<?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="review-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">medsovet</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинский Совет</journal-title><trans-title-group xml:lang="en"><trans-title>Meditsinskiy sovet = Medical Council</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2079-701X</issn><issn pub-type="epub">2658-5790</issn><publisher><publisher-name>REMEDIUM GROUP Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21518/ms2025-166</article-id><article-id custom-type="elpub" pub-id-type="custom">medsovet-9132</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>АКТУАЛЬНЫЕ ПРОБЛЕМЫ ЭНДОКРИНОЛОГИИ И КАРДИОЛОГИИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CURRENT ISSUES IN ENDOCRINOLOGY AND CARDIOLOGY</subject></subj-group></article-categories><title-group><article-title>Приоритеты эффективного и безопасного контроля гликемии: алоглиптин в лечении сахарного диабета 2-го типа</article-title><trans-title-group xml:lang="en"><trans-title>Priorities in effective and safe glycemic control: Alogliptin in type 2 diabetes mellitus treatment</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9007-4123</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бирюкова</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Biryukova</surname><given-names>E. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Бирюкова Елена Валерьевна, д.м.н., профессор кафедры эндокринологии и диабетологии </p><p>127006, Россия, Москва, ул. Долгоруковская, д. 4 </p></bio><bio xml:lang="en"><p>Elena V. Biryukova, Dr. Sci. (Med.), Professor of the Department of Endocrinology and Diabetology</p><p>4, Dolgorukovskaya St., Moscow, 127006, Russia</p></bio><email xlink:type="simple">lena@obsudim.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2125-622X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Соловьева</surname><given-names>И. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Solovyeva</surname><given-names>I. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Соловьева Инна Владимировна, ассистент кафедры эндокринологии и диабетологии; заведующая отделением эндокринологии</p><p>127006, Россия, Москва, ул. Долгоруковская, д. 4 </p><p>111123, Россия, Москва, ул. Новогиреевская, д. 1 </p></bio><bio xml:lang="en"><p>Inna V. Solovyeva, Assistant of the Department of Endocrinology and Diabetology; Head of the Endocrinology Department</p><p>4, Dolgorukovskaya St., Moscow, 127006, Russia</p><p>1, Novogireevskaya St., Moscow, 111123, Russia </p></bio><email xlink:type="simple">Inna.dell.85@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2600-7193</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Аверкова</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Averkova</surname><given-names>I. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Аверкова Ирина Александровна, ассистент кафедры эндокринологии и диабетологии</p><p>127006, Россия, Москва, ул. Долгоруковская, д. 4 </p></bio><bio xml:lang="en"><p>Irina A. Averkova, Assistant of the Department of Endocrinology and Diabetology</p><p>4, Dolgorukovskaya St., Moscow, 127006, Russia</p></bio><email xlink:type="simple">irinadok@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Российский университет медицины (РосУниМед)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Russian University of Medicine (ROSUNIMED)</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Российский университет медицины (РосУниМед);&#13;
Московский клинический научный центр имени А.С. Логинова</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Russian University of Medicine (ROSUNIMED);&#13;
