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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">ometendo</journal-id><journal-title-group><journal-title xml:lang="ru">Ожирение и метаболизм</journal-title><trans-title-group xml:lang="en"><trans-title>Obesity and metabolism</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2071-8713</issn><issn pub-type="epub">2306-5524</issn><publisher><publisher-name>Endocrinology Research Centre</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14341/omet13124</article-id><article-id custom-type="elpub" pub-id-type="custom">ometendo-13124</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group></article-categories><title-group><article-title>Минеральные нарушения у пациентов с хроническими заболеваниями печени. Часть 1: эпидемиология и патофизиология</article-title><trans-title-group xml:lang="en"><trans-title>Mineral disorders in patients with chronic liver disease. Part 1: epidemiology and pathophysiology</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2669-9457</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Горбачева</surname><given-names>А. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Gorbacheva</surname><given-names>A. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Горбачева Анна Максимовна, к.м.н.</p><p>115478, Москва, ул. Дм. Ульянова, д. 11</p><p>ResearcherID: HKO-2637-2023</p><p> </p><p>Scopus Author ID: 57190977461</p></bio><bio xml:lang="en"><p>Anna M. Gorbacheva, MD, PhD</p><p>11 Dm.Ulyanova street, 115478, Moscow</p><p>ResearcherID: HKO-2637-2023</p><p> </p><p>Scopus Author ID: 57190977461</p></bio><email xlink:type="simple">ann.gorbachewa@yandex.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/0000-0001-5952-5846</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бибик</surname><given-names>Е. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Bibik</surname><given-names>E. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Бибик Екатерина Евгеньевна, к.м.н.</p><p>115478, Москва, ул. Дм. Ульянова, д. 11</p><p>ResearcherID: AAY-3052-2020</p><p> </p><p>Scopus Author ID: 57195679482</p></bio><bio xml:lang="en"><p>Ekaterina E. Bibik, MD, PhD</p><p>11 Dm.Ulyanova street, 115478, Moscow</p><p>ResearcherID: AAY-3052-2020</p><p> </p><p>Scopus Author ID: 57195679482</p></bio><email xlink:type="simple">bibik.ekaterina@endocrincentr.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/0000-0002-7285-6874</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лавренюк</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Lavreniuk</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Лавренюк Анастасия Андреевна</p><p>115478, Москва, ул. Дм. Ульянова, д. 11</p><p>ResearcherID: ABF-4392-2022</p><p> </p><p>Scopus Author ID: 7101843976</p></bio><bio xml:lang="en"><p>Anastasia A. Lavreniuk, MD</p><p>11 Dm.Ulyanova street, 115478, Moscow</p><p>ResearcherID: ABF-4392-2022</p><p> </p><p>Scopus Author ID: 7101843976</p></bio><email xlink:type="simple">lavrenyuk.anastasiya@endocrincentr.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/0000-0001-6667-062X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Еремкина</surname><given-names>А. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Eremkina</surname><given-names>A. K.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Еремкина Анна Константиновна, к.м.н.</p><p>115478, Москва, ул. Дм. Ульянова, д. 11</p><p>ResearcherID: R-8848-2019</p><p> </p><p>Scopus Author ID: 57197775339</p></bio><bio xml:lang="en"><p>Anna K. Eremkina, MD, PhD</p><p>11 Dm.Ulyanova street, 115478, Moscow</p><p>ResearcherID: R-8848-2019</p><p> </p><p>Scopus Author ID: 57197775339</p></bio><email xlink:type="simple">eremkina.anna@endocrincentr.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/0000-0002-0532-9126</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Тихонов</surname><given-names>И. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Tikhonov</surname><given-names>I. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Тихонов Игорь Николаевич</p><p>Scopus Author ID: 57200597669</p></bio><bio xml:lang="en"><p>Igor N. Tikhonov, MD</p><p>ResearcherID: ABC-4408-2020</p><p> </p><p>Scopus Author ID: 57200597669</p></bio><email xlink:type="simple">antihbs@gmail.com</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9717-9742</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Мокрышева</surname><given-names>Н. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Mokrysheva</surname><given-names>N. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Мокрышева Наталья Георгиевна, д.м.н., профессор</p><p>115478, Москва, ул. Дм. Ульянова, д. 11 </p><p>ResearcherID: AAY-3761-2020</p><p> </p><p>Scopus Author ID: 35269746000</p></bio><bio xml:lang="en"><p>Natalia G. Mokrysheva, MD, PhD, Professor</p><p>11 Dm.Ulyanova street, 115478, Moscow</p><p>ResearcherID: AAY-3761-2020</p><p> </p><p>Scopus Author ID: 35269746000</p></bio><email xlink:type="simple">mokrisheva.natalia@endocrincentr.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Национальный медицинский исследовательский центр эндокринологии</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Endocrinology Research Center</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ИКМ им. Н.В. Склифосовского Первого МГМУ имени И.М.Сеченова</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Federal State Autonomous Educational Institution of Higher Education I.M. Sechenov First Moscow State Medical&#13;
University of the Ministry of Health of the Russian Federation (Sechenov University)</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>06</day><month>09</month><year>2024</year></pub-date><volume>21</volume><issue>4</issue><fpage>373</fpage><lpage>381</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Горбачева А.М., Бибик Е.Е., Лавренюк А.А., Еремкина А.К., Тихонов И.Н., Мокрышева Н.Г., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Горбачева А.М., Бибик Е.Е., Лавренюк А.А., Еремкина А.К., Тихонов И.Н., Мокрышева Н.Г.</copyright-holder><copyright-holder xml:lang="en">Gorbacheva A.M., Bibik E.E., Lavreniuk A.A., Eremkina A.K., Tikhonov I.N., Mokrysheva N.G.