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Association between NF-kB polymorphism and age-related macular degeneration in a high-altitude population

OBJECTIVE: To investigate the association between the nuclear factor kappa B (NF-kB) gene polymorphism and age-related macular degeneration (AMD) in a high-altitude population. METHODS: Fifty-five patients with AMD and 57 control subjects were recruited from the Qinghai Provincial People’s Hospital,...

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Detalles Bibliográficos
Autores principales: Xin, Yan, Zefeng, Kang, Ling, Li, Ruijuan, Guan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186772/
https://www.ncbi.nlm.nih.gov/pubmed/34101738
http://dx.doi.org/10.1371/journal.pone.0251931
Descripción
Sumario:OBJECTIVE: To investigate the association between the nuclear factor kappa B (NF-kB) gene polymorphism and age-related macular degeneration (AMD) in a high-altitude population. METHODS: Fifty-five patients with AMD and 57 control subjects were recruited from the Qinghai Provincial People’s Hospital, China. Genomic DNA was extracted from the blood sample of each participant. Four NF-kB polymorphisms (rs3774959, rs3774932, rs3774937, and rs230526) were genotyped using a MassARRAY system. The genotype and allele frequencies were compared between the case and control groups using the chi-squared test or Fisher’s exact test. RESULTS: There was no significant difference in sex, age, hypertension, diabetes, blood lipid level or smoking and drinking status between the AMD and control groups (P > 0.05). The genotype distributions of four NF-kB polymorphisms were in accordance with Hardy-Weinberg equilibrium in the control group (P > 0.05). The frequencies of genotype AA of rs3774932 and genotype CC of rs3774937 were nominally significantly higher in the AMD group than in the control group (P = 0.046 and 0.023, respectively), although these associations did not survive the Bonferroni correction (corrected P > 0.05). Genotype distributions of rs3774959 and rs230526 were not significantly different between the two groups (P = 0.08 and 0.16, respectively). No significant difference in the allele frequencies of the four polymorphisms was found between the AMD and control groups (P > 0.05). CONCLUSIONS: Genotype AA of rs3774932 and genotype CC of rs3774937 in NF-kB might be risk factors for AMD.