<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">RUDN Journal of Medicine</journal-id><journal-title-group><journal-title xml:lang="en">RUDN Journal of Medicine</journal-title><trans-title-group xml:lang="ru"><trans-title>Вестник Российского университета дружбы народов. Серия: Медицина</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2313-0245</issn><issn publication-format="electronic">2313-0261</issn><publisher><publisher-name xml:lang="en">Peoples’ Friendship University of Russia named after Patrice Lumumba (RUDN University)</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">39711</article-id><article-id pub-id-type="doi">10.22363/2313-0245-2024-28-1-153-171</article-id><article-id pub-id-type="edn">ZTVZEJ</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>CARDIOLOGY</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>КАРДИОЛОГИЯ</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Hypolypidemic therapy in the XXI century: what is new?</article-title><trans-title-group xml:lang="ru"><trans-title>Гиполипидемическая терапия в XXI веке: что нового?</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2072-5511</contrib-id><contrib-id contrib-id-type="spin">7700-0707</contrib-id><name-alternatives><name xml:lang="en"><surname>Ob’edkova</surname><given-names>Natalya Yu.</given-names></name><name xml:lang="ru"><surname>Объедкова</surname><given-names>Н. Ю.</given-names></name></name-alternatives><email>obedkovany@kursksmu.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0005-7029-2541</contrib-id><name-alternatives><name xml:lang="en"><surname>Usacheva</surname><given-names>Diana N.</given-names></name><name xml:lang="ru"><surname>Усачева</surname><given-names>Д. Н.</given-names></name></name-alternatives><email>obedkovany@kursksmu.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6290-1195</contrib-id><contrib-id contrib-id-type="spin">4371-7708</contrib-id><name-alternatives><name xml:lang="en"><surname>Mal</surname><given-names>Galina S.</given-names></name><name xml:lang="ru"><surname>Маль</surname><given-names>Г. С.</given-names></name></name-alternatives><email>obedkovany@kursksmu.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0566-1476</contrib-id><name-alternatives><name xml:lang="en"><surname>Ob’edkov</surname><given-names>Evgenij G.</given-names></name><name xml:lang="ru"><surname>Объедков</surname><given-names>Е. Г.</given-names></name></name-alternatives><email>obedkovany@kursksmu.net</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Kursk State Medical University</institution></aff><aff><institution xml:lang="ru">Курский государственный медицинский университет</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2024-06-29" publication-format="electronic"><day>29</day><month>06</month><year>2024</year></pub-date><volume>28</volume><issue>2</issue><issue-title xml:lang="en">CARDIOLOGY</issue-title><issue-title xml:lang="ru">КАРДИОЛОГИЯ</issue-title><fpage>153</fpage><lpage>171</lpage><history><date date-type="received" iso-8601-date="2024-06-29"><day>29</day><month>06</month><year>2024</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Ob’edkova N.Y., Usacheva D.N., Mal G.S., Ob’edkov E.G.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2024, Объедкова Н.Ю., Усачева Д.Н., Маль Г.С., Объедков Е.Г.</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Ob’edkova N.Y., Usacheva D.N., Mal G.S., Ob’edkov E.G.</copyright-holder><copyright-holder xml:lang="ru">Объедкова Н.Ю., Усачева Д.Н., Маль Г.С., Объедков Е.Г.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by-nc/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://journals.rudn.ru/medicine/article/view/39711">https://journals.rudn.ru/medicine/article/view/39711</self-uri><abstract xml:lang="en"><p style="text-align: justify;"><italic>Relevance.</italic> The leading position in mortality throughout the world is occupied by cardiovascular diseases, caused be atherosclerosis process. Statins used to be the gold standard of lipid-lowering therapy for a long time due to their high efficacy, optimal tolerance and safety. Nowadays it has been proved that statins reduce low-density lipoprotein levels in high doses by more than 50 %, in medium doses for about 30–49 %. However, often achieving the target level of lipoproteins is not possible due to a variety of reasons, what became a motivation for creating new drugs. The evidence base for the newest lipid-lowering drugs, some of which have already been approved for clinical use according to the publications in the scientific databases Scopus, PubMed, Web of Science for last 10 years. Main results of the most significant clinical trials of drugs’ effectiveness and safety are described including medicines: alirocumab, inclisiran, bococizumab, pelacarsen, mipomersen, bempedoic acid, lomitapide, evinocumab and also methods of