Advances in Clinical and Experimental Medicine
2020, vol. 29, nr 9, September, p. 1057–1063
doi: 10.17219/acem/125397
Publication type: original article
Language: English
License: Creative Commons Attribution 3.0 Unported (CC BY 3.0)
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Enzyme activity and genetic polymorphisms in patients with type II diabetes mellitus
1 Department of Biochemistry, Medical Faculty, Hatay Mustafa Kemal University, Turkey
2 Department of Biochemistry, Pharmacy Faculty, Mersin University, Turkey
3 Department of Medical Biology, Medical Faculty, Hatay Mustafa Kemal University, Turkey
4 Department of Biophysics, Medical Faculty, Mersin University, Turkey
5 Department of Gastroenterology, Samsun Training and Research Hospital, Turkey
Abstract
Background. Diabetes mellitus (DM) has become more and more common and has a high morbidity and mortality rate worldwide. It is a multifactorial chronic disease affected by both genetic and environmental factors.
Objectives. To evaluate the association between antioxidant enzyme activities and their genetic variations and the level of malondialdehyde (MDA) in type II diabetes patients living in the Adıyaman province in the southeast part of Turkey.
Material and Methods. One hundred patients diagnosed with type II DM (T2DM) and 100 healthy controls were included in the study. Malondialdehyde levels and antioxidant enzyme activities were measured spectrophometrically. DNA isolation was performed and genotyping was carried out using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP).
Results. Our results revealed no significant differences in genotype distributions and allele frequencies of all polymorphisms between groups (p > 0.05). Significantly elevated MDA levels and a significant reduction in catalase (CAT) and paraoxonase (PON) enzyme activities were observed in patients compared to the control group in terms of study groups and genetic variations (p < 0.05). Moreover, CAT activity was reduced in TT genotype in terms of CAT -262 C/T polymorphism in patients (p < 0.05). Paraoxonase activity was observed to be lower in MM genotype in both groups (p < 0.05).
Conclusion. CAT -262 C/T polymorphism may be one of the factors that lead to severe clinical situation in DM. Our results suggest that TT genotype may be more prone to lipid peroxidation.
Key words
diabetes mellitus, oxidative stress, cat, malondialdehyde, paraoxonase
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