METABOLISM AND OBESITY: ROLE OF LEPTIN RECEPTOR GENE

Background. Currently more than 119 obesity-related polymorphisms is known to participate in adult obesity. One of them is LEPR Q223R. Many researches shown association of this polymorphism with adult obesity. However, the role of LEPR Q223R in adolescent overweight and obesity is the matter of disp...

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Veröffentlicht in:Acta biomedica scientifica 2017-11, Vol.2 (5), p.56-62
Hauptverfasser: Иевлева, Ксения, Ievleva, Kseniya, Баирова, Татьяна, Bairova, Tatyana, Рычкова, Любовь, Rychkova, Lyubov, Шенеман, Екатерина, Sheneman, Ekaterina, Храмова, Елена, Hramova, Elena, Колесникова, Любовь, Kolesnikova, Lyubov
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Sprache:eng
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Zusammenfassung:Background. Currently more than 119 obesity-related polymorphisms is known to participate in adult obesity. One of them is LEPR Q223R. Many researches shown association of this polymorphism with adult obesity. However, the role of LEPR Q223R in adolescent overweight and obesity is the matter of dispute. Aim: to determine association of polymorphism Q223R of LEPR gene with some biochemical and hormonal measurements of blood in female adolescents with normal weight and with overweight and obesity. Materials and methods. A total of 103 female adolescents (14-17 years of age) was examined. All girls were divided into 2 groups: 43 girls with normal weight (SDS BM 10.311 ± 0.585), and 65 girls with overweight and obesity (SDS BMI 2.255± 0.739) (р < 0.0001). Height, weight, BM1, SDS BM1 were measured. Laboratory tests included triglycerides, total cholesterol and its fraction, TTH, free thyroxin and leptin. All girls were genotyped on carrier of LEPR Q223R. Statistical analysis was provided by software Statistica 8.0 using nonparametric Mann - Whitney methods and Chi-square test with Yates correction. Results. Significant association of carrying RR-genotype with increase of SDS BM1 (p = 0.006), THS (p = 0.006) and decrease of free thyroxin was shown in control group. Conclusion. Our results showed the association of R-allele with increase of SDS BM1, THS and decrease T4 free in control group.
ISSN:2541-9420
2587-9596
DOI:10.12737/article_59e85cb55584e4.51145791