文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

年龄相关性黄斑变性患者替代途径补体蛋白的血浆水平与补体因子H Tyr⁴⁰²His多态性无关。

Plasma levels of complement proteins from the alternative pathway in patients with age-related macular degeneration are independent of Complement Factor H Tyr⁴⁰²His polymorphism.

作者信息

Silva Aldacilene Souza, Teixeira Anderson Gustavo, Bavia Lorena, Lin Fabio, Velletri Roberta, Belfort Rubens, Isaac Lourdes

机构信息

Department of Immunology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.

出版信息

Mol Vis. 2012;18:2288-99. Epub 2012 Aug 30.


DOI:
PMID:22969267
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3436886/
Abstract

PURPOSE: To investigate the influence of the Factor H (CFH) Tyr⁴⁰²His polymorphism on the plasma levels of the alternative pathway proteins CFH, C3, Factor B (FB), Factor D (FD), and Factor I (FI) and the inflammatory marker C-reactive protein (CRP) in 119 patients with age-related macular degeneration (AMD) and 152 unrelated control individuals. METHODS: Patients with AMD and the control group were separated according to CFH polymorphism, age, and gender. Plasma complement proteins and CRP concentrations were determined with enzyme-linked immunosorbent assay, immunodiffusion, or nephelometry. RESULTS: Significant differences in the concentrations of FD and FI were observed between the patients with AMD and the control individuals. We observed significantly reduced FD plasma levels in patients with AMD. We also identified a significant decrease in CFH plasma levels in female patients with AMD in relation to female controls. Plasma FI levels were significantly increased in patients with AMD compared to the control group. Regarding gender, a significant increase in FI plasma levels was observed in male patients. Finally, we found no significant correlation between the CFH Tyr(402)His polymorphism and the CFH, C3, FB, FD, FI, and CRP plasma levels. CONCLUSIONS: Patients with AMD present altered levels of FD and FI in a manner independent of this CFH polymorphism, and gender apparently contributes to the plasma levels of these two proteins in patients with AMD and control individuals.

摘要

目的:研究119例年龄相关性黄斑变性(AMD)患者和152例无关对照个体中,补体因子H(CFH)Tyr⁴⁰²His多态性对替代途径蛋白CFH、C3、因子B(FB)、因子D(FD)、因子I(FI)以及炎症标志物C反应蛋白(CRP)血浆水平的影响。 方法:根据CFH多态性、年龄和性别对AMD患者和对照组进行分组。采用酶联免疫吸附测定、免疫扩散或散射比浊法测定血浆补体蛋白和CRP浓度。 结果:观察到AMD患者和对照个体之间FD和FI浓度存在显著差异。我们发现AMD患者的FD血浆水平显著降低。我们还发现,与女性对照组相比,AMD女性患者的CFH血浆水平显著降低。与对照组相比,AMD患者的血浆FI水平显著升高。在性别方面,男性患者的血浆FI水平显著升高。最后,我们发现CFH Tyr(402)His多态性与CFH、C3、FB、FD、FI和CRP血浆水平之间无显著相关性。 结论:AMD患者的FD和FI水平发生改变,且与这种CFH多态性无关,性别显然会影响AMD患者和对照个体中这两种蛋白的血浆水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec99/3436886/9edbe233ecde/mv-v18-2288-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec99/3436886/ed364efa60fe/mv-v18-2288-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec99/3436886/48e1ac2525ce/mv-v18-2288-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec99/3436886/9edbe233ecde/mv-v18-2288-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec99/3436886/ed364efa60fe/mv-v18-2288-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec99/3436886/48e1ac2525ce/mv-v18-2288-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec99/3436886/9edbe233ecde/mv-v18-2288-f3.jpg

相似文献

[1]
Plasma levels of complement proteins from the alternative pathway in patients with age-related macular degeneration are independent of Complement Factor H Tyr⁴⁰²His polymorphism.

Mol Vis. 2012

[2]
Activation of the alternative complement pathway in vitreous is controlled by genetics in age-related macular degeneration.

Invest Ophthalmol Vis Sci. 2012-9-25

[3]
Plasma complement components and activation fragments: associations with age-related macular degeneration genotypes and phenotypes.