therapeutic lipoprotein apheresis. Dyslipidemia pathogenetic points are considered like inhibition of proprotein convertase subtilisin-kexin type 9, suppression of genes synthesizing lipoprotein (a) by antisense oligonucleotides, cholesterol synthesis suppression by inactivation of adenosine triphosphate-citrate lyase enzyme; the action of microsomal inhibitors of triglyceride transfer protein. <italic>Conclusion</italic>. Searching for new lipid-lowering rational regimens is still ongoing, therefore it is necessary to carefully analyze effectiveness and safety profile for the newest drugs. Some of them like inhibition of proprotein convertase subtilisin-kexin type 9 are actively used in medicine today, while others, the most promising, will be in the future. Ensuring of atherogenic lipoproteins complete control will subsequently make a significant contribution to the primary and secondary cardiovascular diseases prevention, which will save many human lives.</p></abstract><trans-abstract xml:lang="ru"><p style="text-align: justify;"><italic>Актуальность</italic>.<bold> </bold>Лидирующие позиции по смертности во всем мире занимают сердечно-сосудистые заболевания, патогенетически обусловленные процессами атеросклероза. Статины длительное время считали золотым стандартом гиполипидемической терапии в связи с высокой эффективностью, относительно хорошей переносимостью и безопасностью. На данный момент доказано, что терапия статинами в высоких дозах снижает уровень холестерина липопротеинов низкой плотности более чем на 50 %, а в средних — примерно на 30–49 %. Однако, в некоторых случаях достичь целевой уровень липопротеинов в целом не представляется возможным ввиду различных причин, что послужило мотивацией к созданию новых гиполипидемических средств. В статье представлена доказательная база новейших препаратов с липидснижающим действием, часть из которых уже одобрена к клиническому применению на основании публикаций в индексируемых научных базах Scopus, PubMed, Web of Science за последние 10 лет. Представлены основные результаты наиболее значимых клинических испытаний эффективности и безопасности таких препаратов, как алирокумаб, инклисиран, бокоцизумаб, пелакарсен, мипомерсен, бемпедоевая кислота, ломитапид, эвинокумаб, а также методики терапевтического афереза липопротеинов. Рассматриваются точки приложения, воздействующие на патогенетические звенья дислипидемиий: ингибирование пропротеиновой конвертазы субтилизин-кексин 9 типа, подавление генов, синтезирующих липопротеин (а) антисмысловыми олигонуклеотидами, супрессия синтеза холестерина путем инактивации фермента аденозинтрифосфат-цитратлиазы (АТФ-цитратлиазы), действие микросомальных ингибиторов белка переноса триглицеридов.<italic> Выводы. </italic>Поиск новых рациональных схем гиполипидемической терапии все еще продолжается, потому необходимо тщательно анализировать профиль эффективности и безопасности новейших препаратов. Некоторые из них, например, ингибиторы пропротеиновой конвертазы субтилизин-кексин типа 9, активно используются в медицине уже сегодня, за другими, самыми перспективными, — будущее. Обеспечение полного контроля над атерогенными липопротеинами впоследствии внесет значительный вклад в первичную и вторичную профилактику сердечно-сосудистых заболеваний, обусловленных атеросклерозом, что спасет множество человеческих жизней.</p></trans-abstract><kwd-group xml:lang="en"><kwd>coronary heart disease</kwd><kwd>dyslipidemia</kwd><kwd>iPCSK9</kwd><kwd>inclisiran</kwd><kwd>pelacarsen</kwd><kwd>bempedoic acid</kwd><kwd>evinocumab</kwd><kwd>lomitapide</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>ишемическая болезнь сердца</kwd><kwd>дислипидемия</kwd><kwd>иPCSK9</kwd><kwd>инклисиран</kwd><kwd>пелакарсен</kwd><kwd>бемпедоевая кислота</kwd><kwd>эвинокумаб</kwd><kwd>ломитапид</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">Chilbert MR, VanDuyn D, Salah S, Clark CM, Ma Q. Combination Therapy of Ezetimibe and Rosuvastatin for Dyslipidemia: Current Insights. Drug Des Devel Ther. 2022;16:2177–2186. doi: 10.2147/DDDT.S332352</mixed-citation><mixed-citation xml:lang="ru">Chilbert M.R., VanDuyn D., Salah S., Clark C.M., Ma Q. Combination Therapy of Ezetimibe and Rosuvastatin for Dyslipidemia: Current Insights // Drug Des. Devel. Ther. 2022. № 16. С. 2177-2186. doi: 10.2147/DDDT.S332352</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">Lee SA, Kim W, Hong TJ, Ahn Y, Kim MH, Hong SJ, Kim BS, Kim SY, Chae IH, Kim BJ, Rhee MY, Shin JH, Kang TS, Cho JM, Kim JS, Lee CW. Effects of Fixed-dose Combination of Low-intensity Rosuvastatin and Ezetimibe Versus Moderate-­intensity Rosuvastatin Monotherapy on Lipid Profiles in Patients With Hypercholesterolemia: A Randomized, Double-­blind, Multicenter, Phase III Study. Clin Ther. 2021;43(9):1573–1589. doi: 10.1016/j.clinthera.2021.07.016</mixed-citation><mixed-citation