<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">medgen</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинская генетика</journal-title><trans-title-group xml:lang="en"><trans-title>Medical Genetics</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2073-7998</issn><publisher><publisher-name>Publishing House «Genius Media» LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.25557/2073-7998.2026.01.3-11</article-id><article-id custom-type="elpub" pub-id-type="custom">medgen-3372</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>НАУЧНЫЙ ОБЗОР</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEW</subject></subj-group></article-categories><title-group><article-title>Генетический полиморфизм системы метаболизма этанола</article-title><trans-title-group xml:lang="en"><trans-title>Genetic polymorphism of the ethanol metabolism system</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Иванова</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Ivanova</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>630089, г.  Новосибирск, ул. Б. Богаткова, д. 175/1</p></bio><bio xml:lang="en"><p>175/1, B. Bogatkova st., Novosibirsk, 630089</p></bio><email xlink:type="simple">ivanova_a_a@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Максимов</surname><given-names>В. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Maksimov</surname><given-names>V. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>630089, г.  Новосибирск, ул. Б. Богаткова, д. 175/1</p></bio><bio xml:lang="en"><p>175/1, B. Bogatkova st., Novosibirsk, 630089</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Научно-исследовательский институт терапии и профилактической медицины – филиал ФГБНУ «Федеральный исследовательский центр Институт цитологии и генетики Сибирского отделения Российской академии наук»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Research Institutе of Internal and Preventive Medicine −Branch of the  &#13;
Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2026</year></pub-date><pub-date pub-type="epub"><day>09</day><month>02</month><year>2026</year></pub-date><volume>25</volume><issue>1</issue><fpage>3</fpage><lpage>11</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Иванова А.А., Максимов В.Н., 2026</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="ru">Иванова А.А., Максимов В.Н.</copyright-holder><copyright-holder xml:lang="en">Ivanova A.A., Maksimov V.N.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.medgen-journal.ru/jour/article/view/3372">https://www.medgen-journal.ru/jour/article/view/3372</self-uri><abstract><p>Чрезмерное употребление алкоголя является этиологическим фактором развития алкогольного поражения печени (алкогольный стеатогепатит, алкогольный цирроз печени), а также фактором риска обострений ряда заболеваний печени и желудочно-кишечного тракта, как приобретенных (гепатит, цирроз печени вирусной этиологии, панкреатит и т.д.), так и генетически обусловленных (синдром Жильбера, поражение печени при альфа-1-антитрипсиновой недостаточности, муковисцидозе и др.). Основной путь метаболизма этанола в организме человека − оксидативный путь алкогольдегидрогеназы и альдегиддегидрогеназы. Гены, кодирующие ферменты данного пути, обладают значительным полиморфизмом, что приводит к разной степени активности ферментов как у отдельных индивидуумов, так и у целых этнических групп. Обзор посвящен современным исследованиям и актуальным представлениям о метаболизме этилового спирта и вариантах нуклеотидной последовательности, которые могут повлиять на него.