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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="en"><front><journal-meta><journal-id journal-id-type="publisher-id">farmaec</journal-id><journal-title-group><journal-title xml:lang="en">FARMAKOEKONOMIKA. Modern Pharmacoeconomics and Pharmacoepidemiology</journal-title><trans-title-group xml:lang="ru"><trans-title>ФАРМАКОЭКОНОМИКА. Современная фармакоэкономика и фармакоэпидемиология</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2070-4909</issn><issn pub-type="epub">2070-4933</issn><publisher><publisher-name>IRBIS LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.17749/2070-4909/farmakoekonomika.2023.200</article-id><article-id custom-type="elpub" pub-id-type="custom">farmaec-895</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="en"><subject>ORIGINAL ARTICLES</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОРИГИНАЛЬНЫЕ ПУБЛИКАЦИИ</subject></subj-group></article-categories><title-group><article-title>The role of ferritin in liver disease assessment</article-title><trans-title-group xml:lang="ru"><trans-title>Роль ферритина в оценке заболеваний печени</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2964-9167</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Радченко</surname><given-names>В. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Radchenko</surname><given-names>V. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н., профессор 2-й кафедры (терапии усовершенствования врачей) ФГБВОУ ВО «Военно-медицинская академия им. С.М. Кирова» Минобороны России</p><p>ул. Академика Лебедева, д. 6, Санкт-Петербург 194044</p></bio><bio xml:lang="en"><p>Dr. Med. Sc., Professor, Chair 2 (Advanced Medical Training in Therapy), Kirov Military Medical Academy</p><p>6 Academician Lebedev Str., Saint Petersburg 194044</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1095-8787</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гриневич</surname><given-names>В. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Grinevich</surname><given-names>V. B.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н., профессор, заведующий 2-й кафедрой (терапии усовершенствования врачей) ФГБВОУ ВО «Военно-медицинская академия им. С.М. Кирова» Минобороны России</p><p>ул. Делегатская, д. 20, стр.1, Москва 127473</p></bio><bio xml:lang="en"><p>Dr. Med. Sc., Professor, Chief of Chair 2 (Advanced Medical Training in Therapy), Kirov Military Medical Academy</p><p>9А bldg 1 Vuchetich Str., Moscow 127206</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2785-6699</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Иванюк</surname><given-names>Е. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Ivanyuk</surname><given-names>E. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>к.м.н., доцент 2-й кафедры (терапии усовершенствования врачей) ФГБВОУ ВО «Военно-медицинская академия им. С.М. Кирова» Минобороны России</p><p>ул. Делегатская, д. 20, стр.1, Москва 127473</p></bio><bio xml:lang="en"><p>MD, PhD, Associate Professor, Chair 2 (Advanced Medical Training in Therapy), Kirov Military Medical Academy</p><p>9А bldg 1 Vuchetich Str., Moscow 127206</p></bio><email xlink:type="simple">ivanyuk-es@yandex.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лазебник</surname><given-names>Л. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Lazebnik</surname><given-names>L. B.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н., профессор кафедры поликлинической терапии ФГБОУ ВО «Московский государственный медико-стоматологический университет им. А.И. Евдокимова» Минздрава России</p><p>ул. Делегатская, д. 20, стр.1, Москва 127473</p></bio><bio xml:lang="en"><p>Dr. Med. Sc., Professor, Chair of Polyclinic Therapy, Yevdokimov Moscow State University of Medicine and Dentistry</p><p>9А bldg 1 Vuchetich Str., Moscow 127206</p></bio><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Федеральное государственное бюджетное военное образовательное учреждение высшего образования «Военно-медицинская академия им. С.М. Кирова» Министерства обороны Российской Федерации<country>Россия</country></aff><aff xml:lang="en">Kirov Military Medical Academy<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru">Федеральное государственное бюджетное образовательное учреждение высшего образования «Московский государственный медико-стоматологический университет им. А.