xml:lang="ru">Lee S.A., Kim W., Hong T.J., Ahn Y., Kim M.H., Hong S.J., Kim B.S., Kim S.Y., Chae I.H., Kim B.J., Rhee M.Y., Shin J.H., Kang T.S., Cho J.M., Kim J.S., Lee C.W. Effects of Fixed-dose Combination of Low-intensity Rosuvastatin and Ezetimibe Versus Moderate-­intensity Rosuvastatin Monotherapy on Lipid Profiles in Patients With Hypercholesterolemia: A Randomized, Double-­blind, Multicenter, Phase III Study // Clin Ther. 2021. V. 43. № 9. P. 1573-1589. doi: 10.1016/j.clinthera.2021.07.016</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">Ob’edkova NYu, Mal’ GS, Selihova EM, Ob’edkov EG. Progression of hyperlipidemia as a result of a new coronavirus infection in patients with coronary heart disease. Innova. 2023;(31):59–62. (In Russian).</mixed-citation><mixed-citation xml:lang="ru">Объедкова Н.Ю., Маль Г.С., Селихова Е.М., Объедков Е.Г. Прогрессирование гиперлипидемии как результат перенесенной новой коронавирусной инфекции у больных ишемической болезнью сердца // Innova. 2023. № . 31. С. 59-62.</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">Medvedeva EA, Grigorenko EA, Mitkovskaya NP. Innovative lipid-­lowering therapy: experience of inclisiran use in the Republic of Belarus. Russian Journal of Cardiology. 2023;28(4):5417. (In Russian). doi: 10.15829/1560-4071-2023-5417</mixed-citation><mixed-citation xml:lang="ru">Медведева Е.А., Григоренко Е.А., Митьковская Н.П. Инновационная гиполипидемическая терапия: опыт применения инклизирана в Республике Беларусь // Российский кардиологический журнал. 2023. T. 28. № 4. C. 5417. doi: 10.15829/1560-4071-2023-5417</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">Diaz R, Li QH, Bhatt DL, Bittner VA, Baccara-­Dinet MT, Goodman SG, Jukema JW, Kimura T, Parkhomenko A, Pordy R, Reiner Ž, Roe MT, Szarek M, Tse HF, White HD, Zahger D, Zeiher AM, Schwartz GG, Steg PG; ODYSSEY OUTCOMES Committees and Investigators. Intensity of statin treatment after acute coronary syndrome, residual risk, and its modification by alirocumab: insights from the ODYSSEY OUTCOMES trial. Eur J Prev Cardiol. 2021;28(1):33–43. doi: 10.1177/2047487320941987</mixed-citation><mixed-citation xml:lang="ru">Diaz R., Li QH, Bhatt D.L., Bittner V.A., Baccara-­Dinet M.T., Goodman S.G., Jukema J.W., Kimura T., Parkhomenko A., Pordy R., Reiner Ž., Roe M.T., Szarek M., Tse H.F., White H.D., Zahger D., Zeiher A.M., Schwartz G.G., Steg P.G.; ODYSSEY OUTCOMES Committees and Investigators. Intensity of statin treatment after acute coronary syndrome, residual risk, and its modification by alirocumab: insights from the ODYSSEY OUTCOMES trial // Eur. J. Prev. Cardiol. 2021. V. 28. № 1. P. 33-43. doi: 10.1177/2047487320941987</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">Jukema JW, Szarek M, Zijlstra LE, de Silva HA, Bhatt DL, Bittner VA, Diaz R, Edelberg JM, Goodman SG, Hanotin C, Harrington RA, Karpov Y, Moryusef A., Pordy R, Prieto JC, Roe MT, White HD, Zeiher AM, Schwartz GG, Steg PG; ODYSSEY OUTCOMES Committees and Investigators. Alirocumab in Patients With Polyvascular Disease and Recent Acute Coronary Syndrome: ODYSSEY OUTCOMES Trial. J Am Coll Cardiol. 2019;74(9):1167–1176. doi: 10.1016/j.jacc.2019.03.013</mixed-citation><mixed-citation xml:lang="ru">Jukema J.W., Szarek M., Zijlstra L.E., de Silva H.A., Bhatt D.L., Bittner V.A., Diaz R., Edelberg J.M., Goodman S.G., Hanotin C., Harrington R.A., Karpov Y., Moryusef A., Pordy R., Prieto J.C., Roe M.T., White H.D., Zeiher A.M., Schwartz G.G., Steg P.G.; ODYSSEY OUTCOMES Committees and Investigators. Alirocumab in Patients With Polyvascular Disease and Recent Acute Coronary Syndrome: ODYSSEY OUTCOMES Trial // J. Am. Coll. Cardiol. 2019. V. 74. № 9. P. 1167-1176. doi: 10.1016/j.jacc.2019.03.013</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">Räber L, Ueki Y, Otsuka T, Losdat S, Häner JD, Lonborg J, Fahrni G, Iglesias JF, van Geuns RJ, Ondracek AS, Radu Juul Jensen MD, Zanchin C, Stortecky S, Spirk D, Siontis GCM, Saleh L, Matter CM, Daemen J, Mach F, Heg D, Windecker S, Engstrøm T, Lang IM, Koskinas KC; PACMAN-AMI collaborators. Effect of Alirocumab Added to High-­Intensity Statin Therapy on Coronary Atherosclerosis in Patients With Acute Myocardial Infarction: The PACMAN-AMI Randomized Clinical Trial. JAMA. 2022;10;327(18):1771–1781. doi: 10.1001/jama.2022.5218</mixed-citation><mixed-citation xml:lang="ru">Räber L., Ueki Y., Otsuka T., Losdat S., Häner J.D., Lonborg J., Fahrni G., Iglesias J.F., van Geuns R.J., Ondracek A.S., Radu Juul Jensen M.D., Zanchin C., Stortecky S., Spirk D., Siontis G.C.M., Saleh L., Matter C.M., Daemen J., Mach F., Heg D., Windecker S., Engstrøm T., Lang I.M., Koskinas K.C.; PACMAN-AMI collaborators. Effect of Alirocumab Added to High-­Intensity Statin Therapy on Coronary Atherosclerosis in Patients With Acute Myocardial Infarction: The PACMAN-AMI Randomized Clinical Trial // JAMA. 2022. № 10;327(18). P. 1771-1781. doi: 10.1001/jama.2022.5218</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">Pérez de Isla L, Díaz-­Díaz JL, Romero MJ, Muñiz-­Grijalvo O, Mediavilla JD, Argüeso R, Sánchez Muñoz-­Torrero JF, Rubio P, Álvarez-­Baños P, Ponte P, Mañas D, Suárez Gutierrez L, Cepeda JM, Casañas M, Fuentes F, Guijarro C, Ángel Barba M, Saltijeral Cerezo A, Padró T, Mata P; SAFEHEART Study Group. Alirocumab and Coronary Atherosclerosis in Asymptomatic Patients with Familial Hypercholesterolemia: The ARCHITECT Study. Circulation. 