Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/14969
Title: Distribution of MTHFR C677T Gene Polymorphism in Healthy North Macedonian Population
Authors: Brezovska Kavrakova, Julijana 
Tosheska Trajkovska, Katerina 
Kostovska, Irena 
Spasovski, Dejan 
Petkovska, Lidija 
Shubeska Stratrova, Slavica 
Keywords: mutation of methylentetrahydrofolate reductase
frequency
Macedonian population
Issue Date: Jul-2021
Publisher: Macedonian Association of Anatomists
Journal: Journal of Morphological Sciences
Abstract: Methylenetetrahydrofolate reductase (MTHFR) is a key enzyme of folate pathway and mutation of the enzyme methylentetrahydrofolate reductase MTHFR C677T gene. But whether it has influence on the level of total homocysteine is still under debate . Several polymorphisms have been reported in MTHFR gene, but C677T polymorphism is the most studied and it has been reported to be a risk factor for several diseases/disorders. Also, extensive studies have been conducted in various ethnic groups. The pre sent study was designed to explore the frequency of MTHFR C 677T polymorphism in North Macedonian healthy population. The study group consisted of 123 healthy subjects, benevolent blood donors, who were declared to be healthy by a medical doctor from the N ational Institute for Transfusion Medicine in R. N. Macedonia. The MTHFR gene polymorphism was analyzed by the polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP). Our analysis showed that the measurement of the population - genetic parameters of the allelic frequency at the T variable nucleotide had the allelic frequency 0.314. The global prevalence of TT genotype was Hardy - Weinberg's custom with a p value of 0.866, which was excluded from the p value of x 2 test. The remain ing parameters, however, indicated the genetically balanced population and they were important for the reliability of the analysis. In the M acedonian population the lowest frequency has the genotype TT and the highest has genotype CT
URI: http://hdl.handle.net/20.500.12188/14969
Appears in Collections:Faculty of Medicine: Journal Articles

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