<?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">tiblj</journal-id><journal-title-group><journal-title xml:lang="ru">Туберкулез и болезни легких</journal-title><trans-title-group xml:lang="en"><trans-title>Tuberculosis and Lung Diseases</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2075-1230</issn><issn pub-type="epub">2542-1506</issn><publisher><publisher-name>Медицинские знания и технологии</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.58838/2075-1230-2025-103-6-104-116</article-id><article-id custom-type="elpub" pub-id-type="custom">tiblj-1939</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>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group></article-categories><title-group><article-title>Возможности фармакогенетического тестирования в лечении туберкулеза</article-title><trans-title-group xml:lang="en"><trans-title>Potential of Pharmacogenetic Testing in Tuberculosis Treatment</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>Д. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Ivanova</surname><given-names>D. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Иванова Диана Александровна - Д. м. н., ученый секретарь, врач-фтизиатр; врач-терапевт городского клинико-диагностического центра, профессор кафедры фтизиатрии </p><p>107014, г. Москва, ул. Стромынка, д. 10, стр. 1Тел.: +7 (499) 269-14-10</p></bio><bio xml:lang="en"><p>Diana A. Ivanova - Doctor of Medical Sciences, Academic Secretary, Phthisiologist, General Practitioner of City Clinical Diagnostic Center, Professor of Phthisiology Department </p><p>10 Build. 1, Stromynka St., Moscow 107014Phone: +7 (499) 269-14-10</p></bio><email xlink:type="simple">d-ivanova@list.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>Николенко</surname><given-names>Н. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Nikolenko</surname><given-names>N. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Николенко Николай Юрьевич - К. фарм. н., научный сотрудник научно-клинического отдела</p><p>107014, г. Москва, ул. Стромынка, д. 10, стр. 1Тел.: +7 (499) 269-14-10</p></bio><bio xml:lang="en"><p>Nikolay Yu. Nikolenko - Candidate of Pharmacological Sciences, Researcher of Research Clinical Department</p><p>10 Build. 1, Stromynka St., Moscow 107014Phone: +7 (499) 269-14-10</p></bio><email xlink:type="simple">nynikolenko@me.com</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кудлай</surname><given-names>Д. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Galkina</surname><given-names>K. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кудлай Дмитрий Анатольевич - Член-корреспондент РАН, д. м. н., профессор кафедры фармакологии Института фармации; ведущий научный сотрудник лаборатории персонализированной медициныи молекулярной иммунологии № 71 ФГБУ «ГНЦ Институт иммунологии» ФМБА России; профессор кафедры фармакогнозии и промышленной фармации факультета фундаментальной медицины ФГБОУ ВО МГУ имени М.В. Ломоносова</p><p>119991, г. Москва, ул. Трубецкая, д. 8, стр. 2Тел. +7 (499) 248-05-53</p></bio><bio xml:lang="en"><p>Kseniya Yu. Galkina - Candidate of Biological Sciences, Leading Researcher of Department of Laboratory Diagnostics of Tuberculosis and Pathomorphology</p><p>10 Build. 1, Stromynka St., Moscow 107014Phone: +7 (499) 269-14-10</p></bio><email xlink:type="simple">D624254@gmail.com</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Галкина</surname><given-names>К. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Yurovskaya</surname><given-names>E. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Галкина Ксения Юрьевна - К. б. н., ведущий научный сотрудник отдела проблем лабораторной диагностики туберкулеза и патоморфологии</p><p>107014, г. Москва, ул. Стромынка, д. 10, стр. 1Тел.: +7 (499) 269-14-10</p></bio><bio xml:lang="en"><p>Ekaterina I. Yurovskaya - Phthisiologist of Pulmonary Tuberculosis Department no. 6 of Clinic no. 2</p><p>10 Build. 1, Stromynka St., Moscow 107014Phone: +7 (499) 269-14-10</p></bio><email xlink:type="simple">ksyu.galkina.79@list.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Юровская</surname><given-names>Е. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Mitrofanova</surname><given-names>Yu. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Юровская Екатерина Игоревна - Врач-фтизиатр туберкулезного легочного отделения № 6 Клиники № 2</p><p>107014, г. Москва, ул. Стромынка, д. 10, стр. 1Тел.: +7 (499) 269-14-10</p></bio><bio xml:lang="en"><p>Yulia Yu. Mitrofanova - Researcher of Research Clinical Department</p><p>10 Build. 1, Stromynka St., Moscow 107014Phone: +7 (499) 269-14-10</p></bio><email xlink:type="simple">dr.the_end_tb@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Митрофанова</surname><given-names>Ю. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Kudlay</surname><given-names>D. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Митрофанова Юлия Юрьевна - Научный сотрудник научно-клинического отдела</p><p>107014, г. Москва, ул. Стромынка, д. 10, стр. 1Тел.: +7 (499) 269-14-10</p></bio><bio xml:lang="en"><p>Dmitry A. Kudlay - Correspondent Member of RAS, Doctor of Medical Sciences, Professor of Pharmacology Department of Pharmacy Institute, Leading Researcher of Laboratory of Personalized Medicine and Molecular Immunology no. 71, Immunology Research Institute by the Russian Federal Medical Biological Agency, Professor of Department of Pharmacognosy and Industrial Pharmacy, Fundamental Medicine Faculty, Lomonosov Moscow State University</p><p>8 Bd. 2, Trubetskaya St., Moscow, 119991Phone: +7 (499) 248-05-53</p></bio><email xlink:type="simple">yuyumit@yandex.ru</email><xref ref-type="aff" rid="aff-4"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ГБУЗ «Московский городской научно-практический центр борьбы с туберкулезом Департамента здравоохранения города Москвы»; ФГБОУ ДПО «Российская медицинская академия непрерывного профессионального образования» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Moscow Research and Clinical Center for Tuberculosis Control of the Moscow Government Department of Health; Russian Medical Academy of On-going Professional Education, Russian Ministry of Health</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ГБУЗ «Московский городской научно-практический центр борьбы с туберкулезом Департамента здравоохранения города Москвы»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Moscow Research and Clinical Center for Tuberculosis Control of the Moscow Government Department of Health</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>ФГАОУ ВО «Первый МГМУ им. И. М. Сеченова&#13;
