AI Article Synopsis

  • * The study investigates genetic links to primary RPL by analyzing two specific gene SNPs, rs1051740 (related to detoxification) and rs1799983 (related to blood vessel function), in a case-control format involving 63 RPL patients and 50 controls.
  • * Results showed a significantly higher frequency of mutated SNP alleles in RPL patients compared to controls, suggesting these genetic polymorphisms may play a role in primary RPL within the Venezuelan admixed

Article Abstract

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 ( < 0.05). Double-mutated homozygotes were encountered only in RPL patients ( < 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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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11049659PMC
http://dx.doi.org/10.3390/cimb46040217DOI Listing

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