High plasma microfibrillar-associated protein 4 is associated with reduced surgical repair in abdominal aortic

Jes Sanddal Lindholt1, Mathilde Madsen2, Katrine Lindequist Kirketerp-Møller2

  • 1Cardiovascular Research Unit, Viborg Hospital, Viborg, Denmark.

Abstract

Insights

Plasma microfibrillar-associated protein 4 (pMFAP4) may serve as a biomarker for abdominal aortic aneurysms (AAA). High pMFAP4 levels are linked to a lower chance of AAA surgical repair, suggesting a potential prognostic role.

Area of Science:

  • Biochemistry
  • Vascular Biology
  • Biomarker Discovery

Background:

  • Abdominal aortic aneurysms (AAA) require effective biomarkers for prognosis and treatment selection.
  • Microfibrillar-associated protein 4 (MFAP4) is an extracellular matrix protein highly expressed in the aorta and implicated in tissue remodeling diseases.

Purpose of the Study:

  • To investigate the potential of plasma MFAP4 (pMFAP4) as a diagnostic and prognostic biomarker for AAA.
  • To assess the association between pMFAP4 levels and AAA progression and the need for surgical intervention.

Main Methods:

  • Analysis of plasma samples from 504 male AAA patients and 188 controls.
  • Measurement of pMFAP4 levels using Alphalisa.
  • Statistical analyses including Mann-Whitney U test, Spearman's correlation, multiple logistic regression, and competing risk regression.

Main Results:

  • A significant negative correlation was observed between pMFAP4 and aorta growth rate (Spearman's ρ = -0.14, P = .0074), though not significant in multiple linear regression.
  • Immunohistochemistry suggested a tendency for decreased pMFAP4 in AAA.
  • Competing risk regression revealed that patients in the upper tertile of pMFAP4 had a 51% reduced risk of undergoing later surgical repair (HR = 0.51, P = .001).

Conclusions:

  • Elevated plasma MFAP4 levels are associated with a reduced likelihood of surgical repair in patients with abdominal aortic aneurysms.
  • These findings suggest pMFAP4 may have a role in the prognosis of AAA, warranting further validation in independent cohorts.