2023;147(19):1436–1443. doi: 10.1161/CIRCULATIONAHA.122.062557</mixed-citation><mixed-citation xml:lang="ru">Pérez de Isla L., Díaz-­Díaz J.L., Romero M.J., Muñiz-­Grijalvo O., Mediavilla J.D., Argüeso R., Sánchez Muñoz-­Torrero J.F., Rubio P., Álvarez-­Baños P., Ponte P., Mañas D., Suárez Gutierrez L., Cepeda J.M., Casañas M., Fuentes F., Guijarro C., Ángel Barba M., Saltijeral Cerezo A., Padró T., Mata P.; SAFEHEART Study Group. Alirocumab and Coronary Atherosclerosis in Asymptomatic Patients with Familial Hypercholesterolemia: The ARCHITECT Study // Circulation. 2023. V. 147. № 19. P. 1436-1443. doi: 10.1161/CIRCULATIONAHA.122.062557</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">Henry P, Cariou B, Farnier M, Lakhdari SL, Detournay B. Lipid-lowering efficacy and safety of alirocumab in a real-life setting in France: Insights from the ODYSSEY APPRISE study. Arch Cardiovasc Dis. 2023;116(1):3–8. doi: 10.1016/j.acvd.2022.10.004</mixed-citation><mixed-citation xml:lang="ru">Henry P., Cariou B., Farnier M., Lakhdari S.L., Detournay B. Lipid-lowering efficacy and safety of alirocumab in a real-life setting in France: Insights from the ODYSSEY APPRISE study // Arch Cardiovasc Dis. 2023. V. 116. № 1. P. 3-8. doi: 10.1016/j.acvd.2022.10.004</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">Sopenko IV, Rasova SA, Semenikhina PA, Ulanova TV. Modern aspects of hypolipidemic therapy: safety and efficiency. IScience. 2021;(6–3(74));102–110 (In Russian).</mixed-citation><mixed-citation xml:lang="ru">Сопенко И.В., Расова С.А., Семенихина П.А., Уланова Т.В. Современные аспекты гиполипидемической терапии: безопасность и эффективность // Актуальные научные исследования в современном мире. 2021. № (6-3(74)). C. 102-110. EDN: IVAHTT</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">Shikaleva AA, Maximov ML, Kiseleva NM. Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors in the treatment of dyslipidemia. Meditsinskiy sovet    =    Medical Council. 2020;(21):12–18. (In Russian) doi: 10.21518/2079-701X-2020-21-12-18</mixed-citation><mixed-citation xml:lang="ru">Шикалева А.А., Максимов М.Л., Киселева Н.М. Ингибиторы пропротеин конвертазы субтилизин/кексин типа 9 (PCSK9) в лечении дислипидемии // Медицинский совет. 2020. № 21. С. 12-18. doi: 10.21518/2079-701X-2020-21-12-18</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">Raal FJ, Kallend D, Ray KK, Turner T, Koenig W, Wright RS, Wijngaard PLJ, Curcio D, Jaros MJ, Leiter LA, Kastelein JJP.; ORION‑9 Investigators. Inclisiran for the Treatment of Heterozygous Familial Hypercholesterolemia. N Engl J Med. 2020;382(16):1520–1530. doi: 10.1056/NEJMoa1913805</mixed-citation><mixed-citation xml:lang="ru">Raal F.J., Kallend D., Ray K.K., Turner T., Koenig W., Wright R.S., Wijngaard P.L.J., Curcio D., Jaros M.J., Leiter L.A., Kastelein J.J.P.; ORION-9 Investigators. Inclisiran for the Treatment of Heterozygous Familial Hypercholesterolemia // N. Engl. J. Med. 2020. V. 382. № 16. P. 1520-1530. doi: 10.1056/NEJMoa1913805</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">Ennezat PV, Guerbaai RA, Maréchaux S, Le Jemtel TH, François P. Extent of Low-density Lipoprotein Cholesterol Reduction and All-cause and Cardiovascular Mortality Benefit: A Systematic Review and Meta-analysis. J Cardiovasc Pharmacol. 2023;81(1):35–44. doi: 10.1097/FJC.0000000000001345</mixed-citation><mixed-citation xml:lang="ru">Ennezat P.V., Guerbaai R.A., Maréchaux S., Le Jemtel T.H., François P. Extent of Low-density Lipoprotein Cholesterol Reduction and All-cause and Cardiovascular Mortality Benefit: A Systematic Review and Meta-analysis // J. Cardiovasc. Pharmacol. 2023. V. 81. N 1. P. 35-44. doi: 10.1097/FJC.0000000000001345</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">Kudina EV, Samkova IA, Larina VN. Hypolipidemic therapy: evidence-­based effectiveness and new perspectives. Consilium Medicum. 2020;22(10): 55–60. (In Russian). doi.org/10.26442/20751753.2020.10.200292</mixed-citation><mixed-citation xml:lang="ru">Кудина Е.В., Самкова И.А., Ларина В.Н. Гиполипидемическая терапия: доказанная эффективность и новые перспективы // Consilium Medicum. 