</p></abstract><trans-abstract xml:lang="en"><p>Excessive alcohol consumption is an etiologic factor in the development of alcoholic liver disease (alcoholic steatohepatitis, alcoholic liver cirrhosis), as well as a risk factor for exacerbations of a number of liver and gastrointestinal diseases, both acquired (hepatitis, viral liver cirrhosis, pancreatitis, etc.) and genetically determined (Gilbert’s syndrome, liver damage in alpha-1-antitrypsin deficiency, cystic fibrosis, etc.). The main pathway of ethanol metabolism in the human body is the oxidative pathway of alcohol dehydrogenase and aldehyde dehydrogenase. The genes encoding the enzymes of this pathway have significant polymorphism, which leads to different degrees of enzyme activity both among individuals and among entire ethnic groups. The review is devoted to modern research and current ideas about the metabolism of ethyl alcohol and nucleotide variants that can affect it. </p></trans-abstract><kwd-group xml:lang="ru"><kwd>ADH</kwd><kwd>ALDH</kwd><kwd>цирроз</kwd><kwd>этиловый спирт</kwd><kwd>однонуклеотидный вариант</kwd><kwd>ADH1B</kwd><kwd>ADH1C</kwd><kwd>ALDH2</kwd></kwd-group><kwd-group xml:lang="en"><kwd>ADH</kwd><kwd>ALDH</kwd><kwd>cirrhosis</kwd><kwd>ethyl alcohol</kwd><kwd>single nucleotide variant</kwd><kwd>ADH1B</kwd><kwd>ADH1C</kwd><kwd>ALDH2</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Литературный обзор подготовлен в рамках государственного задания FWNR-2024-0004</funding-statement><funding-statement xml:lang="en">The review was prepared within the framework of state assignment FWNR-2024-0004.</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Im P.K., Wright N., Yang L. et аl. Alcohol consumption and risks of more than 200 diseases in Chinese men. Nat Med. 2023;29(6):14761486. https://doi.org/10.1038/s41591-023-02383-8.</mixed-citation><mixed-citation xml:lang="en">Im P.K., Wright N., Yang L. et аl. Alcohol consumption and risks of more than 200 diseases in Chinese men. Nat Med. 2023;29(6):14761486. https://doi.org/10.1038/s41591-023-02383-8.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Paquot N. Le métabolisme de l’alcool [The metabolism of alcohol]. Rev Med Liege. 2019;74(5-6):265-267.</mixed-citation><mixed-citation xml:lang="en">Paquot N. Le métabolisme de l’alcool [The metabolism of alcohol]. Rev Med Liege. 2019;74(5-6):265-267.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Kubiak-Tomaszewska G., Tomaszewski P., Pachecka J. et аl. Molecular mechanisms of ethanol biotransformation: enzymes of oxidative and nonoxidative metabolic pathways in human. Xenobiotica. 2020;50(10):1180-1201. https://doi.org/10.1080/00498254.2020.1761571.</mixed-citation><mixed-citation xml:lang="en">Kubiak-Tomaszewska G., Tomaszewski P., Pachecka J. et аl.  Molecular mechanisms of ethanol biotransformation: enzymes of oxidative and nonoxidative metabolic pathways in human. Xenobiotica. 2020;50(10):11801201. https://doi.org/10.1080/00498254.2020.1761571.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Hyun J., Han J., Lee C. et аl. Pathophysiological Aspects of Alcohol Metabolism in the Liver. Int J Mol Sci. 2021;22(11):5717. https://doi.org/10.3390/ijms22115717.</mixed-citation><mixed-citation xml:lang="en">Hyun J., Han J., Lee C. et аl. Pathophysiological Aspects of Alcohol Metabolism in the Liver. Int J Mol Sci. 2021;22(11):5717. https://doi.org/10.3390/ijms22115717.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Cederbaum A.I. Alcohol metabolism. Clin Liver Dis. 2012;16(4):667-85. https://doi.org/10.1016/j.cld.2012.08.002.</mixed-citation><mixed-citation xml:lang="en">Cederbaum A.I. Alcohol metabolism. Clin Liver Dis. 2012;16(4):667-85. https://doi.org/10.1016/j.cld.2012.08.002.