И. Евдокимова» Министерства здравоохранения Российской Федерации<country>Россия</country></aff><aff xml:lang="en">Yevdokimov Moscow State University of Medicine and Dentistry<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2023</year></pub-date><pub-date pub-type="epub"><day>10</day><month>11</month><year>2023</year></pub-date><volume>16</volume><issue>3</issue><fpage>432</fpage><lpage>446</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Radchenko V.G., Grinevich V.B., Ivanyuk E.S., Lazebnik L.B., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Радченко В.Г., Гриневич В.Б., Иванюк Е.С., Лазебник Л.Б.</copyright-holder><copyright-holder xml:lang="en">Radchenko V.G., Grinevich V.B., Ivanyuk E.S., Lazebnik L.B.</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.pharmacoeconomics.ru/jour/article/view/895">https://www.pharmacoeconomics.ru/jour/article/view/895</self-uri><abstract><sec><title>Background</title><p>Background. Ferritin is an important integral and diagnostic marker of liver diseases. In 1/3 of patients with nonalcoholic fatty liver disease (NAFLD), manifestations of hyperferritinemia are revealed. Increased ferritin level indicates the severity of the disease course and affects the prognosis.</p></sec><sec><title>Objective</title><p>Objective: to determine the prevalence and character of hyperferritinemia manifestations in NAFLD patients and to evaluate the effectiveness of its correction with human placenta hydrolysate.</p></sec><sec><title>Material and methods</title><p>Material and methods. We examined 158 patients aged from 20 to 63 years (92 men and 66 women). There were no significant differences in age between men and women. The control group consisted of 20 practically healthy individuals. Molecular mechanisms of peptide components of human placenta hydrolysate (Laennec®) impact on pathophysiological processes of serum ferritin disorders, iron metabolism indicators, and inflammation manifestations were analyzed.</p></sec><sec><title>Results</title><p>Results. Nineteen peptides potentially important for regulation of iron homeostasis were identified in Laennec® composition. These peptides contribute to the elimination of iron metabolism disorders by regulating the levels of hepcidin (the main hormone of iron homeostasis), reducing ferritin synthesis, as well as exhibiting anti-inflammatory, and immunomodulatory effects. The efficacy of the drug monotherapy in patients with hyperferritinemia was shown.</p></sec><sec><title>Conclusion</title><p>Conclusion. Laennec® was found to be one of the medicines contributing to the reduction of hyperferritinemia manifestations, iron metabolism disorders, and systemic inflammatory process in NAFLD.</p></sec></abstract><trans-abstract xml:lang="ru"><sec><title>Актуальность</title><p>Актуальность. Ферритин является важным интегральным и диагностическим маркером заболеваний печени. У 1/3 пациентов с неалкогольной жировой болезнью печени (НАЖБП) выявлены проявления гиперферритинемии. Повышение уровня ферритина свидетельствует о тяжести течения и влияет на прогноз заболевания.</p></sec><sec><title>Цель</title><p>Цель: определение частоты и характера проявлений гиперферритинемии у больных НАЖБП и оценка эффективности ее коррекции гидролизатом плаценты человека.</p></sec><sec><title>Материал и методы</title><p>Материал и методы. Обследованы 158 больных НАЖБП возрасте от 20 до 63 лет (92 мужчины и 66 женщин). Достоверных различий по возрасту между мужчинами и женщинами не выявлено. Группа контроля составила 20 практически здоровых лиц. Проведен анализ молекулярных механизмов действия пептидных компонентов гидролизата плаценты человека (препарат Лаеннек®) на патофизиологические процессы нарушения содержания ферритина в сыворотке крови, показатели обмена железа, проявления воспаления.</p></sec><sec><title>Результаты</title><p>Результаты. В составе препарата Лаеннек® идентифицированы 19 пептидов, потенциально важных для регулировки гомеостаза железа. Регулируя уровни гепцидина (основного гормона гомеостаза железа), снижая синтез ферритина, а также проявляя противовоспалительные и иммуномодулирующие эффекты, эти пептиды способствуют устранению нарушений обмена железа. Показана эффективность применения препарата у больных НАЖБП с гиперферритинемией в виде монотерапии.