Abstract | PURPOSE: METHODS: RESULTS: Vitreous Cyr61 levels were significantly higher in active PDR patients, quiescent PDR patients, and diabetic macular edema patients compared with non-diabetic control patients (P < 0.01). Pretreatment of bevacizumab significantly suppressed vitreous vascular endothelial growth factor levels; however, it did not inhibit vitreous Cyr61 levels in active PDR patients. Cysteine-rich 61 was strongly detected in endothelial cells and myofibroblasts within active PDR membranes but not in idiopathic epiretinal membrane. CONCLUSION: Vitreous Cyr61 levels were related to different states of PDR and correlated with vascular endothelial growth factor levels in PDR patients. Pretreatment of bevacizumab did not inhibit vitreous Cyr61 levels in active PDR patients. Cysteine-rich 61 might mediate angiogenesis and post-angiogenic fibrosis in PDR.
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Authors | Jian Jang You, Chung May Yang, Muh Shy Chen, Chang-Hao Yang |
Journal | Retina (Philadelphia, Pa.)
(Retina)
Vol. 32
Issue 1
Pg. 103-11
(Jan 2012)
ISSN: 1539-2864 [Electronic] United States |
PMID | 21822163
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Angiogenesis Inhibitors
- Antibodies, Monoclonal, Humanized
- CCN1 protein, human
- Cysteine-Rich Protein 61
- Vascular Endothelial Growth Factor A
- Bevacizumab
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Topics |
- Angiogenesis Inhibitors
(therapeutic use)
- Antibodies, Monoclonal, Humanized
(therapeutic use)
- Bevacizumab
- Case-Control Studies
- Cysteine-Rich Protein 61
(metabolism)
- Diabetic Retinopathy
(drug therapy, metabolism)
- Female
- Humans
- Intravitreal Injections
- Macular Edema
(metabolism)
- Male
- Middle Aged
- Risk Factors
- Vascular Endothelial Growth Factor A
(metabolism)
- Vitreous Body
(metabolism)
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