Invest Ophthalmol Vis Sci. 2009-12

[4]
Risk alleles in CFH and ARMS2 are independently associated with systemic complement activation in age-related macular degeneration.

Ophthalmology. 2011-11-30

[5]
Age-related macular degeneration and modification of systemic complement factor H production through liver transplantation.

Ophthalmology. 2013-4-4

[6]
Complement factor H polymorphism, complement activators, and risk of age-related macular degeneration.

JAMA. 2006-7-19

[7]
Dual roles of different redox forms of complement factor H in protecting against age related macular degeneration.

Free Radic Biol Med. 2018-9-22

[8]
C-reactive protein levels and complement factor H polymorphism interaction in age-related macular degeneration and its progression.

Ophthalmology. 2010-6-3

[9]
Joint association of complement component 3 and CC-cytokine ligand2 (CCL2) or complement component 3 and CFH polymorphisms in age-related macular degeneration.

Ophthalmic Genet. 2017

[10]
Association of genetic variants rs641153 (), rs2230199 (), and rs1410996 () with age-related macular degeneration in a Brazilian population.

Exp Biol Med (Maywood). 2021-11

引用本文的文献

[1]
Effect of Target-Mediated Disposition on Iptacopan Clinical Pharmacokinetics in Participants with Normal or Impaired Hepatic Function.

Clin Pharmacol Ther. 2025-5

[2]
Adipsin and adipocyte-derived C3aR1 regulate thermogenic fat in a sex-dependent fashion.

JCI Insight. 2024-5-7

[3]
C-reactive protein-complement factor H axis as a biomarker of activity in early and intermediate age-related macular degeneration.

Front Immunol. 2024

[4]
Recent Advances in Our Understanding of Age-Related Macular Degeneration: Mitochondrial Dysfunction, Redox Signaling, and the Complement System.

Aging Dis. 2024-1-24

[5]
CRISPR Manipulation of Age-Related Macular Degeneration Haplotypes in the Complement System: Potential Future Therapeutic Applications/Avenues.

Int J Mol Sci. 2024-1-30

[6]
Genetic Aspects of Age-Related Macular Degeneration and Their Therapeutic Potential.

Int J Mol Sci. 2022-10-31

[7]
Age-Related Maculopathy Susceptibility 2 and Complement Factor H Polymorphism and Intraocular Complement Activation in Neovascular Age-Related Macular Degeneration.

Ophthalmol Sci. 2022-4-30

[8]
Local factor H production by human choroidal endothelial cells mitigates complement deposition: implications for macular degeneration.

J Pathol. 2022-5

[9]
Plasma C-C Chemokine Concentrations in Intermediate Age-Related Macular Degeneration.

Front Med (Lausanne). 2021-11-18

[10]
Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration.

Am J Hum Genet. 2021-8-5

本文引用的文献

[1]
A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degeneration.

PLoS One. 2011-10-12

[2]
Complement factor D in age-related macular degeneration.

Invest Ophthalmol Vis Sci. 2011-11-11

[3]
Complement factor H binds malondialdehyde epitopes and protects from oxidative stress.

Nature. 2011-10-5

[4]
Oxidation-specific epitopes are danger-associated molecular patterns recognized by pattern recognition receptors of innate immunity.

Circ Res. 2011-1-21

[5]
Lack of association of CFD polymorphisms with advanced age-related macular degeneration.

Mol Vis. 2010-11-3

[6]
Association of complement factor H Y402H polymorphism and age-related macular degeneration in Brazilian patients.

Acta Ophthalmol. 2010-7-6

[7]
The role of complement Factor H in age-related macular degeneration: a review.

Surv Ophthalmol. 2010

[8]
Treatment of neovascular age-related macular degeneration in patients with diabetes.

Clin Ophthalmol. 2008-6

[9]
Plasma complement components and activation fragments: associations with age-related macular degeneration genotypes and phenotypes.

Invest Ophthalmol Vis Sci. 2009-12

[10]
Chlamydia pneumoniae infection, complement factor H variants and age-related macular degeneration.

Br J Ophthalmol. 2009-3

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索