</p></sec><sec><title>Заключение</title><p>Заключение. Установлено, что Лаеннек® является одним из препаратов, способствующих уменьшению проявлений гиперферритинемии, нарушений обмена железа, системного воспалительного процесса при НАЖБП.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>Неалкогольная жировая болезнь печени</kwd><kwd>НАЖБП</kwd><kwd>ферритин</kwd><kwd>нарушение обмена железа</kwd><kwd>системное воспаление</kwd><kwd>инсулинорезистентность</kwd><kwd>пептиды гидролизата плаценты человека</kwd><kwd>Лаеннек</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Nonalcoholic fatty liver disease</kwd><kwd>NAFLD</kwd><kwd>ferritin</kwd><kwd>iron metabolism disorder</kwd><kwd>systemic inflammation</kwd><kwd>insulin resistance</kwd><kwd>human placenta hydrolysate peptides</kwd><kwd>Laennec</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">Harrison P.M., Arosio P. The ferritins: molecular properties, iron storage function and cellular regulation. Biochim Biophys Acta. 1996; 1275 (3): 161–203. https://doi.org/10.1016/0005-2728(96)00022-9.</mixed-citation><mixed-citation xml:lang="en">Harrison P.M., Arosio P. The ferritins: molecular properties, iron storage function and cellular regulation. Biochim Biophys Acta. 1996; 1275 (3): 161–203. https://doi.org/10.1016/0005-2728(96)00022-9.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">MacKenzie E.L., Iwasaki K., Tsuji Y. Intracellular iron transport and storage: from molecular mechanisms to health implications. Antioxid Redox Signal. 2008; 10 (6): 997–1030. https://doi.org/10.1089/ars.2007.1893. PMC 2932529.</mixed-citation><mixed-citation xml:lang="en">MacKenzie E.L., Iwasaki K., Tsuji Y. Intracellular iron transport and storage: from molecular mechanisms to health implications. Antioxid Redox Signal. 2008; 10 (6): 997–1030. https://doi.org/10.1089/ars.2007.1893. PMC 2932529.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Harrison P.M., Ford G.C., Rice D.W., et al. Production and characterization of recombinant heteropolymers of human ferritin H and L chains. Biochem Soc Transact. 1987; 15: 744–8.</mixed-citation><mixed-citation xml:lang="en">Harrison P.M., Ford G.C., Rice D.W., et al. Production and characterization of recombinant heteropolymers of human ferritin H and L chains. Biochem Soc Transact. 1987; 15: 744–8.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Beaton M.D., Adams P.C. Treatment of hyperferritinemia. Ann Hepatol. 2012; 11 (3): 294–300.</mixed-citation><mixed-citation xml:lang="en">Beaton M.D., Adams P.C. Treatment of hyperferritinemia. Ann Hepatol. 2012; 11 (3): 294–300.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Knovich M.A., Storey J.A., Coffman L.G., et al. Ferritin for the clinician. Blood Rev. 2009; 23 (3): 95–104. https://doi.org/10.1016/j.blre.2008.08.001.</mixed-citation><mixed-citation xml:lang="en">Knovich M.A., Storey J.A., Coffman L.G., et al. Ferritin for the clinician. Blood Rev. 2009; 23 (3): 95–104. https://doi.org/10.1016/j.blre.2008.08.001.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Khosravi M.J., Chan M.A., Bellem A.C., Diamandis Е.Р. A sensitive time-resolved immunofluorometric assay of ferritin in serum with monoclonal antibodies. Clin Chim Acta. 1988; 175 (3): 267–75. https://doi.org/10.1016/0009-8981(88)90102-7.</mixed-citation><mixed-citation xml:lang="en">Khosravi M.J., Chan M.A., Bellem A.C., Diamandis Е.Р. A sensitive time-resolved immunofluorometric assay of ferritin in serum with monoclonal antibodies. Clin Chim Acta. 1988; 175 (3): 267–75. https://doi.org/10.1016/0009-8981(88)90102-7.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Matzner Y., Konijn A.M., Schlomai Z., Ben-Bassat H. Differential effect of isolated placental isoferritins on in vitro T-lymphocyte function. Brit J Haematol. 1985; 59 (3): 443–8. https://doi.org/10.1111/j.1365-2141.1985.tb07331.x.</mixed-citation><mixed-citation xml:lang="en">Matzner Y., Konijn A.M., Schlomai Z., Ben-Bassat H. Differential effect of isolated placental isoferritins on in vitro T-lymphocyte function. Brit J Haematol. 1985; 59 (3): 443–8. https://doi.org/10.1111/j.1365-2141.1985.tb07331.x.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Diamandis E.P. Immunoassays with time-resolved fluorescence spectroscopy: principles and applications. Clin Biochem. 1988; 21 (3): 139–50. https://doi.org/10.1016/0009-9120(88)90001-x.</mixed-citation><mixed-citation xml:lang="en">Diamandis E.P. Immunoassays with time-resolved fluorescence spectroscopy: principles and applications. Clin Biochem. 