</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.omet-endojournals.ru/jour/article/view/13124">https://www.omet-endojournals.ru/jour/article/view/13124</self-uri><abstract><p>Хронические заболевания печени относятся к значимым проблемам здравоохранения во всем мире, а их последствия обуславливают развитие различных минеральных нарушений, которые встречаются у 75% пациентов. Среди минеральных нарушений, развивающихся при хронических заболеваниях печени, наибольшее клиническое значение имеет остеопороз (до 30% больных). Переломы случаются, по разным данным, у 7–35% пациентов. Существует представление о целом ряде механизмов, влияющих на состояние минерального обмена при хронических заболеваниях печени: от нарушения метаболизма витамина D до синтеза провоспалительных цитокинов и функции кишечной микробиоты. На сегодняшний день эти процессы остаются недостаточно изученными: так, не до конца ясны аспекты, касающиеся функционирования околощитовидных желез при хронических заболеваниях печени; нет четкого представления о преобладающих процессах в костной ткани (анти- или прорезорбтивных). Это обусловливает несовершенство профилактических и терапевтических подходов при минеральных нарушениях вследствие хронических заболеваний печени и необходимости дальнейших исследований в этом направлении. Первая часть настоящего обзора посвящена вопросам эпидемиологии и патофизиологии нарушений минерального обмена при данных состояниях; вторая часть обзора будет касаться современных терапевтических подходов</p></abstract><trans-abstract xml:lang="en"><p>Chronic liver disease is a significant public health problem worldwide, and its consequences lead to the development of various mineral disorders, which occur in 75% of patients. Osteoporosis (up to 30% of patients) has the greatest clinical significance among the mineral disorders that develop in chronic liver disease. Fractures occur, according to different data, in 7-35% of patients. There are number of mechanisms influencing the state of mineral metabolism in chronic liver diseases: from the disturbance of vitamin D metabolism to the synthesis of pro-inflammatory cytokines and the function of intestinal microbiota. To date, these processes remain insufficiently studied: for example, aspects concerning the functioning of parathyroid glands in chronic liver diseases are not completely clear; there is no clear idea about the predominant processes in bone tissue (anti- or proresorptive). This determines the imperfection of prophylactic and therapeutic approaches in mineral disorders due to chronic liver diseases and the need for further research in this direction. The first part of this review focuses on the epidemiology and pathophysiology of mineral metabolism disorders in these conditions; the second part of the review will focus on current therapeutic approaches</p></trans-abstract><kwd-group xml:lang="ru"><kwd>Цирроз печени</kwd><kwd>остеопороз</kwd><kwd>витамин D</kwd></kwd-group><kwd-group xml:lang="en"><kwd>liver cirrhosis</kwd><kwd>osteoporosis</kwd><kwd>vitamin D</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа проведена в рамках гранта РНФ №24-25-00348 «Нарушения метаболизма витамина D и особенности костного ремоделирования у пациентов с циррозом печени различной этиологии»</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Cheemerla S, Balakrishnan M. Global Epidemiology of Chronic Liver Disease. Clin Liver Dis (Hoboken). 2021;17(5):365-370. doi: https://doi.org/10.1002/cld.1061</mixed-citation><mixed-citation xml:lang="en">Cheemerla S, Balakrishnan M. Global Epidemiology of Chronic Liver Disease. Clin Liver Dis (Hoboken). 2021;17(5):365-370. doi: https://doi.org/10.1002/cld.1061</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Sepanlou SG, Safiri S, Bisignano C, et al. The global, regional, and national burden of cirrhosis by cause in 195 countries and territories, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet Gastroenterol Hepatol. 2020;5(3). doi: https://doi.org/10.1016/S2468-1253(19)30349-8</mixed-citation><mixed-citation xml:lang="en">Sepanlou SG, Safiri S, Bisignano C, et al. The global, regional, and national burden of cirrhosis by cause in 195 countries and territories, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet Gastroenterol Hepatol. 2020;5(3). doi: https://doi.org/10.1016/S2468-1253(19)30349-8</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Giouleme O, Vyzantiadis T, Nikolaidis N, et al. Pathogenesis of osteoporosis in liver cirrhosis. Hepatogastroenterology. 2006;53(72):938-943</mixed-citation><mixed-citation xml:lang="en">Giouleme O, Vyzantiadis T, Nikolaidis N, et al. Pathogenesis of osteoporosis in liver cirrhosis. Hepatogastroenterology. 2006;53(72):938-943</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Zheng JP, Miao HX, Zheng SW, et al. Risk factors for osteoporosis in liver cirrhosis patients measured by transient elastography. Medicine (United States). 2018;97(20). doi: https://doi.org/10.1097/MD.0000000000010645</mixed-citation><mixed-citation xml:lang="en">Zheng JP, Miao HX, Zheng SW, et al. Risk factors for osteoporosis in liver cirrhosis patients measured by transient elastography. Medicine (United States). 2018;97(20). doi: https://doi.org/10.1097/MD.0000000000010645</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Patel N, Muñoz SJ. Bone disease in cirrhosis. Clin Liver Dis (Hoboken). 2015;6(4). doi: https://doi.org/10.1002/cld.498</mixed-citation><mixed-citation xml:lang="en">Patel N, Muñoz SJ. Bone disease in cirrhosis. Clin Liver Dis (Hoboken). 2015;6(4). doi: https://doi.org/10.1002/cld.498</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Nakchbandi IA. Osteoporosis and fractures in liver disease: Relevance, pathogenesis and therapeutic implications. World J Gastroenterol. 2014;20(28). doi: https://doi.org/10.3748/wjg.v20.i28.9427</mixed-citation><mixed-citation xml:lang="en">Nakchbandi IA. Osteoporosis and fractures in liver disease: Relevance, pathogenesis and therapeutic implications. World J Gastroenterol. 2014;20(28). doi: https://doi.org/10.3748/wjg.v20.i28.9427</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Compston JE, McClung MR, Leslie WD. Osteoporosis. The Lancet. 2019;393(10169):364-376. doi: https://doi.org/10.1016/S0140-6736(18)32112-3</mixed-citation><mixed-citation xml:lang="en">Compston JE, McClung MR, Leslie WD. Osteoporosis. The Lancet. 2019;393(10169):364-376. doi: https://doi.org/10.1016/S0140-6736(18)32112-3</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Merli M, Berzigotti A, Zelber-Sagi S, et al. EASL Clinical Practice Guidelines on nutrition in chronic liver disease. J Hepatol. 2019;70(1). doi: https://doi.org/10.1016/j.jhep.2018.06.024</mixed-citation><mixed-citation xml:lang="en">Merli M, Berzigotti A, Zelber-Sagi S, et al. EASL Clinical Practice Guidelines on nutrition in chronic liver disease. J Hepatol. 2019;70(1). doi: https://doi.org/10.1016/j.jhep.2018.06.024</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Leidig-Bruckner G, Hosch S, Dodidou P, et al. Frequency and predictors of osteoporotic fractures after cardiac or liver transplantation: A follow-up study. Lancet. 