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本文引用的文献

1
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.一项关于年龄相关性黄斑变性的大型全基因组关联研究突出了罕见变异和常见变异的作用。
Nat Genet. 2016 Feb;48(2):134-43. doi: 10.1038/ng.3448. Epub 2015 Dec 21.
2
Impact of the common genetic associations of age-related macular degeneration upon systemic complement component C3d levels.年龄相关性黄斑变性常见基因关联对全身补体成分C3d水平的影响。
PLoS One. 2014 Mar 27;9(3):e93459. doi: 10.1371/journal.pone.0093459. eCollection 2014.
3
A functional variant in the CFI gene confers a high risk of age-related macular degeneration.CFI 基因中的功能性变异赋予了年龄相关性黄斑变性的高风险。
Nat Genet. 2013 Jul;45(7):813-7. doi: 10.1038/ng.2640. Epub 2013 May 19.
4
Seven new loci associated with age-related macular degeneration.七个与年龄相关性黄斑变性相关的新基因座。
Nat Genet. 2013 Apr;45(4):433-9, 439e1-2. doi: 10.1038/ng.2578. Epub 2013 Mar 3.
5
The pivotal role of the complement system in aging and age-related macular degeneration: hypothesis re-visited.补体系统在衰老和年龄相关性黄斑变性中的关键作用:重新审视假说。
Prog Retin Eye Res. 2010 Mar;29(2):95-112. doi: 10.1016/j.preteyeres.2009.11.003. Epub 2009 Dec 2.
6
Plasma complement components and activation fragments: associations with age-related macular degeneration genotypes and phenotypes.血浆补体成分及激活片段:与年龄相关性黄斑变性的基因型和表型的关联
Invest Ophthalmol Vis Sci. 2009 Dec;50(12):5818-27. doi: 10.1167/iovs.09-3928. Epub 2009 Aug 6.
7
Systemic complement activation in age-related macular degeneration.年龄相关性黄斑变性中的全身补体激活
PLoS One. 2008 Jul 2;3(7):e2593. doi: 10.1371/journal.pone.0002593.
8
Variation in complement factor 3 is associated with risk of age-related macular degeneration.补体因子3的变异与年龄相关性黄斑变性的风险相关。
Nat Genet. 2007 Oct;39(10):1200-1. doi: 10.1038/ng2131. Epub 2007 Sep 2.
9
Complement C3 variant and the risk of age-related macular degeneration.补体C3变体与年龄相关性黄斑变性的风险
N Engl J Med. 2007 Aug 9;357(6):553-61. doi: 10.1056/NEJMoa072618. Epub 2007 Jul 18.
10
Individuals homozygous for the age-related macular degeneration risk-conferring variant of complement factor H have elevated levels of CRP in the choroid.补体因子H的年龄相关性黄斑变性风险赋予变体的纯合个体脉络膜中CRP水平升高。
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年龄相关性黄斑变性患者房水中的局部补体激活

Local complement activation in aqueous humor in patients with age-related macular degeneration.

作者信息

Schick T, Steinhauer M, Aslanidis A, Altay L, Karlstetter M, Langmann T, Kirschfink M, Fauser S

机构信息

Department of Ophthalmology, University Hospital of Cologne, Cologne, Germany.

Laboratory for Experimental Immunology of the Eye, Department of Ophthalmology, University Hospital of Cologne, Cologne, Germany.

出版信息

Eye (Lond). 2017 May;31(5):810-813. doi: 10.1038/eye.2016.328. Epub 2017 Jan 27.

DOI:10.1038/eye.2016.328
PMID:28128795
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5437332/
Abstract

PurposeTo investigate complement activation in aqueous humor and in plasma of patients with neovascular age-related macular degeneration (nAMD).Patients and methodsAqueous humor and EDTA-plasma of 31 nAMD patients and 30 age-matched controls was collected. The levels of the complement factor 3 (C3), the regulators factor H (FH), and factor I (FI), and of the complement activation products Ba, C3a, and the terminal complement complex (sC5b-9) were measured. Associations between complement levels and phenotype were determined using Mann-Whitney U-test.ResultsIn plasma, no significant differences were found between the nAMD group and the control group. In aqueous humor, significantly increased levels of Ba (P=0.002), and C3a (P=0.002) indicate local complement activation in nAMD patients and a trend for a concomitant upregulation of the complement regulators FH (P=0.02) and FI (P=0.04).ConclusionsOur findings provide strong evidence for a local complement dysregulation in nAMD patients.

摘要

目的

研究新生血管性年龄相关性黄斑变性(nAMD)患者房水和血浆中的补体激活情况。

患者与方法

收集31例nAMD患者及30例年龄匹配的对照者的房水和乙二胺四乙酸(EDTA)抗凝血浆。检测补体因子3(C3)、调节因子H(FH)、因子I(FI)以及补体激活产物Ba、C3a和末端补体复合物(sC5b-9)的水平。采用曼-惠特尼U检验确定补体水平与表型之间的关联。

结果

在血浆中,nAMD组与对照组之间未发现显著差异。在房水中,Ba(P=0.002)和C3a(P=0.002)水平显著升高,表明nAMD患者存在局部补体激活,同时补体调节因子FH(P=0.02)和FI(P=0.04)有上调趋势。

结论

我们的研究结果为nAMD患者局部补体失调提供了有力证据。