
It has been proposed that preeclampsia is a metabolic syndrome of pregnancy. The polymorphisms PstI and MaeIII of INS, NsiI of INSR and Ala513Pro and Gly972Arg of IRS1 have been associated with metabolic syndrome; moreover, the products of these genes are functionally contiguous during insulin signaling. The aim of this study was to assess whether these polymorphisms are associated with preeclampsia.46 normotensive pregnant women and 43 preeclamptic patients were included in the study to develop a clinical, biochemical and genotypic profile of preeclampsia. Clinical evaluation consisted of measurement of blood pressure, height and weight. Peripheral blood samples were collected for determination of fasting glucose and insulin concentrations and for extraction of genomic DNA. Proteinuria was determined. Polymorphisms were detected using PCR-RFLP.The normotensive and preeclampsia groups did not differ significantly in clinical and biochemical traits, except for systolic and diastolic blood pressure (p 0.05).The lack of an association between preeclampsia and the polymorphisms studied suggests that other genes whose products do not have direct functional interaction with metabolic syndrome or epigenetic factors may play a role in preeclampsia.
Adult, Blood Glucose, Blood Pressure, DNA, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, Receptor, Insulin, Young Adult, Cross-Sectional Studies, Haplotypes, Pre-Eclampsia, Pregnancy, Insulin Receptor Substrate Proteins, Humans, Insulin, Female, Mexico, Alleles, Polymorphism, Restriction Fragment Length
Adult, Blood Glucose, Blood Pressure, DNA, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, Receptor, Insulin, Young Adult, Cross-Sectional Studies, Haplotypes, Pre-Eclampsia, Pregnancy, Insulin Receptor Substrate Proteins, Humans, Insulin, Female, Mexico, Alleles, Polymorphism, Restriction Fragment Length
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