2001;357(9253). doi: https://doi.org/10.1016/S0140-6736(00)03641-2</mixed-citation><mixed-citation xml:lang="en">Leidig-Bruckner G, Hosch S, Dodidou P, et al. Frequency and predictors of osteoporotic fractures after cardiac or liver transplantation: A follow-up study. Lancet. 2001;357(9253). doi: https://doi.org/10.1016/S0140-6736(00)03641-2</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Navasa M, Monegal A, Guañabens N, et al. Bone fractures in liver transplant patients. Rheumatology. 1994;33(1). doi: https://doi.org/10.1093/rheumatology/33.1.52</mixed-citation><mixed-citation xml:lang="en">Navasa M, Monegal A, Guañabens N, et al. Bone fractures in liver transplant patients. Rheumatology. 1994;33(1). doi: https://doi.org/10.1093/rheumatology/33.1.52</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Топчеева О.Н., Дроздов В.Н., Эмбутниекс Ю.В., Вяжевич Ю.В. Минеральная плотность костной ткани у больных циррозом печени // Терапевтическая гастроэнетрология. — 2009. — №8. — С. 51-55.</mixed-citation><mixed-citation xml:lang="en">Topcheeva ON, Drozdov VN, Embutnieks YV, Vyazhevich YV. Mineral’naya plotnost’ kostnoj tkani u bol’nyh cirrozom pecheni // Terapevticheskaya gastroenetrologiya. 2009;8:51-55 (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Топчеева О.Н. Особенности нарушения минеральной плотности костной ткани у больных циррозом печени различной этиологии: Дисс. … мед. наук. — М., 2010. – 115с.</mixed-citation><mixed-citation xml:lang="en">Topcheeva ON. Osobennosti narusheniya mineral’noj plotnosti kostnoj tkani u bol’nyh cirrozom pecheni razlichnoj etiologii: Diss. … med. nauk. M. 2010:115 (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Киргуева О.И. Состояние костной ткани у мужчин, страдающих циррозом печени: Дисс. … мед. наук. — Волгоград, 2017. — 124 с.</mixed-citation><mixed-citation xml:lang="en">Kirgueva OI. Sostoyanie kostnoj tkani u muzhchin, stradayushchih cirrozom pecheni: Diss. … med. nauk. Volgograd. 2017:124 (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Ehnert S, Aspera-Werz RH, Ruoß M, et al. Hepatic Osteodystrophy- Molecular Mechanisms Proposed to Favor Its Development. Int J Mol Sci. 2019;20(10). doi: https://doi.org/10.3390/ijms20102555</mixed-citation><mixed-citation xml:lang="en">Ehnert S, Aspera-Werz RH, Ruoß M, et al. Hepatic Osteodystrophy- Molecular Mechanisms Proposed to Favor Its Development. Int J Mol Sci. 2019;20(10). doi: https://doi.org/10.3390/ijms20102555</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Wintermeyer E, Ihle C, Ehnert S, et al. Crucial role of vitamin D in the musculoskeletal system. Nutrients. 2016;8(6). doi: https://doi.org/10.3390/nu8060319</mixed-citation><mixed-citation xml:lang="en">Wintermeyer E, Ihle C, Ehnert S, et al. Crucial role of vitamin D in the musculoskeletal system. Nutrients. 2016;8(6). doi: https://doi.org/10.3390/nu8060319</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Holick MF. Vitamin D: A D-lightful solution for health. In: Journal of Investigative Medicine. 2011;59. doi: https://doi.org/10.2310/JIM.0b013e318214ea2d</mixed-citation><mixed-citation xml:lang="en">Holick MF. Vitamin D: A D-lightful solution for health. In: Journal of Investigative Medicine. 2011;59. doi: https://doi.org/10.2310/JIM.0b013e318214ea2d</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Nussler AK, Wildemann B, Freude T, et al. Chronic CCl4 intoxication causes liver and bone damage similar to the human pathology of hepatic osteodystrophy: A mouse model to analyse the liver-bone axis. Arch Toxicol. 2014;88(4). doi: https://doi.org/10.1007/s00204-013-1191-5</mixed-citation><mixed-citation xml:lang="en">Nussler AK, Wildemann B, Freude T, et al. Chronic CCl4 intoxication causes liver and bone damage similar to the human pathology of hepatic osteodystrophy: A mouse model to analyse the liver-bone axis. Arch Toxicol. 2014;88(4). doi: https://doi.org/10.1007/s00204-013-1191-5</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Hochrath K, Ehnert S, Ackert-Bicknell CL, et al. Modeling hepatic osteodystrophy in Abcb4 deficient mice. Bone. 2013;55(2). doi: https://doi.org/10.1016/j.bone.2013.03.012</mixed-citation><mixed-citation xml:lang="en">Hochrath K, Ehnert S, Ackert-Bicknell CL, et al. Modeling hepatic osteodystrophy in Abcb4 deficient mice. Bone. 2013;55(2). doi: https://doi.org/10.1016/j.bone.2013.03.012</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Chongthavornvasana S, Lertudomphonwanit C, Mahachoklertwattana P, Korwutthikulrangsri M. Determination of Optimal Vitamin D Dosage in Children with Cholestasis. BMC Pediatr. 2023;23(1). doi: https://doi.org/10.1186/s12887-023-04113-y</mixed-citation><mixed-citation xml:lang="en">Chongthavornvasana S, Lertudomphonwanit C, Mahachoklertwattana P, Korwutthikulrangsri M. Determination of Optimal Vitamin D Dosage in Children with Cholestasis. BMC Pediatr. 2023;23(1). doi: https://doi.org/10.1186/s12887-023-04113-y</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Abdel-Rahman N, Sharawy MH, Megahed N, El-Awady MS. Vitamin D3 abates BDL-induced cholestasis and fibrosis in rats via regulating Hedgehog pathway. Toxicol Appl Pharmacol. 2019;380. doi: https://doi.org/10.1016/j.taap.2019.114697</mixed-citation><mixed-citation xml:lang="en">Abdel-Rahman N, Sharawy MH, Megahed N, El-Awady MS. Vitamin D3 abates BDL-induced cholestasis and fibrosis in rats via regulating Hedgehog pathway. Toxicol Appl Pharmacol. 2019;380. doi: https://doi.org/10.1016/j.taap.2019.114697</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao XY, Li J, Wang JH, et al. Vitamin D serum level is associated with Child-Pugh score and metabolic enzyme imbalances, but not viral load in chronic hepatitis B patients. Medicine (United States). 2016;95(27). doi: https://doi.org/10.1097/MD.0000000000003926</mixed-citation><mixed-citation xml:lang="en">Zhao XY, Li J, Wang JH, et al. Vitamin D serum level is associated with Child-Pugh score and metabolic enzyme imbalances, but not viral load in chronic hepatitis B patients. Medicine (United States). 2016;95(27). doi: https://doi.org/10.1097/MD.0000000000003926</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Arteh J, Narra S, Nair S. Prevalence of vitamin D deficiency in chronic liver disease. Dig Dis Sci. 2010;55(9). doi: https://doi.org/10.1007/s10620-009-1069-9</mixed-citation><mixed-citation xml:lang="en">Arteh J, Narra S, Nair S. Prevalence of vitamin D deficiency in chronic liver disease. Dig Dis Sci. 2010;55(9). doi: https://doi.org/10.1007/s10620-009-1069-9</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">DeLuca HF. History of the discovery of vitamin D and its active metabolites. Bonekey Rep. 2014;3. doi: https://doi.org/10.1038/bonekey.2013.213</mixed-citation><mixed-citation xml:lang="en">DeLuca HF. History of the discovery of vitamin D and its active metabolites. Bonekey Rep. 2014;3. doi: https://doi.org/10.1038/bonekey.2013.213</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Shinchuk L, Holick MF. Vitamin D and rehabilitation: Improving functional outcomes. Nutrition in Clinical Practice. 