(Сеченовский Университет)» МЗ РФ; ФГБОУ ВПО «Московский государственный университет имени М.В. Ломоносова»; ФГБУ «ГНЦ Институт иммунологии» ФМБА России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Moscow Research and Clinical Center for Tuberculosis Control of the Moscow Government Department of Health</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-4"><aff xml:lang="ru"><institution>ГБУЗ «Московский городской научно-практический центр борьбы с туберкулезом Департамента здравоохранения города Москвы»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>I.M. Sechenov First Moscow State Medical University&#13;
(Sechenov University), Russian Ministry of Health; Lomonosov Moscow State University; Immunology Research Institute by the Russian Federal Medical Biological Agency</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>10</day><month>01</month><year>2026</year></pub-date><volume>103</volume><issue>6</issue><fpage>104</fpage><lpage>116</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Иванова Д.А., Николенко Н.Ю., Кудлай Д.А., Галкина К.Ю., Юровская Е.И., Митрофанова Ю.Ю., 2026</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="ru">Иванова Д.А., Николенко Н.Ю., Кудлай Д.А., Галкина К.Ю., Юровская Е.И., Митрофанова Ю.Ю.</copyright-holder><copyright-holder xml:lang="en">Ivanova D.A., Nikolenko N.Y., Galkina K.Y., Yurovskaya E.I., Mitrofanova Y.Y., Kudlay D.A.</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.tibl-journal.com/jour/article/view/1939">https://www.tibl-journal.com/jour/article/view/1939</self-uri><abstract><p>Фармакогенетическое тестирование – наиболее перспективный инструмент персонализированной медицины, направленный на повышение эффективности и безопасности лечения, особенно у сложных коморбидных пациентов. Проведен анализ 122 публикаций, посвященных теоретическим и прикладным аспектам применения фармакогенетического тестирования при лечении больных туберкулезом. Рассмотрена роль генетических полиморфизмов в ответе на лечение, представлены данные о белках, участвующих в процессах фармакокинетики и фармакодинамики основных противотуберкулезных препаратов, и кодирующих эти белки генах. Проанализирован перечень наиболее значимых маркеров, связанных с риском нежелательных реакций при лечении лекарственно-чувствительного и лекарственно-устойчивого туберкулеза, охарактеризованы перспективы их применения в клинической практике. В списке литературы отражены 56 ключевых публикаций, на которые имеются ссылки в тексте. </p></abstract><trans-abstract xml:lang="en"><p>Pharmacogenetic testing is the most promising tool in personalized medicine aimed at enhancing effectiveness and safety of treatment, especially in complicated cases with comorbidities. The review analyzes 122 publications devoted to theoretical and applied aspects of pharmacogenetic testing in the treatment of tuberculosis patients. It considers the role of genetic polymorphisms in the response to treatment, and presents data on proteins involved in pharmacokinetics and pharmacodynamics of main anti-tuberculosis drugs and the genes encoding these proteins. The review analyzes the list of the most significant markers associated with the risk of adverse reactions during treatment of drug-sensitive and drug-resistant tuberculosis, and it characterizes prospects for their use in clinical practice. The list of references contains 56 key publications cited in the text. </p></trans-abstract><kwd-group xml:lang="ru"><kwd>фармакогенетическое тестирование</kwd><kwd>лечение туберкулеза</kwd><kwd>противотуберкулезные препараты</kwd><kwd>фармакогенетический маркер</kwd><kwd>генетический полиморфизм</kwd></kwd-group><kwd-group xml:lang="en"><kwd>pharmacogenetic testing</kwd><kwd>tuberculosis treatment</kwd><kwd>anti-tuberculosis drugs</kwd><kwd>pharmacogenetic marker</kwd><kwd>genetic polymorphism</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Алыменко М.А., Валиев Р.Ш., Валиев Н.Р., Трагира И.Н., Полоников А.В., Балобанова Н.П., Батищев А.В., Коломиец В.М., Маль Г.С., Волкова С.Н., Козлов В.В., Сусликова Е.И., Попова Е.В. Влияние полиморфизма гена МDR1 (ABCB1) на риск развития гепатотоксических реакций у больных туберкулезом легких // Антибиотики и Химиотерапия. – 2023. – Т. 68, № 7-8. – С. 62-69. https://doi.org/10.37489/0235-2990-2023-68-7-8-62-69</mixed-citation><mixed-citation xml:lang="en">Alymenko М.А., Valiev R.S., Valiev N.R., Tragira I.N., Polonikov А.V., Balobanova N.Р., Batishchev A.V., Kolomiets V.М., Mal G.S., Volkova S.N., Kozlov V.V., Suslikova E.I., Popova E.V. The effect of polymorphism of the MDR1 (ABCB1) gene on the risk of hepatotoxic reactions in patients with pulmonary tuberculosis. Antibiotics and Chemotherapy, 2023, vol. 68, no. 7-8, pp. 62-69. (In Russ.) https://doi.org/10.37489/0235-2990-2023-68-7-8-62-69</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Захаров А.В., Еремеев В.В., Чумоватов Н.В., Полякова А.С., Шепелькова Г.С., Комиссарова О.Г., Романов В.В., Эргешов А.Э. Клинико-генетические ассоциации полиморфных аллелей гена CYP3A4 у больных туберкулезом легких с лекарственной устойчивостью возбудителя // Вестник ЦНИИТ. – 2024. – Т. 8, № 4. – С. 17-30. https://doi.org/10.57014/2587-6678-2024-8-4-17-30</mixed-citation><mixed-citation xml:lang="en">Zakharov A.V., Yeremeev V.V., Chumovatov N.V., Polyakova A.S., Shepelkova G.S., Komissarova O.G., Romanov V.V., Ergeshov A.E. Clinical and genetic associations of polymorphic alleles of the CYP3A4 gene in drug-resistant pulmonary TB. Vestnik TSNIIT, 2024, vol. 8, no. 4, pp. 17-30. (In Russ.) https://doi.org/10.57014/2587-6678-2024-8-4-17-30</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Иванова Д.А., Галкина К.Ю., Борисов С.Е., Сафонова С.Г., Кудлай Д.А. Фармакогенетические методы в оценке риска гепатотоксических реакций при лечении впервые выявленных больных туберкулезом // Туберкулез и социально значимые заболевания. – 2018. – Т. 6, № 3. – С. 43-48.