2020. V. 22. № 10. P. 55-60. doi.org/10.26442/20751753.2020.10.200292</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">Ray KK, Troquay RPT, Visseren FLJ, Leiter LA, Scott Wright R, Vikarunnessa S, Talloczy Z, Zang X, Maheux P, Lesogor A, Landmesser U. Long-term efficacy and safety of inclisiran in patients with high cardiovascular risk and elevated LDL cholesterol (ORION‑3): results from the 4‑year open-label extension of the ORION‑1 trial. Lancet Diabetes Endocrinol. 2023;11(2):109–119. doi: 10.1016/S2213-8587(22)00353-9</mixed-citation><mixed-citation xml:lang="ru">Ray K.K., Troquay R.P.T., Visseren F.L.J., Leiter L.A., Scott Wright R., Vikarunnessa S., Talloczy Z., Zang X., Maheux P., Lesogor A., Landmesser U. Long-term efficacy and safety of inclisiran in patients with high cardiovascular risk and elevated LDL cholesterol (ORION-3): results from the 4-year open-label extension of the ORION-1 trial // Lancet Diabetes Endocrinol. 2023. V. 11. № 2. P. 109-119. doi: 10.1016/S2213-8587(22)00353-9</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">Ray KK, Kallend D, Leiter LA, Raal FJ, Koenig W, Jaros MJ, Schwartz GG, Landmesser U, Garcia Conde L, Wright RS; ORION‑11 Investigators. Effect of inclisiran on lipids in primary prevention: the ORION‑11 trial. Eur Heart J. 2022;43(48):5047–5057. doi: 10.1093/eurheartj/ehac615</mixed-citation><mixed-citation xml:lang="ru">Ray K.K., Kallend D., Leiter L.A., Raal F.J., Koenig W., Jaros M.J., Schwartz G.G., Landmesser U., Garcia Conde L., Wright R.S.; ORION-11 Investigators. Effect of inclisiran on lipids in primary prevention: the ORION-11 trial // Eur. Heart J. 2022. V. 43. № 48. P. 5047-5057. doi: 10.1093/eurheartj/ehac615</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">Reijman MD, Schweizer A, Peterson ALH, Bruckert E, Stratz C, Defesche JC, Hegele RA, Wiegman A. Rationale and design of two trials assessing the efficacy, safety, and tolerability of inclisiran in adolescents with homozygous and heterozygous familial hypercholesterolaemia. Eur J Prev Cardiol. 2022;29(9):1361–1368. doi: 10.1093/eurjpc/zwac025</mixed-citation><mixed-citation xml:lang="ru">Reijman M.D., Schweizer A., Peterson A.L.H., Bruckert E., Stratz C., Defesche J.C., Hegele R.A., Wiegman A. Rationale and design of two trials assessing the efficacy, safety, and tolerability of inclisiran in adolescents with homozygous and heterozygous familial hypercholesterolaemia // Eur. J. Prev. Cardiol. 2022. V. 29. № 9. P. 1361-1368. doi: 10.1093/eurjpc/zwac025</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">Zyryanov SK, Butranova OI. New opportunities for lowering low-density lipoprotein cholesterol: comparative characteristics of PCSK9‑targeted therapy. Russian Journal of Cardiology. 2022;27(11):5271. (In Russian). doi: 10.15829/1560-4071-2022-5271</mixed-citation><mixed-citation xml:lang="ru">Зырянов С.К., Бутранова О.И. Новые возможности снижения уровня холестерина липопротеидов низкой плотности: сравнительные характеристики PCSK9-таргетной терапии // Российский кардиологический журнал. 2022. Vol. 27. № 11. P. 5271. doi: 10.15829/1560-4071-2022-5271</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">Grześk G, Dorota B, Wołowiec Ł, Wołowiec A, Osiak J, Kozakiewicz M, Banach J. Safety of PCSK9 inhibitors. Biomed Pharmacother. 2022;156:113957. doi: 10.1016/j.biopha.2022</mixed-citation><mixed-citation xml:lang="ru">Grześk G., Dorota B., Wołowiec Ł., Wołowiec A., Osiak J., Kozakiewicz M., Banach J. Safety of PCSK9 inhibitors // Biomed Pharmacother. 2022. V. 156. P. 113957. doi: 10.1016/j.biopha.2022</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">Sosnowska B, Surma S, Banach M. Targeted Treatment against Lipoprotein (a): The Coming Breakthrough in Lipid Lowering Therapy. Pharmaceuticals (Basel). 2022;15(12):1573. doi: 10.3390/ph15121573</mixed-citation><mixed-citation xml:lang="ru">Sosnowska B., Surma S., Banach M. Targeted Treatment against Lipoprotein (a): The Coming Breakthrough in Lipid Lowering Therapy // Pharmaceuticals (Basel). 2022. V. 15. № 12. P. 1573. doi: 10.3390/ph15121573</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">Kosmas CE, Bousvarou MD, Papakonstantinou EJ, Tsamoulis D, Koulopoulos A, Echavarria Uceta R, Guzman E, Rallidis LS. Novel Pharmacological Therapies for the Management of Hyperlipoproteinemia(a). Int J Mol Sci. 2023;24(17):13622. doi: 10.3390/ijms241713622</mixed-citation><mixed-citation xml:lang="ru">Kosmas C.E., Bousvarou M.D., Papakonstantinou E.J., Tsamoulis D., Koulopoulos A., Echavarria Uceta R., Guzman E., Rallidis L.S. Novel Pharmacological Therapies for the Management of Hyperlipoproteinemia(a) // Int. J. Mol.Sci. 2023. V. 24. № 17. P. 13622. doi: 10.3390/ijms241713622</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">Korneva VA, Kuznetsova TY, Julius U. Modern Approaches to Lower Lipoprotein(a) Concentrations and Consequences for Cardiovascular Diseases. Biomedicines. 