Key result
Mutated mEPH and NOS3 alleles are linked to primary recurrent pregnancy loss in Venezuelan women.
Why the study?
Information on possible genetic links to recurrent pregnancy loss in admixed populations was scarce and contradictory.
Are gene polymorphisms rs1051740 (mEPH) and rs1799983 (NOS3) associated with primary recurrent pregnancy loss in admixed Venezuelan women?
Case-Control (n=113)
Are gene polymorphisms rs1051740 (mEPH) and rs1799983 (NOS3) associated with primary recurrent pregnancy loss in admixed Venezuelan women?
p-value: p=< 0.05
Genetic polymorphisms rs1051740 (mEPH) and rs1799983 (NOS3) are significantly associated with primary recurrent pregnancy loss in the Venezuelan admixed population.
mEPH/NOS3 variants associated with recurrent pregnancy loss in Venezuelan women; leaves open causality and need for prospective validation.
Recurrent pregnancy loss (RPL) affects around 2% of women of reproductive age. Primary RPL is defined by ≥2 pregnancy losses and no normal birth delivery. In secondary RPL, the losses are after a normal pregnancy and delivery. Most cases have no clear aetiology, although primary cases are the most complex. Several gene single nucleotide polymorphisms (SNPs) have been associated with RPL. The frequency of some SNPs is increased in women suffering from RLP from Asian or Caucasian races; however, in admixed populations, the information on possible genetic links is scarce and contradictory. This study aimed to assess the frequency of two SNPs present in two different enzymes involved in medical conditions observed during pregnancy. It is a case–control study. Microsomal epoxy hydrolase (mEPH) is involved in detoxifying xenobiotics, is present in the ovaries, and is hormonally regulated. The endothelial nitric oxide synthase (NOS3) that forms nitric is involved in vascular tone. Two SNPs, rs1051740 (mEPH) and rs1799983 (NOS3), were assessed. The study included 50 controls and 63 primary RPL patients. The frequency of mutated alleles in both SNPs was significantly higher in patients (p < 0.05). Double-mutated homozygotes were encountered only in RPL patients (p < 0.05). Genetic polymorphisms rs1051740 and rs1799983 may be involved in primary RPL in the Venezuelan admix population. Genetic studies could provide crucial information on the aetiology of primary RPL.
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Peña et al. (2024) conducted a case-control in Primary recurrent pregnancy loss (n=113). mEPH (rs1051740) and NOS3 (rs1799983) gene polymorphisms vs. Controls without primary recurrent pregnancy loss was evaluated on Frequency of mutated alleles in rs1051740 and rs1799983 (p=< 0.05). The frequency of mutated alleles in mEPH (rs1051740) and NOS3 (rs1799983) was significantly higher in Venezuelan women with primary recurrent pregnancy loss compared to controls (p < 0.05).
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