</mixed-citation><mixed-citation xml:lang="en">Ivanova D.A., Galkina K.Yu., Borisov S.E., Safonova S.G., Kudlay D.A. Pharmacogenetic methods in assessing the risk of hepatotoxic reactions in the treatment of new tuberculosis patients. Tuberculosis and Socially Significant Diseases, 2018, vol. 6, no. 3, pp. 43-48. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Иванова Д.А., Юровская Е.И., Галкина К.Ю. Фармакогенетические маркеры в лечении больных туберкулезом с множественной лекарственной устойчивостью возбудителя // Фармакогенетика и фармакогеномика. – 2025. – № 2. – С. 23-29. https://doi.org/10.37489/2588-0527-2025-2-23-29</mixed-citation><mixed-citation xml:lang="en">Ivanova D.A., Yurovskaya E.I., Galkina K.Yu. Pharmacogenetic markers in the treatment of patients with multidrug-resistant tuberculosis. Pharmacogenetics and Pharmacogenomics, 2025, no. 2, pp. 23-29. (In Russ.) https://doi.org/10.37489/2588-0527-2025-2-23-29</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Краснова Н.М., Евдокимова Н.Е., Егорова А.А., Филиппова О.И., Алексеева Е.А., Рудых З.А., Чертовских Я.В., Венгеровский А.И., Кравченко А.Ф., Сычев Д.А. Влияние типа ацетилирования на частоту гепатотоксичности изониазида у пациентов с впервые выявленным туберкулезом органов дыхания // Антибиотики и Химиотерапия. – 2020. – Т. 65, № 7-8. – С. 31-36. https://doi.org/10.37489/0235-2990-2020-65-7-8-31-36</mixed-citation><mixed-citation xml:lang="en">Krasnova N.M., Evdokimova N.E., Egorova A.A., Filippova O.I., Alekseeva E.A., Rudykh Z.A., Chertovskykh Y.V., Vengerovskii A.I., Kravchenko A.F., Sychev D.A. Influence of the acetylation type on the incidence of isoniazid-induced hepatotoxicity in patients with newly diagnosed pulmonary tuberculosis. Antibiotics and Chemotherapy, 2020, vol. 65, no. 7-8, pp. 31-36. (In Russ.) https://doi.org/10.37489/0235-2990-2020-65-7-8-31-36</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Краснова Н.М., Николаев В.М., Татаринова О.В., Прокопьев Е.С., Венгеровский А.И., Сычев Д.А. Зависимость режима дозирования от скорости ацетилирования изониазида у пациентов с впервые выявленным туберкулезом легких // Экспериментальная и клиническая фармакология. – 2024. – Т. 87, № 8. – С. 20-25. https://doi.org/10.30906/0869-2092-2024-87-8-20-25</mixed-citation><mixed-citation xml:lang="en">Krasnova N.M., Nikolaev V.M., Tatarinova O.V., Prokopyev E.S., Vengerovskii A.I., Sychev D.A. Dependence of the dosing regimen on the rate of isoniazid acetylation in patients with newly diagnosed pulmonary tuberculosis. Eksperimentalnaya i Klinicheskaya Farmakologiya, 2024, vol. 87, no. 8, pp. 20-25. (In Russ.) https://doi.org/10.30906/0869-2092-2024-87-8-20-25</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Можокина Г.Н., Казаков А.В., Елистратова Н.А., Попов С.А. Ферменты биотрансформации ксенобиотиков и персонификация режимов лечения больных туберкулезом // Туберкулез и болезни легких. – 2016. – Т. 94, № 4. – С. 6-12. https://doi.org/10.21292/2075-1230-2016-94-4-6-12</mixed-citation><mixed-citation xml:lang="en">Mozhokina G.N., Kazakov A.V., Elistratova N.A., Popov S.A. Biotransformation enzymes for xenobiotics and personalization of treatment regimens for tuberculosis patients. Tuberculosis and Lung Diseases, 2016, vol. 94, no. 4, pp. 6-12. (In Russ.) https://doi.org/10.21292/2075-1230-2016-94-4-6-12</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Прикладная фармакогенетика: Монография / под ред. Д.А. Сычева. – Тверь: ООО «Издательство «Триада», 2021.</mixed-citation><mixed-citation xml:lang="en">Prikladnaya farmakogenetika: Monografiya. [Applied Pharmacogenetics. Monograph]. D.A Sychev, eds., Tver, OOO Izdatelstvo Triada Publ., 2021.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Степанова Н.А. Персонализированные подходы к повышению эффективности и безопасности фармакотерапии туберкулеза органов дыхания: автореф. дисс. ...докт. мед. наук / Н. А. Степанова. – Москва, 2022. URL: https://critub.ru/wp-content/uploads/AvtoreferatStepanovaNA-na-sajt.pdf [Дата обращения 27.09.2025].</mixed-citation><mixed-citation xml:lang="en">Stepanova N.A. Personalizirovannyye podkhody k povysheniyu effektivnosti i bezopasnosti farmakoterapii tuberkuleza organov dykhaniya. Avtoref. diss. dokt. med. nauk. [Personalized approaches to improving the effectiveness and safety of pharmacotherapy of respiratory tuberculosis. Synopsis of Doct. Diss.]. Moscow, 2022. Available: https://critub.ru/wp-content/uploads/AvtoreferatStepanovaNA-na-sajt.pdf Accessed September 27, 2025</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Тюлькова Т. Е., Ткачук А. П., Акмалова К. А., Абдуллаев Ш. П., Мирзаев К. Б., Сычев Д. А., Мануйлов В. А. Генетический полиморфизм, влияющий на метаболизм противотуберкулезных препаратов // Фармакогенетика и фармакогеномика. – 2024. – № 2. – С. 37-45. https://doi.org/ 10.37489/2588-527-2024-2-37-45</mixed-citation><mixed-citation xml:lang="en">Tyulkova T.E., Tkachuk A.P., Akmalova K.A., Abdullaev Sh.P., Mirzaev K.B., Sychev D.A., Manuylov V.A. Genetic polymorphisms affect the metabolism of antituberculosis drugs. Pharmacogenetics and Pharmacogenomics, 2024, no. 2, pp. 37-45. (In Russ.) https://doi.org/10.37489/2588-0527-2024-2-37-45</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Юнусбаева М.М., Бородина Л.Я., Билалов Ф.С., Шарипов Р.А., Юнусбаев Б.Б. Исследование влияния полиморфизма генов CYP3A5, CYP2B6 и NAT2 на эффективность лечения туберкулеза с множественной лекарственной устойчивостью // Фармакогенетика и фармакогеномика. – 2020. – № 2. – С. 26-27. https://doi.org/10.37489/2588-0527-2020-2-26-27</mixed-citation><mixed-citation xml:lang="en">Yunusbaeva M.M., Borodina L.Ya., Bilalov F.S., Sharipov R.A., Yunusbaev B.B. A study of the influence of CYP3A5, CYP2B6 and NAT2 gene polymorphism on the effectiveness of treatment for multidrug-resistant tuberculosis Pharmacogenetics and Pharmacogenomics, 2020, no. 2, pp. 26-27. (In Russ.) https://doi.org/10.37489/2588-0527-2020-2-26-27</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Ahmad J., Dellinger A., Nicoletti P., Barnhart H.X., Ghabril M., Fontana R.J., et al. Clinical and HLA associations of fluoroquinolone-induced liver injury: results from the drug-induced liver injury network // The American Journal of Gastroenterology. – 2025. – № 10. – Р. 14309. https://doi.org/10.14309/ajg.0000000000003457</mixed-citation><mixed-citation xml:lang="en">Ahmad J., Dellinger A., Nicoletti P., Barnhart H.X., Ghabril M., Fontana R.J. et al. Clinical and HLA associations of fluoroquinolone-induced liver injury: results from the drug-induced liver injury network. The American Journal of Gastroenterology, 2025, no. 10, pp. 14309. https://doi.org/10.14309/ajg.0000000000003457</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Ahmed S., Zhou Z., Zhou J., Chen S.Q. Pharmacogenomics of drug metabolizing enzymes and transporters: relevance to precision medicine // Genomics, Proteomics &amp; Bioinformatics. – 2016. – Vol. 14, №. 