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<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">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">10.21518/2079-701X-2020-7-122-128</article-id><article-id custom-type="elpub" pub-id-type="custom">medsovet-5663</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>ДРУГИЕ ПРОБЛЕМЫ ЭНДОКРИНОЛОГИИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>OTHER PROBLEMS OF ENDOCRINOLOGY</subject></subj-group></article-categories><title-group><article-title>Пероральные бисфосфонаты как терапия выбора у пациентов с умеренным риском переломов</article-title><trans-title-group xml:lang="en"><trans-title>Oral bisphosphonates as the therapy of choice in patients with moderate risk of fractures</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1886-124X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Марченкова</surname><given-names>Л. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Marchenkova</surname><given-names>L. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Марченкова Лариса Александровна, к.м.н., заведующая отделом соматической реабилитации, активного долголетия и репродуктивного здоровья</p><p>121099, Россия, Москва, ул. Новый Арбат, д. 32</p></bio><bio xml:lang="en"><p>Larisa A. Marchenkova, Cand. of Sci. (Med.), Head of Department of Somatic Rehabilitation, Active Longevity and Reproductive Health, Lead Researcher,</p><p>32, Novyy Arbat St., Moscow, 121099, Russia</p></bio><email xlink:type="simple">MarchenkovaLA@nmicrk.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/0000-0003-3767-8475</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Макарова</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Makarova</surname><given-names>E. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Макарова Екатерина Владимировна, научный сотрудник отдела соматической реабилитации, активного долголетия и репродуктивного здоровья</p><p>121099, Россия, Москва, ул. Новый Арбат, д. 32</p></bio><bio xml:lang="en"><p>Ekaterina V. Makarova, Researcher, Department of Somatic Rehabilitation, Active Longevity and Reproductive Health</p><p>32, Novyy Arbat St., Moscow, 121099, Russia</p></bio><email xlink:type="simple">rue-royal@inbox.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Национальный медицинский исследовательский центр реабилитации и курортологии<country>Россия</country></aff><aff xml:lang="en">National Medical Research Center of Rehabilitation and Balneology<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2020</year></pub-date><pub-date pub-type="epub"><day>28</day><month>05</month><year>2020</year></pub-date><volume>0</volume><issue>7</issue><fpage>122</fpage><lpage>128</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Марченкова Л.А., Макарова Е.В., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Марченкова Л.А., Макарова Е.В.</copyright-holder><copyright-holder xml:lang="en">Marchenkova L.A., Makarova E.V.</copyright-holder><license 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/5663">https://www.med-sovet.pro/jour/article/view/5663</self-uri><abstract><p>У специалиста, занимающегося остеопорозом (ОП), сегодня есть доступ к качественным диагностическим алгоритмам, позволяющим определить риск переломов и необходимость назначения лечения, а также возможность выбрать современную лекарственную терапию, которая будет наиболее подходящей, максимально комфортной и безопасной. Такой современный алгоритм выбора терапии ОП основан на оценке степени риска перелома пациента, который определяется наличием и тяжестью перенесенных низкоэнергетических переломов, уровнем минеральной плотности кости (МПК), а также 10-летней вероятностью переломов по калькулятору FRAX. Пациенты с умеренным риском остеопорозных переломов – наиболее спорная категория больных в отношении выбора и оценки прогноза лечения, поскольку они либо не имеют переломов в анамнезе, либо перенесли всего один низкоэнергетический перелом на фоне остеопении или нормальной МПК. В таких случаях в качестве стартовой терапии ОП рекомендуются пероральные бисфос- фонаты (БФ) с планируемой длительностью лечения 5 лет. Алендровая кислота – наиболее известный и назначаемый пероральный БФ, отличающийся финансовой доступностью и благоприятным профилем клинической эффективности при