Associations of Mthfr C677t Polymorphism With Insulin Resistance, Results of Nurse Study (Nursing Unacquainted Related Stress Etiologies) Publisher



Kheradmand M¹ ; Maghbooli Z² ; Salemi S³ ; Sanjari M^{4, 5} Show Affiliations
Source: Journal of Diabetes and Metabolic Disorders Published:2017

Abstract

Background: The insulin resistance syndrome is one of the major contributors of metabolic syndrome, diabetes Type 2 and atherosclerotic cardiovascular disease. A common mutation (677C to T; Ala to Val) in the methylenetetrahydrofolate reductase (MTHFR) gene is associated with decreased specific MTHFR activity and elevation of the homocysteine. The aim of this study is investigation of association between MTHFR 677C > T polymorphism with insulin resistance by using HOMA (Homeostasis Model Assessment) index in nurses who are potentially prone to develop insulin resistance because of unfavorable effects of shift work. Method: Nursing Unacquainted Related Stress Etiologies Study (Nurse Study) was conducted in five different educational hospitals of Tehran University of Medical Science (TUMS). The nurses aged 22-57 who have been referred by the matron were recruited. A self-administered questionnaire was completed. Anthropometric measurements including weight, height, waist and hip circumference in addition to blood pressure were measured. Insulin resistance and Insulin sensitivity were measured using the homeostatic model assessment (HOMA) and quantitative insulin sensitivity check index (QUICKI) respectively. The detection of MTHFR C677T polymorphism in exon four of MTHFR gene was performed by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis using HINFI restriction enzyme digestion. Result: A total of 273 subjects were recruited in the study. CT genotype were detected in 51.6% (129) subjects and CC and TT genotype were seen in 9.2% (25) and 35.2% (96) subjects respectively. Participants with TT genotype (9.65 ± 4.00) have significantly lower insulin level than participants with CT genotype (14.12 ± 15.34) (p-value: 0.01). The same significant difference was observed for HOMA index (p-value: 0.03). Result showed that HOMA is lower in subjects who are taking supplements. Conclusion: Result of this study showed subjects with TT genotype had significantly lower HOMA compare to CT genotype and the same pattern was seen for insulin level. We also found subjects taking supplement have lower HOMA compared to others regardless of their genotype. © 2017 The Author(s).