Loginov Moscow Clinical Scientific Center</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>24</day><month>05</month><year>2025</year></pub-date><volume>0</volume><issue>6</issue><fpage>256</fpage><lpage>264</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Бирюкова Е.В., Соловьева И.В., Аверкова И.А., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Бирюкова Е.В., Соловьева И.В., Аверкова И.А.</copyright-holder><copyright-holder xml:lang="en">Biryukova E.V., Solovyeva I.V., Averkova I.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.med-sovet.pro/jour/article/view/9132">https://www.med-sovet.pro/jour/article/view/9132</self-uri><abstract><p>Сахарный диабет 2-го типа (СД2) – тяжелое заболевание, связанное с развитием серьезных хронических осложнений при отсутствии целевого гликемического контроля. Обсуждение вопросов эффективного и доступного лечения СД2 чрезвычайно актуально. В последние годы наблюдается существенное расширение арсенала сахароснижающих лекарственных препаратов, что обусловлено углублением понимания механизмов развития сахарного диабета. Раскрыто значение энтероинсулярной оси, инкретиновой системы (глюкагоноподобного пептида 1-го типа (ГПП-1), глюкозозависимого инсулинотропного полипептида (ГИП)) в регуляции углеводного обмена. Ингибиторы дипептидилпептидазы-4 (иДПП-4), также известные как глиптины, относятся к классу сахароснижающих препаратов с инкретиновой активностью. Обсуждаются механизмы действия иДПП-4, подчеркнуты преимущества этой группы препаратов. Глиптины воздействуют на ведущий патофизиологический дефект СД2 – дисфункцию β-клеток поджелудочной железы. Наиболее важным для их сахароснижающего действия является ГПП-1. Ингибиторы ДПП-4 продлевают период полувыведения и доступность эндогенного ГПП-1, подавляя ДПП-4. Прием иДПП-4 не сопровождается развитием гипогликемии или увеличением массы тела, их назначение включено в алгоритмы лечения заболевания на ранних стадиях СД2. Статья посвящена выбору оптимального препарата из группы иДПП-4. Представлены результаты клинических исследований эффективности, переносимости и безопасности алоглиптина, приводятся данные сравнительных исследований с другими сахароснижающими препаратами. Обсуждаются терапевтические преимущества алоглиптина. Препарат показал свою эффективность в качестве монотерапии и в составе комбинированной терапии СД2. Рассматриваются преимущества комбинации алоглиптина и метформина. Разнонаправленное действие этих препаратов на патогенетические механизмы развития СД2 приводит к усилению фармакологических эффектов. Подчеркивается важность рациональных комбинаций сахароснижающих препаратов. Содержащаяся в обзоре информация об эффективном и безопасном контроле гликемии у пациентов с СД2 должна помочь в принятии решений специалистами сферы здравоохранения в повседневной клинической работе.</p></abstract><trans-abstract xml:lang="en"><p>Type 2 diabetes mellitus (T2DM) is a severe disease associated with the development of serious chronic complications without targeted glycemic control. Discussion of issues of effective and affordable treatment of T2DM is of the most immediate interest. Recent years have seen a significant expansion of the glucose-lowering drug arsenal, which resulted from a deeper insight into the mechanisms of diabetes mellitus development. The significance of the entero-insular axis (EIA), the incretin system (glucagon-like peptide type 1 (GLP-1), glucose-dependent insulinotropic polypeptide (GIP)) in the regulation of carbohydrate metabolism has been discovered. Inhibitors of dipeptidyl peptidase-4 (DPP-4is), also known as “gliptins”, belong to the group of incretin-based glucose-lowering drugs. The article discusses the mechanisms of action of DPP-4is and highlights the advantages of this group of drugs. Gliptins act on the major pathophysiological defect in T2DM – pancreatic β-cell dysfunction. GLP-1 is the most important for their glucose-lowering action. DPP-4is extend the half-life and availability of endogenous GLP-1 by inhibiting DPP-4. The use of DPP-4is is not accompanied by the development of hypoglycemia or weight gain, and is included in the algorithms for treating the