лечении ОП. Эффективность лечения пероральными БФ во многом определяется переносимостью препарата и приверженностью пациентов лечению. Нежелательные эффекты, особенно со стороны верхних отделов желудочно-кишечного тракта (ЖКТ) и отсутствие мотивации пациентов были признаны в качестве основных причин низкой приверженности терапии ОП. Благодаря низкой частоте развития нежелательных явлений и удобной для приема фармакологической форме, способствующим повышению комлаентности лечения, буферный раствор алендроната в растворимых шипучих таблетках может иметь предпочтения у больных с уме- ренным риском переломов. Солюбизированый в буферном растворе алендронат в значительно меньшей степени контактирует со слизистой пищевода и желудка, минимизируя контакт между частицами препарата и слизистой оболочкой верхних отделов ЖКТ и уменьшая в итоге местный раздражающий эффект и вероятность возникновения гастро-эзофагеального рефлюкса.</p></abstract><trans-abstract xml:lang="en"><p>Nowadays clinicians have access to high-quality diagnostic algorithms to determine the risk of fractures and the need for treatment, as well as the ability to choose the most advanced drug therapy that will be the most suitable, comfortable and safe for the patient with osteoporosis. This algorithm for the selection of therapy is based on an assessment of the fracture risk, which is determined by the presence and severity of low-energy fractures, the level of bone mineral density (BMD), and the 10-year probability of fractures. Patients with a moderate risk of osteoporotic fractures are the most controversial category of patients regarding the choice and assessment of the prognosis of treatment, since they either have no history of fractures or have suffered only one low-energy fracture due to osteopenia or normal BMD. In such cases, oral bisphosphonates with a planned treatment duration of 5 years were recommended as starting therapy for osteoporosis. Alendronic acid is the most well-known and widely prescribed oral bisphosphonate, characterized by financial availability and a favorable profile of clinical efficacy in the treatment of osteoporosis. The effectiveness of treatment with oral bisphosphonates is largely determined by the tolerability of the drug and patient adherence to treatment. Gastrointestinal side effects and the lack of patient motivation are the main reasons for the low adherence to anti-osteoporotic therapy. Due to the low incidence of adverse events and the convenient pharmacological form for enhancing treatment compliance, alendronate buffer solution in soluble effervescent tablets may be preferred in patients with a moderate risk of fractures. Solubilized in a buffer solution alendronate less contacts the mucous membrane of the esophagus and stomach, minimizing contact between the particles of the drug and the mucous membrane of the upper gastrointestinal tract, and ultimately reducing the local irritating effect and the likelihood of gastroesophageal reflux.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>остеопороз</kwd><kwd>алендронат</kwd><kwd>риск переломов</kwd><kwd>персонализованная медицина</kwd><kwd>комплаентность</kwd><kwd>нежелательные лекарственные явления</kwd></kwd-group><kwd-group xml:lang="en"><kwd>osteoporosis</kwd><kwd>alendronate</kwd><kwd>fracture risk</kwd><kwd>personalized medicine</kwd><kwd>compliance</kwd><kwd>adverse drug effects</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">Kanis J.A., Harvey N.C., McCloskey E., Bruyère O., Veronese N., Lorentzon M. et al. Algorithm for the management of patients at low, high and very high risk of osteoporotic fractures. Osteoporos Int. 2020;31:1–12. doi: 10.1007/s00198-019-05176-3.</mixed-citation><mixed-citation xml:lang="en">Kanis J.A., Harvey N.C., McCloskey E., Bruyère O., Veronese N., Lorentzon M. et al. Algorithm for the management of patients at low, high and very high risk of osteoporotic fractures. Osteoporos Int. 2020;31:1–12. doi: 10.1007/s00198-019-05176-3.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Piscitelli P., Chitano G., Greco M., Benvenuto M., Sbenagla E., Coli G. et al. Pharmaco-economic issues in the treatment of severe osteoporosis. Clin Cases Miner Bone Metab. 2010;7(1):61–64. Available at: https://pubmed.ncbi.nlm.nih.gov/22461294-pharmaco-economic-issues-in-the-treatmentof-severe-osteoporosis.