Plasma matrix metalloproteinase-9 and ACE-inhibitor-induced improvement of urinary albumin excretion in non-diabetic, microalbuminuric subjects

J Renin Angiotensin Aldosterone Syst. 2007 Dec;8(4):177-80. doi: 10.3317/jraas.2007.029.

Abstract

Introduction: Elevated plasma matrix metalloproteinase-9 (MMP-9) levels have been suggested to precede the development of microalbuminuria. As angiotensin-converting enzyme (ACE) inhibitors effectively reduce urinary albumin excretion (UAE), in the present study we have investigated the potential association of plasma MMP-9 levels with UAE and treatment effects of ACE-inhibition.

Material and methods: In a placebo-controlled randomised trial we determined plasma MMP-9 levels at baseline and after three months of randomisation to either placebo (n=202) or fosinopril (20 mg/day, n=204) treatment.

Results: Baseline plasma MMP-9 levels were not related to baseline UAE (r=-0.008, p=0.871). Three months of fosinopril treatment effectively reduced UAE compared to placebo treatment (-10.4+/-2.4 vs. 1.8+/-1.3 mg/24 hours, p<0.001, respectively). However, fosinopril treatment failed to significantly change plasma MMP-9 levels compared to placebo (-0.47+/-7.68 vs. 0.06+/-9.20, p=0.646, respectively). In addition, the change in UAE was not related with change in MMP-9 levels.

Conclusion: The effective reduction of UAE with fosinopril was not related to plasma MMP-9 levels.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Albuminuria / blood*
  • Albuminuria / drug therapy*
  • Angiotensin-Converting Enzyme Inhibitors / therapeutic use*
  • Diabetes Mellitus / blood*
  • Female
  • Fosinopril / therapeutic use*
  • Humans
  • Male
  • Matrix Metalloproteinase 9 / blood*
  • Middle Aged
  • Placebos

Substances

  • Angiotensin-Converting Enzyme Inhibitors
  • Placebos
  • Matrix Metalloproteinase 9
  • Fosinopril