2007;22(3). doi: https://doi.org/10.1177/0115426507022003297</mixed-citation><mixed-citation xml:lang="en">Shinchuk L, Holick MF. Vitamin D and rehabilitation: Improving functional outcomes. Nutrition in Clinical Practice. 2007;22(3). doi: https://doi.org/10.1177/0115426507022003297</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Booth DR, Ding N, Parnell GP, et al. Cistromic and genetic evidence that the vitamin D receptor mediates susceptibility to latitudedependent autoimmune diseases. Genes Immun. 2016;17(4):213-219. doi: https://doi.org/10.1038/gene.2016.12</mixed-citation><mixed-citation xml:lang="en">Booth DR, Ding N, Parnell GP, et al. Cistromic and genetic evidence that the vitamin D receptor mediates susceptibility to latitudedependent autoimmune diseases. Genes Immun. 2016;17(4):213-219. doi: https://doi.org/10.1038/gene.2016.12</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Christensen MHE, Apalset EM, Nordbø Y, Varhaug JE, Mellgren G, Lien EA. 1,25-Dihydroxyvitamin D and the Vitamin D Receptor Gene Polymorphism Apa1 Influence Bone Mineral Density in Primary Hyperparathyroidism. PLoS One. 2013;8(2). doi: https://doi.org/10.1371/journal.pone.0056019</mixed-citation><mixed-citation xml:lang="en">Christensen MHE, Apalset EM, Nordbø Y, Varhaug JE, Mellgren G, Lien EA. 1,25-Dihydroxyvitamin D and the Vitamin D Receptor Gene Polymorphism Apa1 Influence Bone Mineral Density in Primary Hyperparathyroidism. PLoS One. 2013;8(2). doi: https://doi.org/10.1371/journal.pone.0056019</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Christakos S, Dhawan P, Porta A, Mady LJ, Seth T. Vitamin D and intestinal calcium absorption. Mol Cell Endocrinol. 2011;347(1-2). doi: https://doi.org/10.1016/j.mce.2011.05.038</mixed-citation><mixed-citation xml:lang="en">Christakos S, Dhawan P, Porta A, Mady LJ, Seth T. Vitamin D and intestinal calcium absorption. Mol Cell Endocrinol. 2011;347(1-2). doi: https://doi.org/10.1016/j.mce.2011.05.038</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Veldurthy V, Wei R, Oz L, Dhawan P, Jeon YH, Christakos S. Vitamin D, calcium homeostasis and aging. Bone Res. 2016;4. doi: https://doi.org/10.1038/boneres.2016.41</mixed-citation><mixed-citation xml:lang="en">Veldurthy V, Wei R, Oz L, Dhawan P, Jeon YH, Christakos S. Vitamin D, calcium homeostasis and aging. Bone Res. 2016;4. doi: https://doi.org/10.1038/boneres.2016.41</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Shymanskyi I, Lisakovska O, Mazanova A, Labudzynskyi D, Veliky M. Vitamin D3 modulates impaired crosstalk between RANK and glucocorticoid receptor signaling in bone marrow cells after chronic prednisolone administration. Front Endocrinol (Lausanne). 2018;9(JUN). doi: https://doi.org/10.3389/fendo.2018.00303</mixed-citation><mixed-citation xml:lang="en">Shymanskyi I, Lisakovska O, Mazanova A, Labudzynskyi D, Veliky M. Vitamin D3 modulates impaired crosstalk between RANK and glucocorticoid receptor signaling in bone marrow cells after chronic prednisolone administration. Front Endocrinol (Lausanne). 2018;9(JUN). doi: https://doi.org/10.3389/fendo.2018.00303</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Wacker M, Holiack MF. Vitamin D-effects on skeletal and extraskeletal health and the need for supplementation. Nutrients. 2013;5(1). doi: https://doi.org/10.3390/nu5010111</mixed-citation><mixed-citation xml:lang="en">Wacker M, Holiack MF. Vitamin D-effects on skeletal and extraskeletal health and the need for supplementation. Nutrients. 2013;5(1). doi: https://doi.org/10.3390/nu5010111</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Takahashi N, Udagawa N, Suda T. Vitamin D endocrine system and osteoclasts. Bonekey Rep. 2014;3. doi: https://doi.org/10.1038/bonekey.2014.17</mixed-citation><mixed-citation xml:lang="en">Takahashi N, Udagawa N, Suda T. Vitamin D endocrine system and osteoclasts. Bonekey Rep. 2014;3. doi: https://doi.org/10.1038/bonekey.2014.17</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Prié D, Forand A, Francoz C, et al. Plasma Fibroblast Growth Factor 23 Concentration Is Increased and Predicts Mortality in Patients on the Liver-Transplant Waiting List. PLoS One. 2013;8(6). doi: https://doi.org/10.1371/journal.pone.0066182</mixed-citation><mixed-citation xml:lang="en">Prié D, Forand A, Francoz C, et al. Plasma Fibroblast Growth Factor 23 Concentration Is Increased and Predicts Mortality in Patients on the Liver-Transplant Waiting List. PLoS One. 2013;8(6). doi: https://doi.org/10.1371/journal.pone.0066182</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">He X, Shen Y, Ma X, et al. The association of serum FGF23 and non-alcoholic fatty liver disease is independent of vitamin D in type 2 diabetes patients. Clin Exp Pharmacol Physiol. 2018;45(7). doi: https://doi.org/10.1111/1440-1681.12933</mixed-citation><mixed-citation xml:lang="en">He X, Shen Y, Ma X, et al. The association of serum FGF23 and non-alcoholic fatty liver disease is independent of vitamin D in type 2 diabetes patients. Clin Exp Pharmacol Physiol. 2018;45(7). doi: https://doi.org/10.1111/1440-1681.12933</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Bihari C, Lal D, Thakur M, et al. Suboptimal Level of Bone-Forming Cells in Advanced Cirrhosis are Associated with Hepatic Osteodystrophy. Hepatol Commun. 2018;2(9). doi: https://doi.org/10.1002/hep4.1234</mixed-citation><mixed-citation xml:lang="en">Bihari C, Lal D, Thakur M, et al. Suboptimal Level of Bone-Forming Cells in Advanced Cirrhosis are Associated with Hepatic Osteodystrophy. Hepatol Commun. 2018;2(9). doi: https://doi.org/10.1002/hep4.1234</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Lavi-Moshayoff V, Wasserman G, Meir T, Silver J, Naveh- Many T. PTH increases FGF23 gene expression and mediates the high-FGF23 levels of experimental kidney failure: A bone parathyroid feedback loop. Am J Physiol Renal Physiol. 2010;299(4). doi: https://doi.org/10.1152/ajprenal.00360.2010</mixed-citation><mixed-citation xml:lang="en">Lavi-Moshayoff V, Wasserman G, Meir T, Silver J, Naveh- Many T. PTH increases FGF23 gene expression and mediates the high-FGF23 levels of experimental kidney failure: A bone parathyroid feedback loop. Am J Physiol Renal Physiol. 