disease in the early stages of T2DM. The article is devoted to the choice of the right drug from the DPP-4is group. It presents the results of clinical studies evaluating the efficacy, tolerability and safety of alogliptin, and data from studies comparing alogliptin with other glucose-lowering drugs. The therapeutic advantages of alogliptin are discussed. The drug has shown its effectiveness as monotherapy and as part of combination therapy in T2DM. The advantages of alogliptin and metformin combination are considered. The multi-directional action of these drugs on the pathogenetic mechanisms of T2DM leads to an increase in pharmacological effects. The importance of rational combinations of glucose-lowering drugs is emphasized. The information provided in the review concerning effective and safe glycemic control in patients with T2DM should help health professionals to make decisions in their daily clinical practice.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>гликированный гемоглобин</kwd><kwd>сахароснижающая терапия</kwd><kwd>гипогликемии</kwd><kwd>ингибиторы ДПП-4</kwd><kwd>алоглиптин</kwd></kwd-group><kwd-group xml:lang="en"><kwd>glycated hemoglobin</kwd><kwd>glucose-lowering therapy</kwd><kwd>hypoglycemia</kwd><kwd>DPP-4is</kwd><kwd>alogliptin</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">Lovic D, Piperidou A, Zografou I, Grassos H, Pittaras A, Manolis A. The Growing Epidemic of Diabetes Mellitus. Curr Vasc Pharmacol. 2020;18(2):104–109. https://doi.org/10.2174/1570161117666190405165911.</mixed-citation><mixed-citation xml:lang="en">Lovic D, Piperidou A, Zografou I, Grassos H, Pittaras A, Manolis A. The Growing Epidemic of Diabetes Mellitus. Curr Vasc Pharmacol. 2020;18(2):104–109. https://doi.org/10.2174/1570161117666190405165911.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Gerstein HC, Santaguida P, Raina P, Morrison KM, Balion C, Hunt D et al. Annual incidence and relative risk of diabetes in people with various categories of dysglycemia: a systematic overview and meta-analysis of prospective studies. Diabetes Res Clin Pract. 2007;78(3):305–312. https://doi.org/10.1016/j.diabres.2007.05.004.</mixed-citation><mixed-citation xml:lang="en">Gerstein HC, Santaguida P, Raina P, Morrison KM, Balion C, Hunt D et al. Annual incidence and relative risk of diabetes in people with various categories of dysglycemia: a systematic overview and meta-analysis of prospective studies. Diabetes Res Clin Pract. 2007;78(3):305–312. https://doi.org/10.1016/j.diabres.2007.05.004.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">DeMarsilis A, Reddy N, Boutari C, Filippaios A, Sternthal E, Katsiki N, Mantzoros C. Pharmacotherapy of type 2 diabetes: An update and future directions. Metabolism. 2022;137:155332. https://doi.org/10.1016/j.metabol.2022.155332.</mixed-citation><mixed-citation xml:lang="en">DeMarsilis A, Reddy N, Boutari C, Filippaios A, Sternthal E, Katsiki N, Mantzoros C. Pharmacotherapy of type 2 diabetes: An update and future directions. Metabolism. 2022;137:155332. https://doi.org/10.1016/j.metabol.2022.155332.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Lu X, Xie Q, Pan X, Zhang R, Zhang X, Peng G et al. Type 2 diabetes mellitus in adults: pathogenesis, prevention and therapy. Signal Transduct Target Ther. 2024;9(1):262. https://doi.org/10.1038/s41392-024-01951-9.</mixed-citation><mixed-citation xml:lang="en">Lu X, Xie Q, Pan X, Zhang R, Zhang X, Peng G et al. Type 2 diabetes mellitus in adults: pathogenesis, prevention and therapy. Signal Transduct Target Ther. 2024;9(1):262. https://doi.org/10.1038/s41392-024-01951-9.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Rizzo M, Nauck MA, Mantzoros CS. Incretin-based therapies in 2021 – Current status and perspectives for the future. Metabolism. 2021;122:154843. https://doi.org/10.1016/j.metabol.2021.154843.