2021;9(9):1271. doi: 10.3390/biomedicines9091271</mixed-citation><mixed-citation xml:lang="ru">Korneva V.A., Kuznetsova T.Y., Julius U. Modern Approaches to Lower Lipoprotein(a) Concentrations and Consequences for Cardiovascular Diseases // Biomedicines. 2021. V. 9. № 9. P. 1271. doi: 10.3390/biomedicines9091271</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">Chan DC, Watts GF. The Promise of PCSK9 and Lipoprotein(a) as Targets for Gene Silencing Therapies. Clin Ther. 2023; S0149–2918(23)00258–8. doi: 10.1016/j.clinthera.2023.07.008</mixed-citation><mixed-citation xml:lang="ru">Chan D.C., Watts G.F. The Promise of PCSK9 and Lipoprotein(a) as Targets for Gene Silencing Therapies // Clin. Ther. 2023. V. S0149-2918(23)00258-8. doi: 10.1016/j.clinthera.2023.07.008</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">Tsimikas S, Karwatowska-­Prokopczuk E, Gouni-­Berthold I, Tardif JC, Baum SJ, Steinhagen-­Thiessen E, Shapiro MD, Stroes ES, Moriarty PM, Nordestgaard BG, Xia S, Guerriero J, Viney NJ, O’Dea L, Witztum JL; AKCEA-APO(a)-LRx Study Investigators. Lipoprotein(a) Reduction in Persons with Cardiovascular Disease. N Engl J Med. 2020;382(3):244–255. doi: 10.1056/NEJMoa1905239</mixed-citation><mixed-citation xml:lang="ru">Tsimikas S., Karwatowska-­Prokopczuk E., Gouni-­Berthold I., Tardif J.C., Baum S.J., Steinhagen-­Thiessen E., Shapiro M.D., Stroes E.S., Moriarty P.M., Nordestgaard B.G., Xia S., Guerriero J., Viney N.J., O’Dea L., Witztum J.L.; AKCEA-APO(a)-LRx Study Investigators. Lipoprotein(a) Reduction in Persons with Cardiovascular Disease // N. Engl. J. Med. 2020. V. 382. № 3. P. 244-255. doi: 10.1056/NEJMoa1905239</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">Chambergo-­Michilot D, Alur A, Kulkarni S, Agarwala A. Mipomersen in Familial Hypercholesterolemia: An Update on Health-­Related Quality of Life and Patient-­Reported Outcomes. Vasc Health Risk Manag. 2022;18:73–80. doi: 10.2147/VHRM.S191965</mixed-citation><mixed-citation xml:lang="ru">Chambergo-­Michilot D., Alur A., Kulkarni S., Agarwala A. Mipomersen in Familial Hypercholesterolemia: An Update on Health-­Related Quality of Life and Patient-­Reported Outcomes // Vasc. Health Risk Manag. 2022. V. 18. P. 73-80. doi: 10.2147/VHRM.S191965</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">Nurmohamed NS, Navar AM, Kastelein JJP. New and Emerging Therapies for Reduction of LDL–Cholesterol and Apolipoprotein B: JACC Focus Seminar 1/4. J Am Coll Cardiol. 2021;77(12):1564–1575. doi: 10.1016/j.jacc.2020.11.079</mixed-citation><mixed-citation xml:lang="ru">Nurmohamed N.S., Navar A.M., Kastelein J.J.P. New and Emerging Therapies for Reduction of LDL-Cholesterol and Apolipoprotein B: JACC Focus Seminar 1/4 // J. Am. Coll. Cardiol. 2021. V. 77. № 12. P. 1564-1575. doi: 10.1016/j.jacc.2020.11.079</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">Tummala R, Gupta M, Devanabanda AR, Bandyopadhyay D, Aronow WS, Ray KK, Mamas M, Ghosh RK. Bempedoic acid and its role in contemporary management of hyperlipidemia in atherosclerosis. Ann Med. 2022;54(1):1287–1296. doi: 10.1080/07853890.2022.2059559</mixed-citation><mixed-citation xml:lang="ru">Tummala R., Gupta M., Devanabanda A.R., Bandyopadhyay D., Aronow W.S., Ray K.K., Mamas M., Ghosh R.K. Bempedoic acid and its role in contemporary management of hyperlipidemia in atherosclerosis // Ann. Med. 2022. V. 54. № 1. P. 1287-1296. doi: 10.1080/07853890.2022.2059559</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">Ruscica M, Sirtori CR, Carugo S, Banach M, Corsini A. Bempedoic Acid: for Whom and When. Curr Atheroscler Rep. 2022;24(10):791–801. doi: 10.1007/s11883-022-01054-2</mixed-citation><mixed-citation xml:lang="ru">Ruscica M., Sirtori C.R., Carugo S., Banach M., Corsini A. Bempedoic Acid: for Whom and When // Curr Atheroscler Rep. 2022. V. 24. № 10. P. 791-801. doi: 10.1007/s11883-022-01054-2</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">Jialal I, Ramakrishnan N. Bempedoic acid: a novel oral LDL-cholesterol lowering agent. Int J Physiol Pathophysiol Pharmacol. 2022;14(2):84–89.</mixed-citation><mixed-citation xml:lang="ru">Jialal I, Ramakrishnan N. Bempedoic acid: a novel oral LDL-cholesterol lowering agent. Int. J. Physiol. Pathophysiol. Pharmacol. 