2010;299(4). doi: https://doi.org/10.1152/ajprenal.00360.2010</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Silver J, Naveh-Many T. FGF23 and the parathyroid glands. Pediatric Nephrology. 2010;25(11). doi: https://doi.org/10.1007/s00467-010-1565-3</mixed-citation><mixed-citation xml:lang="en">Silver J, Naveh-Many T. FGF23 and the parathyroid glands. Pediatric Nephrology. 2010;25(11). doi: https://doi.org/10.1007/s00467-010-1565-3</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Fisher L, Fisher A. Vitamin D and Parathyroid Hormone in Outpatients With Noncholestatic Chronic Liver Disease. Clinical Gastroenterology and Hepatology. 2007;5(4). doi: https://doi.org/10.1016/j.cgh.2006.10.015</mixed-citation><mixed-citation xml:lang="en">Fisher L, Fisher A. Vitamin D and Parathyroid Hormone in Outpatients With Noncholestatic Chronic Liver Disease. Clinical Gastroenterology and Hepatology. 2007;5(4). doi: https://doi.org/10.1016/j.cgh.2006.10.015</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Islam MZ, Viljakainen HT, Kärkkäinen MUM, Saarnio E, Laitinen K, Lamberg-Allardt C. Prevalence of vitamin D deficiency and secondary hyperparathyroidism during winter in pre-menopausal Bangladeshi and Somali immigrant and ethnic Finnish women: associations with forearm bone mineral density. Br J Nutr. 2012;107(2):277-283. doi: https://doi.org/10.1017/S0007114511002893</mixed-citation><mixed-citation xml:lang="en">Islam MZ, Viljakainen HT, Kärkkäinen MUM, Saarnio E, Laitinen K, Lamberg-Allardt C. Prevalence of vitamin D deficiency and secondary hyperparathyroidism during winter in pre-menopausal Bangladeshi and Somali immigrant and ethnic Finnish women: associations with forearm bone mineral density. Br J Nutr. 2012;107(2):277-283. doi: https://doi.org/10.1017/S0007114511002893</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Narayanasamy K, Karthick R, Raj AK. High Prevalent Hypovitaminosis D Is Associated with Dysregulation of Calcium-parathyroid Hormone-vitamin D Axis in Patients with Chronic Liver Diseases. J Clin Transl Hepatol. 2019;7(1):15-20. doi: https://doi.org/10.14218/JCTH.2018.00018</mixed-citation><mixed-citation xml:lang="en">Narayanasamy K, Karthick R, Raj AK. High Prevalent Hypovitaminosis D Is Associated with Dysregulation of Calcium-parathyroid Hormone-vitamin D Axis in Patients with Chronic Liver Diseases. J Clin Transl Hepatol. 2019;7(1):15-20. doi: https://doi.org/10.14218/JCTH.2018.00018</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Duarte MP, Farias ML, Coelho HS, et al. Calcium-parathyroid hormone-vitamin D axis and metabolic bone disease in chronic viral liver disease. J Gastroenterol Hepatol. 2001;16(9):1022-1027. doi: https://doi.org/10.1046/j.1440-1746.2001.02561.x</mixed-citation><mixed-citation xml:lang="en">Duarte MP, Farias ML, Coelho HS, et al. Calcium-parathyroid hormone-vitamin D axis and metabolic bone disease in chronic viral liver disease. J Gastroenterol Hepatol. 2001;16(9):1022-1027. doi: https://doi.org/10.1046/j.1440-1746.2001.02561.x</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Marek B, Kajdaniuk D, Niedziołka D, et al. Growth hormone/insulinlike growth factor-1 axis, calciotropic hormones and bone mineral density in young patients with chronic viral hepatitis. Endokrynol Pol. 2015;66(1):22-29. doi: https://doi.org/10.5603/EP.2015.0005</mixed-citation><mixed-citation xml:lang="en">Marek B, Kajdaniuk D, Niedziołka D, et al. Growth hormone/insulinlike growth factor-1 axis, calciotropic hormones and bone mineral density in young patients with chronic viral hepatitis. Endokrynol Pol. 2015;66(1):22-29. doi: https://doi.org/10.5603/EP.2015.0005</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Corey RL, Whitaker MD, Crowell MD, et al. Vitamin D deficiency, parathyroid hormone levels, and bone disease among patients with end-stage liver disease and normal serum creatinine awaiting liver transplantation. Clin Transplant. 2014;28(5). doi: https://doi.org/10.1111/ctr.12351</mixed-citation><mixed-citation xml:lang="en">Corey RL, Whitaker MD, Crowell MD, et al. Vitamin D deficiency, parathyroid hormone levels, and bone disease among patients with end-stage liver disease and normal serum creatinine awaiting liver transplantation. Clin Transplant. 2014;28(5). doi: https://doi.org/10.1111/ctr.12351</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Dibble JB, Sheridan P, Hampshire R, Hardy GJ, Losowsky MS. Evidence for secondary hyperparathyroidism in the osteomalacia associated with chronic liver disease. Clin Endocrinol (Oxf ). 1981;15(4):373-383. doi: https://doi.org/10.1111/j.1365-2265.1981.tb00677.x</mixed-citation><mixed-citation xml:lang="en">Dibble JB, Sheridan P, Hampshire R, Hardy GJ, Losowsky MS. Evidence for secondary hyperparathyroidism in the osteomalacia associated with chronic liver disease. Clin Endocrinol (Oxf ). 1981;15(4):373-383. doi: https://doi.org/10.1111/j.1365-2265.1981.tb00677.x</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Gerhardt A, Greenberg A, Reilly JJ, Van Thiel DH. Hypercalcemia. A complication of advanced chronic liver disease. Arch Intern Med. 1987;147(2):274-277. doi: https://doi.org/10.1001/archinte.147.2.274</mixed-citation><mixed-citation xml:lang="en">Gerhardt A, Greenberg A, Reilly JJ, Van Thiel DH. Hypercalcemia. A complication of advanced chronic liver disease. Arch Intern Med. 1987;147(2):274-277. doi: https://doi.org/10.1001/archinte.147.2.274</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Compston JE, Greer S, Skingle SJ, et al. Early increase in plasma parathyroid hormone levels following liver transplantation. J Hepatol. 1996;25(5):715-718. doi: https://doi.org/10.1016/s0168-8278(96)80243-1</mixed-citation><mixed-citation xml:lang="en">Compston JE, Greer S, Skingle SJ, et al. Early increase in plasma parathyroid hormone levels following liver transplantation. J Hepatol. 1996;25(5):715-718. doi: https://doi.org/10.1016/s0168-8278(96)80243-1</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Prytuła A, Walle J Vande, Van Vlierberghe H, et al. Factors associated with 1,25-dihydroxyvitamin D3 concentrations in liver transplant recipients: a prospective observational longitudinal study. Endocrine. 2016;52(1):93-102. doi: https://doi.org/10.1007/s12020-015-0757-9</mixed-citation><mixed-citation xml:lang="en">Prytuła A, Walle J Vande, Van Vlierberghe H, et al. Factors associated with 1,25-dihydroxyvitamin D3 concentrations in liver transplant recipients: a prospective observational longitudinal study. Endocrine. 2016;52(1):93-102. doi: https://doi.org/10.1007/s12020-015-0757-9</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Klein GL, Soriano H, Shulman RJ, Levy M, Jones G, Langman CB. Hepatic osteodystrophy in chronic cholestasis: evidence for a multifactorial etiology. Pediatr Transplant. 