</mixed-citation><mixed-citation xml:lang="en">Rizzo M, Nauck MA, Mantzoros CS. Incretin-based therapies in 2021 – Current status and perspectives for the future. Metabolism. 2021;122:154843. https://doi.org/10.1016/j.metabol.2021.154843.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Sesti G, Avogaro A, Belcastro S, Bonora BM, Croci M, Daniele G et al. Ten years of experience with DPP-4 inhibitors for the treatment of type 2 diabetes mellitus. Acta Diabetol. 2019;56(6):605–617. https://doi.org/10.1007/s00592-018-1271-3.</mixed-citation><mixed-citation xml:lang="en">Sesti G, Avogaro A, Belcastro S, Bonora BM, Croci M, Daniele G et al. Ten years of experience with DPP-4 inhibitors for the treatment of type 2 diabetes mellitus. Acta Diabetol. 2019;56(6):605–617. https://doi.org/10.1007/s00592-018-1271-3.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Deacon CF. Dipeptidyl peptidase 4 inhibitors in the treatment of type 2 diabetes mellitus. Nat Rev Endocrinol. 2020;16(11):642–653. https://doi.org/10.1038/s41574-020-0399-8.</mixed-citation><mixed-citation xml:lang="en">Deacon CF. Dipeptidyl peptidase 4 inhibitors in the treatment of type 2 diabetes mellitus. Nat Rev Endocrinol. 2020;16(11):642–653. https://doi.org/10.1038/s41574-020-0399-8.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Gallwitz B. Clinical Use of DPP-4 Inhibitors. Front Endocrinol. 2019;10:389. https://doi.org/10.3389/fendo.2019.00389.</mixed-citation><mixed-citation xml:lang="en">Gallwitz B. Clinical Use of DPP-4 Inhibitors. Front Endocrinol. 2019;10:389. https://doi.org/10.3389/fendo.2019.00389.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Hernández C, Bogdanov P, Corraliza L, Garcia-Ramirez M, Sola-Adell C, Arranz JA et al. Topical Administration of GLP-1 Receptor Agonists Prevents Retinal Neurodegeneration in Experimental Diabetes. Diabetes. 2016;65(1):172–187. https://doi.org/10.2337/db15-0443.</mixed-citation><mixed-citation xml:lang="en">Hernández C, Bogdanov P, Corraliza L, Garcia-Ramirez M, Sola-Adell C, Arranz JA et al. Topical Administration of GLP-1 Receptor Agonists Prevents Retinal Neurodegeneration in Experimental Diabetes. Diabetes. 2016;65(1):172–187. https://doi.org/10.2337/db15-0443.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Mari A, Sallas WM, He YL, Watson C, Ligueros-Saylan M, Dunning BE et al. Vildagliptin, a dipeptidyl peptidase-IV inhibitor, improves model-assessed beta-cell function in patients with type 2 diabetes. J Clin Endocrinol Metab. 2005;90(8):4888–4894. https://doi.org/10.1210/jc.2004-2460.</mixed-citation><mixed-citation xml:lang="en">Mari A, Sallas WM, He YL, Watson C, Ligueros-Saylan M, Dunning BE et al. Vildagliptin, a dipeptidyl peptidase-IV inhibitor, improves model-assessed beta-cell function in patients with type 2 diabetes. J Clin Endocrinol Metab. 2005;90(8):4888–4894. https://doi.org/10.1210/jc.2004-2460.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Ahrén B. DPP-4 inhibitors. Best Pract Res Clin Endocrinol Metab. 2007;21(4):517–533. https://doi.org/10.1016/j.beem.2007.07.005.</mixed-citation><mixed-citation xml:lang="en">Ahrén B. DPP-4 inhibitors. Best Pract Res Clin Endocrinol Metab. 2007;21(4):517–533. https://doi.org/10.1016/j.beem.2007.07.005.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Capuano A, Sportiello L, Maiorino MI, Rossi F, Giugliano D, Esposito K. Dipeptidyl peptidase-4 inhibitors in type 2 diabetes therapy – focus on alogliptin. Drug Des Devel Ther. 2013;7:989–1001. https://doi.org/10.2147/DDDT.S37647.</mixed-citation><mixed-citation xml:lang="en">Capuano A, Sportiello L, Maiorino MI, Rossi F, Giugliano D, Esposito K. Dipeptidyl peptidase-4 inhibitors in type 2 diabetes therapy – focus on alogliptin. Drug Des Devel Ther. 2013;7:989–1001. https://doi.org/10.2147/DDDT.S37647.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Johns E, McKay G, Fisher M. Dipeptidyl peptidase-4 (DPP-4) inhibitors. Br J Cardiol. 