</mixed-citation><mixed-citation xml:lang="en">Piscitelli P., Chitano G., Greco M., Benvenuto M., Sbenagla E., Coli G. et al. Pharmaco-economic issues in the treatment of severe osteoporosis. Clin Cases Miner Bone Metab. 2010;7(1):61–64. Available at: https://pubmed.ncbi.nlm.nih.gov/22461294-pharmaco-economic-issues-in-the-treatmentof-severe-osteoporosis.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Насонов Е.Л. (ред.) Российские клинические рекомендации. Ревматология. М.: ГЭОТАР-Медиа; 2017. 464 с. Режим доступа: https://www.rosmedlib.ru/book/ISBN9785970442616.html.</mixed-citation><mixed-citation xml:lang="en">Nasonov E.L. (ed.). Russian clinical recommendations. Rheumatology. Moscow: GEOTAR-Media; 2017. 464 p. (In Russ.) Available at: https://www.rosmedlib.ru/book/ISBN9785970442616.html.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Strom O., Borgstrom F., Kanis J.A., Compston J., Cooper C., McCloskey E.V., Jonsson B. Osteoporosis: burden, health care provision and opportunities in the EU: A report prepared in collaboration with the International Osteoporosis Foundation (IOF) and the European Federation of Pharmaceutical Industry Associations (EFPIA). Arch Osteoporos. 2011;6:59–155. doi: 10.1007/s11657-011-0060-1.</mixed-citation><mixed-citation xml:lang="en">Strom O., Borgstrom F., Kanis J.A., Compston J., Cooper C., McCloskey E.V., Jonsson B. Osteoporosis: burden, health care provision and opportunities in the EU: A report prepared in collaboration with the International Osteoporosis Foundation (IOF) and the European Federation of Pharmaceutical Industry Associations (EFPIA). Arch Osteoporos. 2011;6:59–155. doi: 10.1007/s11657-011-0060-1.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Kanis J.A., Adams J., Borgstrom F., Cooper C., Jonsson A., Preedy D. et al. The cost-effectiveness of alendronate in the management of osteoporosis. Bone. 2008;42(1):4–15. doi: 10.1016/j.bone.2007.10.019.</mixed-citation><mixed-citation xml:lang="en">Kanis J.A., Adams J., Borgstrom F., Cooper C., Jonsson A., Preedy D. et al. The cost-effectiveness of alendronate in the management of osteoporosis. Bone. 2008;42(1):4–15. doi: 10.1016/j.bone.2007.10.019.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Мазуров В.И., Лесняк О.М., Белова К.Ю., Ершова О.Б., Зоткин Е.Г., Марченкова Л.А. et al. Алгоритмы выбора терапии остеопороза при оказании первичной медико-санитарной помощи и организации льготного лекарственного обеспечения отдельных категорий граждан, имеющих право на получение государственной социальной помощи. Системный обзор и резолюция Экспертного совета Российской ассоциации по остеопорозу. Профилактическая медицина. 2019;22(1):57–65. doi: 10.17116/profmed20192201157.</mixed-citation><mixed-citation xml:lang="en">Mazurov V.I., Lesnyak O.M., Belova K.Yu., Ershova O.B., Zotkin E.G., Marchenkova L.A. et al. Algorithm for selection of drug for osteoporosis treatment in primary care and in organization of provision with medicinal products of citizens eligible for state social assistance. Review of the literature and position of Russian Association on Osteoporosis Expert Council. Russian Journal of Preventive Medicine and Public Health = Profilakticheskaya meditsina. 2019;22(1):57–65. (In Russ.) doi: 10.17116/profmed20192201157.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Piscitelli P., Auriemma R., Neglia C., Migliore A. Alendronate: new formulations of an old and effective drug to improve adherence avoiding upper gastrointestinal side effects. Eur Rev Med Pharmacol Sci. 2014;18(24):3788–3796. Available at: https://pubmed.ncbi.nlm.nih.gov/25555868-alendronate-new-formulations-of-an-old-and-effectivedrug-to-improve-adherence-avoiding-upper-gastrointestinal-side-effects.</mixed-citation><mixed-citation xml:lang="en">Piscitelli P., Auriemma R., Neglia C., Migliore A. Alendronate: new formulations of an old and effective drug to improve adherence avoiding upper gastrointestinal side effects. Eur Rev Med Pharmacol Sci. 2014;18(24):3788–3796. Available at: https://pubmed.ncbi.nlm.nih.gov/25555868-alendronate-new-formulations-of-an-old-and-effectivedrug-to-improve-adherence-avoiding-upper-gastrointestinal-side-effects.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Мельниченко Г.