5. – P. 298-313. https://doi.org/10.1016/j.gpb.2016.03.008.</mixed-citation><mixed-citation xml:lang="en">Ahmed S., Zhou Z., Zhou J., Chen S.Q. Pharmacogenomics of drug metabolizing enzymes and transporters: relevance to precision medicine. Genomics, Proteomics &amp; Bioinformatics, 2016, vol. 14, no. 5, pp. 298-313. https://doi.org/10.1016/j.gpb.2016.03.008.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Allegra S., Di Paolo A., Cusato J., Fatiguso G., Arrigoni E., Danesi R., Corcione S., D'Avolio A. Different underlying mechanism might explain the absence of a significant difference in area under the concentration-time curve of linezolid for different ABCB1 genotypes // Therapeutic Drug Monitoring. – 2019. – Vol. 41, № 2. – P. 254-255. https://doi.org/10.1097/FTD.0000000000000</mixed-citation><mixed-citation xml:lang="en">Allegra S., Di Paolo A., Cusato J., Fatiguso G., Arrigoni E., Danesi R., Corcione S., D'Avolio A. Different underlying mechanism might explain the absence of a significant difference in area under the concentration-time curve of linezolid for different ABCB1 genotypes. Therapeutic Drug Monitoring, 2019, vol. 41, no. 2, pp. 254-255. https://doi.org/10.1097/FTD.0000000000000596</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Araujo-Mariz C., Militão de Albuquerque M.F.P., Lopes E.P., Ximenes R.A.A., Lacerda H.R., Miranda-Filho D.B., Lustosa-Martins B.B., Pastor A.F.P., Acioli-Santos B. Hepatotoxicity during TB treatment in people with HIV/AIDS related to NAT2 polymorphisms in Pernambuco, Northeast Brazil // Annals of Hepatology. – 2020. – Vol. 19, № 2. – Р. 153-160. https://doi.org/10.1016/j.aohep.2019.09.008</mixed-citation><mixed-citation xml:lang="en">Araujo-Mariz C., Militão de Albuquerque M.F.P., Lopes E.P., Ximenes R.A.A., Lacerda H.R., Miranda-Filho D.B., Lustosa-Martins B.B., Pastor A.F.P., Acioli-Santos B. Hepatotoxicity during TB treatment in people with HIV/AIDS related to NAT2 polymorphisms in Pernambuco, Northeast Brazil. Annals of Hepatology, 2020, vol. 19, no. 2, pp. 153-160. https:// doi.org/10.1016/j.aohep.2019.09.008</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Azuma J., Ohno M., Kubota R., Yokota S., Nagai T., Tsuyuguchi K., Okuda Y., Takashima T., Kamimura S., Fujio Y., Kawase I. NAT2 genotype guided regimen reduces isoniazid-induced liver injury and early treatment failure in the 6-month four-drug standard treatment of tuberculosis: a randomized controlled trial for pharmacogenetics-based therapy // European Journal of Clinical Pharmacology. – 2013. – Vol. 69, № 5. – Р. 1091-1101. https://doi.org/10.1007/s00228-012-1429-9</mixed-citation><mixed-citation xml:lang="en">Azuma J., Ohno M., Kubota R., Yokota S., Nagai T., Tsuyuguchi K., Okuda Y., Takashima T., Kamimura S., Fujio Y., Kawase I. NAT2 genotype guided regimen reduces isoniazid-induced liver injury and early treatment failure in the 6-month four-drug standard treatment of tuberculosis: a randomized controlled trial for pharmacogenetics-based therapy. European Journal of Clinical Pharmacology, 2013, vol. 69, no. 5, pp. 1091-1101. https:// doi.org/10.1007/s00228-012-1429-9</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Barliana M.I., Afifah N.N., Yunivita V., Ruslami R. Genetic polymorphism related to ethambutol outcomes and susceptibility to toxicity // Frontiers in Genetics. – 2023. – № 14. –Р. 1118102. https://doi.org/10.3389/fgene.2023.1118102</mixed-citation><mixed-citation xml:lang="en">Barliana M.I., Afifah N.N., Yunivita V., Ruslami R. Genetic polymorphism related to ethambutol outcomes and susceptibility to toxicity. Frontiers in Genetics, 2023, no. 14, pp. 1118102. https://doi.org/10.3389/fgene.2023.1118102</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Cai Y., Yi J., Zhou C., Shen X. Pharmacogenetic study of drug-metabolising enzyme polymorphisms on the risk of anti-tuberculosis drug-induced liver injury: a meta-analysis // PLoS One. – 2012. – Vol. 7, № 10. – Р. e47769. https://doi.org/10.1371/journal.pone.0047769</mixed-citation><mixed-citation xml:lang="en">Cai Y., Yi J., Zhou C., Shen X. Pharmacogenetic study of drug-metabolising enzyme polymorphisms on the risk of anti-tuberculosis drug-induced liver injury: a meta-analysis. PLoS One, 2012, vol. 7, no. 10, pp. e47769. https://doi.org/10.1371/journal.pone.0047769</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Cheli S., Fusi M., De Silvestri A., Bonini I., Clementi E., Cattaneo D., Montrasio C., Baldelli S. In linezolid underexposure, pharmacogenetics matters: The role of CYP3A5 // Biomedicine &amp; Pharmacotherapy. – 2021. – № 139. – Р. 111631. https://doi.org/10.1016/j.biopha.2021.111631</mixed-citation><mixed-citation xml:lang="en">Cheli S., Fusi M., De Silvestri A., Bonini I., Clementi E., Cattaneo D., Montrasio C., Baldelli S. In linezolid underexposure, pharmacogenetics matters: The role of CYP3A5. Biomedicine &amp; Pharmacotherapy, 2021, no. 139, pp. 111631. https://doi.org/10.1016/j.biopha.2021.111631</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Clinical Pharmacogenomics (ClinPgx). Available at: https://www.clinpgx.org/ [Accessed 30.09.2025].