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Transferrin receptor levels and polymorphism of its gene in age-related macular degeneration
Author(s) -
Daniel Wysokiński,
Katarzyna Danisz,
Elżbieta Pawłowska,
Mariola Dorecka,
Dorota Romaniuk,
Jacek Robaszkiewicz,
Marta Szaflik,
Jerzy Szaflik,
Janusz Błasiak,
Jacek P. Szaflik
Publication year - 2015
Publication title -
acta biochimica polonica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.452
H-Index - 78
eISSN - 1734-154X
pISSN - 0001-527X
DOI - 10.18388/abp.2014_843
Subject(s) - transferrin , genotype , transferrin receptor , macular degeneration , allele , polymorphism (computer science) , biology , medicine , gene polymorphism , genetics , soluble transferrin receptor , endocrinology , gene , iron deficiency , iron status , anemia , ophthalmology
The aim of the present study was to investigate the association of age related macular degeneration (AMD) risk with some aspects of iron homeostasis: iron concentration in serum, level of soluble transferrin receptor (sTfR), and transferrin receptor (TFRC) genetic variability. Four hundred and ninety one AMD patients and 171 controls were enrolled in the study. Restriction fragment length polymorphism PCR was employed to genotype polymorphisms of the TFRC gene, and colorimetric assays were used to determine the level of iron and sTfR. Multiple logistic regression was applied for all genotype/allele-related analyses and the ANOVA test for iron and sTfR serum level comparison. We found that the genotypes and alleles of the c.-253G > A polymorphism of the TFRC gene were associated with AMD risk and this association was modulated by smoking status, AMD family history, living environment (rural/urban), body mass index and age. The levels of sTfR was higher in AMD patients than controls, whereas concentrations of iron did not differ in these two groups. No association was found between AMD occurrence and the p.Gly142Ser polymorphism of the TRFC gene. The results obtained suggest that transferrin receptor and variability of its gene may influence AMD risk.

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