2017;24:(1). https://doi.org/10.5837/bjc.2017.001.</mixed-citation><mixed-citation xml:lang="en">Johns E, McKay G, Fisher M. Dipeptidyl peptidase-4 (DPP-4) inhibitors. Br J Cardiol. 2017;24:(1). https://doi.org/10.5837/bjc.2017.001.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Panda SP. Role of DPP4 and DPP4i in Glucose Homeostasis and Cardiorenal Syndrome. Endocr Metab Immune Disord Drug Targets. 2023;23(2):179–187. https://doi.org/10.2174/1871530322666220531123116.</mixed-citation><mixed-citation xml:lang="en">Panda SP. Role of DPP4 and DPP4i in Glucose Homeostasis and Cardiorenal Syndrome. Endocr Metab Immune Disord Drug Targets. 2023;23(2):179–187. https://doi.org/10.2174/1871530322666220531123116.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Cho YK, Kang YM, Lee SE, Lee J, Park JY, Lee WJ et al. Efficacy and safety of combination therapy with SGLT2 and DPP4 inhibitors in the treatment of type 2 diabetes: A systematic review and meta-analysis. Diabetes Metab. 2018;44(5):393–401. https://doi.org/10.1016/j.diabet.2018.01.011.</mixed-citation><mixed-citation xml:lang="en">Cho YK, Kang YM, Lee SE, Lee J, Park JY, Lee WJ et al. Efficacy and safety of combination therapy with SGLT2 and DPP4 inhibitors in the treatment of type 2 diabetes: A systematic review and meta-analysis. Diabetes Metab. 2018;44(5):393–401. https://doi.org/10.1016/j.diabet.2018.01.011.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Дедов ИИ, Шестакова МВ, Майоров АЮ, Мокрышева НГ, Андреева ЕН, Безлепкина ОБ и др. Алгоритмы специализированной медицинской помощи больным сахарным диабетом / Под редакцией И.И. Дедова, М.В. Шестаковой, А.Ю. Майорова. 11-й выпуск. Сахарный диабет. 2023;26(2S):1–157. https://doi.org/10.14341/DM13042.</mixed-citation><mixed-citation xml:lang="en">Dedov II, Shestakova MV, Mayorov AYu, Mokrysheva NG, Andreeva EN, Bezlepkina OB et al. Standards of Specialized Diabetes Care / Edited by Dedov I.I., Shestakova M.V., Mayorov A.Yu. 11th Edition. Diabetes Mellitus. 2023;26(2S):1–157. (In Russ.) https://doi.org/10.14341/DM13042.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Lyu X, Zhu X, Zhao B, Du L, Chen D, Wang C et al. Effects of dipeptidyl peptidase-4 inhibitors on beta-cell function and insulin resistance in type 2 diabetes: meta-analysis of randomized controlled trials. Sci Rep. 2017;7:44865. https://doi.org/10.1038/srep44865.</mixed-citation><mixed-citation xml:lang="en">Lyu X, Zhu X, Zhao B, Du L, Chen D, Wang C et al. Effects of dipeptidyl peptidase-4 inhibitors on beta-cell function and insulin resistance in type 2 diabetes: meta-analysis of randomized controlled trials. Sci Rep. 2017;7:44865. https://doi.org/10.1038/srep44865.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Шестакова МВ, Шестакова ЕА, Качко ВА. Особенности применения алоглиптина у различных групп пациентов с сахарным диабетом 2 типа: дополнительные результаты исследования ENTIRE. Проблемы эндокринологии. 2020;66(2):49–60. https://doi.org/10.14341/probl12273.</mixed-citation><mixed-citation xml:lang="en">Shestakova MV, Shestakova EA, Kachko VA. Specific features of the use of alogliptin in various groups of patients with type 2 diabetes mellitus: additional results of the ENTIRE study. Problemy Endokrinologii. 2020;66(2):49–60. (In Russ.) https://doi.org/10.14341/probl12273.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Godinho R, Mega C, Teixeira-de-Lemos E, Carvalho E, Teixeira F, Fernandes R, Reis F. The Place of Dipeptidyl Peptidase-4 Inhibitors in Type 2 Diabetes Therapeutics: A “Me Too” or “the Special One” Antidiabetic Class? J Diabetes Res. 2015;2015:806979. https://doi.org/10.1155/2015/806979.</mixed-citation><mixed-citation xml:lang="en">Godinho R, Mega C, Teixeira-de-Lemos E, Carvalho E, Teixeira F, Fernandes R, Reis F. The Place of Dipeptidyl Peptidase-4 Inhibitors in Type 2 Diabetes Therapeutics: A “Me Too” or “the Special One” Antidiabetic Class? J Diabetes Res. 2015;2015:806979. https://doi.org/10.1155/2015/806979.