А., Белая Ж.Е., Рожинская Л.Я., Торопцова Н.В., Алексеева Л.И., Бирюкова Е.В. и др. Федеральные клинические рекомендации по диагностике, лечению и профилактике остеопороза. Проблемы эндокринологии. 2017;63(6):392–426. doi: 10.14341/probl2017636392-426.</mixed-citation><mixed-citation xml:lang="en">Mel’nichenko G.A., Belaya Z.E., Rozhinskaya L.Y., Toroptsova N.V., Alekseeva L.I., Biryukova E.V., et al. Russian federal clinical guidelines on the diagnostics, treatment, and prevention of osteoporosis. Problemy endokrinologii = Problems of Endocrinology. 2017;63(6):392–426. (In Russ.) doi: 10.14341/probl2017636392-426.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Adler R.A., El-Hajj Fuleihan G., Bauer D.C., Camacho P.M, Clarke B.L., Clines G.A. et al. Managing Osteoporosis in Patients on Long-Term Bisphosphonate Treatment: Report of a Task Force of the American Society for Bone and Mineral Research. J Bone Miner Res. 2016;31(1):16–35. doi: 10.1002/jbmr.2708.</mixed-citation><mixed-citation xml:lang="en">Adler R.A., El-Hajj Fuleihan G., Bauer D.C., Camacho P.M, Clarke B.L., Clines G.A. et al. Managing Osteoporosis in Patients on Long-Term Bisphosphonate Treatment: Report of a Task Force of the American Society for Bone and Mineral Research. J Bone Miner Res. 2016;31(1):16–35. doi: 10.1002/jbmr.2708.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Hagsten B., Svensson O., Gardulf A. Health-related quality of life and selfreported ability concerning ADL and IADL after hip fracture: a randomized trial. Acta Orthop. 2006;77(1):114–119. doi: 10.1080/17453670610045786.</mixed-citation><mixed-citation xml:lang="en">Hagsten B., Svensson O., Gardulf A. Health-related quality of life and selfreported ability concerning ADL and IADL after hip fracture: a randomized trial. Acta Orthop. 2006;77(1):114–119. doi: 10.1080/17453670610045786.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Khalid S., Calderón-Larrañaga S., Hawley S., Ali S., Judge A., Arden N., et al. Comparative anti-fracture effectiveness of different oral anti-osteoporosis therapies based on “real-world” data: a meta-analysis of propensitymatched cohort findings from the UK Clinical Practical Research Database and Catalan SIDIAP Database. Clinical Epidemiology. 2018;10:1417–1431. doi: 10.2147/CLEP.S164112.</mixed-citation><mixed-citation xml:lang="en">Khalid S., Calderón-Larrañaga S., Hawley S., Ali S., Judge A., Arden N., et al. Comparative anti-fracture effectiveness of different oral anti-osteoporosis therapies based on “real-world” data: a meta-analysis of propensitymatched cohort findings from the UK Clinical Practical Research Database and Catalan SIDIAP Database. Clinical Epidemiology. 2018;10:1417–1431. doi: 10.2147/CLEP.S164112.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">McNabb B.L., Vittinghoff E., Schwartz A.V., Eastell R., Bauer D.C., Ensrud K. et al. BMD changes and predictors of increased bone loss in postmenopausal women after a 5-year course of alendronate. J Bone Miner. Res. 2013;28(6):1319–1327. doi: 10.1002/jbmr.1864.</mixed-citation><mixed-citation xml:lang="en">McNabb B.L., Vittinghoff E., Schwartz A.V., Eastell R., Bauer D.C., Ensrud K. et al. BMD changes and predictors of increased bone loss in postmenopausal women after a 5-year course of alendronate. J Bone Miner. Res. 2013;28(6):1319–1327. doi: 10.1002/jbmr.1864.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Levis S., Quandt S.A., Thompson D., Scott J., Schneider D.L., Ross P.D. et al. Alendronate reduces the risk of multiple symptomatic fractures: results from the fracture intervention trial. J Am Geriatr Soc. 2002;50(3):409–415. doi: 10.1046/j.1532-5415.2002.50102.x.</mixed-citation><mixed-citation xml:lang="en">Levis S., Quandt S.A., Thompson D., Scott J., Schneider D.L., Ross P.D. et al. Alendronate reduces the risk of multiple symptomatic fractures: results from the fracture intervention trial. J Am Geriatr Soc. 2002;50(3):409–415. doi: 10.1046/j.1532-5415.2002.50102.x.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Black D.M., Schwartz A.V., Ensrud K.E., Schwartz A.V., Ensrud K.E., Cauley J.A. et al. Effects of continuing or stopping alendronate after 5 years of treatment: the fracture intervention trial long-term extension (FLEX): a randomized trial. JAMA. 2006;296(24):2927–2938. doi: 10.1001/jama.296.24.2927.