Macular Edema in Central Retinal Vein Occlusion Correlates With Aqueous Fibrinogen Alpha Chain

被引:11
|
作者
Cehofski, Lasse Jorgensen [1 ,2 ]
Kojima, Kentaro [3 ]
Kusada, Natsuki [3 ]
Rasmussen, Maja [1 ]
Muttuvelu, Danson Vasanthan [4 ,5 ]
Grauslund, Jakob [1 ,2 ]
Vorum, Henrik [6 ,7 ]
Honore, Bent [7 ,8 ]
机构
[1] Odense Univ Hosp, Dept Ophthalmol, Sdr Blvd 29, DK-5000 Odense, Denmark
[2] Univ Southern Denmark, Dept Clin Res, Odense, Denmark
[3] Kyoto Prefectural Univ Med, Dept Ophthalmol, Kyoto, Japan
[4] Copenhagen Univ Hosp, Dept Ophthalmol, Copenhagen, Denmark
[5] Univ Copenhagen, Fac Hlth & Med Sci, Copenhagen, Denmark
[6] Aalborg Univ Hosp, Dept Ophthalmol, Aalborg, Denmark
[7] Aalborg Univ, Dept Clin Med, Aalborg, Denmark
[8] Aarhus Univ, Dept Biomed, Aarhus, Denmark
关键词
retina; retinal vasculature; mass spectrometry; proteomics; aqueous humor; COMPUTATIONAL PLATFORM; NETWORKS; PROTEINS; IMPLANT; BRANCH;
D O I
10.1167/iovs.64.2.23
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. The global protein profile of the aqueous humor has been found to correlate with the severity of retinal vascular disease. Studying the aqueous humor in central retinal vein occlusion (CRVO) with proteomic techniques may bring insights to the molecular mechanisms underlying the condition.METHODS. Aqueous humor samples from treatment naive patients with CRVO complicated by macular edema (n = 28) and age-matched controls (n = 20) were analyzed by label free quantification liquid chromatography tandem mass spectrometry. Best corrected visual acuity (BCVA) was measured as logMAR, and the severity of macular edema was evaluated as central retinal thickness (CRT) with optical coherence tomography. Control samples were obtained prior to cataract surgery. Significantly changed proteins were identified by a permutation-based calculation with a false discovery rate of 0.05. RESULTS. A total of 177 proteins were differentially expressed in CRVO. Regulated proteins were involved in complement activation, innate immune response, blood coagulation, and cell adhesion. Upregulated proteins that correlated with BCVA and CRT included fibrinogen alpha, beta, and gamma chains, fibronectin, Ig lambda-6 chain C region, Ig alpha-1 chain C region, and complement C7. Downregulated proteins that correlated negatively with BCVA, and CRT, included procollagen C-endopeptidase enhancer 1, clusterin, opticin, reelin, fibrillin-1, and cadherin-2. Monocyte differentiation antigen CD14 and lipopolysaccharide-binding protein were increased in CRVO.CONCLUSIONS. Fibrinogen chains, fibronectin, and immunoglobulin components correlated with BCVA and CRT, suggesting a multifactorial response. Protective anti-angiogenic proteins, including procollagen C-endopeptidase enhancer 1, clusterin, and opticin, were downregulated in CRVO and correlated negatively with BCVA and CRT.
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页数:16
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