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Matrix γ-carboxyglutamate protein and Fetuin-A, in wet type age-related macular degeneration.

Authors :
Javadzadeh A
Ghorbanihaghjo A
Heidari E
Baharivand N
Sadeghi K
Sorkhabi R
Ahoor MH
Source :
International journal of ophthalmology [Int J Ophthalmol] 2015 Jun 18; Vol. 8 (3), pp. 556-9. Date of Electronic Publication: 2015 Jun 18 (Print Publication: 2015).
Publication Year :
2015

Abstract

Aim: To evaluate the high sensitivity C-reactive protein (hsCRP), Fetuin-A and matrix γ-carboxyglutamate protein (MGP) as the main factors for vascular calcification and inflammation in serum of patients with advanced age-related macular degeneration (ARMD) in comparison to healthy controls.<br />Methods: The subjects were 40 patients with choroidal neovascularization (CNV) having a mean age of 70.9±9.1y and a matched group of 49 apparently healthy control subjects. The ARMD was diagnosed using a slit-lamp with superfield lens, fundus photography and fluorescein angiography. Measurement of hsCRP was done by nephelometry method. Levels of Fetuin-A and MGP were measured by enzyme-linked immunosorbent assay (ELISA) technique.<br />Results: hsCRP [0.45(0.07-2.63) mg/L vs 0.25(0.03-1.2) mg/L, P=0.02)] and Fetuin-A levels (50.27±5.04 vs 44.99±10.28 ng/mL, P=0.009) were higher in the patients than in the control groups. We could not find significant difference in MGP level between two groups (P=0.08). There was not a significant correlation between MGP with Fetuin-A and hsCRP among the patients (P=0.7, P=0.9 respectively). A significant negative correlation of hsCRP with Fetuin-A was observed in both case and control groups (P=0.004, r=-0.33 and P=0.001, r=-0.54, respectively).<br />Conclusion: Although our study shows that serum hsCRP and Fetuin-A is increased in CNV patients as well as negatively correlated with both study groups, their direct role on pathogenesis of ARMD required future studies.

Details

Language :
English
ISSN :
2222-3959
Volume :
8
Issue :
3
Database :
MEDLINE
Journal :
International journal of ophthalmology
Publication Type :
Academic Journal
Accession number :
26086007
Full Text :
https://doi.org/10.3980/j.issn.2222-3959.2015.03.21