2022. V. 14. № 2. P. 84-89. URL: https://pubmed.ncbi.nlm.nih.gov/35619668/</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">Ballantyne CM, Bays H, Catapano AL, Goldberg A, Ray KK, Saseen JJ. Role of Bempedoic Acid in Clinical Practice. Cardiovasc Drugs Ther. 2021;35(4):853–864. doi: 10.1007/s10557-021-07147-5</mixed-citation><mixed-citation xml:lang="ru">Ballantyne C.M., Bays H., Catapano A.L., Goldberg A., Ray K.K., Saseen J.J. Role of Bempedoic Acid in Clinical Practice // Cardiovasc Drugs Ther. 2021. V. 35. № 4. P. 853-864. doi: 10.1007/s10557-021-07147-5</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">Cicero AFG, Fogacci F, Hernandez AV, Banach M; Lipid and Blood Pressure Meta-­Analysis Collaboration (LBPMC) Group and the International Lipid Expert Panel (ILEP). Efficacy and safety of bempedoic acid for the treatment of hypercholesterolemia: A systematic review and meta-analysis. PLoS Med. 2020;17(7): e1003121. doi: 10.1371/journal.pmed.1003121</mixed-citation><mixed-citation xml:lang="ru">Cicero A.F.G., Fogacci F., Hernandez A.V., Banach M., Lipid and Blood Pressure Meta-­Analysis Collaboration (LBPMC) Group and the International Lipid Expert Panel (ILEP). Efficacy and safety of bempedoic acid for the treatment of hypercholesterolemia: A systematic review and meta-analysis // PLoS Med. 2020. V. 17. № 7. P. e1003121. doi: 10.1371/journal.pmed.1003121</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">Ray KK, Bays HE, Catapano AL, Lalwani ND, Bloedon LT, Sterling LR, Robinson PL, Ballantyne CM; CLEAR Harmony Trial. Safety and Efficacy of Bempedoic Acid to Reduce LDL Cholesterol. N Engl J Med. 2019;380(11):1022–1032. doi: 10.1056/NEJMoa1803917</mixed-citation><mixed-citation xml:lang="ru">Ray K.K., Bays H.E., Catapano A.L., Lalwani N.D., Bloedon L.T., Sterling L.R., Robinson P.L., Ballantyne C.M. CLEAR Harmony Trial. Safety and Efficacy of Bempedoic Acid to Reduce LDL Cholesterol // N. Engl. J. Med. 2019. V. 380. № 11. P. 1022-1032. doi: 10.1056/NEJMoa1803917</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">Stefanutti C. Lomitapide-a Microsomal Triglyceride Transfer Protein Inhibitor for Homozygous Familial Hypercholesterolemia. Curr Atheroscler Rep. 2020;22(8):38. doi: 10.1007/s11883-020-00858-4</mixed-citation><mixed-citation xml:lang="ru">Stefanutti C. Lomitapide-a Microsomal Triglyceride Transfer Protein Inhibitor for Homozygous Familial Hypercholesterolemia // Curr. Atheroscler. Rep. 2020. V. 22. № 8. P. 38. doi: 10.1007/s11883-020-00858-4</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">Zheng Y, Hu Y, Han Z, Yan F, Zhang S, Yang Z, Zhao F, Li L, Fan J, Wang R, Luo Y. Lomitapide ameliorates middle cerebral artery occlusion-­induced cerebral ischemia/reperfusion injury by promoting neuronal autophagy and inhibiting microglial migration. CNS Neurosci Ther. 2022;28(12):2183–2194. doi: 10.1111/cns.13961</mixed-citation><mixed-citation xml:lang="ru">Zheng Y., Hu Y., Han Z., Yan F., Zhang S., Yang Z., Zhao F., Li L., Fan J., Wang R., Luo Y. Lomitapide ameliorates middle cerebral artery occlusion-­induced cerebral ischemia/reperfusion injury by promoting neuronal autophagy and inhibiting microglial migration // CNS Neurosci. Ther. 2022. V. 28. № 12. P. 2183-2194. doi: 10.1111/cns.13961</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">Larrey D, D’Erasmo L, O’Brien S, Arca M; Italian Working Group on Lomitapide. Long-term hepatic safety of lomitapide in homozygous familial hypercholesterolaemia. Liver Int. 2023;43(2):413–423. doi: 10.1111/liv.15497</mixed-citation><mixed-citation xml:lang="ru">Larrey D., D’Erasmo L., O’Brien S., Arca M.; Italian Working Group on Lomitapide. Long-term hepatic safety of lomitapide in homozygous familial hypercholesterolaemia // Liver Int. 2023. V. 43. № 2. P. 413-423. doi: 10.1111/liv.15497</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">Cefalù AB, D’Erasmo L, Iannuzzo G, Noto D, Giammanco A, Montali A, Zambon A, Forte F, Suppressa P, Giannini S, Barbagallo CM, Ganci A, Nardi E, Vernuccio F, Caldarella R, Ciaccio M, Arca M, Averna M. Efficacy and safety of lomitapide in familial chylomicronaemia syndrome. Atherosclerosis. 2022;359:13–19. doi: 10.1016/j.atherosclerosis.2022.08.017</mixed-citation><mixed-citation xml:lang="ru">Cefalù A.B., D’Erasmo L., Iannuzzo G., Noto D., Giammanco A., Montali A., Zambon A., Forte F., Suppressa P., Giannini S., Barbagallo C.M., Ganci A., Nardi E., Vernuccio F., Caldarella R., Ciaccio M., Arca M., Averna M. Efficacy and safety of lomitapide in familial chylomicronaemia syndrome // Atherosclerosis. 2022. V. 359. P. 13-19. doi: 10.1016/j.atherosclerosis.2022.08.017</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">D’Erasmo L, Bini S, Arca M. Rare Treatments for Rare Dyslipidemias: New Perspectives in the Treatment of Homozygous Familial Hypercholesterolemia (HoFH) and Familial Chylomicronemia Syndrome (FCS). Curr Atheroscler Rep. 2021;23(11):65. doi: 10.1007/s11883-021-00967-8</mixed-citation><mixed-citation xml:lang="ru">D’Erasmo L., Bini S., Arca M. Rare Treatments for Rare Dyslipidemias: New Perspectives in the Treatment of Homozygous Familial Hypercholesterolemia (HoFH) and Familial Chylomicronemia Syndrome (FCS) // Curr. Atheroscler. Rep. 2021. V. 23. № 11. P. 65. doi: 10.1007/s11883-021-00967-8</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">Sosnowska B, Adach W, Surma S, Rosenson RS, Banach M. Evinacumab, an ANGPTL3 Inhibitor, in the Treatment of Dyslipidemia. J Clin Med. 