1988; 21 (3): 139–50. https://doi.org/10.1016/0009-9120(88)90001-x.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Chang T.Y., Liu K.L., Chang C.S., et al. Ferric citrate supplementation reduces red-blood-cell aggregation and improves CD163+ macrophagemediated hemoglobin metabolism in a rat model of high-fat-dietinduced obesity. Mol Nutr Food Res. 2018; 62 (2). https://doi.org/10.1002/mnfr.201700442.</mixed-citation><mixed-citation xml:lang="en">Chang T.Y., Liu K.L., Chang C.S., et al. Ferric citrate supplementation reduces red-blood-cell aggregation and improves CD163+ macrophagemediated hemoglobin metabolism in a rat model of high-fat-dietinduced obesity. Mol Nutr Food Res. 2018; 62 (2). https://doi.org/10.1002/mnfr.201700442.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Sandnes M., Ulvik R.J., Vorland M., Reikvam H. Hyperferritinemia – a clinical overview. J Clin Med. 2021; 10 (9): 2008. https://doi.org/10.3390/jcm10092008.</mixed-citation><mixed-citation xml:lang="en">Sandnes M., Ulvik R.J., Vorland M., Reikvam H. Hyperferritinemia – a clinical overview. J Clin Med. 2021; 10 (9): 2008. https://doi.org/10.3390/jcm10092008.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Torti F.M., Torti S.V. Regulation of ferritin genes and protein. Blood. 2002; 99 (10): 3505–16. https://doi.org/10.1182/blood.v99.10.35054.</mixed-citation><mixed-citation xml:lang="en">Torti F.M., Torti S.V. Regulation of ferritin genes and protein. Blood. 2002; 99 (10): 3505–16. https://doi.org/10.1182/blood.v99.10.35054.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">George D.K., Goldwurm S., MacDonald G.A., et al. Increased hepatic iron concentration in nonalcoholic steatohepatitis is associated with increased fibrosis. Gastroenterology. 1998; 114 (2): 311–8. https://doi.org/10.1016/s0016-5085(98)70482-2.</mixed-citation><mixed-citation xml:lang="en">George D.K., Goldwurm S., MacDonald G.A., et al. Increased hepatic iron concentration in nonalcoholic steatohepatitis is associated with increased fibrosis. Gastroenterology. 1998; 114 (2): 311–8. https://doi.org/10.1016/s0016-5085(98)70482-2.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Piperno A. Classification and diagnosis of iron overload. Haematologica. 1998; 83 (5): 447–55.</mixed-citation><mixed-citation xml:lang="en">Piperno A. Classification and diagnosis of iron overload. Haematologica. 1998; 83 (5): 447–55.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Deugnier Y., Turlin B., le Quilleuc D., et al. A reappraisal of hepatic siderosis in patients with end-stage cirrhosis: practical implications for the diagnosis of hemochromatosis. Am J Surg Pathol. 1997; 21 (6): 669–75. https://doi.org/10.1097/00000478-199706000-00007.</mixed-citation><mixed-citation xml:lang="en">Deugnier Y., Turlin B., le Quilleuc D., et al. A reappraisal of hepatic siderosis in patients with end-stage cirrhosis: practical implications for the diagnosis of hemochromatosis. Am J Surg Pathol. 1997; 21 (6): 669–75. https://doi.org/10.1097/00000478-199706000-00007.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Громова О.А., Торшин И.Ю., Шаповалова Ю.О. и др. COVID-19 и железодефицитная анемия: взаимосвязи патогенеза и терапии. Акушерство, гинекология и репродукция. 2020; 14 (5): 644–55. https://doi.org/10.17749/2313-7347/ob.gyn.rep.2020.179.</mixed-citation><mixed-citation xml:lang="en">Gromova O.A., Torshin I.Yu., Shapovalova Yu.O., et al. COVID-19 and iron deficiency anemia: relationships of pathogenesis and therapy. Obstetrics, Gynecology and Reproduction. 2020; 14 (5): 644–55 (in Russ.). https://doi.org/10.17749/2313-7347/ob.gyn.rep.2020.179.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Громова О.А., Торшин И.Ю., Минушкин О.Н. и др. Об эффективности и молекулярных механизмах действия препарата «Лаеннек» в лечении патологических состояний печени, связанных с отложением железа в печени. Дело жизни. 2015; 1: 44–51.</mixed-citation><mixed-citation xml:lang="en">Gromova O.A., Torshin I.Yu., Minushkin O.N., et al. On the effectiveness and molecular mechanisms of action of the drug Laennec in the treatment of pathological liver conditions associated with iron deposition in the liver. Delo zhizni. 2015; 1: 44–51 (in Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Минушкин О.Н. Максимов В.