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Association of polymorphisms of complement factor I rs141853578 (G119R) with age-related macular degeneration in Iranian population

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تاریخ
2018
نویسنده
Bonyadi, M
Norouzi, N
Babaei, E
Jabbarpoor Bonyadi, MH
Javadzadeh, A
Yaseri, M
Soheilian, M
Metadata
نمایش پرونده کامل آیتم
چکیده
Background: Age-related macular degeneration (AMD) is a complex disease, and recent studies have shown role of complement system genes in its development. Complement factor I regulates the complement pathways, and relationship between CFI polymorphisms and AMD is controversial. We evaluated the possible association of complement factor I rs141853578 (G119R) variation with advanced AMD in Iranian patients. Materials and methods: We included 371 case-control samples consisting of 220 advanced AMD patients and 151 genetically unrelated healthy controls. Extracted DNA samples amplified to obtain fragment including the polymorphic complement factor I rs141853578 (G119R) region. Results: The distribution of the genotypes was significantly different in the AMD patients compared to that of controls (p = 0.035). The TT genotype frequencies for CFI were significantly higher in AMD group (7.7 vs. 2%, OR 4.67, CI 1.33-16.45, p = 0.016). This significant difference was maintained after adjustment for the effects of age and gender (OR 5.09, CI 1.42-18.20, p = 0.012). The minor allele frequency (T allele) was also significantly higher in AMD patients compared to that of controls (29.3 vs. 21.5% OR 1.51, CI 1.07-2.13, p = 0.018). Conclusion: Current study showed that CFI rs141853578 (G119R) is a risk factor for developing advanced type AMD. This study also suggests that the frequency of G119R polymorphism in our population is not as rare as reported from other populations. é 2018 Springer Science+Business Media B.V., part of Springer Nature
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http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52748
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