2022;12(1):168. doi: 10.3390/jcm12010168</mixed-citation><mixed-citation xml:lang="ru">Sosnowska B., Adach W., Surma S., Rosenson R.S., Banach M. Evinacumab, an ANGPTL3 Inhibitor, in the Treatment of Dyslipidemia // J. Clin. Med. 2022. V. 12. № 1. P. 168. doi: 10.3390/jcm12010168</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">Deng M, Kutrolli E, Sadewasser A, Michel S, Joibari MM, Jaschinski F, Olivecrona G, Nilsson SK, Kersten S. ANGPTL4 silencing via antisense oligonucleotides reduces plasma triglycerides and glucose in mice without causing lymphadenopathy. J Lipid Res. 2022;63(7):100237. doi: 10.1016/j.jlr.2022.100237</mixed-citation><mixed-citation xml:lang="ru">Deng M., Kutrolli E., Sadewasser A., Michel S., Joibari M.M., Jaschinski F., Olivecrona G., Nilsson S.K., Kersten S. ANGPTL4 silencing via antisense oligonucleotides reduces plasma triglycerides and glucose in mice without causing lymphadenopathy // J. Lipid Res. 2022. V. 63. № 7. P. 100237. doi: 10.1016/j.jlr.2022.100237</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">Sun T, Zhan W, Wei L, Xu Z, Fan L, Zhuo Y, Wang C, Zhang J. Circulating ANGPTL3 and ANGPTL4 levels predict coronary artery atherosclerosis severity. Lipids Health Dis. 2021;20(1):154. doi: 10.1186/s12944-021-01580-z</mixed-citation><mixed-citation xml:lang="ru">Sun T., Zhan W., Wei L., Xu Z., Fan L., Zhuo Y., Wang C., Zhang J. Circulating ANGPTL3 and ANGPTL4 levels predict coronary artery atherosclerosis severity // Lipids Health Dis. 2021. V. 20. № 1 P. 154. doi: 10.1186/s12944-021-01580-z</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">Chen R, Lin S, Chen X. The promising novel therapies for familial hypercholesterolemia. J Clin Lab Anal. 2022;36(7): e24552. doi: 10.1002/jcla.24552</mixed-citation><mixed-citation xml:lang="ru">Chen R., Lin S., Chen X. The promising novel therapies for familial hypercholesterolemia // J. Clin. Lab. Anal. 2022. V. 36. № 7. P. e24552. doi: 10.1002/jcla.24552</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">Ahmad Z, Banerjee P, Hamon S, Chan KC, Bouzelmat A, Sasiela WJ, Pordy R, Mellis S, Dansky H, Gipe DA, Dunbar RL. Inhibition of Angiopoietin-­Like Protein 3 With a Monoclonal Antibody Reduces Triglycerides in Hypertriglyceridemia. Circulation. 2019;140(6):470–486. doi: 10.1161/CIRCULATIONAHA.118.039107</mixed-citation><mixed-citation xml:lang="ru">Ahmad Z., Banerjee P., Hamon S., Chan K.C., Bouzelmat A., Sasiela W.J., Pordy R., Mellis S., Dansky H., Gipe D.A., Dunbar R.L. Inhibition of Angiopoietin-­Like Protein 3 With a Monoclonal Antibody Reduces Triglycerides in Hypertriglyceridemia // Circulation. 2019. V. 140. № 6. P. 470-486. doi: 10.1161/CIRCULATIONAHA.118.039107</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">Harada-­Shiba M, Ali S, Gipe DA, Gasparino E, Son V, Zhang Y, Pordy R, Catapano AL. A randomized study investigating the safety, tolerability, and pharmacokinetics of evinacumab, an ANGPTL3 inhibitor, in healthy Japanese and Caucasian subjects. Atherosclerosis. 2020;314:33–40. doi: 10.1016/j.atherosclerosis.2020.10.013</mixed-citation><mixed-citation xml:lang="ru">Harada-­Shiba M., Ali S., Gipe D.A., Gasparino E., Son V., Zhang Y., Pordy R., Catapano A.L. A randomized study investigating the safety, tolerability, and pharmacokinetics of evinacumab, an ANGPTL3 inhibitor, in healthy Japanese and Caucasian subjects // Atherosclerosis. 2020. V. 314. P. 33-40. doi: 10.1016/j.atherosclerosis.2020.10.013</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">Parhofer KG. Apheresis: What Should a Clinician Know? Curr Atheroscler Rep. 2023;25(3):77–83. doi: 10.1007/s11883-023-01081-7</mixed-citation><mixed-citation xml:lang="ru">Parhofer K.G. Apheresis: What Should a Clinician Know? // Curr Atheroscler Rep. 2023. V. 25. № 3. P. 77-83. doi: 10.1007/s11883-023-01081-7</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><citation-alternatives><mixed-citation xml:lang="en">Kayikcioglu M. LDL Apheresis and Lp (a) Apheresis: A Clinician’s Perspective. Curr Atheroscler Rep. 2021;23(4):15. doi: 10.1007/s11883-021-00911-w.</mixed-citation><mixed-citation xml:lang="ru">Kayikcioglu M. LDL Apheresis and Lp (a) Apheresis: A Clinician’s Perspective // Curr. Atheroscler. Rep. 2021. V. 23. № 4. P. 15. doi: 10.1007/s11883-021-00911-w.</mixed-citation></citation-alternatives></ref><ref id="B46"><label>46.</label><citation-alternatives><mixed-citation xml:lang="en">Taylan C, Weber LT. An update on lipid apheresis for familial hypercholesterolemia. Pediatr Nephrol. 2023;38(2):371–382. doi: 10.1007/s00467-022-05541-1</mixed-citation><mixed-citation xml:lang="ru">Taylan C., Weber L.T. An update on lipid apheresis for familial hypercholesterolemia // Pediatr Nephrol. 2023. V. 38. № 2. P. 371-382. doi: 10.1007/s00467-022-05541-1</mixed-citation></citation-alternatives></ref></ref-list></back></article>