А., Пальцев А.И. и др. Рекомендации по применению гидролизата человеческой плаценты при заболеваниях печени. Экспериментальная и клиническая гастроэнтерология. 2016; 12: 75–7.</mixed-citation><mixed-citation xml:lang="en">Minushkin O.N., Maksimov V.A., Paltsev A.I., et al. Recommendations for the use of human placenta hydrolysate in liver diseases. Experimental and Clinical Gastroenterology. 2016; 12: 75–7 (in Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Радченко В.Г., Селиверстов П.В., Иванова В.Ф., Ситкин С.И. Алгоритм лечения неалкогольной жировой болезни печени и роль митохондриальной дисфункции в ее развитии. Фарматека. 2017; 6: 12–9.</mixed-citation><mixed-citation xml:lang="en">Radchenko V.G., Seliverstov P.V., Ivanova V.F., Sitkin S.I. Algorithm of treatment of non-alcoholic fatty of liver disease and the role of mitochondrial dysfunction in its development. Farmateka. 2017; 6: 12–9 (in Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Маянский А.Н., Маянский Д.Н. Очерки о нейтрофиле и макрофаге. 2-е изд. Новосибирск: Наука; 1989: 340 с.</mixed-citation><mixed-citation xml:lang="en">Mayanskiy A.N., Mayanskiy D.N. Essays on neutrophil and macrophage. 2nd ed. Novosibirsk: Nauka; 1989: 340 pp. (in Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Щербинина С.П., Романова Е.А., Левина А.А. и др. Диагностическое значение комплексного исследования показателей метаболизма железа в клинической практике. Гематология и трансфузиология. 2005; 50 (5): 23–8.</mixed-citation><mixed-citation xml:lang="en">Scherbinina S.P., Romanova E.A., Levina A.A., et al. Diagnostic value of a complex study of iron metabolism in clinical practice. Russian Journal of Hematology and Transfusiology. 2005; 50 (5): 23–8 (in Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Громова О.А., Торшин И.Ю., Максимов В.А. и др. Пептиды в составе препарата Лаеннек, способствующие устранению гиперферритинемии и перегрузки железом. ФАРМАКОЭКОНОМИКА. Современная фармакоэкономика и фармакоэпидемиология. 2020; 13 (4): 413–25. https://doi.org/10.17749/2070-4909/farmakoekonomika.2020.070.</mixed-citation><mixed-citation xml:lang="en">Gromova O.A., Torshin I.Yu., Maksimov V.A., et al. Peptides contained in the composition of Laennec that contribute to the treatment of hyperferritinemia and iron overload disorders. FARMAKOEKONOMIKA. Sovremennaya farmakoekonomika i farmakoepidemiologiya / FARMAKOEKONOMIKA. Modern Pharmacoeconomics and Pharmacoepidemiology. 2020; 13 (4): 413–25 (in Russ.). https://doi.org/10.17749/2070-4909/farmakoekonomika. 2020.070.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Радченко В.Г., Лазебник Л.Б., Гриневич В.Б., Радченко Д.В. Препарат плаценты Лаеннек как универсальный регулятор. М.: Тинкомаркетинг; 2022: 260 с.</mixed-citation><mixed-citation xml:lang="en">Radchenko V.G., Lazebnik L.B., Grinevich V.B., Radchenko D.V. Placenta preparation Laennec as a universal regulator. Мoscow: Timkomarketing; 2022: 260 pp. (in Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Токарев Ю.Н., Сеттарова Д.А., Сметанина Н.С. и др. Болезни перегрузки железом (гемохроматозы): руководство для врачей. М.: Медпрактика-М; 2004: 328 с.</mixed-citation><mixed-citation xml:lang="en">Tokarev Yu.N., Settarova D.A., Smetanina N.S., et al. Diseases of iron overload (hemochromatosis): a guide for doctors. Мoscow: Medpraktika-М; 2004: 328 pp. (in Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Ramm G.A., Ruddell R.G. Iron homeostasis, hepatocellular injury, and fibrogenesis in hemochromatosis; the role of inflammation in a noninflammatory liver disease. Semin Liver Dis. 2010; 30 (3): 271–87. https://doi.org/10.1055/s-0030-1255356.</mixed-citation><mixed-citation xml:lang="en">Ramm G.A., Ruddell R.G. Iron homeostasis, hepatocellular injury, and fibrogenesis in hemochromatosis; the role of inflammation in a noninflammatory liver disease. Semin Liver Dis. 2010; 30 (3): 271–87. https://doi.org/10.1055/s-0030-1255356.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Смирнов О.А., Радченко В.Г., Кальм Е.И. Клинико-морфологические особенности хронического гепатита при гемосидерозе печени. Российский медицинский журнал. 2003; 1: 20–2.</mixed-citation><mixed-citation xml:lang="en">Смирнов О.А., Радченко В.Г., Кальм Е.И. Клинико-морфологические особенности хронического гепатита при гемосидерозе печени. Medical Journal of the Russian Federation. 