</mixed-citation><mixed-citation xml:lang="en">Black D.M., Schwartz A.V., Ensrud K.E., Schwartz A.V., Ensrud K.E., Cauley J.A. et al. Effects of continuing or stopping alendronate after 5 years of treatment: the fracture intervention trial long-term extension (FLEX): a randomized trial. JAMA. 2006;296(24):2927–2938. doi: 10.1001/jama.296.24.2927.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Black D.M., Cummings S.R., Karpf D.B., Cauley J.A., Thompson D.E., Nevitt M.C. et al. Randomised trial of effect of alendronate on risk of fracture in women with existing vertebral fractures. The Lancet. 1996;348(9041):1535–1541. doi: 10.1016/S0140-6736(96)07088-2.</mixed-citation><mixed-citation xml:lang="en">Black D.M., Cummings S.R., Karpf D.B., Cauley J.A., Thompson D.E., Nevitt M.C. et al. Randomised trial of effect of alendronate on risk of fracture in women with existing vertebral fractures. The Lancet. 1996;348(9041):1535–1541. doi: 10.1016/S0140-6736(96)07088-2.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Black D.M., Bauer D.C., Schwartz A.V., Cummings S.R., Rosen C.J. Continuing bisphosphonate treatment for osteoporosis – for whom and for how long? N Engl J Med. 2012;366(22):2051–2053. doi: 10.1056/NEJMp1202623.</mixed-citation><mixed-citation xml:lang="en">Black D.M., Bauer D.C., Schwartz A.V., Cummings S.R., Rosen C.J. Continuing bisphosphonate treatment for osteoporosis – for whom and for how long? N Engl J Med. 2012;366(22):2051–2053. doi: 10.1056/NEJMp1202623.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Orwoll E., Ettinger M., Weiss S., Miller P., Kendler D., Graham J. et al. Alendronate for the treatment of osteoporosis in men. N Engl J Med. 2000;343(9):604–610. doi: 10.1056/NEJM200008313430902.</mixed-citation><mixed-citation xml:lang="en">Orwoll E., Ettinger M., Weiss S., Miller P., Kendler D., Graham J. et al. Alendronate for the treatment of osteoporosis in men. N Engl J Med. 2000;343(9):604–610. doi: 10.1056/NEJM200008313430902.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Greenspan S.L., Nelson J.B., Trump D.L., Resnick N.M. Effect of once-weekly oral alendronate on bone loss in men receiving androgen deprivation therapy for prostate cancer: a randomized trial. Ann Intern Med. 2007;146(6):416–424. doi: 10.7326/0003-4819-146-6-200703200-00006.</mixed-citation><mixed-citation xml:lang="en">Greenspan S.L., Nelson J.B., Trump D.L., Resnick N.M. Effect of once-weekly oral alendronate on bone loss in men receiving androgen deprivation therapy for prostate cancer: a randomized trial. Ann Intern Med. 2007;146(6):416–424. doi: 10.7326/0003-4819-146-6-200703200-00006.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Lespessailles E. Bisphosphonates and glucocorticoid-induced osteoporosis: efficacy and tolerability. Joint Bone Spine. 2013;80(3):258–264. doi: 10.1016/j.jbspin.2012.08.005.</mixed-citation><mixed-citation xml:lang="en">Lespessailles E. Bisphosphonates and glucocorticoid-induced osteoporosis: efficacy and tolerability. Joint Bone Spine. 2013;80(3):258–264. doi: 10.1016/j.jbspin.2012.08.005.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Sawka A.M., Papaioannou A., Adachi J.D., Gafni A., Hanley D.A., Thabane L. Does alendronate reduce the risk of fracture in men? A meta-analysis incorporating prior knowledge of anti-fracture efficacy in women. BMC Musculoskelet Disord. 2005;6:39. doi: 10.1186/1471-2474-6-39.</mixed-citation><mixed-citation xml:lang="en">Sawka A.M., Papaioannou A., Adachi J.D., Gafni A., Hanley D.A., Thabane L. Does alendronate reduce the risk of fracture in men? A meta-analysis incorporating prior knowledge of anti-fracture efficacy in women. BMC Musculoskelet Disord. 2005;6:39. doi: 10.1186/1471-2474-6-39.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Kanis J.A., Cooper C., Hiligsmann M., Rabenda V., Reginster J.-Y., Rizzoli R. Partial adherence: a new perspective on health economic assessment in osteoporosis. Osteoporos Int. 2011;22(10):2565–2573. doi: 10.1007/s00198-011-1668-0.</mixed-citation><mixed-citation xml:lang="en">Kanis J.A., Cooper C., Hiligsmann M., Rabenda V., Reginster J.