AI Article Synopsis

  • The study examines the relationship between specific genetic variations (polymorphisms) in matrix metalloproteinases MMP-2 and MMP-9 and the occurrence of aortic valve calcification (AVC) in individuals.
  • It involved 92 AVC patients and 92 healthy individuals from western Iran, using various methods to analyze gene variations and the serum levels of these enzymes.
  • Results indicated that AVC patients had higher frequencies of risk alleles (A for MMP-2 and T for MMP-9) and elevated levels of MMP-2 and MMP-9 compared to healthy controls, suggesting a link between these factors and increased cardiovascular disease risk.

Article Abstract

Matrix metalloproteinase (MMP) enzyme gene polymorphisms MMP-2-1575G/A and MMP-9-1562C/T promoter polymorphism, their serum levels, and activity are associated with aortic valve calcification (AVC). The synergistic link between the risk of AVC and the alleles T and A of MMP-9 and MMP-2 was investigated, respectively. Ninety-two cases with AVC and 92 healthy individuals from the west of Iran were included, and MMP- 2-1575G/A and MMP-9-1562C/T promoter polymorphisms were detected using PCR-RFLP. The serum levels and activity of MMP-2 and -9 were assessed using ELISA and gelatin zymography methods, respectively. In addition, serum biochemical markers, including FBS, urea and creatinine, cholesterol, triglyceride, HDL, LDL, calcium, phosphorus, and blood pressure: systolic blood pressure and diastolic blood pressure were measured. Heart valve calcification disease was associated with a comparatively higher frequency of the A allele of the MMP2-1575 variation ( = 0.002). In addition, the frequency of T allele of the MMP9-1562 variant was higher than the control group ( = 0.007). MMP-2 and MMP-9 serum levels and activities were observed to be considerably higher in the experimental group than in the control group ( < 0.001). Patients are more susceptible to cardiovascular disease than the control group due to elevated serum levels and activity of MMP-2 and MMP-9.

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Source
http://dx.doi.org/10.1089/gtmb.2023.0370DOI Listing

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