2003; 1: 20–2 (in Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Houstis N., Rosen E.D., Lander E.S. Reactive oxygen species have a causal role in multiple forms of insulin resistance. Nature. 2006; 440 (7086): 944–8. https://doi.org/10.1038/nature04634.</mixed-citation><mixed-citation xml:lang="en">Houstis N., Rosen E.D., Lander E.S. Reactive oxygen species have a causal role in multiple forms of insulin resistance. Nature. 2006; 440 (7086): 944–8. https://doi.org/10.1038/nature04634.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Sumida Y., Kanemasa K., Fukumoto K., et al. Effect of iron reduction by phlebotomy in Japanese patients with non-alcoholic steatohepatitis: a pilot study. Hepatol Res. 2006; 36 (4): 315–21. https://doi.org/10.1016/j.hepres.2006.08.003.</mixed-citation><mixed-citation xml:lang="en">Sumida Y., Kanemasa K., Fukumoto K., et al. Effect of iron reduction by phlebotomy in Japanese patients with non-alcoholic steatohepatitis: a pilot study. Hepatol Res. 2006; 36 (4): 315–21. https://doi.org/10.1016/j.hepres.2006.08.003.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Bottomley S. Secondary iron overload disorders. Sem Hematol. 1998; 35 (1): 77–86.</mixed-citation><mixed-citation xml:lang="en">Bottomley S. Secondary iron overload disorders. Sem Hematol. 1998; 35 (1): 77–86.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Tilg H., Hotamisligil G.S. Nonalcoholic fatty liver disease: cytokineadipokine interplay and regulation of insulin resistance. Gastroenterology. 2006; 131 (3): 934–45. https://doi.org/10.1053/j.gastro.2006.05.054.</mixed-citation><mixed-citation xml:lang="en">Tilg H., Hotamisligil G.S. Nonalcoholic fatty liver disease: cytokineadipokine interplay and regulation of insulin resistance. Gastroenterology. 2006; 131 (3): 934–45. https://doi.org/10.1053/j.gastro.2006.05.054.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Tacke F., Nuraldeen R., Koch A., et al. Iron parameters determine the prognosis of critically ill patients. Crit Care Med. 2016; 44 (6): 1049–58. https://doi.org/10.1097/CCM.0000000000001607.</mixed-citation><mixed-citation xml:lang="en">Tacke F., Nuraldeen R., Koch A., et al. Iron parameters determine the prognosis of critically ill patients. Crit Care Med. 2016; 44 (6): 1049–58. https://doi.org/10.1097/CCM.0000000000001607.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Ruscitti P., Di Benedetto P., Berardicurti O., et al. Pro-inflammatory properties of H-ferritin on human macrophages, ex vivo and in vitro observations. Sci Rep. 2020; 10 (1): 12232. https://doi.org/10.1038/s41598-020-69031-w.</mixed-citation><mixed-citation xml:lang="en">Ruscitti P., Di Benedetto P., Berardicurti O., et al. Pro-inflammatory properties of H-ferritin on human macrophages, ex vivo and in vitro observations. Sci Rep. 2020; 10 (1): 12232. https://doi.org/10.1038/s41598-020-69031-w.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Veas F. (Ed.) Acute phase proteins – regulation and functions of acute phase proteins. InTech; 2011: 380 pp. https://doi.org/10.5772/756.</mixed-citation><mixed-citation xml:lang="en">Veas F. (Ed.) Acute phase proteins – regulation and functions of acute phase proteins. InTech; 2011: 380 pp. https://doi.org/10.5772/756.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Moirand R., Mortaji A.M., Loréal O., et al. A new syndrome of liver iron overload with normal transferrin saturation. Lancet. 1997; 349 (9045): 95–7. https://doi.org/10.1016/S0140-6736(96)06034-5.</mixed-citation><mixed-citation xml:lang="en">Moirand R., Mortaji A.M., Loréal O., et al. A new syndrome of liver iron overload with normal transferrin saturation. Lancet. 1997; 349 (9045): 95–7. https://doi.org/10.1016/S0140-6736(96)06034-5.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Cohen L.A., Gutierrez L., Weiss A., et al. Serum ferritin is derived primarily from macrophages through a nonclassical secretory pathway. Blood. 2010; 116 (9): 1574–84. https://doi.org/10.1182/blood-2009-11-253815.</mixed-citation><mixed-citation xml:lang="en">Cohen L.A., Gutierrez L., Weiss A., et al. Serum ferritin is derived primarily from macrophages through a nonclassical secretory pathway. Blood. 2010; 116 (9): 1574–84. https://doi.org/10.1182/ blood-2009-11-253815.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Orino K., Lehman L., Tsuji Y., et al. Ferritin and the response to oxidative stress. Biochem J. 2001; 357 (Pt. 1): 241–7. https://doi.org/10.1042/0264-6021:3570241.