</mixed-citation><mixed-citation xml:lang="en">Clinical Pharmacogenomics (ClinPgx). Available: https://www.clinpgx.org/ Accessed September 30, 2025</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Fernandes D.C., Santos N.P., Moraes M.R., Braga A.C., Silva C.A., Ribeiro-dos-Santos A., Santos S. Association of the CYP2B6 gene with anti-tuberculosis drug-induced hepatotoxicity in a Brazilian Amazon population // International journal of infectious diseases. – 2015. – № 33. – P. 28-31. https://doi.org/10.1016/j.ijid.2014.04.011</mixed-citation><mixed-citation xml:lang="en">Fernandes D.C., Santos N.P., Moraes M.R., Braga A.C., Silva C.A., Ribeiro-dos-Santos A., Santos S. Association of the CYP2B6 gene with anti-tuberculosis drug-induced hepatotoxicity in a Brazilian Amazon population. International Journal of Infectious Diseases, 2015, no. 33, pp. 28-31. https://doi.org/10.1016/j.ijid.2014.04.011</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Garrabou G., Soriano À., Pinós T., Casanova-Mollà J., Pacheu-Grau D., Morén C., et al. Influence of Mitochondrial Genetics on the Mitochondrial Toxicity of Linezolid in Blood Cells and Skin Nerve Fibers // Antimicrobial Agents and Chemotherapy. – 2017. – Vol. 61, № 9. – Р. e00542-17. https://doi.org/10.1128/AAC.00542-17</mixed-citation><mixed-citation xml:lang="en">Garrabou G., Soriano À., Pinós T., Casanova-Mollà J., Pacheu-Grau D., Morén C. et al. Influence of mitochondrial genetics on the mitochondrial toxicity of linezolid in blood cells and skin nerve fibers. Antimicrobial Agents and Chemotherapy, 2017, vol. 61, no. 9, pp. e00542-17. https://doi.org/10.1128/AAC.00542-17</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Haas D.W., Abdelwahab M.T., van Beek S.W., Baker P., Maartens G., Bradford Y., et al. Pharmacogenetics of Between-Individual Variability in Plasma Clearance of Bedaquiline and Clofazimine in South Africa // The Journal of Infectious Diseases. – 2022. – Vol. 226, № 1. – P. 147-156. https://doi.org/10.1093/infdis/jiac024</mixed-citation><mixed-citation xml:lang="en">Haas D.W., Abdelwahab M.T., van Beek S.W., Baker P., Maartens G., Bradford Y. et al. Pharmacogenetics of between-individual variability in plasma clearance of bedaquiline and clofazimine in South Africa. The Journal of Infectious Diseases, 2022, vol. 226, no. 1, pp. 147-156. https://doi.org/10.1093/infdis/jiac024</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Headriawan A., Pramono A.A., Sukadi A., et al. NAT2 Gene rs1041983 is associated with anti-tuberculosis drug induced hepatotoxicity among pediatric tuberculosis in Bandung, Indonesia // The Application of Clinical Genetics. – 2021. – № 14. – P. 297-303. https://doi.org/10.2147/TACG.S303668</mixed-citation><mixed-citation xml:lang="en">Headriawan A., Pramono A.A., Sukadi A. et al. NAT2 Gene rs1041983 is associated with anti-tuberculosis drug induced hepatotoxicity among pediatric tuberculosis in Bandung, Indonesia. The Application of Clinical Genetics, 2021, no. 14, pp. 297-303. https://doi.org/10.2147/TACG.S303668</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Hoa P.Q., Kim H.K., Jang T.W., Seo H., Oh J.Y., Kim H.C., et al. Population pharmacokinetic model of rifampicin for personalized tuberculosis pharmacotherapy: Effects of SLCO1B1 polymorphisms on drug exposure // International Journal of Antimicrobial Agents. – 2024. – Vol. 63, № 2. – Р. 107034. https://doi.org/10.1016/j.ijantimicag.2023.107034</mixed-citation><mixed-citation xml:lang="en">Hoa P.Q., Kim H.K., Jang T.W., Seo H., Oh J.Y., Kim H.C. et al. Population pharmacokinetic model of rifampicin for personalized tuberculosis pharmacotherapy: Effects of SLCO1B1 polymorphisms on drug exposure. International Journal of Antimicrobial Agents, 2024, vol. 63, no. 2, pp. 107034. https://doi.org/10.1016/j.ijantimicag.2023.107034</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Hussain Z., Zhu J., Ma X. Metabolism and hepatotoxicity of pyrazinamide, an antituberculosis drug // Drug Metabolism and Disposition: the Biological Fate of Chemicals. – 2021. – Vol. 49, № 8. – P. 679-682. https://doi.org/10.1124/dmd.121.000389</mixed-citation><mixed-citation xml:lang="en">Hussain Z., Zhu J., Ma X. Metabolism and hepatotoxicity of pyrazinamide, an antituberculosis drug. Drug Metabolism and Disposition: the Biological Fate of Chemicals, 2021, vol. 49, no. 8, pp. 679-682. https://doi.org/10.1124/dmd.121.000389</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Jiang M., Yang J., Yang L., Wang L, Wang T., Han S. et al. An association study of HLA with levofloxacin-induced severe cutaneous adverse drug reactions in Han Chinese // iScience. – 2023. – Vol. 26, № 8. – Р. е107391. https://doi.org/10.1016/j.isci.2023.107391</mixed-citation><mixed-citation xml:lang="en">Jiang M., Yang J., Yang L., Wang L, Wang T., Han S. et al. An association study of HLA with levofloxacin-induced severe cutaneous adverse drug reactions in Han Chinese. iScience, 2023, vol. 26, no. 8, pp. е107391. https://doi.org/10.1016/j.isci.2023.107391</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Kivrane A., Ulanova V., Grinberga S., Sevostjanovs E., Viksna A., Ozere I., Bogdanova I., Zolovs M., Ranka R. Exploring Variability in Rifampicin Plasma Exposure and Development of Anti-Tuberculosis Drug-Induced Liver Injury among Patients with Pulmonary Tuberculosis from the Pharmacogenetic Perspective // Pharmaceutics. – 2024. – Vol. 16, № 3. – Р. 388. https://doi.org/10.3390/pharmaceutics16030388</mixed-citation><mixed-citation xml:lang="en">Kivrane A., Ulanova V., Grinberga S., Sevostjanovs E., Viksna A., Ozere I., Bogdanova I., Zolovs M., Ranka R. Exploring variability in rifampicin plasma exposure and development of anti-tuberculosis drug-induced liver injury among patients with pulmonary tuberculosis from the pharmacogenetic perspective. Pharmaceutics, 2024, vol. 16, no. 3, pp. 388. https://doi.org/10.3390/pharmaceutics16030388</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Lopez-Medina A.I., Campos-Staffico A.M., Chahal C.A., Volkers I., Jacoby J.P., Berenfeld O., Luzum J.A. Genetic risk factors for drug-induced long QT syndrome: findings from a large real-world case-control study // Pharmacogenomics. – 2024. – Vol. 25, №3. – Р.117-131. https://doi.org/10.2217/pgs-2023-0229</mixed-citation><mixed-citation xml:lang="en">Lopez-Medina A.I., Campos-Staffico A.M., Chahal C.A., Volkers I., Jacoby J.P., Berenfeld O., Luzum J.A. Genetic risk factors for drug-induced long QT syndrome: findings