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肺炎衣原体感染、补体因子H变体与年龄相关性黄斑变性

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

作者信息

Shen D, Tuo J, Patel M, Herzlich A A, Ding X, Chew E Y, Chan C-C

机构信息

10 Center Drive, 10/10N103, National Institutes of Health/National Eye Institute, Bethesda, MD 20892-1857, USA.

出版信息

Br J Ophthalmol. 2009 Mar;93(3):405-8. doi: 10.1136/bjo.2008.145383. Epub 2008 Nov 7.

Abstract

BACKGROUND/AIMS: Impaired inhibition of the alternative complement pathway by complement factor H (CFH) is linked to age-related macular degeneration (AMD) based on the strong association between CFH variant and AMD. Chlamydia pneumoniae (C pneumoniae) infection can trigger the alternative pathway, but the evidence for an association between C pneumoniae and AMD is contradictory. This study investigated whether C pneumoniae infection is associated with AMD and whether the presence of C pneumonia modulates AMD risk conferred by CFH variants.

METHODS

Genomic DNA extracted from peripheral blood of 148 advanced AMD patients and 162 controls was subjected to Taqman and PCR-RFLP for the CFH polymorphism and PCR for the C pneumoniae gene. Genomic DNA was also examined from microdissected macular cells from 59 AMD and 16 age-matched non-AMD archived slides. chi(2) testing was performed for case-control analysis.

RESULTS

C pneumoniae infection was associated with increased risk of AMD (OR = 2.17, p<0.017). A CFH variant was also linked to increased risk of AMD (OR = 1.98, p<0.0001). However, no relationship was found between risk-conferring CFH variant and C pneumoniae (OR = 1.81, p = 0.08).

CONCLUSION

There is a possible association between AMD and C pneumoniae infection, although CFH may not be directly involved in the pathogenesis of C pneumoniae infection-mediated AMD.

摘要

背景/目的:基于补体因子H(CFH)变异与年龄相关性黄斑变性(AMD)之间的强关联,CFH对替代补体途径抑制作用受损与AMD相关。肺炎衣原体(C肺炎)感染可触发替代途径,但关于C肺炎与AMD之间关联的证据相互矛盾。本研究调查了C肺炎感染是否与AMD相关,以及C肺炎的存在是否调节CFH变异赋予的AMD风险。

方法

从148例晚期AMD患者和162例对照的外周血中提取基因组DNA,进行Taqman和PCR-RFLP检测CFH多态性,PCR检测C肺炎基因。还从59例AMD和16例年龄匹配的非AMD存档玻片的显微切割黄斑细胞中检测基因组DNA。进行卡方检验用于病例对照分析。

结果

C肺炎感染与AMD风险增加相关(OR = 2.17,p<0.017)。CFH变异也与AMD风险增加相关(OR = 1.98,p<0.0001)。然而,在赋予风险的CFH变异与C肺炎之间未发现关联(OR = 1.81,p = 0.08)。

结论

AMD与C肺炎感染之间可能存在关联,尽管CFH可能不直接参与C肺炎感染介导的AMD的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ab7/2746818/5f9be7ca3fa2/nihms-139169-f0001.jpg

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