2013
DOI: 10.1111/aogs.12155
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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, regar… Show more

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Cited by 17 publications
(21 citation statements)
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“…A single nucleotide polymorphism (SNP), C633T in the HRG-gene causes a change from a proline to a serine at amino acid 186 in the protein, and the allele frequencies in a mixedhas been associated with several aspects of fertility. For instance, an increased prevalence of the minor T-allele was detected among women with primary recurrent miscarriage [Lindgren et al 2013], and among patients undergoing in vitro fertilization (IVF), women homozygous for the minor T-allele had lower pregnancy success rates than women homo-or heterozygous for the major C-allele [Nordqvist et al 2011]. Moreover, homozygous carriers of the minor T-allele received fewer oocytes despite higher levels of administered FSH and had a lower number of fertilized oocytes during IVF treatment [Nordqvist et al 2015].…”
Section: Introductionmentioning
confidence: 99%
“…A single nucleotide polymorphism (SNP), C633T in the HRG-gene causes a change from a proline to a serine at amino acid 186 in the protein, and the allele frequencies in a mixedhas been associated with several aspects of fertility. For instance, an increased prevalence of the minor T-allele was detected among women with primary recurrent miscarriage [Lindgren et al 2013], and among patients undergoing in vitro fertilization (IVF), women homozygous for the minor T-allele had lower pregnancy success rates than women homo-or heterozygous for the major C-allele [Nordqvist et al 2011]. Moreover, homozygous carriers of the minor T-allele received fewer oocytes despite higher levels of administered FSH and had a lower number of fertilized oocytes during IVF treatment [Nordqvist et al 2015].…”
Section: Introductionmentioning
confidence: 99%
“…This group was defined as ‘diagnosed with primary recurrent miscarriage’ (no known children either before or after diagnosis) [19,21], and consisted of 43 women who were compared to controls. Age, BMI and smoking did not differ between the groups, but hypothyroidism was more prevalent (p < 0.001) among cases.…”
Section: Resultsmentioning
confidence: 99%
“…HRG has been reported to exist as at least ten naturally occurring single nucleotide polymorphisms (SNPs) [16,17]. One of the SNPs, the HRG C633T SNP, has been postulated to be of relevance for implantation and a successful pregnancy [18] and there is an increased occurrence of the homozygous T/T genotype in patients with primary recurrent miscarriage [19]. …”
Section: Introductionmentioning
confidence: 99%
“…In the article by Lindgren et al. , the wrong reference categories were used in the logistic regression analysis in Table 3. The correct values are given in Table 3 below:…”
Section: Factors Associated With Recurrent Miscarriage In a Subgroup mentioning
confidence: 99%