Circulating matrix metalloproteinases and their inhibitors in inguinal hernia and abdominal aortic aneurysm

G A Antoniou1, I K Tentes, S A Antoniou

  • 1Department of Vascular Surgery, Demokritos University of Thrace, Alexandroupolis, Greece. antoniou.ga@hotmail.com

Abstract

Insights

Matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) show altered blood levels in patients with abdominal aortic aneurysm and inguinal hernia. These findings suggest a potential link in collagen metabolism underlying these conditions.

Area of Science:

  • Biochemistry
  • Vascular Biology
  • Connective Tissue Disorders

Background:

  • Matrix metalloproteinases (MMPs) and their inhibitors (TIMPs) are implicated in connective tissue degeneration, leading to aortic aneurysms and abdominal wall hernias.
  • Clinical studies show a higher incidence of abdominal hernias in patients with aortic aneurysms, suggesting a potential shared pathology.

Purpose of the Study:

  • To quantify plasma levels of MMP-9, MMP-2, TIMP-1, and TIMP-2 in patients with abdominal aortic aneurysm and inguinal hernia.
  • To investigate potential pathogenic links between these conditions through impaired collagen metabolism.

Main Methods:

  • Plasma samples from 33 male patients with abdominal aortic aneurysm, 91 male patients with inguinal hernia, and 35 healthy male controls were analyzed.
  • Enzyme-linked immunosorbent assay (ELISA) was used to measure concentrations of MMP-9, MMP-2, TIMP-1, and TIMP-2.

Main Results:

  • MMP-9 and MMP-2 levels were lower in patients with both conditions compared to controls, with the lowest levels observed in hernia patients.
  • TIMP-2 levels were elevated in inguinal hernia patients but reduced in aortic aneurysm patients.
  • TIMP-1 showed opposite correlations to TIMP-2, with reduced levels in hernia patients and elevated levels in aneurysm patients.

Conclusions:

  • Distinct patterns of circulating MMP and TIMP levels exist in patients with aortic aneurysms and inguinal hernias compared to healthy individuals.
  • These differing plasma levels suggest distinct pathogenic processes involving MMPs and TIMPs in collagen metabolism for each disease.
  • Further research combining plasma and tissue analysis is needed to explore the common pathogenesis of these diseases.

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