Diabetic retinopathy - Seeing beyond glucose-induced microvascular disease

被引:654
作者
Antonetti, David A.
Barber, Alistair J.
Bronson, Sarah K.
Freeman, Willard M.
Gardner, Thomas W.
Jefferson, Leonard S.
Kester, Mark
Kimball, Scot R.
Krady, J. Kyle
LaNoue, Kathryn F.
Norbury, Christopher C.
Quinn, Patrick G.
Sandirasegarane, Lakshman
Simpson, Ian A.
机构
[1] Penn State Univ, Coll Med, Dept Ophthalmol, Hershey, PA 17033 USA
[2] Penn State Univ, Coll Med, Dept Cellular & Mol Physiol, Hershey, PA 17033 USA
[3] Penn State Univ, Coll Med, Dept Neural & Behav Sci, Hershey, PA 17033 USA
[4] Penn State Univ, Coll Med, Dept Pharmacol, Hershey, PA 17033 USA
关键词
D O I
10.2337/db05-1635
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Diabetic retinopathy remains a frightening prospect to patients and frustrates physicians. Destruction of damaged retina by photocoagulation remains the primary treatment nearly 50 years after its introduction. The diabetes pandemic requires new approaches to understand the pathophysiology and improve the detection, prevention, and treatment of retinopathy. This perspective considers how the unique anatomy and physiology of the retina may predispose it to the metabolic stresses of diabetes. The roles of neural retinal alterations and impaired retinal insulin action in the pathogenesis of early retinopathy and the mechanisms of vision loss are emphasized. Potential means to overcome limitations of current animal models and diagnostic testing are also presented with the goal of accelerating therapies to manage retinopathy in the face of ongoing diabetes.
引用
收藏
页码:2401 / 2411
页数:11
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