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">dbGene. ADH1A alcohol dehydrogenase 1A (class I), alpha polypeptide [ Homo sapiens (human) ]. [Internet]. Available from: https://www.ncbi.nlm.nih.gov/gene/124</mixed-citation><mixed-citation xml:lang="en">dbGene. ADH1A alcohol dehydrogenase 1A (class I), alpha polypeptide [ Homo sapiens (human) ]. [Internet]. Available from: https://www.ncbi.nlm.nih.gov/gene/124</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">dbGene. ADH1B alcohol dehydrogenase 1B (class I), beta polypeptide [ Homo sapiens (human) ]. [Internet]. Available from: https://www.ncbi.nlm.nih.gov/gene/125</mixed-citation><mixed-citation xml:lang="en">dbGene. ADH1B alcohol dehydrogenase 1B (class I), beta polypeptide [ Homo sapiens (human) ]. [Internet]. Available from: https://www.ncbi.nlm.nih.gov/gene/125</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">dbGene. ADH1C alcohol dehydrogenase 1C (class I), gamma polypeptide [ Homo sapiens (human) ]. [Internet]. Available from: https://www.ncbi.nlm.nih.gov/gene/126</mixed-citation><mixed-citation xml:lang="en">dbGene. ADH1C alcohol dehydrogenase 1C (class I), gamma polypeptide [ Homo sapiens (human) ]. [Internet]. Available from: https://www.ncbi.nlm.nih.gov/gene/126</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">dbGene. ADH4 alcohol dehydrogenase 4 (class II), pi polypeptide [ Homo sapiens (human) ]. [Internet]. Available from: https://www. ncbi.nlm.nih.gov/gene/127</mixed-citation><mixed-citation xml:lang="en">dbGene. ADH4 alcohol dehydrogenase 4 (class II), pi polypeptide [ Homo sapiens (human) ]. [Internet]. Available from:   https://www. ncbi.nlm.nih.gov/gene/127</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">dbGene. ADH5 alcohol dehydrogenase 5 (class III), chi polypeptide [ Homo sapiens (human) ]. [Internet]. Available from: https://www. ncbi.nlm.nih.gov/gene/128</mixed-citation><mixed-citation xml:lang="en">dbGene. ADH5 alcohol dehydrogenase 5 (class III), chi polypeptide [ Homo sapiens (human) ]. [Internet]. Available from:   https://www.ncbi.nlm.nih.gov/gene/128</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">dbGene. ADH7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide [ Homo sapiens (human) ]. [Internet]. Available from: https://www.ncbi.nlm.nih.gov/gene/131</mixed-citation><mixed-citation xml:lang="en">dbGene. ADH7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide [ Homo sapiens (human) ]. [Internet]. Available from: https://www.ncbi.nlm.nih.gov/gene/131</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">dbGene. ADH6 alcohol dehydrogenase 6 (class V) [ Homo sapiens (human) ]. [Internet]. Available from: https://www.ncbi.nlm.nih.gov/gene/130</mixed-citation><mixed-citation xml:lang="en">dbGene. ADH6 alcohol dehydrogenase 6 (class V) [ Homo sapiens (human) ]. [Internet]. Available from:  https://www.ncbi.nlm.nih.gov/gene/130</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">dbGene. ALDH1B1 aldehyde dehydrogenase 1 family member B1 [ Homo sapiens (human) ]. [Internet]. Available from: https://www.ncbi.nlm.nih.gov/gene/219</mixed-citation><mixed-citation xml:lang="en">dbGene. ALDH1B1 aldehyde dehydrogenase 1 family member B1 [ Homo sapiens (human) ]. [Internet]. Available from:   https://www.ncbi.nlm.nih.gov/gene/219</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">dbGene. ALDH2 aldehyde dehydrogenase 2 family member [ Homo sapiens (human) ]. [Internet]. Available from: https://www.ncbi.nlm.nih.gov/gene/217</mixed-citation><mixed-citation xml:lang="en">dbGene. ALDH2 aldehyde dehydrogenase 2 family member [ Homo sapiens (human) ]. [Internet]. Available from:   https://www.ncbi.nlm.nih.gov/gene/217</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">dbGene. ALDH1A1 aldehyde dehydrogenase 1 family member A1 [ Homo sapiens (human) ]. [Internet]. Available from: https://www.ncbi.nlm.nih.gov/gene/216</mixed-citation><mixed-citation xml:lang="en">dbGene. ALDH1A1 aldehyde dehydrogenase 1 family member A1 [ Homo sapiens (human) ]. [Internet]. Available from:  https://www.ncbi.nlm.nih.gov/gene/216</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Genome Aggregation Database. [Internet]. Available from: https:// gnomad.broadinstitute.org/</mixed-citation><mixed-citation xml:lang="en">Genome Aggregation Database. [Internet]. Available from:  https://gnomad.broadinstitute.org/</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Долинина Д.