Lim JH, Park SY, Yang JH, Kim MY, Kim MH, Ryu HM. Transforming growth factor‐beta1 (TGF‐β1) gene polymorphisms in Korean patients with pre‐eclampsia. Am J Reprod Immunol 2010; 63: 291–298 Problem The aim of this study was to investigate whether c.869T>C (Leu10Pro) and c.915G>C (Arg25Pro) polymorphisms in exon1 of the transforming growth factor‐beta1 (TGF‐β1) gene are associated with development of pre‐eclampsia (PE) in Korean women. Method of study We analyzed blood samples from 164 patients with PE and 182 healthy pregnant women using the polymerase chain reaction and DNA sequencing. Results The frequencies of the 869CC and combined TC/CC genotypes were higher in patients with PE than in healthy controls. In the PE with intrauterine growth restriction (IUGR), the frequencies of these genotypes were also higher than that in controls. Furthermore, the 869C allele frequency was significantly higher in both PE and IUGR‐complicated PE than in controls. Multivariate analysis showed that the 869TC, CC, and combined TC/CC genotypes were associated with an increased risk of PE compared with the 869TT genotype. In addition, the 869TC, CC, and combined TC/CC genotypes were significantly associated with an increased risk of IUGR‐complicated PE compared with the 869TT genotype. The TGF‐β1 c.915G>C polymorphism was not detected in our population. Conclusion Our findings indicate that the TGF‐β1 c.869T>C polymorphism may be a genetic risk factor for PE and IUGR‐complicated PE.