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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/12468
Title: Systematic review and meta-analysis of the association between complement component 3 and age-related macular degeneration: A HuGE review and meta-analysis
Authors: Ammarin Thakkinstian
Gareth J. McKay
Mark McEvoy
Usha Chakravarthy
Subhabrata Chakrabarti
Giuliana Silvestri
Inderjeet Kaur
Xiaoxin Li
John Attia
Mahidol University
Queen's University Belfast
University of Newcastle, Australia
L.V. Prasad Eye Institute India
Peking University
Hunter Medical Research Institute, Australia
John Hunter Hospital
Keywords: Medicine
Issue Date: 15-Jun-2011
Citation: American Journal of Epidemiology. Vol.173, No.12 (2011), 1365-1369
Abstract: The authors performed a meta-analysis to estimate the magnitude of polymorphism effects for the complement component C3 gene (C3) and their possible mode of action on age-related macular degeneration (AMD). The meta-analysis included 16 and 7 studies for rs2230199 and rs1047286, respectively. Data extraction and risk of bias assessments were performed in duplicate, and heterogeneity and publication bias were explored. There was moderate evidence for association between both polymorphisms and AMD in Caucasians. For rs2230199, patients with CG and GG genotypes were 1.44 (95% confidence interval (CI): 1.33, 1.56) and 1.88 (95% CI: 1.59, 2.23) times more likely to have AMD than patients with the CC genotype. For rs1047286, GA and AA genotypes had 1.27 (95% CI: 1.15, 1.41) and 1.70 (95% CI: 1.27, 2.11) times higher risk of AMD than did GG genotypes. These gene effects suggested an additive model. The population attributable risks for the GG/GC and AA/GA genotypes are approximately 5%-10%. Subgroup analysis by ethnicity indicates that these variants are very infrequent in Asians and that the observed gene effects are based largely on the high frequency within Caucasian populations. This meta-analysis supports the association between C3 and AMD and provides a robust estimate of the genetic risk. © 2011 The Author.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79958789920&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/12468
ISSN: 14766256
00029262
Appears in Collections:Scopus 2011-2015

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