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Research Reports

Evaluating VEGFR1 genetic polymorphisms as a predisposition to AMD in a cohort from northern China

, , , , , , & show all
Pages 388-393 | Received 28 Jul 2015, Accepted 03 Oct 2015, Published online: 25 Feb 2016
 

ABSTRACT

Objective: The association among genetic variants in VEGFR1 and a predisposition to age-related macular degeneration (AMD) in a northern cohort from China was evaluated.

Methods: A retrospective case-control correlation study was conducted on 432 cases and 906 gender-and ethnicity-matched controls. Whole DNA was isolated from peripheral blood samples after the individuals underwent detailed eye examinations. Eight single nucleotide polymorphisms (SNPs) in VEGFR1 genes were genotyped for all individuals using a MALDI-TOF technique. The distribution of genotypes was analyzed for Hardy-Weinberg equilibrium and the relationships among the genotype and allele frequencies with AMD were evaluated by age-adjusted logistic regression analysis. The measurement of linkage disequilibrium (LD) was carried out by Haploview 4.2. Bonferroni testing was employed to correct for multiple comparisons.

Results: Among the SNPs genotyped, p values of six SNPs were less than 0.05 between AMD cases and unaffected controls. However, after Bonferroni correction, the genotype and allele distributions of only two SNPs, rs9554322 and rs9582036 differed significantly between the controls and AMD patients. Further, the rs9554322 CC genotype conferred strong susceptibility to AMD (OR = 6.057, 95% CI: 3.099–11.839). Rs9943922 was also found to be significantly associated with AMD in the distributions for the genotype and allele recessive model (p = 0.004). The specific haplotype CA of rs9582036 and rs9554320 was associated with AMD (p = 0.035), but the correlation did not remain after correction.

Conclusions: The SNPs rs9554322, rs9582036 and rs9943922 were correlated with AMD. Gene variants in VEGFR1 were linked to a pronounced emerging risk for AMD in a population in northern China.

Declaration of interest

The authors report no conflicts of interest. The authors alone are responsible for the writing and content of this article.

Funding

This work was supported by grants from the National Natural Science Foundation of China (NSFC, No.81460093), the External Scientific and Technological Cooperation Programs of NingXia Hui Autonomous Region (2014ZYH65), and the National Basic Research Program of China (973 Program; #2011CB510200).

Additional information

Funding

This work was supported by grants from the National Natural Science Foundation of China (NSFC, No.81460093), the External Scientific and Technological Cooperation Programs of NingXia Hui Autonomous Region (2014ZYH65), and the National Basic Research Program of China (973 Program; #2011CB510200).

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