</mixed-citation><mixed-citation xml:lang="en">Orino K., Lehman L., Tsuji Y., et al. Ferritin and the response to oxidative stress. Biochem J. 2001; 357 (Pt. 1): 241–7. https://doi.org/10.1042/0264-6021:3570241.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Wood J. Guidelines for quantifying iron overload. Hematology Am Soc Hematol Educ Program. 2014; 2014 (1): 210–5. https://doi.org/10.1182/asheducation-2014.1.210.</mixed-citation><mixed-citation xml:lang="en">Wood J. Guidelines for quantifying iron overload. Hematology Am Soc Hematol Educ Program. 2014; 2014 (1): 210–5. https://doi.org/10.1182/asheducation-2014.1.210.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Торшин И.Ю., Громова О.А. Мировой опыт использования гидролизатов плаценты человека в терапии. Экспериментальная и клиническая гастроэнтерология. 2019; 1 (10): 79–89. https://doi.org/10.31146/1682-8658-ecg-170-10-79-89.</mixed-citation><mixed-citation xml:lang="en">Torshin I.Yu., Gromova O.A. Worldwide experience of the therapeutic use of the human placental hydrolytes. Experimental and Clinical Gastroenterology. 2019; 1 (10): 79–89 (in Russ.). https://doi.org/10.31146/1682-8658-ecg-170-10-79-89.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Faber H.R., Bland T., Day C.L., et al. Altered domain closure and iron binding in transferrins: the crystal structure of the Asp60Ser mutant of the amino-terminal half-molecule of human lactoferrin. J Mol Biol. 1996; 256 (2): 352–63. https://doi.org/10.1006/jmbi.1996.0091.</mixed-citation><mixed-citation xml:lang="en">Faber H.R., Bland T., Day C.L., et al. Altered domain closure and iron binding in transferrins: the crystal structure of the Asp60Ser mutant of the amino-terminal half-molecule of human lactoferrin. J Mol Biol. 1996; 256 (2): 352–63. https://doi.org/10.1006/jmbi.1996.0091.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Громова О.А., Торшин И.Ю., Волков А.Ю. и др. Препарат «Лаеннек»: элементный состав и фармакологическое действие. Пластическая хирургия и косметология. 2011; 2: 327–33.</mixed-citation><mixed-citation xml:lang="en">Gromova O.A., Torshin I.Yu., Volkov A.Yu., et al. Preparation Laennec: elemental composition and key role in the pharmacological action. Plasticheskaya khirurgiya i cosmetologiya / Plastic Surgery and Cosmetology. 2011; 2: 327–33 (in Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Chen L.Y., Chang S.D., Sreenivasan G.M. Dysmetabolic hyperferritinemia is assiciated with normal transferrin saturation, mild hepatic iron overload, and elevated hepsidin. Ann Hematol. 2011; 90 (2): 139– 43. https://doi.org/10.1007/s00277-010-1050-x.</mixed-citation><mixed-citation xml:lang="en">Chen L.Y., Chang S.D., Sreenivasan G.M. Dysmetabolic hyperferritinemia is assiciated with normal transferrin saturation, mild hepatic iron overload, and elevated hepsidin. Ann Hematol. 2011; 90 (2): 139– 43. https://doi.org/10.1007/s00277-010-1050-x.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao Q., Garreau I., Sannier F., Piot J.M. Opioid peptides derived from hemoglobin: hemorphins. Biopolymers. 1997; 43 (2): 75–98. https://doi.org/10.1002/(SICI)1097-0282(1997)43:2&lt;75::AIDBIP2&gt;3.0.CO;2-X.</mixed-citation><mixed-citation xml:lang="en">Zhao Q., Garreau I., Sannier F., Piot J.M. Opioid peptides derived from hemoglobin: hemorphins. Biopolymers. 1997; 43 (2): 75–98. https://doi.org/10.1002/(SICI)1097-0282(1997)43:2&lt;75::AIDBIP2&gt;3.0.CO;2-X.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Громова О.А., Торшин И.Ю., Гришина Т.Р., Томилова И.К. Значение использования препаратов железа и его молекулярных синергистов для профилактики и лечения железодефицитной анемии у беременных. Российский вестник акушера-гинеколога. 2015; 15 (4): 85–94. https://doi.org/10.17116/rosakush201515485-94.</mixed-citation><mixed-citation xml:lang="en">Gromova O.A., Torshin I.Iu., Grishina T.R., Tomilova I.K. Value of the use of iron preparations and molecular synergists for the prevention and treatment of iron-deficiency anemia in pregnant women. Russian Bulletin of Obstetrician-Gynecologist. 2015; 15 (4): 85–94 (in Russ.). https://doi.org/10.17116/rosakush201515485-94.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Colucci S., Pagani A., Pettinato M., et al. The immunophilin FKBP12 inhibits hepcidin expression by binding the BMP type I receptor ALK2 in hepatocytes. Blood. 