from a large real-world case-control study. Pharmacogenomics, 2024, vol. 25, no. 3, pp. 117-131. https://doi.org/ 10.2217/pgs-2023-0229</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Mackay E., Platt G., Peloquin C.A., Brooks M.B., Coit J.M., Velásquez G.E., et al. Impact of pharmacogenetics on pharmacokinetics of first-line antituberculosis drugs in the HIRIF Trial // The Journal of Infectious Diseases. – 2025. – Vol. 232, № 2. – P. 258-265. https://doi.org/10.1093/infdis/jiaf195</mixed-citation><mixed-citation xml:lang="en">Mackay E., Platt G., Peloquin C.A., Brooks M.B., Coit J.M., Velásquez G.E. et al. Impact of pharmacogenetics on pharmacokinetics of first-line antituberculosis drugs in the HIRIF Trial. The Journal of Infectious Diseases, 2025, vol. 232, no. 2, pp. 258-265. https://doi.org/10.1093/infdis/jiaf195</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Mahajan R., Tyagi A.K. Pharmacogenomic insights into tuberculosis treatment shows the NAT2 genetic variants linked to hepatotoxicity risk: a systematic review and meta-analysis // BMC Genomics Data. – 2024. – Vol. 25, № 1. – Р. 103. https://doi.org/10.1186/s12863-024-01286-y</mixed-citation><mixed-citation xml:lang="en">Mahajan R., Tyagi A.K. Pharmacogenomic insights into tuberculosis treatment shows the NAT2 genetic variants linked to hepatotoxicity risk: a systematic review and meta-analysis. BMC Genomics Data, 2024, vol. 25, no. 1, pp. 103. https://doi.org/10.1186/s12863-024-01286-y</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Manca A., Calcagno A., D'Avolio A., Cusato J. Pharmacogenetics of first-line antitubercular drugs: an update // Therapeutic Drug Monitoring. – 2025, № 2. – Online ahead of print. https://doi.org/10.1097/FTD.0000000000001378</mixed-citation><mixed-citation xml:lang="en">Manca A., Calcagno A., D'Avolio A., Cusato J. Pharmacogenetics of first-line antitubercular drugs: an update. Therapeutic Drug Monitoring, 2025, no. 2. Online ahead of print. https://doi.org/10.1097/FTD.0000000000001378</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">McDermott J.H., Wolf J., Hoshitsuki K., Huddart R., Caudle K.E., Whirl-Carrillo M., et al. Clinical Pharmacogenetics Implementation Consortium Guideline for the Use of Aminoglycosides Based on MT-RNR1 Genotype // Clin Pharmacol Ther. – 2022. –Vol. 111, № 2. – Р. 366-372. https://doi.org/10.1002/cpt.2309</mixed-citation><mixed-citation xml:lang="en">McDermott J.H., Wolf J., Hoshitsuki K., Huddart R., Caudle K.E., Whirl-Carrillo M. et al. clinical pharmacogenetics implementation consortium guideline for the use of aminoglycosides based on MT-RNR1 genotype. Clin. Pharmacol. Ther., 2022, vol. 111, no. 2, pp. 366-372. https://doi.org/10.1002/cpt.2309</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Naidoo A., Ramsuran V., Chirehwa M., Denti P., McIlleron H., Naidoo K., et al. Effect of genetic variation in UGT1A and ABCB1 on moxifloxacin pharmacokinetics in South African patients with tuberculosis // Pharmacogenomics. – 2018. – Vol. 19, № 1. – Р. 17-29. https://doi.org/10.2217/pgs-2017-0144</mixed-citation><mixed-citation xml:lang="en">Naidoo A., Ramsuran V., Chirehwa M., Denti P., McIlleron H., Naidoo K. et al. Effect of genetic variation in UGT1A and ABCB1 on moxifloxacin pharmacokinetics in South African patients with tuberculosis. Pharmacogenomics, 2018, vol. 19, no. 1, pp. 17-29. https://doi.org/10.2217/pgs-2017-0144</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Oelofse C., Ndong Sima C.A.A., Möller M., Uren C. Pharmacogenetics as part of recommended precision medicine for tuberculosis treatment in African populations: Could it be a reality? // Clinical and Translational Science. – 2023. – Vol. 16, № 7. – P. 1101-1112. https://doi.org/10.1111/cts.13520</mixed-citation><mixed-citation xml:lang="en">Oelofse C., Ndong Sima C.A.A., Möller M., Uren C. Pharmacogenetics as part of recommended precision medicine for tuberculosis treatment in African populations: Could it be a reality? Clinical and Translational Science, 2023, vol. 16, no. 7, pp. 1101-1112. https://doi.org/10.1111/cts.13520</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Pasipanodya J.G., Srivastava S., Gumbo T. Meta-analysis of clinical studies supports the pharmacokinetic variability hypothesis for acquired drug resistance and failure of antituberculosis therapy // Clinical Infectious Diseases. – 2012. – Vol. 55, № 2. – Р. 169-177. https://doi.org/10.1093/cid/cis353</mixed-citation><mixed-citation xml:lang="en">Pasipanodya J.G., Srivastava S., Gumbo T. Meta-analysis of clinical studies supports the pharmacokinetic variability hypothesis for acquired drug resistance and failure of antituberculosis therapy. Clinical Infection Diseases, 2012, vol. 55, no. 2, pp. 169-177. https://doi.org/ 10.1093/cid/cis353</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Peng W., Zhao Z.Z., Jiao L., Wu T., Chen H., Zhang C.Y., et al. Prospective study of ALDH1A1 gene polymorphisms associated with antituberculosis drug-induced liver injury in western Chinese Han population // Microbiol Immunol. – 2021. – Vol. 65, № 4. – Р. 143-153. https://doi.org/10.1111/1348-0421.12877</mixed-citation><mixed-citation xml:lang="en">Peng W., Zhao Z.Z., Jiao L., Wu T., Chen H., Zhang C.Y. et al. Prospective study of ALDH1A1 gene polymorphisms associated with antituberculosis drug-induced liver injury in western Chinese Han population. Microbiol. Immunol., 2021, vol. 65, no. 4, pp. 143-153. https://doi.org/ 10.1111/1348-0421.12877</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Petros Z., Lee M.M., Takahashi A., Zhang Y., Yimer G., Habtewold A., Amogne W., Aderaye G., Schuppe-Koistinen I., Mushiroda T., Makonnen E., Kubo M., Aklillu E. Genome-wide association and replication study of anti-tuberculosis drugs-induced liver toxicity // BMC Genomics. – 2016. – Vol. 17, № 1. – Р. 755. https://doi.org/10.1186/s12864-016-3078-3</mixed-citation><mixed-citation xml:lang="en">Petros Z., Lee M.M., Takahashi A., Zhang Y., Yimer G., Habtewold A., Amogne W., Aderaye G., Schuppe-Koistinen I., Mushiroda T., Makonnen E., Kubo M., Aklillu E. Genome-wide association and replication study of anti-tuberculosis drugs-induced liver toxicity. BMC Genomics, 