Histidine-rich glycoprotein gene polymorphism in patients with recurrent miscarriage.

Abstract:

:Association between the histidine-rich glycoprotein (HRG) C633T single nucleotide polymorphism (SNP) and recurrent miscarriage was investigated in a case-control study. The cases constituted 187 women with recurrent miscarriage that were compared with 395 controls who had delivered a child and had no history of miscarriage. Blood samples were collected from each woman, genomic DNA was extracted and genotyped for the HRG C633T SNP. In the whole study population, the percentage of miscarriage was the same, regardless of genotype (C/C 31.2%, C/T 32.9% and T/T 32.5%). However, an association between homozygous T/T carriers and recurrent miscarriage was detected in a subgroup of women with primary recurrent miscarriage (odds ratio 2.44, 95% CI 1.01-5.92). Our results indicate an important role for the HRG C633T SNP in the occurrence of recurrent miscarriage.

authors

Lindgren KE,Kårehed K,Karypidis H,Hosseini F,Bremme K,Landgren BM,Skjöldebrand-Sparre L,Stavreus-Evers A,Sundström-Poromaa I,Akerud H

doi

10.1111/aogs.12155

subject

Has Abstract

pub_date

2013-08-01 00:00:00

pages

974-7

issue

8

eissn

0001-6349

issn

1600-0412

journal_volume

92

pub_type

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