2017; 130 (19): 2111–20. https://doi.org/10.1182/blood-2017-04-780692.</mixed-citation><mixed-citation xml:lang="en">Colucci S., Pagani A., Pettinato M., et al. The immunophilin FKBP12 inhibits hepcidin expression by binding the BMP type I receptor ALK2 in hepatocytes. Blood. 2017; 130 (19): 2111–20. https://doi.org/10.1182/blood-2017-04-780692.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Jiang S., Wang C.X., Lan L., Zhao D. Vitamin A deficiency aggravates iron deficiency by upregulating the expression of iron regulatory protein-2. Nutrition. 2012; 28 (3): 281–7. https://doi.org/10.1016Zj.nut.2011.08.015.</mixed-citation><mixed-citation xml:lang="en">Jiang S., Wang C.X., Lan L., Zhao D. Vitamin A deficiency aggravates iron deficiency by upregulating the expression of iron regulatory protein-2. Nutrition. 2012; 28 (3): 281–7. https://doi.org/10.1016Zj. nut.2011.08.015.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Лазебник Л.Б., Радченко В.Г., Селиверстов П.В. и др. Современное представление о фиброзе печени и подходах к его лечению у больных неалкогольным стеатогепатитом. Экспериментальная и клиническая гастроэнтерология. 2017; 12: 98–109.</mixed-citation><mixed-citation xml:lang="en">Lazebnik L.B., Radchenko V.G., Seliverstov P.V., et al. The contemporary understanding of liver fibrosis and approaches to treatment in patients with nonalcoholic steatohepatitis. Experimental and Clinical Gastroenterology. 2017; 12: 98–109.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Chen Z., Xu W., Ma W., et al.Clinical laboratory evaluation of COVID-19. Clin Chim Acta. 2021; 519: 172–82. https://doi.org/10.1016/j.cca.2021.04.022.</mixed-citation><mixed-citation xml:lang="en">Chen Z., Xu W., Ma W., et al.Clinical laboratory evaluation of COVID-19. Clin Chim Acta. 2021; 519: 172–82. https://doi.org/10.1016/j.cca.2021.04.022.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Dufrusine B., Di Francesco A., Oddi S., et al. Iron-dependent trafficking of 5-lipoxygenase and impact on human macrophage activation. Front Immunol. 2019; 10: 1347. https://doi.org/10.3389/fimmu.2019.0134.</mixed-citation><mixed-citation xml:lang="en">Dufrusine B., Di Francesco A., Oddi S., et al. Iron-dependent trafficking of 5-lipoxygenase and impact on human macrophage activation. Front Immunol. 2019; 10: 1347. https://doi.org/10.3389/ fimmu.2019.0134.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Davis R.J., Faucher M., Racaniello L.K., et al. Insulin-like growth factor I and epidermal growth factor regulate the expression of transferrin receptors at the cell surface by distinct mechanisms. J Biol Chem. 1987; 262 (27): 13126–34. https://doi.org/10.1016/S00219258(18)45177-0.</mixed-citation><mixed-citation xml:lang="en">Davis R.J., Faucher M., Racaniello L.K., et al. Insulin-like growth factor I and epidermal growth factor regulate the expression of transferrin receptors at the cell surface by distinct mechanisms. J Biol Chem. 1987; 262 (27): 13126–34. https://doi.org/10.1016/S00219258(18)45177-0.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Vera M., Sobrevals L., Zaratiegui M., et al. Liver transduction with a simian virus 40 vector encoding insulin-like growth factor I reduces hepatic damage and the development of liver cirrhosis. Gene Ther. 2007; 14 (3): 203–10. https://doi.org/10.1038/sj.gt.3302858.</mixed-citation><mixed-citation xml:lang="en">Vera M., Sobrevals L., Zaratiegui M., et al. Liver transduction with a simian virus 40 vector encoding insulin-like growth factor I reduces hepatic damage and the development of liver cirrhosis. Gene Ther. 2007; 14 (3): 203–10. https://doi.org/10.1038/sj.gt.3302858.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Villareal D.T., Holloszy J.O., Kohrt W.M. Effects of DHEA replacement on bone mineral density and body composition in elderly women and men. Clin Endocrinol (Oxf). 2000; 53 (5): 561–8. https://doi.org/10.1046/j.1365-2265.2000.01131.x.</mixed-citation><mixed-citation xml:lang="en">Villareal D.T., Holloszy J.O., Kohrt W.M. Effects of DHEA replacement on bone mineral density and body composition in elderly women and men. Clin Endocrinol (Oxf). 2000; 53 (5): 561–8. https://doi.org/10.1046/j.1365-2265.2000.01131.x.</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>