-Y., Rizzoli R. Partial adherence: a new perspective on health economic assessment in osteoporosis. Osteoporos Int. 2011;22(10):2565–2573. doi: 10.1007/s00198-011-1668-0.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Siris E., Harris S.T., Rosen C.J., Barr C.E., Arvensen J.N., Abbott T.A., Silverman S. Adherence to bisphosphonate therapy and fracture rates in osteoporotic women: relationship to vertebral and nonvertebral fractures from 2 US claims databases. Mayo Clin Proc. 2006;81(8):1013–1022. doi: 10.4065/81.8.1013.</mixed-citation><mixed-citation xml:lang="en">Siris E., Harris S.T., Rosen C.J., Barr C.E., Arvensen J.N., Abbott T.A., Silverman S. Adherence to bisphosphonate therapy and fracture rates in osteoporotic women: relationship to vertebral and nonvertebral fractures from 2 US claims databases. Mayo Clin Proc. 2006;81(8):1013–1022. doi: 10.4065/81.8.1013.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Soong Y.-K., Tsai K.-S., Huang H.-Y., Yang R.-S., Chen J.-F., Wu P. C.-H., Huang K.-E. Risk of refracture associated with compliance and persistence with bisphosphonate therapy in Taiwan. Osteoporos Int. 2013;24(2):511–521. doi: 10.1007/s00198-012-1984-z.</mixed-citation><mixed-citation xml:lang="en">Soong Y.-K., Tsai K.-S., Huang H.-Y., Yang R.-S., Chen J.-F., Wu P. C.-H., Huang K.-E. Risk of refracture associated with compliance and persistence with bisphosphonate therapy in Taiwan. Osteoporos Int. 2013;24(2):511–521. doi: 10.1007/s00198-012-1984-z.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Hansen C., Pedersen B.D., Eriksen S.A., Gerstoft F., Vestergaard P. Subjects with osteoporosis to remain at high risk for fracture despite benefit of prior bisphosphonate treatment – a Danish case-control study. Osteoporos Int. 2017;28(1):321–328. doi: 10.1007/s00198-016-3720-6.</mixed-citation><mixed-citation xml:lang="en">Hansen C., Pedersen B.D., Eriksen S.A., Gerstoft F., Vestergaard P. Subjects with osteoporosis to remain at high risk for fracture despite benefit of prior bisphosphonate treatment – a Danish case-control study. Osteoporos Int. 2017;28(1):321–328. doi: 10.1007/s00198-016-3720-6.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Landfeldt E., Ström O., Robbins S., Borgström F. Adherence to treatment of primary osteoporosis and its association to fratures – the Swedish Adherence Register Analysis (SARA). Osteoporos Int. 2012;23(2):433–443. doi: 10.1007/s00198-011-1549-6.</mixed-citation><mixed-citation xml:lang="en">Landfeldt E., Ström O., Robbins S., Borgström F. Adherence to treatment of primary osteoporosis and its association to fratures – the Swedish Adherence Register Analysis (SARA). Osteoporos Int. 2012;23(2):433–443. doi: 10.1007/s00198-011-1549-6.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Лесняк О.М., Беневоленская Л.И. Остеопороз в Российской Федерации: проблемы и перспективы. Научно-практическая ревматология. 2010;48(5):14–18. doi: 10.14412/1995-4484-2010-725.</mixed-citation><mixed-citation xml:lang="en">Lesnyak O.M., Benevolenskaya L.I. Osteoporosis in the Russian Federation: Problems and Perspectives. Nauchno-prakticheskaya revmatologiya = Rheumatology Science and Practice. 2010;48(5):14–18. (In Russ.) doi: 10.14412/1995-4484-2010-725.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Марченкова Л.А., Макарова Е.В., Герасименко М.Ю. Распространенность остеопороза, ассоциирующихся с ним переломов и уровня информированности по проблеме среди пациентов, проходящих медицинскую реабилитацию. Лечащий врач. 2020;(2):54–57. Режим доступа: https://www.lvrach.ru/2020/02/15437500/</mixed-citation><mixed-citation xml:lang="en">Marchenkova L.A., Makarova E.V., Gerasimenko M.Yu. Prevalence of osteoporosis, associated fractures, and level of knowledge about this problem among the patients undergoing medical rehabilitation. Lechashchiy vrach = Therapist. 2020;(2):54–57. (In Russ.) Available https://www.lvrach.ru/2020/02/15437500/</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Марченкова Л.А., Древаль А.В., Прохорова Е.А., Лосева В.А. Приверженность больных постменопаузальным остеопорозом комбинированной терапии алендронатом натрия и колекальциферолом и ее влияние на эффективность лечения. Проблемы эндокринологии. 2014;(4):22–29. doi: 10.14341/probl201460422-29.