Telomeres are complex structures at the end of linear chromosomes that protect the DNA from shortening down in size. Altough their role is not yet fully understood, telomeres have a significant impact on aging. With each cell division, the telomeres shorten to the point, where they become so short, that the cells can no longer divide. The shorter the telomeres become, the more susceptible individual becomes to diseases associated with aging, as well as diseases such as atherosclerosis, diabetes and others. Telomere shortening is also adversely affected by various factors, such as smoking, stress, inactive lifestyles, toxic environmental substances, obesity etc.
In this master’s thesis, we have studied the relationship between telomere length and polymorphisms in the methylenetetrahydrofolate reductase gene (MTHFR). For this purpose, the relative telomere length by monochromatic multiplex quantitative polymerase chain reaction was determined in 183 DNA samples from healthy subjects of two age groups (younger with average age of 23 years and older with average age of 57 years) isolated from whole blood. Competitive allele specific PCR (KASP PCR) was used to genotype the rs1801131 and rs1801133 in gene encoding methylenetetrahydrofolate reductase (MTHFR). With the statistical analysis, we then verified the relationship between the relative length of telomeres and the polymorphisms present. We also wanted to correlate telomere length regarding the gender and age of the subjects. We did not confirm an association between telomere length and selected factors, as the tests did not reach statistical significance. Although two previous studies had evaluated the relation of the telomere lenght and polymorphisms of the MTHFR gene, our study is the first to compare telomere length and MTHFR polymorphisms in both genders and in different age groups.
Our study is one of many that demonstrate the complexity of the telomere length managment and the lack of knowledge in this field, making drawing clinically relevant conclusions difficult. In order to better evaluate if MTHFR polymorphisms affect telomere shortening, longitudinal studies involving a larger number of subjects over a period of time and more extensive clinical data would be required. Data on dietary folate intake would be particularly important. In addition, several folate pathway genes could be included in the study.
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