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Shabnam M, Uddin MM, Islam MK, Hossain T, Fattah SA. Prescribing Patterns of Dipeptidyl Peptidase-4 (DPP-4) Inhibitors in Type-2 Diabetes Mellitus: A Cross-sectional Observational Study. J Green Life Med Col. 2022;7(2):61–67. Available at: https://www.researchgate.net/publication/388353453_Original_Article_on_DPP_IV_Inhibitor.</mixed-citation><mixed-citation xml:lang="en">Shabnam M, Uddin MM, Islam MK, Hossain T, Fattah SA. Prescribing Patterns of Dipeptidyl Peptidase-4 (DPP-4) Inhibitors in Type-2 Diabetes Mellitus: A Cross-sectional Observational Study. J Green Life Med Col. 2022;7(2):61–67. Available at: https://www.researchgate.net/publication/388353453_Original_Article_on_DPP_IV_Inhibitor.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Saisho Y. Alogliptin benzoate for management of type 2 diabetes. Vasc Health Risk Manag. 2015;11:229–243. https://doi.org/10.2147/VHRM.S68564.</mixed-citation><mixed-citation xml:lang="en">Saisho Y. Alogliptin benzoate for management of type 2 diabetes. Vasc Health Risk Manag. 2015;11:229–243. https://doi.org/10.2147/VHRM.S68564.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Scott LJ. Alogliptin: a review of its use in the management of type 2 diabetes mellitus. Drugs. 2010;70(15):2051–2072. https://doi.org/10.2165/11205080-000000000-00000.</mixed-citation><mixed-citation xml:lang="en">Scott LJ. Alogliptin: a review of its use in the management of type 2 diabetes mellitus. Drugs. 2010;70(15):2051–2072. https://doi.org/10.2165/11205080-000000000-00000.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Моргунов ЛЮ. Алоглиптин: эффективность, безопасноcть, новые возможности. Медицинский совет. 2020;(7):42–49. https://doi.org/10.21518/2079-701X-2020-7-42-49.</mixed-citation><mixed-citation xml:lang="en">Morgunov LYu. Alogliptin: efficiency, safety, new possibilities. Meditsinskiy Sovet. 2020;(7):42–49. (In Russ.) https://doi.org/10.21518/2079-701X-2020-7-42-49.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">DeFronzo RA, Fleck PR, Wilson CA, Mekki Q. Efficacy and safety of the dipeptidyl peptidase-4 inhibitor alogliptin in patients with type 2 diabetes and inadequate glycemic control: a randomized, double-blind, placebocontrolled study. Diabetes Care. 2008;31(12):2315–2317. https://doi.org/10.2337/dc08-1035.</mixed-citation><mixed-citation xml:lang="en">DeFronzo RA, Fleck PR, Wilson CA, Mekki Q. Efficacy and safety of the dipeptidyl peptidase-4 inhibitor alogliptin in patients with type 2 diabetes and inadequate glycemic control: a randomized, double-blind, placebocontrolled study. Diabetes Care. 2008;31(12):2315–2317. https://doi.org/10.2337/dc08-1035.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">White WB, Cannon CP, Heller SR, Nissen SE, Bergenstal RM, Bakris GL et al. Alogliptin after acute coronary syndrome in patients with type 2 diabetes. N Engl J Med. 2013;369(14):1327–1335. https://doi.org/10.1056/NEJMoa1305889.</mixed-citation><mixed-citation xml:lang="en">White WB, Cannon CP, Heller SR, Nissen SE, Bergenstal RM, Bakris GL et al. Alogliptin after acute coronary syndrome in patients with type 2 diabetes. N Engl J Med. 2013;369(14):1327–1335. https://doi.org/10.1056/NEJMoa1305889.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Фадеев ВВ. Результаты первого ретроспективного исследования алоглиптина по сравнению с другими пероральными сахароснижающими препаратами у пациентов с сахарным диабетом 2 типа в России ARRIVAL. Эффективная фармакотерапия. 2023;19(12):6–14. https://doi.org/10.33978/2307-3586-2023-19-12-6-14.</mixed-citation><mixed-citation xml:lang="en">Fadeev VV. Results of the First Retrospective Study of Alogliptin Compared with Other Oral Hypoglycemic Drugs in Patients with Type 2 Diabetes Mellitus in Russia ARRIVAL. Effective Pharmacotherapy. 