</mixed-citation><mixed-citation xml:lang="en">Marchenkova L.A. Dreval A.V., Prokhorova E.A., Loseva V.A. The adherence of postmenopausal osteoporosis patients to therapy with combination medication contains alendronic acid and colecalciferol and its impact on the effectiveness of treatment. Problemy endockrinologii = Problems of Endocrinology. 2014;(4):22–29. doi: 10.14341/probl201460422-2</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Cooper A., Drake J., Brankin E. Treatment persistence with once-monthly ibandronate and patient support vs. once-weekly alendronate: results from the PERSIST study. Int J Clin Pract. 2006;60(8):896–905. doi: 10.1111/j.1742-1241.2006.01059.x.</mixed-citation><mixed-citation xml:lang="en">Cooper A., Drake J., Brankin E. Treatment persistence with once-monthly ibandronate and patient support vs. once-weekly alendronate: results from the PERSIST study. Int J Clin Pract. 2006;60(8):896–905. doi: 10.1111/j.1742-1241.2006.01059.x.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Siris E.S., Selby P.L., Saag K.G., Borgstrom F., Herings R.M., Silverman S.L. Impact of osteoporosis treatment adherence on fracture rates in North America and Europe. Am J Med. 2009;122(2):S3–S13. doi: 10.1016/j.amjmed.2008.12.002.</mixed-citation><mixed-citation xml:lang="en">Siris E.S., Selby P.L., Saag K.G., Borgstrom F., Herings R.M., Silverman S.L. Impact of osteoporosis treatment adherence on fracture rates in North America and Europe. Am J Med. 2009;122(2):S3–S13. doi: 10.1016/j.amjmed.2008.12.002.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Abraham S.C., Cruz-Correa M., Lee L., Yardley J.H., Wu T.T. Alendronate-associated esophageal injury: pathologic and endoscopic features. Mod Pathol. 1999.12(12):1152–1157. Available at: https://pubmed.ncbi.nlm.nih.gov/10619269-alendronate-associated-esophageal-injury-pathologic-andendoscopic-</mixed-citation><mixed-citation xml:lang="en">Abraham S.C., Cruz-Correa M., Lee L., Yardley J.H., Wu T.T. Alendronate-associated esophageal injury: pathologic and endoscopic features. Mod Pathol. 1999.12(12):1152–1157. Available at: https://pubmed.ncbi.nlm.nih.gov/10619269-alendronate-associated-esophageal-injury-pathologic-andendoscopic-</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">features. 32. Lufkin E.G., Argueta R., Whitaker M.D., Cameron A.L., Wong V.H., Egan K.S. et al. Pamidronate: an unrecognized problem in gastrointestinal tolerability. Osteoporosis Int. 1994;4(6):320–322. doi: 10.1007/BF01622190.</mixed-citation><mixed-citation xml:lang="en">features. 32. Lufkin E.G., Argueta R., Whitaker M.D., Cameron A.L., Wong V.H., Egan K.S. et al. Pamidronate: an unrecognized problem in gastrointestinal tolerability. Osteoporosis Int. 1994;4(6):320–322. doi: 10.1007/BF01622190.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">De Groen P.C., Lubbe D.F., Hirsch L.J., Daifotis A., Stephenson W., Freedholm D. et al. Esophagitis associated with the use of alendronate. N Engl J Med. 19963;335(14):1016–1021. doi: 10.1056/NEJM199610033351403.</mixed-citation><mixed-citation xml:lang="en">De Groen P.C., Lubbe D.F., Hirsch L.J., Daifotis A., Stephenson W., Freedholm D. et al. Esophagitis associated with the use of alendronate. N Engl J Med. 19963;335(14):1016–1021. doi: 10.1056/NEJM199610033351403.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Gertz B.J., Holland S.D., Kline W.F., Matuszewski B.K., Porras A.G. Clinical pharmacology of alendronate sodium. Osteopor Int. 1993;3:13–16. doi: 10.1007/BF01623002.</mixed-citation><mixed-citation xml:lang="en">Gertz B.J., Holland S.D., Kline W.F., Matuszewski B.K., Porras A.G. Clinical pharmacology of alendronate sodium. Osteopor Int. 1993;3:13–16. doi: 10.1007/BF01623002.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Argenzio R.A., Eisemann J. Mechanisms of acid injury in porcine gastroesophageal mucosa. Am J Vet Res. 1996;57(4):564–573. Available at: https://pubmed.ncbi.nlm.nih.gov/8712526-mechanisms-of-acid-injury-in-porcinegastroesophageal-mucosa.</mixed-citation><mixed-citation xml:lang="en">Argenzio R.A., Eisemann J. Mechanisms of acid injury in porcine gastroesophageal mucosa. Am J Vet Res. 1996;57(4):564–573. Available at: https://pubmed.ncbi.nlm.nih.gov/8712526-mechanisms-of-acid-injury-in-porcinegastroesophageal-mucosa.