Levels of matrix metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 mRNAs in patients with primary hypertension or hypertension-induced atherosclerosis

J Int Med Res. 2012;40(3):986-94. doi: 10.1177/147323001204000317.

Abstract

Objective: Matrix metalloproteinase-9 (MMP-9) and tissue inhibitor of matrix metalloproteinase-1 (TIMP-1) affect degradation of vascular elastin, collagen remodelling and formation of atherosclerotic plaque. This cross-sectional study investigated the levels of MMP-9 and TIMP-1 mRNAs in the blood of patients with primary hypertension with and without hypertension-induced carotid atherosclerosis.

Methods: Hypertensive patients with and without atherosclerosis and age- and gender-matched normotensive subjects were enrolled. MMP-9 and TIMP-1 mRNA were quantified using real-time reverse transcription-polymerase chain reaction.

Results: Hypertensive patients (n = 86) had significantly lower levels of TIMP-1 mRNA than normotensive subjects (n = 43). Hypertensive patients with atherosclerosis (n = 42) showed significantly elevated levels of MMP-9 mRNA compared with both normotensive subjects and hypertensive patients without atherosclerosis (n = 44).

Conclusions: Primary hypertension resulted in decreased TIMP-1 mRNA levels, suggesting a potential mechanism contributing to the degradation of elastin. Hypertension-induced atherosclerosis was associated with significantly increased levels of MMP-9 mRNA, which may enhance both the deposition of types I and III collagen and atherosclerotic plaque formation.

MeSH terms

  • Aged
  • Atherosclerosis / etiology*
  • Base Sequence
  • Case-Control Studies
  • Cross-Sectional Studies
  • DNA Primers
  • Female
  • Humans
  • Hypertension / blood*
  • Hypertension / complications
  • Hypertension / enzymology
  • Male
  • Matrix Metalloproteinase 9 / genetics*
  • Middle Aged
  • RNA, Messenger / genetics*
  • Real-Time Polymerase Chain Reaction
  • Tissue Inhibitor of Metalloproteinase-1 / genetics*
  • Ultrasonography, Doppler

Substances

  • DNA Primers
  • RNA, Messenger
  • Tissue Inhibitor of Metalloproteinase-1
  • Matrix Metalloproteinase 9