Abstract | OBJECTIVE: METHODS: The KIR3DL2 gene A52G in exon 3 and C32T in exon 9 polymorphism were determined by polymerase chain reaction-restricted fragment length polymorphism (PCR-RFLP) in 95 pre-eclampsia and 91 normal pregnant women. RESULTS: There was significant difference between two group in exon 3 in terms of genotypes and allele (P < 0.05). There was a significant difference between two groups regarding the frequencies of exon 9 CC, CT and TT genotypes (P < 0.05). But no significant difference was found between mild pre-eclampsia and severe pre-eclampsia groups in terms of the two SNP loci (P > 0.05). CONCLUSION: The A52G polymorphism in exon 3 and the frequencies of C32T in exon 9 of KIR3DL2 gene polymorphism are associated with the pathogenesis of pre-eclampsia, But it has no correlation with the severity of preeclampsia.
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Authors | Xiao-lan Wang, Wei-yuan Zhang, Qi Wang, Cheng-juan Sun |
Journal | Zhonghua yi xue za zhi
(Zhonghua Yi Xue Za Zhi)
Vol. 89
Issue 21
Pg. 1468-71
(Jun 02 2009)
ISSN: 0376-2491 [Print] China |
PMID | 19953898
(Publication Type: English Abstract, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Alleles
- Exons
- Female
- Gene Frequency
- Genotype
- Humans
- Polymorphism, Restriction Fragment Length
- Pre-Eclampsia
(genetics)
- Pregnancy
- Receptors, KIR3DL2
(genetics)
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