COVID-19 БИЛАН КАСАЛЛАНГАН ЎЗБЕК БЕМОРЛАРИДА, КАСАЛЛИКНИНГ ОҒИРЛИК ДАРАЖАСИ ВА ГОМОЦИСТЕИН КОНЦЕНТРАЦИЯСИГА MTR ГЕНИ rs1805087, MTRR ГЕНИ rs1801394 ПОЛИМОРФИЗМЛАРИНИНГ БОҒЛИҚЛИГИ
Ключевые слова:
MTR, MTRR, rs1805087, rs1801394, ёввойи аллел, минор аллел фолат цикли, гипергомоцистеинемия, эндотелиал дисфункция.Аннотация
SARS-CoV-2 инфекцияси кўзғатган COVID-19 нинг энг оғир асоратларидан бири, гиперкоагулопатия индуцирлаган хаётий мухим органларни ишемик бузилиши хисобланиб, у сабабли COVID-19 билан касалланган беморларда ногиронлик ва ўлим холатлари кўплаб кузатилмоқда. Шу сабабли, гиперкоагулопатияга сабабчи бўлувчи факторларни чуқур ўрганиш орқали, бу паталогик жараёни ривожланишига мойиллиги бор беморларни саралаб олиб уларда махсус пролифактив ва терапевтик амалиётлар ўтказиш орқали юқорида келтирилган мажрухлик ва ўлим кўрсаткичларини камайтириш мумкин. Гиперкоагулопатияга сабаб бўлувчифакторлардан бири, бу тромбофил генлар хисобланганMTR ва MTRR генларини полиморфизмлари бўлиб, уларни COVID-19 билан касалланган ўзбек беморларида ўрганиш, бу генларнинг турли аллеларини шу ўрганилган беморларда гомоцистеин миқдорига ўзаро боғлиқлиги, хамда COVID-19 патогенезидаги қандай ахамиятга эга эканлигини тушунишга ёрдам бериши мумкин.
Библиографические ссылки
Brandalize AP, Bandinelli E, Borba JB, Félix TM, Roisenberg I, Schüler-Faccini L. Polymorphisms in genes MTHFR, MTR and MTRR are not risk factors for cleft lip/palate in South Brazil. Braz J Med Biol Res. 2007 Jun;40(6):787-91. doi: 10.1590/s0100-879x2006005000112. PMID: 17581676.
Armando D'Angelo, Jacob Selhub; Homocysteine and Thrombotic Disease. Blood 1997; 90 (1): 1–11. doi: https://doi.org/10.1182/blood.V90.1.1.
Vidmar Golja M, Šmid A, Karas Kuželički N, Trontelj J, Geršak K, Mlinarič-Raščan I. Folate Insufficiency Due to MTHFR Deficiency Is Bypassed by 5-Methyltetrahydrofolate. J Clin Med. 2020 Sep 2;9(9):2836. doi: 10.3390/jcm9092836. PMID: 32887268; PMCID: PMC7564482.
Zheng Y, Cantley LC. Toward a better understanding of folate metabolism in health and disease. J Exp Med. 2019 Feb 4;216(2):253-266. doi: 10.1084/jem.20181965. Epub 2018 Dec 26. PMID: 30587505; PMCID: PMC6363433.
Lu H, Stratton CW, Tang YW. Outbreak of pneumonia of unknown etiology in Wuhan, China: the mystery and the miracle // J. Med. Virol.-2020.-№92(4).-B.401–402
Zhu N.etal., ‘ANovelCoronavirusfromPatientswithPneumoniainChina, 2019’, N. Engl. J. Med., vol. 382, no. 8, pp. 727–733, Feb. 2020, doi: 10.1056/NEJMoa2001017
Lu R., Zhao X., Li J. et al. Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding. Lancet. 2020;395(10224):565-574; doi: 10.1016/S0140-6736(20)30251-8
Fu Y, Cheng Y, Wu Y. Understanding SARS-CoV-2-Mediated Inflammatory Responses: From Mechanisms to Potential Therapeutic Tools. Virol Sin. 2020;35(3):266-271. doi:10.1007/s12250-020-00207-4
Savla SR, Prabhavalkar KS, Bhatt LK. Cytokine storm associated coagulation complications in COVID-19 patients: Pathogenesis and Management. Expert Rev Anti Infect Ther. 2021;19(11):1397-1413. doi:10.1080/14787210.2021.1915129.
Ludwig ML, Matthews RG. Structure-based perspectives on B12-dependent enzymes. Annu Rev Biochem 1997; 66: 269-313.
Laraqui A, Allami A, Carrié A, Coiffard AS, Benkouka F, Benjouad A, Bendriss A, Kadiri N, Bennouar N, Benomar A, Guedira A, Raisonnier A, Fellati S, Srairi JE, Benomar M. Influence of methionine synthase (A2756G) and methionine synthase reductase (A66G) polymorphisms on plasma homocysteine levels and relation to risk of coronary artery disease. Acta Cardiol. 2006 Feb;61(1):51-61. doi: 10.2143/AC.61.1.2005140. PMID: 16485733.
Chen J., Stampfer M.J., Ma J., Selhub J., Malinow M.R., HennekensC.H.. et al. (2001) Influence of a methionine synthase (D919G) polymorphism on plasma homocysteine and folate levels and relation to risk of myocardial infarction. Atherosclerosis 154, 667–672 10.1016/S0021-9150(00)00469-X
Ma LM, Yang HP, Yang XW, Ruan LH. Methionine synthase A2756G polymorphism influences pediatric acute lymphoblastic leukemia risk: a meta-analysis. Biosci Rep. 2019 Jan 15;39(1):BSR20181770. doi: 10.1042/BSR20181770. PMID: 30559146; PMCID: PMC6331679.