2016, vol. 17, no. 1, pp. 755. https://doi.org/10.1186/s12864-016-3078-3</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Rens N.E., Uyl-de Groot C.A., Goldhaber-Fiebert J.D., Croda J., Andrews J.R. Cost-effectiveness of a pharmacogenomic test for stratified isoniazid dosing in treatment of active tuberculosis // Clinical Infectious Diseases. – 2020. – № 71. – Р. 3136-3143. https://doi.org/10.1093/cid/ciz1212</mixed-citation><mixed-citation xml:lang="en">Rens N.E., Uyl-de Groot C.A., Goldhaber-Fiebert J.D., Croda J., Andrews J.R. Cost-effectiveness of a pharmacogenomic test for stratified isoniazid dosing in treatment of active tuberculosis. Clinical Infection Diseases, 2020, no. 71, pp. 3136-3143. https://doi.org/10.1093/cid/ciz1212</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Richardson M., Kirkham J., Dwan K., Sloan D.J., Davies G., Jorgensen A.L. NAT2 variants and toxicity related to anti-tuberculosis agents: a systematic review and meta-analysis // International Journal of Tuberculosis and Lung Disease. – 2019. – Vol. 23, № 3. – Р. 293-305. https://doi.org/10.5588/ijtld.18.0324</mixed-citation><mixed-citation xml:lang="en">Richardson M., Kirkham J., Dwan K., Sloan D.J., Davies G., Jorgensen A.L. NAT2 variants and toxicity related to anti-tuberculosis agents: a systematic review and meta-analysis. International Journal Tuberculosis and Lung Disease, 2019, vol. 23, no. 3, pp. 293-305. https://doi.org/10.5588/ijtld.18.0324</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Santoso S.B., Pribadi P., Irham L.M. Isoniazid-induced liver injury risk level in different variants of N-acetyltransferase 2 (NAT2) polymorphisms: a literature review // Pharmacia. – 2023. – Vol.70, № 4. – Р. 973-981. https://doi.org/10.3897/pharmacia.70.e109869</mixed-citation><mixed-citation xml:lang="en">Santoso S.B., Pribadi P., Irham L.M. Isoniazid-induced liver injury risk level in different variants of N-acetyltransferase 2 (NAT2) polymorphisms: a literature review. Pharmacia, 2023, vol. 70, no. 4, pp. 973-981. https://doi.org/10.3897/pharmacia.70.e109869</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Schiuma M., Dinegro S., Battini V., Torre A., Covizzi A., Civati A., et al. NAT2 acetylation status predicts hepatotoxicity during antituberculosis therapy: cumulative risk analysis of a multiethnic cohort // International Journal of Molecular Sciences. – 2025.– Vol. 26, № 8. – Р. 3881. https://doi.org/10.3390/ijms26083881</mixed-citation><mixed-citation xml:lang="en">Schiuma M., Dinegro S., Battini V., Torre A., Covizzi A., Civati A. et al. NAT2 acetylation status predicts hepatotoxicity during antituberculosis therapy: cumulative risk analysis of a multiethnic cohort. International Journal of Molecular Sciences, 2025, vol. 26, no. 8, pp. 3881. https://doi.org/10.3390/ijms26083881</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Sherwin K.B.S, de Kock L., Diacon A.H., Werely C.J., Xia H., Rosenkranz B., van der Merwe L., Donald P.R. N-Acetyltransferase genotypes and the pharmacokinetics and tolerability of para-aminosalicylic acid in patients with drug-resistant pulmonary tuberculosis // Antimicrob Agents Chemotherю – 2015. – Vol. 59, № 7. –Р. 4129-4138. https://doi.org/10.1128/aac.04049-14</mixed-citation><mixed-citation xml:lang="en">Sherwin K.B.S, de Kock L., Diacon A.H., Werely C.J., Xia H., Rosenkranz B., van der Merwe L., Donald P.R. N-Acetyltransferase genotypes and the pharmacokinetics and tolerability of para-aminosalicylic acid in patients with drug-resistant pulmonary tuberculosis. Antimicrob. Agents Chemother., 2015, vol. 59, no. 7, pp. 4129-4138. https://doi.org/10.1128/aac.04049-14</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Sileshi T., Makonnen E., Telele N.F., Barclay V., Zumla A., Aklillu E. Variability in plasma rifampicin concentrations and role of SLCO1B1, ABCB1, AADAC2 and CES2 genotypes in Ethiopian patients with tuberculosis // Infect Dis (Lond). – 2024. – Vol. 56, № 4. – P. 308-319. https://doi.org/10.1080/23744235.2024.2309348</mixed-citation><mixed-citation xml:lang="en">Sileshi T., Makonnen E., Telele N.F., Barclay V., Zumla A., Aklillu E. Variability in plasma rifampicin concentrations and role of SLCO1B1, ABCB1, AADAC2 and CES2 genotypes in Ethiopian patients with tuberculosis. Infect. Dis. (Lond.), 2024, vol. 56, no. 4, pp. 308-319. https://doi.org/10.1080/23744235.2024.2309348</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Spahn C., Toda N., Groat B., Aimer O., Rogers S., Oni-Orisan A., Monte A., Hakooz N. and the Pharmacogenomics Global Research Network Publications Committee. Transforming pharmacovigilance with pharmacogenomics: toward personalized risk management // Clinical Pharmacology &amp; Therapeutics. – 2025. – Vol. 18, № 6. – Р. 1286-1296. https://doi.org/10.1002/cpt.70095.</mixed-citation><mixed-citation xml:lang="en">Spahn C., Toda N., Groat B., Aimer O., Rogers S., Oni-Orisan A., Monte A., Hakooz N. and the Pharmacogenomics Global Research Network Publications Committee. Transforming pharmacovigilance with pharmacogenomics: toward personalized risk management. Clinical Pharmacology &amp; Therapeutics, 2025, vol. 18, no. 6, pp. 1286-1296. https://doi.org/10.1002/cpt.70095.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Sundell J., Bienvenu E., Birgersson S., Äbelö A., Ashton M. Population pharmacokinetics and pharmacogenetics of ethambutol in adult patients coinfected with tuberculosis and HIV // Antimicrob Agents Chemother. – 2020. – Vol. 64, №2. – Р. e01583-19. https://doi.org/10.1128/AAC.01583-19</mixed-citation><mixed-citation xml:lang="en">Sundell J., Bienvenu E., Birgersson S., Äbelö A., Ashton M. Population pharmacokinetics and pharmacogenetics of ethambutol in adult patients coinfected with tuberculosis and HIV. Antimicrob. Agents Chemother., 2020, vol. 64, no. 2, pp. e01583-19. https://doi.org/10.1128/AAC.01583-19</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Tarazjani A.D., Jouabadi S.M., Jouabadi S.M., Naderi E., Sturkenboom M., Ahmadizar F. Genetic polymorphism and risk of anti-tuberculosis drug-induced liver injury (AT-DILI): a systematic review and meta-analysis. 2025. Available at: https://www.medrxiv.org/collection/pharmacology-andtherapeutics?page=2 [Accessed 21.11.2025].