Complement, Age-Related Macular Degeneration and a Vision of the Future

被引:117
作者
Gehrs, Karen M. [2 ]
Jackson, Jared R. [2 ]
Brown, Eric N. [2 ]
Allikmets, Rando [3 ,4 ]
Hageman, Gregory S. [1 ]
机构
[1] Univ Utah, Dept Ophthalmol & Visual Sci, John A Moran Eye Ctr, Salt Lake City, UT 84132 USA
[2] Univ Iowa, Dept Ophthalmol & Visual Sci, Iowa City, IA USA
[3] Columbia Univ, Dept Ophthalmol, New York, NY 10027 USA
[4] Columbia Univ, Dept Pathol & Cell Biol, New York, NY USA
基金
美国国家卫生研究院;
关键词
RANDOMIZED CLINICAL-TRIAL; DENSE DEPOSIT DISEASE; FACTOR-H POLYMORPHISM; BLUE-MOUNTAINS-EYE; BEAVER DAM EYE; SUBFOVEAL CHOROIDAL NEOVASCULARIZATION; KRYPTON LASER PHOTOCOAGULATION; HIGH-DOSE SUPPLEMENTATION; BODY-MASS INDEX; PHOTODYNAMIC THERAPY;
D O I
10.1001/archophthalmol.2010.18
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Age-related macular degeneration (AMD) is one of the most well-characterized late-onset, complex trait diseases. Remarkable advances in our understanding of the genetic and biological foundations of this disease were derived from a recent convergence of scientific and clinical data. Importantly, the more recent identification of AMD-associated variations in a number of complement pathway genes has provided strong support for earlier, paradigm-shifting studies that suggested that aberrant function of the complement system plays a key role in disease etiology. Collectively, this wealth of information has provided an impetus for the development of powerful tools to accurately diagnose disease risk and progression and complement-based therapeutics that will ultimately delay or prevent AMD. Indeed, we are poised to witness a new era of a personalized approach toward the assessment, management, and treatment of this debilitating, chronic disease. Arch Ophthalmol. 2010;128(3):349-358
引用
收藏
页码:349 / 358
页数:10
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