О., Солопекин Н.В., Толстикова А.В., Щетинина А.Ю. Этнотерриториальные вариации характера распределения генов биотрансформации этанола в популяциях тюркоязычных народов Западной Сибири. Медицинская генетика. 2016; 15(4): 32-35.</mixed-citation><mixed-citation xml:lang="en">Dolinina D.O., Solopekin N.V., Tolstikova A.V., Shchetinina A.Y. Etnoterritorial’nyye variatsii kharaktera raspredeleniya genov biotransformatsii etanola v populyatsiyakh tyurkoyazychnykh narodov Zapadnoy Sibiri [Ethnoterritorial variations of character distribution genes of ethanol’s biotransformation in turkic peoples of Western Siberia]. Meditsinskaya genetika [Medical Genetics]. 2016;15(4):32-35. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Марусин А.В., Степанов В.А., Спиридонова М.Г. и др. Ассоциации генетического полиморфизма этанол-метаболизирующих ферментов ADH1B, ADH7 и CYP2E1 с алкоголизмом и с риском развития коронарного атеросклероза в русской популяции. Генетика человека и патология. 2004; 7:118-125.</mixed-citation><mixed-citation xml:lang="en">Marusin A.V., Stepanov V.A., Spiridonova M.G., et al. Assotsiatsii geneticheskogo polimorfizma etanol-metaboliziruyushchikh fermentov ADH1B, ADH7 i CYP2E1 s alkogolizmom i s riskom razvitiya koronarnogo ateroskleroza v russkoy populyatsii [Associations of genetic polymorphism of ethanol-metabolizing enzymes ADH1B, ADH7, and CYP2E1 with alcoholism and the risk of coronary atherosclerosis in the Russian population]. Genetika cheloveka i patologiya [Human Genetics and Pathology]. 2004; 7:118-125. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Edenberg H.J., McClintick J.N.. Alcohol Dehydrogenases, Aldehyde Dehydrogenases, and Alcohol Use Disorders: A Critical Review. Alcohol Clin Exp Res. 2018;42(12):2281-2297. https://doi.org/10.1111/acer.13904.</mixed-citation><mixed-citation xml:lang="en">Edenberg H.J., McClintick J.N.. Alcohol Dehydrogenases, Aldehyde Dehydrogenases, and Alcohol Use Disorders: A Critical Review. Alcohol Clin Exp Res. 2018;42(12):2281-2297. https://doi.org/10.1111/acer.13904.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Фасхутдинова Г.Г., Казанцева А.В., Асадуллин А.Р. и др. Анализ ассоциаций полиморфных локусов генов ADH1B, ADH1C, PDYN с хроническим алкоголизмом. Медицинская генетика. 2011; 10(7): 12-19.</mixed-citation><mixed-citation xml:lang="en">Faskhutdinova G.G., Kazantseva A.V., Asadullin A.R. et al. Analiz assotsiatsiy polimorfnykh lokusov genov ADH1B, ADH1C, PDYN s khronicheskim alkogolizmom [Analysis of associations of polymorphic loci of the ADH1B, ADH1C, PDYN genes with chronic alcoholism]. Meditsinskaya genetika [Medical Genetics]. 2011; 10(7): 12-19. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Jennings M.V., Martínez-Magaña J.J., Courchesne-Krak N.S. et аl. A phenome-wide association and Mendelian randomisation study of alcohol use variants in a diverse cohort comprising over 3 million individuals. EBioMedicine. 2024;103:105086. https://doi.org/10.1016/j.ebiom.2024.105086.</mixed-citation><mixed-citation xml:lang="en">Jennings M.V., Martínez-Magaña J.J., Courchesne-Krak N.S. et аl. A phenome-wide association and Mendelian randomisation study of alcohol use variants in a diverse cohort comprising over 3 million individuals. EBioMedicine. 2024;103:105086. https://doi.org/10.1016/j.ebiom.2024.105086.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Way M., McQuillin A., Saini J. et аl. Genetic variants in or near ADH1B and ADH1C affect susceptibility to alcohol dependence in a British and Irish population. Addict Biol. 2015;20(3):594-604. https://doi.org/10.1111/adb.12141.</mixed-citation><mixed-citation xml:lang="en">Way M., McQuillin A., Saini J. et аl.  Genetic variants in or near ADH1B and ADH1C affect susceptibility to alcohol dependence in a British and Irish population. Addict Biol. 2015;20(3):594-604. https://doi.org/10.1111/adb.12141.