2002;6(2):136-140. doi: https://doi.org/10.1034/j.1399-3046.2002.01060.x</mixed-citation><mixed-citation xml:lang="en">Klein GL, Soriano H, Shulman RJ, Levy M, Jones G, Langman CB. Hepatic osteodystrophy in chronic cholestasis: evidence for a multifactorial etiology. Pediatr Transplant. 2002;6(2):136-140. doi: https://doi.org/10.1034/j.1399-3046.2002.01060.x</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Marie PJ, Kassem M. Osteoblasts in osteoporosis: Past, emerging, and future anabolic targets. Eur J Endocrinol. 2011;165(1). doi: https://doi.org/10.1530/EJE-11-0132</mixed-citation><mixed-citation xml:lang="en">Marie PJ, Kassem M. Osteoblasts in osteoporosis: Past, emerging, and future anabolic targets. Eur J Endocrinol. 2011;165(1). doi: https://doi.org/10.1530/EJE-11-0132</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Ruiz-Gaspà S, Martinez-Ferrer A, Guañabens N, et al. Effects of bilirubin and sera from jaundiced patients on osteoblasts: Contribution to the development of osteoporosis in liver diseases. Hepatology. 2011;54(6). doi: https://doi.org/10.1002/hep.24605</mixed-citation><mixed-citation xml:lang="en">Ruiz-Gaspà S, Martinez-Ferrer A, Guañabens N, et al. Effects of bilirubin and sera from jaundiced patients on osteoblasts: Contribution to the development of osteoporosis in liver diseases. Hepatology. 2011;54(6). doi: https://doi.org/10.1002/hep.24605</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Nuti R, Brandi ML, Checchia G, et al. Guidelines for the management of osteoporosis and fragility fractures. Intern Emerg Med. 2019;14(1). doi: https://doi.org/10.1007/s11739-018-1874-2</mixed-citation><mixed-citation xml:lang="en">Nuti R, Brandi ML, Checchia G, et al. Guidelines for the management of osteoporosis and fragility fractures. Intern Emerg Med. 2019;14(1). doi: https://doi.org/10.1007/s11739-018-1874-2</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Delgado-Calle J, Sato AY, Bellido T. Role and mechanism of action of sclerostin in bone. Bone. 2017;96. doi: https://doi.org/10.1016/j.bone.2016.10.007</mixed-citation><mixed-citation xml:lang="en">Delgado-Calle J, Sato AY, Bellido T. Role and mechanism of action of sclerostin in bone. Bone. 2017;96. doi: https://doi.org/10.1016/j.bone.2016.10.007</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Rhee Y, Kim WJ, Han KJ, Lim SK, Kim SH. Effect of liver dysfunction on circulating sclerostin. J Bone Miner Metab. 2014;32(5). doi: https://doi.org/10.1007/s00774-013-0524-z</mixed-citation><mixed-citation xml:lang="en">Rhee Y, Kim WJ, Han KJ, Lim SK, Kim SH. Effect of liver dysfunction on circulating sclerostin. J Bone Miner Metab. 2014;32(5). doi: https://doi.org/10.1007/s00774-013-0524-z</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Reid IR. Targeting Sclerostin in Postmenopausal Osteoporosis: Focus on Romosozumab and Blosozumab. BioDrugs. 2017;31(4). doi: https://doi.org/10.1007/s40259-017-0229-2</mixed-citation><mixed-citation xml:lang="en">Reid IR. Targeting Sclerostin in Postmenopausal Osteoporosis: Focus on Romosozumab and Blosozumab. BioDrugs. 2017;31(4). doi: https://doi.org/10.1007/s40259-017-0229-2</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Guañabens N, Parés A. Osteoporosis in chronic liver disease. Liver International. 2018;38(5). doi: https://doi.org/10.1111/liv.13730</mixed-citation><mixed-citation xml:lang="en">Guañabens N, Parés A. Osteoporosis in chronic liver disease. Liver International. 2018;38(5). doi: https://doi.org/10.1111/liv.13730</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Kimura K, Terasaka T, Iwata N, et al. Combined effects of androgen and growth hormone on osteoblast marker expression in mouse C2C12 and MC3T3-E1 cells induced by bone morphogenetic protein. J Clin Med. 2017;6(1). doi: https://doi.org/10.3390/jcm6010006</mixed-citation><mixed-citation xml:lang="en">Kimura K, Terasaka T, Iwata N, et al. Combined effects of androgen and growth hormone on osteoblast marker expression in mouse C2C12 and MC3T3-E1 cells induced by bone morphogenetic protein. J Clin Med. 2017;6(1). doi: https://doi.org/10.3390/jcm6010006</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Qiu T, Crane JL, Xie L, Xian L, Xie H, Cao X. IGF-I induced phosphorylation of PTH receptor enhances osteoblast to osteocyte transition. Bone Res. 2018;6(1). doi: https://doi.org/10.1038/s41413-017-0002-7</mixed-citation><mixed-citation xml:lang="en">Qiu T, Crane JL, Xie L, Xian L, Xie H, Cao X. IGF-I induced phosphorylation of PTH receptor enhances osteoblast to osteocyte transition. Bone Res. 2018;6(1). doi: https://doi.org/10.1038/s41413-017-0002-7</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Guerra-Menéndez L, Sádaba MC, Puche JE, et al. IGF-I increases markers of osteoblastic activity and reduces bone resorption via osteoprotegerin and RANK-ligand. J Transl Med. 2013;11(1). doi: https://doi.org/10.1186/1479-5876-11-271</mixed-citation><mixed-citation xml:lang="en">Guerra-Menéndez L, Sádaba MC, Puche JE, et al. IGF-I increases markers of osteoblastic activity and reduces bone resorption via osteoprotegerin and RANK-ligand. J Transl Med. 2013;11(1). doi: https://doi.org/10.1186/1479-5876-11-271</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Krishnan V. Regulation of bone mass by Wnt signaling. Journal of Clinical Investigation. 2006;116(5):1202-1209. doi: https://doi.org/10.1172/JCI28551</mixed-citation><mixed-citation xml:lang="en">Krishnan V. Regulation of bone mass by Wnt signaling. Journal of Clinical Investigation. 2006;116(5):1202-1209. doi: https://doi.org/10.1172/JCI28551</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Nasu M, Sugimoto T, Chihara M, Hiraumi M, Kurimoto F, Chihara K. Effect of natural menopause on serum levels of IGF-I and IGFbinding proteins: Relationship with bone mineral density and lipid metabolism in perimenopausal women. Eur J Endocrinol. 1997;136(6). doi: https://doi.org/10.1530/eje.0.1360608</mixed-citation><mixed-citation xml:lang="en">Nasu M, Sugimoto T, Chihara M, Hiraumi M, Kurimoto F, Chihara K. Effect of natural menopause on serum levels of IGF-I and IGFbinding proteins: Relationship with bone mineral density and lipid metabolism in perimenopausal women. Eur J Endocrinol. 1997;136(6). doi: https://doi.org/10.1530/eje.0.1360608</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">de la Garza RG, Morales-Garza LA, Martin-Estal I, Castilla-Cortazar I. Insulin-Like Growth Factor-1 Deficiency and Cirrhosis Establishment. J Clin Med Res. 2017;9(4). doi: https://doi.org/10.14740/jocmr2761w</mixed-citation><mixed-citation xml:lang="en">de la Garza RG, Morales-Garza LA, Martin-Estal I, Castilla-Cortazar I. Insulin-Like Growth Factor-1 Deficiency and Cirrhosis Establishment. J Clin Med Res. 2017;9(4). doi: https://doi.org/10.14740/jocmr2761w</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Cemborain A, Castilla-Cortázar I, García M, et al. Osteopenia in rats with liver cirrhosis: Beneficial effects of IGF-I treatment. J Hepatol. 