Articles | Open Access | DOI: https://doi.org/10.37547/TAJMSPR/Volume03Issue06-07

The Role Of rs1799883 Polymorphism Of The FABP2 Gene In The Pathogenesis Of Nosological Syntropy Of Gallstone Disease And Metabolic Syndrome

Raximov Anvar Pulatboevich , Assistant, Urgench Branch Of The Tashkent Medical Academy, Urgench, Uzbekistan
Ismailov O’ktam Safaevich , Doctor Of Medical Sciences, Professor, Tashkent Medical Academy, Tashkent, Uzbekistan
Batirov Davronbek Yusupovich , Candidate Of Medical Sciences, Associate Professor, Urgench Branch Of The Tashkent Medical Academy, Urgench, Uzbekistan

Abstract

Objective: to study the role of the rs1799883 polymorphism of the FABP2 gene in the pathogenesis of gallstone disease in combination with MS. Material and methods. Molecular genetic studies were carried out in the Department of Molecular Medicine and Cell Technologies of the RSNPMC Hematology.

The analysis of the associations of the rs1799883 polymorphisms of the FABP2 gene was carried out using a case-control model.

The main group consisted of 118 patients with cholelithiasis in combination with MS living in the Khorezm region.

Results: As a result of our research, we identified a significant association of the homozygous genotype for the Thr allele with the development of gallstone disease in combination with MS. The indicator of the ratio of the chances of developing gallstone disease in combination with MS in carriers of this genotype was OR = 2.9 at 95% CI: 1.122- 7.424. The relative risk of disease was RR = 2.5 with 95% CI: 1.11-5.76.

Conclusion: Our results allow us to conclude that the homozygous Thr/Thr genotype plays an important role in the formation of gallstone disease and obesity in people of Uzbek nationality.

Keywords

Gallstone disease, metabolic syndrome, FABP2, Ala54Thr, polymorphism, gene, allele, genotype, pathogenesis, obesity

References

Akhmedov, V.A., & Gaus, O.V. (2019). Modern ideas about the mechanisms of development and management tactics of patients with cholelithiasis associated with metabolic syndrome. Medical Alphabet, 2 (13), 52-56.

Dorofeeva S.G., Konoplya E.N., Mansimova O.V., Shelukhina A.N., Anyushonkov O.S. (2020). Cholelithiasis: modern concepts of aetiology and pathogenesis. Integrative trends in medicine and education. 2. pp. 21-25.

Zelenskaya, E.M., Koh, N.V., Slepukhina, A.A., & Lifshits, G.I. (2017). Nutrigenetic test in clinical practises: goals and opportunities. Clinical practice, (3 (31)).

Sagdatova, A. A., Zulkarneev, R. Kh., Khusnutdinova, E. K., Nurgalieva, A. Kh., & Zagidullin, Sh. Z. (2017). Multifactorial clinical and genetic model of the development of gallstone disease. Practical medicine, (6 (107)).

Khokhlacheva, N.A., Kosareva, T.S., & Lukashevich, A.P. (2020). New approaches to the study of the prevalence of gallstone disease. Archive of Internal Medicine, 10 (4 (54)).

Shutova, E. V. (2016). Apolipoprotein e gene polymorphism and lipid metabolism disorders in children with cholelithiasis. Child health, (5 (73)).

Baratta, F., Pastori, D., Cocomello, N., Colantoni, A., Ferro, D., Angelico, F., & Del Ben, M. (2021). Sex-Related Differences in the Association between Metabolic Syndrome and Gallstone Disease. International journal of environmental research and public health, 18(4), 1958.

Chauhan, T., Mittal, R. D., & Mittal, B. (2020). Association of Common Single Nucleotide Polymorphisms of Candidate Genes with Gallstone Disease: A Meta-Analysis. Indian Journal of Clinical Biochemistry, 35(3), 290-311.

Li, L., Qiao, X., Wang, X., Liu, D., Xue, Q., Han, L., ... & Yang, J. (2019). The association between apolipoprotein E and gallstone disease: an updated meta-analysis. BMC medical genetics, 20(1), 1-9.

Sheng, B., Zhao, Q., Ma, M., & Zhang, J. (2020). An inverse association of weight and the occurrence of asymptomatic gallbladder stone disease in hypercholesterolemia patients: a case-control study. Lipids in Health and Disease, 19(1), 1-10.

Stender, S., Frikke-Schmidt, R., Benn, M., Nordestgaard, B. G., & Tybjærg-Hansen, A. (2013). Low-density lipoprotein cholesterol and risk of gallstone disease: a Mendelian randomization study and meta-analyses. Journal of hepatology, 58(1), 126-133.

Zhang, H., Wu, J., & Yu, L. (2014). Association of Gln27Glu and Arg16Gly polymorphisms in Beta2-adrenergic receptor gene with obesity susceptibility: a meta-analysis. PLoS One, 9(6), e100489.

Бородина, С. В., Гаппарова, К. М., Зайнудинов, З. М., & Григорьян, О. Н. (2016). Генетические предикторы развития ожирения. Ожирение и метаболизм, 13(2).

Feher Turkovic, L., Pizent, A., Dodig, S., Pavlovic, M., & Pasalic, D. (2012). FABP 2 gene polymorphism and metabolic syndrome in elderly people of Croatian descent. Biochemia Medica, 22(2), 217-224.

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Pulatboevich, R. A. ., Safaevich, I. O. ., & Yusupovich, B. D. . (2021). The Role Of rs1799883 Polymorphism Of The FABP2 Gene In The Pathogenesis Of Nosological Syntropy Of Gallstone Disease And Metabolic Syndrome. The American Journal of Medical Sciences and Pharmaceutical Research, 3(06), 46–51. https://doi.org/10.37547/TAJMSPR/Volume03Issue06-07