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Ayuso P., García-Martín E., Cornejo-García J.A. et аl. Genetic Variants of Alcohol Metabolizing Enzymes and Alcohol-Related Liver Cirrhosis Risk. J Pers Med. 2021;11(5):409. https://doi.org/10.3390/jpm11050409.</mixed-citation><mixed-citation xml:lang="en">Ayuso P., García-Martín E., Cornejo-García J.A. et аl. Genetic Variants of Alcohol Metabolizing Enzymes and Alcohol-Related Liver Cirrhosis Risk. J Pers Med. 2021;11(5):409. https://doi.org/10.3390/jpm11050409.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Zeng E., Sookoian S., Pirola C.J. et аl. ADH1B∗2 Is Associated With Reduced Severity of Nonalcoholic Fatty Liver Disease in Adults, Independent of Alcohol Consumption. Gastroenterology. 2020;159(3):929-943. https://doi.org/10.1053/j.gastro.2020.05.054.</mixed-citation><mixed-citation xml:lang="en">Zeng E., Sookoian S., Pirola C.J. et аl. ADH1B∗2 Is Associated With Reduced Severity of Nonalcoholic Fatty Liver Disease in Adults, Independent of Alcohol Consumption. Gastroenterology. 2020;159(3):929-943. https://doi.org/10.1053/j.gastro.2020.05.054.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Yokoyama A., Taniki N., Hara S. et аl. Slow-metabolizing ADH1B and inactive heterozygous ALDH2 increase vulnerability to fatty liver in Japanese men with alcohol dependence. J Gastroenterol. 2018;53(5):660-669. https://doi.org/10.1007/s00535-017-1402-6.</mixed-citation><mixed-citation xml:lang="en">Yokoyama A., Taniki N., Hara S. et аl.  Slow-metabolizing ADH1B and inactive heterozygous ALDH2 increase vulnerability to fatty liver in Japanese men with alcohol dependence. J Gastroenterol. 2018;53(5):660-669. https://doi.org/10.1007/s00535-017-1402-6.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Иванов В.П., Кущева Н.С. Влияние полиморфизма генов ферментов метаболизма этанола на риск развития алкогольных психозов. Наркология. 2013; 12(8): 51-54.</mixed-citation><mixed-citation xml:lang="en">Ivanov V.P., Kushcheva N.S. Vliyaniye polimorfizma genov fermentov metabolizma etanola na risk razvitiya alkogol’nykh psikhozov [The influence of polymorphism of genes encoding ethanol metabolism enzymes on the risk of developing alcoholic psychoses]. Narkologiya [Narcology]. 2013; 12(8): 51-54. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Tóth R., Fiatal S., Petrovski B. et аl. Combined effect of ADH1B RS1229984, RS2066702 and ADH1C RS1693482/ RS698 alleles on alcoholism and chronic liver diseases. Dis Markers. 2011;31(5):26777. https://doi.org/10.3233/DMA-2011-0828.</mixed-citation><mixed-citation xml:lang="en">Tóth R., Fiatal S., Petrovski B. et аl. Combined effect of ADH1B RS1229984, RS2066702 and ADH1C RS1693482/ RS698 alleles on alcoholism and chronic liver diseases. Dis Markers. 2011;31(5):26777. https://doi.org/10.3233/DMA-2011-0828.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Hoang Y.T.T., Nguyen Y.T., Vu L.T. et аl. Association of ADH1B rs1229984, ADH1C rs698, and ALDH2 rs671 with Alcohol abuse and Alcoholic Cirrhosis in People Living in Northeast Vietnam. Asian Pac J Cancer Prev. 2023;24(6):2073-2082. https://doi.org/10.31557/APJCP.2023.24.6.2073.</mixed-citation><mixed-citation xml:lang="en">Hoang Y.T.T., Nguyen Y.T., Vu L.T. et аl.  Association of ADH1B rs1229984, ADH1C rs698, and ALDH2 rs671 with Alcohol abuse and Alcoholic Cirrhosis in People Living in Northeast Vietnam. Asian Pac J Cancer Prev. 2023;24(6):2073-2082. https://doi.org/10.31557/APJCP.2023.24.6.2073.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Zeng D., Huang Q., Yu Z., Wu H. Association between aldehyde dehydrogenase 2 gene rs671 G&gt;A polymorphism and alcoholic liver cirrhosis in southern Chinese Hakka population. J Clin Lab Anal. 2021;35(7):e23855. https://doi.org/10.1002/jcla.23855.