1998;28(1). doi: https://doi.org/10.1016/S0168-8278(98)80211-0</mixed-citation><mixed-citation xml:lang="en">Cemborain A, Castilla-Cortázar I, García M, et al. Osteopenia in rats with liver cirrhosis: Beneficial effects of IGF-I treatment. J Hepatol. 1998;28(1). doi: https://doi.org/10.1016/S0168-8278(98)80211-0</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Adamek A, Kasprzak A. Insulin-like growth factor (IGF) system in liver diseases. Int J Mol Sci. 2018;19(5). doi: https://doi.org/10.3390/ijms19051308</mixed-citation><mixed-citation xml:lang="en">Adamek A, Kasprzak A. Insulin-like growth factor (IGF) system in liver diseases. Int J Mol Sci. 2018;19(5). doi: https://doi.org/10.3390/ijms19051308</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Golds G, Houdek D, Arnason T. Male Hypogonadism and Osteoporosis: The Effects, Clinical Consequences, and Treatment of Testosterone Deficiency in Bone Health. Int J Endocrinol. 2017;2017. doi: https://doi.org/10.1155/2017/4602129</mixed-citation><mixed-citation xml:lang="en">Golds G, Houdek D, Arnason T. Male Hypogonadism and Osteoporosis: The Effects, Clinical Consequences, and Treatment of Testosterone Deficiency in Bone Health. Int J Endocrinol. 2017;2017. doi: https://doi.org/10.1155/2017/4602129</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Seeman E. The structural and biomechanical basis of the gain and loss of bone strength in women and men. Endocrinol Metab Clin North Am. 2003;32(1). doi: https://doi.org/10.1016/S0889-8529(02)00078-6</mixed-citation><mixed-citation xml:lang="en">Seeman E. The structural and biomechanical basis of the gain and loss of bone strength in women and men. Endocrinol Metab Clin North Am. 2003;32(1). doi: https://doi.org/10.1016/S0889-8529(02)00078-6</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Naseem S, Hussain T, Manzoor S. Interleukin-6: A promising cytokine to support liver regeneration and adaptive immunity in liver pathologies. Cytokine Growth Factor Rev. 2018;39. doi: https://doi.org/10.1016/j.cytogfr.2018.01.002</mixed-citation><mixed-citation xml:lang="en">Naseem S, Hussain T, Manzoor S. Interleukin-6: A promising cytokine to support liver regeneration and adaptive immunity in liver pathologies. Cytokine Growth Factor Rev. 2018;39. doi: https://doi.org/10.1016/j.cytogfr.2018.01.002</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Wu Q, Zhou X, Huang D, Ji Y, Kang F. IL-6 enhances osteocytemediated osteoclastogenesis by promoting JAK2 and RANKL activity in vitro. Cellular Physiology and Biochemistry. 2017;41(4). doi: https://doi.org/10.1159/000465455</mixed-citation><mixed-citation xml:lang="en">Wu Q, Zhou X, Huang D, Ji Y, Kang F. IL-6 enhances osteocytemediated osteoclastogenesis by promoting JAK2 and RANKL activity in vitro. Cellular Physiology and Biochemistry. 2017;41(4). doi: https://doi.org/10.1159/000465455</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Nakchbandi IA, Mitnick MA, Lang R, Gundberg C, Kinder B, Insogna K. Circulating levels of interleukin-6 soluble receptor predict rates of bone loss in patients with primary hyperparathyroidism. Journal of Clinical Endocrinology and Metabolism. 2002;87(11). doi: https://doi.org/10.1210/jc.2001-011814</mixed-citation><mixed-citation xml:lang="en">Nakchbandi IA, Mitnick MA, Lang R, Gundberg C, Kinder B, Insogna K. Circulating levels of interleukin-6 soluble receptor predict rates of bone loss in patients with primary hyperparathyroidism. Journal of Clinical Endocrinology and Metabolism. 2002;87(11). doi: https://doi.org/10.1210/jc.2001-011814</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Blaschke M, Koepp R, Cortis J, et al. IL-6, IL-1β, and TNF-α only in combination influence the osteoporotic phenotype in Crohn’s patients via bone formation and bone resorption. Advances in Clinical and Experimental Medicine. 2018;27(1). doi: https://doi.org/10.17219/acem/67561</mixed-citation><mixed-citation xml:lang="en">Blaschke M, Koepp R, Cortis J, et al. IL-6, IL-1β, and TNF-α only in combination influence the osteoporotic phenotype in Crohn’s patients via bone formation and bone resorption. Advances in Clinical and Experimental Medicine. 2018;27(1). doi: https://doi.org/10.17219/acem/67561</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Norris CA, He M, Kang LI, et al. Synthesis of IL-6 by hepatocytes is a normal response to common hepatic stimuli. PLoS One. 2014;9(4). doi: https://doi.org/10.1371/journal.pone.0096053</mixed-citation><mixed-citation xml:lang="en">Norris CA, He M, Kang LI, et al. Synthesis of IL-6 by hepatocytes is a normal response to common hepatic stimuli. PLoS One. 2014;9(4). doi: https://doi.org/10.1371/journal.pone.0096053</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Shimada M, Matsumata T, Taketomi A, et al. The role of interleukin-6, interleukin-16, tumor necrosis factor-alpha and endotoxin in hepatic resection. Hepatogastroenterology. 1995;42(5):691-697</mixed-citation><mixed-citation xml:lang="en">Shimada M, Matsumata T, Taketomi A, et al. The role of interleukin-6, interleukin-16, tumor necrosis factor-alpha and endotoxin in hepatic resection. Hepatogastroenterology. 1995;42(5):691-697</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">Hernandez-Barragan A, Montes-de-Oca-Angeles D, Lemus- Peña M, et al. Serum determination of IL-1β and IL-1RA in patients with chronic liver diseases. Ann Hepatol. 2022;27. doi: https://doi.org/10.1016/j.aohep.2022.100864</mixed-citation><mixed-citation xml:lang="en">Hernandez-Barragan A, Montes-de-Oca-Angeles D, Lemus- Peña M, et al. Serum determination of IL-1β and IL-1RA in patients with chronic liver diseases. Ann Hepatol. 2022;27. doi: https://doi.org/10.1016/j.aohep.2022.100864</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Ruscitti P, Cipriani P, Carubbi F, et al. The role of IL-1β in the bone loss during rheumatic diseases. Mediators Inflamm. 2015;2015. doi: https://doi.org/10.1155/2015/782382</mixed-citation><mixed-citation xml:lang="en">Ruscitti P, Cipriani P, Carubbi F, et al. The role of IL-1β in the bone loss during rheumatic diseases. Mediators Inflamm. 