Abstract

Background: Matrix metalloproteinase 9 (MMP-9) and tissue inhibitor of metalloproteinases 1 (TIMP-1) are regulating enzymes of the extracellular matrix. A systemic imbalance of MMP-9 and TIMP-1, thought to reflect an imbalance of the extracellular matrix homeostasis, is previously associated with polypoidal choroidal vasculopathy (PCV) in Asian patients. Previous studies suggest inter-ethnical differences in the genetic background and etiology of PCV. To further explore this issue, we studied the plasma levels of MMP-9 and TIMP-1 in Caucasian patients with PCV and compared to healthy age-matched controls. Methods: For this prospective case-control study, 60 participants were recruited who were either patients with PCV (n = 26) or healthy controls (n = 34). All participants underwent detailed clinical examination. We sampled fresh venous blood, isolated plasma, and quantified plasma concentrations of the extracellular matrix regulators MMP-9 and TIMP-1 using electrochemiluminescence immunoassays. Results: Plasma levels of MMP-9 (p = 0.4), TIMP-1 (p = 0.9), and MMP-9/TIMP-1 ratio (p = 0.4) did not differ significantly between patients with PCV and healthy controls. No differences appeared after adjusting for influencing co-variates in multivariate analyses. Conclusion: We demonstrate that Caucasian patients with PCV do not have altered levels of plasma MMP-9 or plasma TIMP-1. These findings suggest no strong evidence of a systemic imbalance of the extracellular matrix homeostasis in Caucasian patients with PCV. Our findings are in line with studies of other aspects of PCV that are also subject to significant inter-ethnical differences.

Highlights

  • Polypoidal choroidal vasculopathy (PCV) is a distinct clinical entity characterized by polypoidal abnormalities of vessels originating from the choroid, described as aneurismal type 1 neovascularization in the literature [1,2]

  • Patients with polypoidal choroidal vasculopathy (PCV) and healthy control did not differ in plasma Matrix metalloproteinase 9 (MMP-9) (p = 0.4), tissue inhibitor of metalloproteinases 1 (TIMP-1) (p = 0.9), or MMP-9/TIMP-1 ratio (p = 0.4) (Figure 1)

  • We found no association between PCV and altered plasma levels of MMP-9, TIMP-1, or the MMP-9/TIMP-1 ratio (Table 2)

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Summary

Introduction

Polypoidal choroidal vasculopathy (PCV) is a distinct clinical entity characterized by polypoidal abnormalities of vessels originating from the choroid, described as aneurismal type 1 neovascularization in the literature [1,2]. In Asian patients with PCV, a higher MMP-9 and no difference in TIMP-1 points towards an imbalance in the extracellular matrix homeostasis. Considering the inter-ethnical differences in the elastin gene and association to PCV [11,12,13], which may be suggestive of an etiological difference in the involvement of extracellular matrix, we hypothesized if the association between PCV and MMP-9 would be present in Caucasian patients with PCV. Our aim with this prospective clinic-based case-control study was to quantify plasma levels of MMP-9 and its inhibitor tissue inhibitor of metalloproteinases 1 (TIMP-1, known as metalloproteinase inhibitor 1) in patients with PCV and compare to healthy age-matched control individuals in a Caucasian population

Study Design
Participants
Participant Recruitment and Data Collection
Quantification of Plasma MMP-9 and TIMP-1
Data Analysis and Statistics
Results
Discussion
Full Text
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