2006
DOI: 10.1136/bjo.2006.090852
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Verteporfin photodynamic therapy induced apoptosis in choroidal neovascular membranes

Abstract: Verteporfin PDT leads to selective and effective damage of EC within CNV. Both patent and occluded vessels were lined by apoptotic EC. This finding and the increased expression of proliferation marker at later time points suggest that revascularisation after PDT is caused by angiogenesis rather than recanalisation.

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Cited by 22 publications
(14 citation statements)
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References 19 publications
(30 reference statements)
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“…Recently, recurrence of CNV after PDT has been demonstrated to be due to angiogenesis and not recanalization. 11 This use of bevacizumab immediately after PDT on the same day therefore blocks this immediate upregulation of angiogenic mediators and theoretically blocks recurrence of CNV by angiogenesis. Clinical studies in adults have shown a decreased need for retreatments, as well as better visual results with this combination of PDT and antiangiogenic drugs compared to PDT alone.…”
Section: Discussionmentioning
confidence: 99%
“…Recently, recurrence of CNV after PDT has been demonstrated to be due to angiogenesis and not recanalization. 11 This use of bevacizumab immediately after PDT on the same day therefore blocks this immediate upregulation of angiogenic mediators and theoretically blocks recurrence of CNV by angiogenesis. Clinical studies in adults have shown a decreased need for retreatments, as well as better visual results with this combination of PDT and antiangiogenic drugs compared to PDT alone.…”
Section: Discussionmentioning
confidence: 99%
“…Photodynamic therapy is based on EC damage leading to vascular occlusion 23 24. However, enhanced VEGF expression25 and VEGF predominance over endogenous angiogenesis inhibitors, namely pigment epithelium-derived factor (PEDF)26 and endostatin,27 early after PDT, possibly restarts the angiogenesis cascade.…”
Section: Discussionmentioning
confidence: 99%
“…50 This might explain why endostatin was diminished in the early post-PDT period when endothelial cells were severely damaged, [30][31][32] but enhanced thereafter when healthy endothelial cells were found. Increased infiltration with leucocytes and macrophages (unpublished data) producing proteolytic enzymes may also contribute to enhanced release of endostatin.…”
Section: Discussionmentioning
confidence: 99%
“…[30][31][32] In .90% of the cases, however, a recurrence is seen within 3 months. [2][3][4][5][6] Enhanced VEGF expression 17 and predominance over pigment epithelium-derived factor 19 might contribute to this rebound effect.…”
Section: Discussionmentioning
confidence: 99%