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C 反应蛋白及炎症在年龄相关性黄斑变性发病机制中的作用。

The role of CRP and inflammation in the pathogenesis of age-related macular degeneration.

机构信息

Institute of Medical Biochemistry, Clinical Center of Serbia and Farmaceutical Faculty, University of Belgrade, Belgrade, Serbia.

出版信息

Biochem Med (Zagreb). 2012;22(1):39-48. doi: 10.11613/bm.2012.005.

DOI:10.11613/bm.2012.005
PMID:22384518
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4062327/
Abstract

Age-related macular degeneration (AMD) is a complex, degenerative and progressive disease involving the multiple genetic and environmental factors that can result in severe visual loss. The etiology of AMD is not well understood. Many theories exist and feature mechanisms of oxidative stress, atherosclerotic-like changes, genetic predisposition and inflammation. The most recent clinical studies appointed to a great role of inflammation and C-reactive protein (CRP) in the pathogenesis of AMD. There is a large body of evidence indicating the association of CRP with endothelial dysfunction, oxidative stress and production of reactive oxygen species (ROS), as well as with lipid status disorder in AMD patients. According to recent studies, CRP is definitely not only the inflammatory marker but also a mediator of development of the vascular disorders in the retinal circulation. The results obtained from the present studies may help our understanding the pathogenesis of the retinal vascular disease associated with high levels of CRP.

摘要

年龄相关性黄斑变性(AMD)是一种复杂的、退行性的和进行性疾病,涉及多种遗传和环境因素,可导致严重的视力丧失。AMD 的病因尚不清楚。存在许多理论,其特征在于氧化应激、动脉粥样硬化样变化、遗传易感性和炎症的机制。最近的临床研究指出炎症和 C 反应蛋白(CRP)在 AMD 发病机制中的重要作用。大量证据表明 CRP 与 AMD 患者的内皮功能障碍、氧化应激和活性氧(ROS)的产生以及脂质状态紊乱有关。根据最近的研究,CRP 不仅是炎症标志物,还是视网膜循环中血管紊乱发展的介质。本研究获得的结果可能有助于我们了解与 CRP 水平升高相关的视网膜血管疾病的发病机制。

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本文引用的文献

1
New insights in the pathophysiology of inflammation.炎症病理生理学的新见解。
Biochem Med (Zagreb). 2011;21(3):243-4. doi: 10.11613/bm.2011.033.
2
Lipids, lipoproteins, and age-related macular degeneration.脂质、脂蛋白与年龄相关性黄斑变性
J Lipids. 2011;2011:802059. doi: 10.1155/2011/802059. Epub 2011 Jul 28.
3
Disease-causing mutations in genes of the complement system.补体系统基因中的致病突变。
Am J Hum Genet. 2011 Jun 10;88(6):689-705. doi: 10.1016/j.ajhg.2011.05.011.
4
Emerging therapies for the treatment of neovascular age related macular degeneration.治疗新生血管性年龄相关性黄斑变性的新兴疗法。
Semin Ophthalmol. 2011 May;26(3):149-55. doi: 10.3109/08820538.2011.570846.
5
Genetics of age-related macular degeneration: current concepts, future directions.年龄相关性黄斑变性的遗传学:当前概念与未来方向
Semin Ophthalmol. 2011 May;26(3):77-93. doi: 10.3109/08820538.2011.577129.
6
A review and meta-analysis of the association between C-reactive protein and age-related macular degeneration.C 反应蛋白与年龄相关性黄斑变性相关性的综述和荟萃分析。
Surv Ophthalmol. 2011 May-Jun;56(3):184-94. doi: 10.1016/j.survophthal.2010.08.007. Epub 2011 Mar 21.
7
The association of lipoprotein parameters and C-reactive protein in patients with age-related macular degeneration.脂蛋白参数与年龄相关性黄斑变性患者 C 反应蛋白的相关性。
Ophthalmic Res. 2011;46(3):125-32. doi: 10.1159/000323815. Epub 2011 Feb 18.
8
Diabetes mellitus and early age-related macular degeneration.糖尿病与早发性年龄相关性黄斑变性。
Arch Ophthalmol. 2011 Feb;129(2):196-9. doi: 10.1001/archophthalmol.2010.355.
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Clinical risk factors for age-related macular degeneration: a systematic review and meta-analysis.与年龄相关的黄斑变性的临床危险因素:系统评价和荟萃分析。
BMC Ophthalmol. 2010 Dec 13;10:31. doi: 10.1186/1471-2415-10-31.
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CD36 plays an important role in the clearance of oxLDL and associated age-dependent sub-retinal deposits.CD36在氧化型低密度脂蛋白(oxLDL)的清除以及相关的年龄依赖性视网膜下沉积物中发挥着重要作用。
Aging (Albany NY). 2010 Dec;2(12):981-9. doi: 10.18632/aging.100218.