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Peter C.P., Handt L.K., Smith S.M. Esophageal irritation due to alendronate sodium tablets (possible mechanisms). Dig Dis Sci. 1998;43(9):1998–2002. doi: 10.1023/A:1018894827961.</mixed-citation><mixed-citation xml:lang="en">Peter C.P., Handt L.K., Smith S.M. Esophageal irritation due to alendronate sodium tablets (possible mechanisms). Dig Dis Sci. 1998;43(9):1998–2002. doi: 10.1023/A:1018894827961.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Epstein S., Geusens R., Fisher J.E., Hill S., Roy S., Rodan G. et al. Desitegration profiles of alendronate formulations: implications for clinical safety and efficacy. J Applied Res. 2005;5(2):253–265. Available at: https://jrnlappliedresearch.com/articles/Vol5Iss2/Epstein.pdf.</mixed-citation><mixed-citation xml:lang="en">Epstein S., Geusens R., Fisher J.E., Hill S., Roy S., Rodan G. et al. Desitegration profiles of alendronate formulations: implications for clinical safety and efficacy. J Applied Res. 2005;5(2):253–265. Available at: https://jrnlappliedresearch.com/articles/Vol5Iss2/Epstein.pdf.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Kanis J.A., Reginster J.Y., Kaufman J.M., Ringe J.-D., Adachi J.D., Hiligsmann M. et al. A reappraisal of generic bisphosphonates in osteoporosis. Osteoporos Int. 2012;23:213–221. doi: 10.1007/s00198-011-1796-6.</mixed-citation><mixed-citation xml:lang="en">Kanis J.A., Reginster J.Y., Kaufman J.M., Ringe J.-D., Adachi J.D., Hiligsmann M. et al. A reappraisal of generic bisphosphonates in osteoporosis. Osteoporos Int. 2012;23:213–221. doi: 10.1007/s00198-011-1796-6.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Grima D.T., Papaioannou A., Airia P., Ioannidis G., Adachi J.D. Adverse events, bone mineral density and discontinuation associated with generic alendronate among postmenopausal women previously tolerant of brand alendronate: a retrospective cohort study. BMC Musculoskelet Disord. 2010;11:68. doi: 10.1186/1471-2474-11-68.</mixed-citation><mixed-citation xml:lang="en">Grima D.T., Papaioannou A., Airia P., Ioannidis G., Adachi J.D. Adverse events, bone mineral density and discontinuation associated with generic alendronate among postmenopausal women previously tolerant of brand alendronate: a retrospective cohort study. BMC Musculoskelet Disord. 2010;11:68. doi: 10.1186/1471-2474-11-68.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Ström O., Landfeldt E. The association between automatic generic substitution and treatment persistence with oral bisphosphonates. Osteoporos Int. 2012;23(8):2201–2209. doi: 10.1007/s00198-011-1850-4.</mixed-citation><mixed-citation xml:lang="en">Ström O., Landfeldt E. The association between automatic generic substitution and treatment persistence with oral bisphosphonates. Osteoporos Int. 2012;23(8):2201–2209. doi: 10.1007/s00198-011-1850-4.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Hodges L.A., Connolly S.M., Winter J., Schmidt T., Stevens H.N.E., Hayward M., Wilson C.G. Modulation of gastric pH by a buffered soluble effervescent formulation: a possible means of improving gastric tolerability of alendronate. Int J Pharm. 2012;432:57–62. doi: 10.1016/j.ijpharm.2012.04.073.</mixed-citation><mixed-citation xml:lang="en">Hodges L.A., Connolly S.M., Winter J., Schmidt T., Stevens H.N.E., Hayward M., Wilson C.G. Modulation of gastric pH by a buffered soluble effervescent formulation: a possible means of improving gastric tolerability of alendronate. Int J Pharm. 2012;432:57–62. doi: 10.1016/j.ijpharm.2012.04.073.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Gomez Acotto C., Antonelli C., Flynn D., McDaid D., Roldan E.J. Upper gastrointestinal tract transit times of tablet and drinkable solution formulations of alendronate: a bioequivalence and a quantitative, randomized study using video deglutition. Calcif Tissue Int. 2012;91(5):325–334. doi: 10.1007/s00223-012-9639-9.</mixed-citation><mixed-citation xml:lang="en">Gomez Acotto C., Antonelli C., Flynn D., McDaid D., Roldan E.J. Upper gastrointestinal tract transit times of tablet and drinkable solution formulations of alendronate: a bioequivalence and a quantitative, randomized study using video deglutition. Calcif Tissue Int. 2012;91(5):325–334. doi: 10.1007/s00223-012-9639-9.</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>