</mixed-citation><mixed-citation xml:lang="en">Tarazjani A.D., Jouabadi S.M., Jouabadi S.M., Naderi E., Sturkenboom M., Ahmadizar F. Genetic polymorphism and risk of anti-tuberculosis drug-induced liver injury (AT-DILI): a systematic review and meta-analysis. 2025. Available: https://www.medrxiv.org/collection/pharmacology-andtherapeutics?page=2 Accessed November 21, 2025</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Ulanova V., Kivrane A., Viksna A., Pahirko L., Freimane L., Sadovska D., et al. Effect of NAT2, GSTM1 and CYP2E1 genetic polymorphisms on plasma concentration of isoniazid and its metabolites in patients with tuberculosis, and the assessment of exposure-response relationships // Front Pharmacol. – 2024. – № 15. – Р. 1332752. https://doi.org/10.3389/fphar.2024.1332752.</mixed-citation><mixed-citation xml:lang="en">Ulanova V., Kivrane A., Viksna A., Pahirko L., Freimane L., Sadovska D. et al. Effect of NAT2, GSTM1 and CYP2E1 genetic polymorphisms on plasma concentration of isoniazid and its metabolites in patients with tuberculosis, and the assessment of exposure-response relationships. Front. Pharmacol., 2024, no. 15, pp. 1332752. https://doi.org/10.3389/fphar.2024.1332752.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Verma R., da Silva K.E., Rockwood N., Wasmann R.E., Yende N., Song T., Kim E., Denti P., Wilkinson R.J., Andrews J.R. A Nanopore sequencing-based pharmacogenomic panel to personalize tuberculosis drug dosing //American Journal of Respiratory and Critical Care Medicine. – 2024. – Vol. 209, № 12. – Р. 1486-1496. https://doi.org/10.1164/rccm.202309-1583OC.</mixed-citation><mixed-citation xml:lang="en">Verma R., da Silva K.E., Rockwood N., Wasmann R.E., Yende N., Song T., Kim E., Denti P., Wilkinson R.J., Andrews J.R. A Nanopore sequencing-based pharmacogenomic panel to personalize tuberculosis drug dosing. American Journal of Respiratory and Critical Care Medicine, 2024, vol. 209, no. 12, pp. 1486-1496. https://doi.org/10.1164/rccm.202309-1583OC.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">VigiAccess. Available at: https://www.vigiaccess.org/ [Accessed 21.11.2025].</mixed-citation><mixed-citation xml:lang="en">VigiAccess. Available: https://www.vigiaccess.org/ Accessed November 21, 2025</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Weiner M., Gelfond J., Johnson-Pais T.L., Engle M., Peloquin C.A., Johnson J.L., Sizemore E.E., Mac Kenzie W.R. Elevated plasma moxifloxacin concentrations and SLCO1B1 g.-11187G&gt;A polymorphism in adults with pulmonary tuberculosis // Antimicrobial Agents and Chemotherapy. – 2018. – Vol. 62, № 5. – Р. e01802 01817.</mixed-citation><mixed-citation xml:lang="en">Weiner M., Gelfond J., Johnson-Pais T.L., Engle M., Peloquin C.A., Johnson J.L., Sizemore E.E., Mac Kenzie W.R. Elevated plasma moxifloxacin concentrations and SLCO1B1 g.-11187G&gt;A polymorphism in adults with pulmonary tuberculosis. Antimicrobial Agents and Chemotherapy, 2018, vol. 62, no. 5, pp. e01802 01817.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">WHO. Global Tuberculosis Report 2024. – Geneva: World Health Organization. – 2024. – P. 1-68. Available at: https://worldhealthorg.shinyapps.io/tb_profiles/ [Accessed 21.10.2025]</mixed-citation><mixed-citation xml:lang="en">WHO, Global Tuberculosis Report 2024. Geneva, World Health Organization. 2024, pp. 1-68. Available: https://worldhealthorg.shinyapps.io/tb_profiles/ Accessed October 21, 2025</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Yang S., Hwang S.J., Park J.Y., Chung E.K., Lee J.I. Association of genetic polymorphisms of CYP2E1, NAT2, GST and SLCO1B1 with the risk of anti-tuberculosis drug-induced liver injury: a systematic review and meta-analysis // BMJ Open. – 2019. – Vol. 9, № 8. – Р. e027940. https://doi.org/10.1136/bmjopen-2018-027940</mixed-citation><mixed-citation xml:lang="en">Yang S., Hwang S.J., Park J.Y., Chung E.K., Lee J.I. Association of genetic polymorphisms of CYP2E1, NAT2, GST and SLCO1B1 with the risk of anti-tuberculosis drug-induced liver injury: a systematic review and meta-analysis. BMJ Open, 2019, vol. 9, no. 8, pp. e027940. https://doi.org/ 0.1136/bmjopen-2018-027940</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang M., Wang S., Wilffert B., Tong R., van Soolingen D., van den Hof S., Alffenaar J.W. The association between the NAT2 genetic polymorphisms and risk of DILI during anti-TB treatment: a systematic review and meta-analysis // Br J Clin Pharmacol. – 2018. – Vol. 84, № 12. – Р. 2747-2760. https://doi.org/10.1111/bcp.13722</mixed-citation><mixed-citation xml:lang="en">Zhang M., Wang S., Wilffert B., Tong R., van Soolingen D., van den Hof S., Alffenaar J.W. The association between the NAT2 genetic polymorphisms and risk of DILI during anti-TB treatment: a systematic review and meta-analysis. Br. J. Clin. Pharmacol., 2018, vol. 84, no. 12, pp. 2747-2760. https://doi.org/10.1111/bcp.13722</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang X.H., Xie Y., Xu Q.G., Cao K., Xu K., Jin Z.B., Li Y., Wei S.H. Mitochondrial mutations in ethambutol-induced optic neuropathy // Front Cell Dev Biol. – 2021. – № 9. – Р. 754676. https://doi.org/10.3389/fcell.2021.754676</mixed-citation><mixed-citation xml:lang="en">Zhang X.H., Xie Y., Xu Q.G., Cao K., Xu K., Jin Z.B., Li Y., Wei S.H. Mitochondrial mutations in ethambutol-induced optic neuropathy. Front. Cell Dev. Biol., 2021, no. 9, pp. 754676. https://doi.org/10.3389/fcell.2021.754676</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Zou J., Chen S., Rao W., Fu L, Zhang J., Liao Y., et al. Population pharmacokinetic modeling of bedaquiline among multidrug-resistant pulmonary tuberculosis patients from China // Antimicrob Agents Chemother. – 2022. – Vol. 66, №10. – Р. e0081122. https://doi.org/10.1128/aac.00811-22</mixed-citation><mixed-citation xml:lang="en">Zou J., Chen S., Rao W., Fu L, Zhang J., Liao Y. et al. Population pharmacokinetic modeling of bedaquiline among multidrug-resistant pulmonary tuberculosis patients from China. Antimicrob. Agents Chemother., 2022, vol. 66, no. 10, pp. e0081122. https://doi.org/10.1128/aac.00811-22</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>
