87 — 9 (47) 2022 — Ismailov O.S., Batirov D.Yu., Rakhimov A.P., Azadov B.R., Yusupov D.D., MOLECULAR GENETIC INTERRELATION OF GALLSTONE DISEASE AND METABOLIC SYNDROME
MOLECULAR GENETIC INTERRELATION OF GALLSTONE DISEASE AND METABOLIC SYNDROME
Ismailov O.S., Ministry of Health of the Republic of Uzbekistan. Office of science and educational institutions.
Batirov D.Yu., Urgench branch of the Tashkent Medical Academy
Rakhimov A.P., Urgench branch of the Tashkent Medical Academy
Azadov B.R., Urgench branch of the Tashkent Medical Academy
Yusupov D.D., Urgench branch of the Tashkent Medical Academy
Resume
This research work was carried out on the basis of the Department of Faculty and Hospital Surgery of the Urgench branch of the Tashkent Medical Academy in the surgical departments of the Khorezm Regional Diversified Medical Center based on clinical analysis and diagnostic results of patients with cholelithiasis with MS and cholelithiasis without metabolic disorders. Molecular genetic studies were carried out in the Department of Molecular Medicine and Cell Technologies of the RSNPMC of Hematology. Association analysis of the rs1042713 and rs1042714 polymorphisms of the ADRB2 gene was carried out using a case-control model.
The results obtained by the authors allow us to conclude that the homozygous Glu/Glu genotype plays an important role in the pathogenesis of nosological syntropy of cholelithiasis and metabolic syndrome. The risk of developing cholelithiasis with MS when carrying this genotypic variant of the ADRB2 gene can significantly increase by more than 3.5 times. The homozygous Gln/Gln genotype indicates a protective effect in the formation of cholelithiasis with a combination of MS.
Polymorphism rs 1042713 of the ADRB2 gene does not allow the use of this locus as a genetic marker for predicting the risk of developing MS in patients with cholelithiasis.
Keywords: molecular genetic relationship of cholelithiasis, metabolic syndrome, Glu/Glu homozygous genotype, ADRB2 genotypic variant
First page
514
Last page
519
For citation: Ismailov O.S., Batirov D.Yu., Rakhimov A.P., Azadov B.R., Yusupov D.D., MOLECULAR GENETIC INTERRELATION OF GALLSTONE DISEASE AND METABOLIC SYNDROME //New Day in Medicine 9 (47)2022 514-519 https://l.clck.bar/b5281
LIST OF REFERENCES:
- Ахмедов В.А., Гаус О.В. Современные представления о механизмах развития и тактике ведения больных желчнокаменной болезнью, ассоциированной с метаболическим синдромом. // Медицинский алфавит. – 2019. – № 2(13). – С. 52-56
- Дорофеева С.Г., Конопля Е.Н., Мансимова О.В., Шелухина А.Н., Анюшонков О.С. Желчнокаменная болезнь: современные представления об этиологии и патогенезе // Интегративные тенденции в медицине и образовании. – 2020. – Т. 2. С. 21-25.
- Зеленская Е.М., Кох Н.В., Слепухина А.А., Лифшиц Г.И. Нутригенетический тест в клинической практике: цели и возможности // Клиническая практика. – 2017. – № 3 (31). – С. 76-82.
- Сагдатова А.А., Зулкарнеев Р.Х., Хуснутдинова Э.К., Нургалиева А.Х., Загидуллин Ш.З. Многофакторная клинико-генетическая модель развития желчнокаменной болезни // Практическая медицина. – 2017. – № 6 (107). – С.108-112.
- Хохлачева Н.А., Косарева Т.С., Лукашевич А.П. Новые подходы в изучении распространенности желчнокаменной болезни // Архив внутренней медицины. – 2020. – Т. 10, №4 (54). – С.281-287.
- Baratta F., Pastori D., Cocomello N., Colantoni A., Ferro D., Angelico F., Del Ben M. Sex-Related Differences in the Association between Metabolic Syndrome and Gallstone Disease. // Int J Environ Res Public Health. 2021 Feb 18;18(4):1958.
- Chauhan T., Mittal R.D., Mittal B. Association of Common Single Nucleotide Polymorphisms of Candidate Genes with Gallstone Disease: A Meta-Analysis. // Indian J ClinBiochem. 2020 Jul;35(3):290-311.
- Li L., Qiao X., Wang X., Liu D., Xue Q., Han L., Dai F., Ma G., Yang Z., Zhang T., Yang S., Cai S., Gao M., Yang J. The association between apolipoprotein E and gallstone disease: an updated meta-analysis. // BMC Med Genet. 2019 Jun 14;20(1):109.
- Sheng B., Zhao Q., Ma M., Zhang J. An inverse association of weight and the occurrence of asymptomatic gallbladder stone disease in hypercholesterolemia patients: a case-control study. // Lipids Health Dis. 2020 Oct 23;19(1):228.
- Stender S., Frikke-Schmidt R., Benn M., Nordestgaard B.G., Tybjærg-Hansen A. Low-density lipoprotein cholesterol and risk of gallstone disease: a Mendelian randomization study and meta-analyses. // J Hepatol. 2013 Jan;58(1):126-33.
- Zhang H., Wu J., Yu L. Association of Gln27Glu and Arg16Gly polymorphisms in Beta2-adrenergic receptor gene with obesity susceptibility: a meta-analysis. PLoS One. 2014 Jun 24;9(6):e100489. doi: 10.1371/journal.pone.0100489. PMID: 24960039; PMCID: PMC4069060
- Borodina S.V., Gapparova K.M., Zainudinov Z.M., Grigorian O.N. Genetic predictors of obesity development. // Obesity and metabolism. 2016; 13(2):7-13. doi: 10.14341/OMET201627-13.
- Mihai S. Jalba George G. Rhoads Kitaw Demissie. Association of Codon 16 and Codon 27 β2‐Adrenergic Receptor Gene Polymorphisms with Obesity: A Meta‐analysis. First published: 06 September 2012 https://doi.Org/10.1038/oby.2008.327Citations: 41 2098 vol. 16 № 9 | september 2008 | www.obesityjournal.org.
- Jalba M.S., Rhoads G.G., Demissie K. (2008) Ассоциация полиморфизмов гена бета 2-адренорецептора кодона 16 и кодона 27 с ожирением: метаанализ. Ожирение (Серебряная весна) 16 : 2096–2106. [ PubMed ] [ Google Scholar.