2015;2015. doi: https://doi.org/10.1155/2015/782382</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Dinarello CA. Overview of the IL-1 family in innate inflammation and acquired immunity. Immunol Rev. 2018;281(1). doi: https://doi.org/10.1111/imr.12621</mixed-citation><mixed-citation xml:lang="en">Dinarello CA. Overview of the IL-1 family in innate inflammation and acquired immunity. Immunol Rev. 2018;281(1). doi: https://doi.org/10.1111/imr.12621</mixed-citation></citation-alternatives></ref><ref id="cit74"><label>74</label><citation-alternatives><mixed-citation xml:lang="ru">Nakamura I, Jimi E. Regulation of Osteoclast Differentiation and Function by Interleukin-1. Vitam Horm. 2006;74. doi: https://doi.org/10.1016/S0083-6729(06)74015-8</mixed-citation><mixed-citation xml:lang="en">Nakamura I, Jimi E. Regulation of Osteoclast Differentiation and Function by Interleukin-1. Vitam Horm. 2006;74. doi: https://doi.org/10.1016/S0083-6729(06)74015-8</mixed-citation></citation-alternatives></ref><ref id="cit75"><label>75</label><citation-alternatives><mixed-citation xml:lang="ru">Lorenzo J, Horowitz M, Choi Y. Osteoimmunology: Interactions of the bone and immune system. Endocr Rev. 2008;29(4). doi: https://doi.org/10.1210/er.2007-0038</mixed-citation><mixed-citation xml:lang="en">Lorenzo J, Horowitz M, Choi Y. Osteoimmunology: Interactions of the bone and immune system. Endocr Rev. 2008;29(4). doi: https://doi.org/10.1210/er.2007-0038</mixed-citation></citation-alternatives></ref><ref id="cit76"><label>76</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao S, Jiang J, Jing Y, et al. The concentration of tumor necrosis factor-α determines its protective or damaging effect on liver injury by regulating Yap activity. Cell Death Dis. 2020;11(1). doi: https://doi.org/10.1038/s41419-020-2264-z</mixed-citation><mixed-citation xml:lang="en">Zhao S, Jiang J, Jing Y, et al. The concentration of tumor necrosis factor-α determines its protective or damaging effect on liver injury by regulating Yap activity. Cell Death Dis. 2020;11(1). doi: https://doi.org/10.1038/s41419-020-2264-z</mixed-citation></citation-alternatives></ref><ref id="cit77"><label>77</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao B, Grimes SN, Li S, Hu X, Ivashkiv LB. TNF-induced osteoclastogenesis and inflammatory bone resorption are inhibited by transcription factor RBP-J. Journal of Experimental Medicine. 2012;209(2). doi: https://doi.org/10.1084/jem.20111566</mixed-citation><mixed-citation xml:lang="en">Zhao B, Grimes SN, Li S, Hu X, Ivashkiv LB. TNF-induced osteoclastogenesis and inflammatory bone resorption are inhibited by transcription factor RBP-J. Journal of Experimental Medicine. 2012;209(2). doi: https://doi.org/10.1084/jem.20111566</mixed-citation></citation-alternatives></ref><ref id="cit78"><label>78</label><citation-alternatives><mixed-citation xml:lang="ru">Boyce BF, Li P, Yao Z, et al. TNFα and pathologic bone resorption. Keio Journal of Medicine. 2005;54(3). doi: https://doi.org/10.2302/kjm.54.127</mixed-citation><mixed-citation xml:lang="en">Boyce BF, Li P, Yao Z, et al. TNFα and pathologic bone resorption. Keio Journal of Medicine. 2005;54(3). doi: https://doi.org/10.2302/kjm.54.127</mixed-citation></citation-alternatives></ref><ref id="cit79"><label>79</label><citation-alternatives><mixed-citation xml:lang="ru">Stojic J, Kukla M, Grgurevic I. The Intestinal Microbiota in the Development of Chronic Liver Disease: Current Status. Diagnostics. 2023;13(18). doi: https://doi.org/10.3390/diagnostics13182960</mixed-citation><mixed-citation xml:lang="en">Stojic J, Kukla M, Grgurevic I. The Intestinal Microbiota in the Development of Chronic Liver Disease: Current Status. Diagnostics. 2023;13(18). doi: https://doi.org/10.3390/diagnostics13182960</mixed-citation></citation-alternatives></ref><ref id="cit80"><label>80</label><citation-alternatives><mixed-citation xml:lang="ru">Liu J, Yang D, Wang X, et al. Gut Microbiota Targeted Approach in the Management of Chronic Liver Diseases. Front Cell Infect Microbiol. 2022;12. doi: https://doi.org/10.3389/fcimb.2022.774335</mixed-citation><mixed-citation xml:lang="en">Liu J, Yang D, Wang X, et al. Gut Microbiota Targeted Approach in the Management of Chronic Liver Diseases. Front Cell Infect Microbiol. 2022;12. doi: https://doi.org/10.3389/fcimb.2022.774335</mixed-citation></citation-alternatives></ref><ref id="cit81"><label>81</label><citation-alternatives><mixed-citation xml:lang="ru">Jeong H, Kim D. Bone Diseases in Patients with Chronic Liver Disease. Int J Mol Sci. 2019;20(17):4270. doi: https://doi.org/10.3390/ijms20174270</mixed-citation><mixed-citation xml:lang="en">Jeong H, Kim D. Bone Diseases in Patients with Chronic Liver Disease. Int J Mol Sci. 2019;20(17):4270. doi: https://doi.org/10.3390/ijms20174270</mixed-citation></citation-alternatives></ref><ref id="cit82"><label>82</label><citation-alternatives><mixed-citation xml:lang="ru">Yang YJ, Kim DJ. An overview of the molecular mechanisms contributing to musculoskeletal disorders in chronic liver disease: Osteoporosis, sarcopenia, and osteoporotic sarcopenia. Int J Mol Sci. 2021;22(5):1-33. doi: https://doi.org/10.3390/ijms22052604</mixed-citation><mixed-citation xml:lang="en">Yang YJ, Kim DJ. An overview of the molecular mechanisms contributing to musculoskeletal disorders in chronic liver disease: Osteoporosis, sarcopenia, and osteoporotic sarcopenia. Int J Mol Sci. 2021;22(5):1-33. doi: https://doi.org/10.3390/ijms22052604</mixed-citation></citation-alternatives></ref><ref id="cit83"><label>83</label><citation-alternatives><mixed-citation xml:lang="ru">Sumida K, Shrestha P, Mallisetty Y, et al. Incident Diuretic Use and Subsequent Risk of Bone Fractures: A Large Nationwide Observational Study of US Veterans. Mayo Clin Proc. 2024;99(6):913-926. doi: https://doi.org/10.1016/j.mayocp.2023.09.018</mixed-citation><mixed-citation xml:lang="en">Sumida K, Shrestha P, Mallisetty Y, et al. Incident Diuretic Use and Subsequent Risk of Bone Fractures: A Large Nationwide Observational Study of US Veterans. Mayo Clin Proc. 2024;99(6):913-926. doi: https://doi.org/10.1016/j.mayocp.2023.09.018</mixed-citation></citation-alternatives></ref><ref id="cit84"><label>84</label><citation-alternatives><mixed-citation xml:lang="ru">van der Burgh AC, Oliai Araghi S, Zillikens MC, et al. The impact of thiazide diuretics on bone mineral density and the trabecular bone score: the Rotterdam Study. Bone. 2020;138. doi: https://doi.org/10.1016/j.bone.2020.115475</mixed-citation><mixed-citation xml:lang="en">van der Burgh AC, Oliai Araghi S, Zillikens MC, et al. The impact of thiazide diuretics on bone mineral density and the trabecular bone score: the Rotterdam Study. Bone. 2020;138. doi: https://doi.org/10.1016/j.bone.2020.115475</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>