2023;19(12):6–14. (In Russ.) https://doi.org/10.33978/2307-3586-2023-19-12-6-14.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">McCreight LJ, Bailey CJ, Pearson ER. Metformin and the gastrointestinal tract. Diabetologia. 2016;59(3):426–435. https://doi.org/10.1007/s00125-015-3844-9.</mixed-citation><mixed-citation xml:lang="en">McCreight LJ, Bailey CJ, Pearson ER. Metformin and the gastrointestinal tract. Diabetologia. 2016;59(3):426–435. https://doi.org/10.1007/s00125-015-3844-9.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">LaMoia TE, Shulman GI. Cellular and Molecular Mechanisms of Metformin Action. Endocr Rev. 2021;42(1):77–96. https://doi.org/10.1210/endrev/bnaa023.</mixed-citation><mixed-citation xml:lang="en">LaMoia TE, Shulman GI. Cellular and Molecular Mechanisms of Metformin Action. Endocr Rev. 2021;42(1):77–96. https://doi.org/10.1210/endrev/bnaa023.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Del Prato S, Camisasca R, Wilson C, Fleck P. Durability of the efficacy and safety of alogliptin compared with glipizide in type 2 diabetes mellitus: a 2-year study. Diabetes Obes Metab. 2014;16(12):1239–1246. https://doi.org/10.1111/dom.12377.</mixed-citation><mixed-citation xml:lang="en">Del Prato S, Camisasca R, Wilson C, Fleck P. Durability of the efficacy and safety of alogliptin compared with glipizide in type 2 diabetes mellitus: a 2-year study. Diabetes Obes Metab. 2014;16(12):1239–1246. https://doi.org/10.1111/dom.12377.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Ji L, Li L, Kuang J, Yang T, Kim DJ, Kadir AA et al. Efficacy and safety of fixeddose combination therapy, alogliptin plus metformin, in Asian patients with type 2 diabetes: A phase 3 trial. Diabetes Obes Metab. 2017;19(5):754–758. https://doi.org/10.1111/dom.12875.</mixed-citation><mixed-citation xml:lang="en">Ji L, Li L, Kuang J, Yang T, Kim DJ, Kadir AA et al. Efficacy and safety of fixeddose combination therapy, alogliptin plus metformin, in Asian patients with type 2 diabetes: A phase 3 trial. Diabetes Obes Metab. 2017;19(5):754–758. https://doi.org/10.1111/dom.12875.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Khunti S, Khunti K, Seidu S. Therapeutic inertia in type 2 diabetes: prevalence, causes, consequences and methods to overcome inertia. Ther Adv Endocrinol Metab. 2019;10:2042018819844694. https://doi.org/10.1177/2042018819844694.</mixed-citation><mixed-citation xml:lang="en">Khunti S, Khunti K, Seidu S. Therapeutic inertia in type 2 diabetes: prevalence, causes, consequences and methods to overcome inertia. Ther Adv Endocrinol Metab. 2019;10:2042018819844694. https://doi.org/10.1177/2042018819844694.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Davies MJ, Drexel H, Jornayvaz FR, Pataky Z, Seferović PM, Wanner C. Cardiovascular outcomes trials: a paradigm shift in the current management of type 2 diabetes. Cardiovasc Diabetol. 2022;21(1):144. https://doi.org/10.1186/s12933-022-01575-9.</mixed-citation><mixed-citation xml:lang="en">Davies MJ, Drexel H, Jornayvaz FR, Pataky Z, Seferović PM, Wanner C. Cardiovascular outcomes trials: a paradigm shift in the current management of type 2 diabetes. Cardiovasc Diabetol. 2022;21(1):144. https://doi.org/10.1186/s12933-022-01575-9.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Koufakis T, Zografou I, Doumas M, Kotsa K. The Current Place of DPP4 Inhibitors in the Evolving Landscape of Type 2 Diabetes Management: Is It Time to Bid Adieu? Am J Cardiovasc Drugs. 2023;23(6):601–608. https://doi.org/10.1007/s40256-023-00610-8.</mixed-citation><mixed-citation xml:lang="en">Koufakis T, Zografou I, Doumas M, Kotsa K. The Current Place of DPP4 Inhibitors in the Evolving Landscape of Type 2 Diabetes Management: Is It Time to Bid Adieu? Am J Cardiovasc Drugs. 2023;23(6):601–608. https://doi.org/10.1007/s40256-023-00610-8.</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>