</mixed-citation><mixed-citation xml:lang="en">Zeng D., Huang Q., Yu Z., Wu H. Association between aldehyde dehydrogenase 2 gene rs671 G&gt;A polymorphism and alcoholic liver cirrhosis in southern Chinese Hakka population. J Clin Lab Anal. 2021;35(7):e23855. https://doi.org/10.1002/jcla.23855.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Shang D., Wang P., Tang W. et аl. Genetic Variations of ALDH (rs671) Are Associated With the Persistence of HBV Infection Among the Chinese Han Population. Front Med (Lausanne). 2022;9:811639. https://doi.org/10.3389/fmed.2022.811639.</mixed-citation><mixed-citation xml:lang="en">Shang D., Wang P., Tang W. et аl. Genetic Variations of ALDH (rs671) Are Associated With the Persistence of HBV Infection Among the Chinese Han Population. Front Med (Lausanne). 2022;9:811639. https://doi.org/10.3389/fmed.2022.811639.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Tsai M.C., Yang S.S., Lin C.C. et аl. Association of Heavy Alcohol Intake and ALDH2 rs671 Polymorphism With Hepatocellular Carcinoma and Mortality in Patients With Hepatitis B Virus-Related Cirrhosis. JAMA Netw Open. 2022;5(7):e2223511. https://doi.org/10.1001/jamanetworkopen.2022.23511.</mixed-citation><mixed-citation xml:lang="en">Tsai M.C., Yang S.S., Lin C.C. et аl. Association of Heavy Alcohol Intake and ALDH2 rs671 Polymorphism With Hepatocellular Carcinoma and Mortality in Patients With Hepatitis B Virus-Related Cirrhosis. JAMA Netw Open. 2022;5(7):e2223511. https://doi.org/10.1001/jamanetworkopen.2022.23511.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Chen Y., Liu H., Yu Z. et аl. ALDH2 Polymorphism rs671 *1/*2 Genotype is a Risk Factor for the Development of Alcoholic Liver Cirrhosis in Hakka Alcoholics. Int J Gen Med. 2022;15:4067-4077. https://doi.org/10.2147/IJGM.S356761.</mixed-citation><mixed-citation xml:lang="en">Chen Y., Liu H., Yu Z. et аl. ALDH2 Polymorphism rs671 *1/*2 Genotype is a Risk Factor for the Development of Alcoholic Liver Cirrhosis in Hakka Alcoholics. Int J Gen Med. 2022;15:4067-4077. https://doi.org/10.2147/IJGM.S356761.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Abe H., Aida Y., Seki N. et аl. Aldehyde dehydrogenase 2 polymorphism for development to hepatocellular carcinoma in East Asian alcoholic liver cirrhosis. J Gastroenterol Hepatol. 2015;30(9):1376-83. https://doi.org/10.1111/jgh.12948.</mixed-citation><mixed-citation xml:lang="en">Abe H., Aida Y., Seki N. et аl. Aldehyde dehydrogenase 2 polymorphism for development to hepatocellular carcinoma in East Asian alcoholic liver cirrhosis. J Gastroenterol Hepatol. 2015;30(9):1376-83. https://doi.org/10.1111/jgh.12948.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Linneberg A., Gonzalez-Quintela A., Vidal C. et аl. Genetic determinants of both ethanol and acetaldehyde metabolism influence alcohol hypersensitivity and drinking behaviour among Scandinavians. Clin Exp Allergy. 2010;40(1):123-30. https://doi.org/10.1111/j.1365-2222.2009.03398.x.</mixed-citation><mixed-citation xml:lang="en">Linneberg A., Gonzalez-Quintela A., Vidal C. et аl. Genetic determinants of both ethanol and acetaldehyde metabolism influence alcohol hypersensitivity and drinking behaviour among Scandinavians. Clin Exp Allergy. 2010;40(1):123-30. https://doi.org/10.1111/j.1365-2222.2009.03398.x.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Luo X., Kranzler H.R., Zuo L. et аl. ADH4 gene variation is associated with alcohol and drug dependence: results from family controlled and population-structured association studies. Pharmacogenet Genomics. 2005;15(11):755-68. https://doi.org/10.1097/01.fpc.0000180141.77036.dc.</mixed-citation><mixed-citation xml:lang="en">Luo X., Kranzler H.R., Zuo L. et аl. ADH4 gene variation is associated with alcohol and drug dependence: results from family controlled and populationstructured association studies. Pharmacogenet Genomics. 2005;15(11):75568. https://doi.org/10.1097/01.fpc.0000180141.77036.dc.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