Al Farra HY. Methionine synthase polymorphisms (MTR 2756 A>G and MTR 2758 C>G) frequencies and distribution in the Jordanian population and their correlation with neural tube defects in the population of the northern part of Jordan. Indian J HumGenet. 2010 Sep;16(3):138-43. doi: 10.4103/0971-6866.73405. PMID: 21206701; PMCID: PMC3009424.
Hobbs C.A., Sherman S.L., Yi P., Hopkins S.E.,Torfs C.P., Hine R.J., Pogribna M., Rozen R., James S.J.Polymorphisms in Genes Involved in Folate Metabolismas Maternal Risk Factors for Down syndrome // Am. J.Hum.Genet.2000.Vol.67,№3.P.623–630.doi:10.1086/303055OhrvikVE.
Susan J. Duthie, Sabrina Narayanan, Gillian M. Brand, Lynn Pirie, George Grant, Impact of Folate Deficiency on DNA Stability, The Journal of Nutrition, Volume 132, Issue 8, August 2002, Pages 2444S–2449S, https://doi.org/10.1093/jn/132.8.2444S
Miller AL. The methylation, neurotransmitter, and antioxidant connections between folate and depression. Altern Med Rev. 2008 Sep;13(3):216-26. PMID: 18950248.
Kronenberg G, Harms C, Sobol RW, Cardozo-Pelaez F, Linhart H, Winter B, Balkaya M, Gertz K, Gay SB, Cox D, Eckart S, Ahmadi M, Juckel G, Kempermann G, Hellweg R, Sohr R, Hörtnagl H, Wilson SH, Jaenisch R, Endres M. Folate deficiency induces neurodegeneration and brain dysfunction in mice lacking uracil DNA glycosylase. J Neurosci. 2008 Jul 9;28(28):7219-30. doi: 10.1523/JNEUROSCI.0940-08.2008. PMID: 18614692; PMCID: PMC3844834.
Diane M. Ward, Opal S. et al. Altered sterol metabolism in budding yeast affects mitochondrial iron–sulfur (Fe-S) cluster synthesis Received for publication, January 5, 2018, and in revised form, May 11, 2018. DOI 10.1074/jbc.RA118.001781 Cox 2018 Ward et al. Published under exclusive license by The American Society for Biochemistry and Molecular Biology, Inc.
Shi S, Qin M, Shen B, et al. Association of Cardiac Injury With Mortality in Hospitalized Patients With COVID-19 in Wuhan, China [published online ahead of print, 2020 Mar 25]. JAMACardiol. 2020;e200950. doi:10.1001/jamacardio.2020.0950.
Фетисова И.Н. Полиморфизм генов фолатногоцикла и болезни человека // Вестник Ивановской медицинскойакадемии.2006.Т.11,№1-2.С.77–82
Доброхотова Ю.Э., Джобава Э.М., АминтаеваЛ.А., Алиева А.Н., Артизанова А.П., Болкунова Н.В. Эндотелиальнаядисфункция:гомоцистеин и оксид азота у беременных групп высокого риска. Современные подходы к терапии. Роль фолиевой кислоты//Проблемы репродукции. 2010.T.16,№6.С.98–103
Yakub M, Moti N, Parveen S, Chaudhry B, Azam I, Iqbal MP. Polymorphisms in MTHFR, MS and CBS genes and homocysteine levels in a Pakistani population. PLoS One. 2012;7(3):e33222. doi: 10.1371/journal.pone.0033222. Epub 2012 Mar 21. PMID: 22470444; PMCID: PMC3310006.
Caccamo D, Gorgone G, Currò M, Parisi G, Di Iorio W, Menichetti C, Belcastro V, Parnetti L, Rossi A, Pisani F, Ientile R, Calabresi P. Effect of MTHFR polymorphisms on hyperhomocysteinemia in levodopa-treated Parkinsonian patients. Neuromolecular Med. 2007;9(3):249-54. doi: 10.1007/s12017-007-8006-x. PMID: 17914182.
Lucock M. Folic Acid: Nutritional Biochemistry, Molecular Biology, and Role in Disease Processes. Mol. Genet. Metab. 2000;71:121–138. doi: 10.1006/mgme.2000.3027.
Eloranta J.J., Zaïr Z.M., Hiller C., Häusler S., Stieger B., Kullak-Ublick G.A. Vitamin D3 and its nuclear receptor increase the expression and activity of the human proton-coupled folate transporter. Mol. Pharmacol. 2009;76:1062–1071. doi: 10.1124/mol.109.055392.
Gropper S.S., Smith J.L. Advanced Nutrition and Human Metabolism. 7th ed. Cengage Learning; Belmont, CA, USA: 2017.
Ikizler T.A. A Patient with CKD and Poor Nutritional Status. Clin. J. Am. Soc. Nephrol. 2013;8:2174–2182. doi: 10.2215/CJN.04630513.
Meisel E, Efros O, Bleier J, Beit Halevi T, Segal G, Rahav G, Leibowitz A, Grossman E. Folate Levels in Patients Hospitalized with Coronavirus Disease 2019. Nutrients. 2021 Mar 2;13(3):812. doi: 10.3390/nu13030812. PMID: 33801194; PMCID: PMC8001221.