Single Nucleotide Polymorphisms from CSF2, FLT1, TFPI and TLR9 Genes Are Associated with Prelabor Rupture of Membranes

被引:6
|
作者
Wujcicka, Wioletta Izabela [1 ]
Kacerovsky, Marian [2 ,3 ]
Krekora, Michal [4 ,5 ]
Kaczmarek, Piotr [6 ]
Grzesiak, Mariusz [5 ,7 ]
机构
[1] Polish Mothers Mem Hosp Res Inst, Sci Lab Ctr Med Lab Diagnost & Screening, 281-289 Rzgowska St, PL-93338 Lodz, Poland
[2] Charles Univ Prague, Univ Hosp Hradec Kralove, Fac Med Hradec Kralove, Dept Obstet & Gynecol, Simkova 870, Hradec Kralove 50003, Czech Republic
[3] Univ Hosp Hradec Kralove, Biomed Res Ctr, Hradec Kralove 50003, Czech Republic
[4] Polish Mothers Mem Hosp, Dept Obstet & Gynecol, Res Inst, PL-93338 Lodz, Poland
[5] Med Univ Lodz, Dept Gynecol & Obstet, 281-289 Rzgowska St, PL-93338 Lodz, Poland
[6] Polish Mothers Mem Hosp, Lab Prenatal Fetal & Maternal Diagnost, Res Inst, PL-93338 Lodz, Poland
[7] Polish Mothers Mem Hosp, Dept Perinatol Obstet & Gynecol, Res Inst, PL-93338 Lodz, Poland
关键词
prelabor rupture of membranes (PROM); pPROM; tPROM; hemostasis; angiogenesis; pregnancy; genotyping; single nucleotide polymorphism (SNP); restriction fragment length polymorphism (RFLP); PRETERM PREMATURE RUPTURE; MEAN PLATELET VOLUME; TOLL-LIKE RECEPTORS; TISSUE FACTOR; AMNIOTIC-FLUID; PROMOTES ANGIOGENESIS; PERINATAL OUTCOMES; MYCOPLASMA-HOMINIS; ENDOTHELIAL-CELLS; FETAL MEMBRANES;
D O I
10.3390/genes12111725
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A prelabor rupture of membranes (PROM) and its subtypes, preterm PROM (pPROM) and term PROM (tPROM), are associated with disturbances in the hemostatic system and angiogenesis. This study was designed to demonstrate the role of single nucleotide polymorphisms (SNPs), localized in CSF2 (rs25881), FLT1 (rs722503), TFPI (C-399T) and TLR9 (rs352140) genes, in PROM. A population of 360 women with singleton pregnancy consisted of 180 PROM cases and 180 healthy controls. A single-SNP analysis showed a similar distribution of genotypes in the studied polymorphisms between the PROM or the pPROM women and the healthy controls. Double-SNP TT variants for CSF2 and FLT1 polymorphisms, CC variants for TLR9 and TFPI SNPs, TTC for CSF2, FLT1 and TLR9 polymorphisms, TTT for FLT1, TLR9 and TFPI SNPs and CCCC and TTTC complex variants for all tested SNPs correlated with an increased risk of PROM after adjusting for APTT, PLT parameters and/or pregnancy disorders. The TCT variants for the CSF2, FLT1 and TLR9 SNPs and the CCTC for the CSF2, FLT1, TLR9 and TFPI polymorphisms correlated with a reduced risk of PROM when corrected by PLT and APTT, respectively. We concluded that the polymorphisms of genes, involved in hemostasis and angiogenesis, contributed to PROM.
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页数:23
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