COMPLEMENT FACTOR P IN CHOROIDAL NEOVASCULAR MEMBRANES OF PATIENTS WITH AGE-RELATED MACULAR DEGENERATION

被引:8
作者
Wolf-Schnurrbusch, Ute E. K. [1 ]
Stuck, Anna K. [1 ]
Hess, Roberto [1 ]
Wolf, Sebastian [1 ,2 ]
Enzmann, Volker [1 ]
机构
[1] Univ Bern, Inselspital, Dept Ophthalmol, CH-3010 Bern, Switzerland
[2] Univ Bern, Sch Med, Dept Pathol, CH-3010 Bern, Switzerland
来源
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES | 2009年 / 29卷 / 07期
关键词
complement; Factor P; AMD; CNV; immunocytochemistry; alternative pathway; FACTOR-H POLYMORPHISM; RISK; PATHOGENESIS; INFLAMMATION; PROPERDIN; VARIANT; INDIVIDUALS; PATHWAY; DISEASE;
D O I
10.1097/IAE.0b013e3181a2f40f
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To evaluate whether complement Factor P (properdin) was present in surgically removed choroidal neovascular membranes of patients with age-related macular degeneration (AMD) and to investigate whether associated pre- and postoperative clinical characteristics can be correlated. Methods: The study population consisted of 26 AMD patients (26 eyes) with the exclusion criterion of prior treatment of the choroidal neovascular membranes. Factor P was detected immunocytochemically on paraffin sections (7 mu m) by a polyclonal rabbit antihuman antibody. Results: Eleven of 22 assessable membranes showed a positive reaction for Factor P. The average percentage of Factor P-positive cells per membrane ranged from 0.65% to 4.09%. The duration of visual loss was significantly longer (8.6 +/- 2.7 vs. 3.9 +/- 0.8 months), and the size of postoperative measured area of atrophic retinal pigment epithelium was larger (27.6 +/- 7.6 vs. 15.0 +/- 6.9 mm(2)) in patients with Factor P-positive membranes compared with Factor P-negative ones. Conclusion: Factor P was expressed in 50% of choroidal neovascular membranes of patients with AMD. The group with Factor P-positive membranes differed significantly from the Factor P-negative group in key clinical outcomes. Additional studies need to investigate the role of Factor P in the development of AMD for potential therapeutic intervention.
引用
收藏
页码:966 / 973
页数:8
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