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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">ssmu</journal-id><journal-title-group><journal-title xml:lang="ru">Бюллетень сибирской медицины</journal-title><trans-title-group xml:lang="en"><trans-title>Bulletin of Siberian Medicine</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1682-0363</issn><issn pub-type="epub">1819-3684</issn><publisher><publisher-name>Siberian State Medical University, the Ministry of Healthcare of the Russian Federation</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.20538/1682-0363-2023-4-48-56</article-id><article-id custom-type="elpub" pub-id-type="custom">ssmu-5417</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>ОРИГИНАЛЬНЫЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL PAPERS</subject></subj-group></article-categories><title-group><article-title>Распространенность некоторых терапевтических заболеваний в зависимости от уровней адипокинов у людей до 45 лет</article-title><trans-title-group xml:lang="en"><trans-title>Prevalence of some internal diseases depending on the adipokine level in people under 45 years of age</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2268-4186</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Каштанова</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kashtanova</surname><given-names>E. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Каштанова Елена Владимировна – д-р биол. наук, доцент, зав. лабораторией клинических биохимических и гормональных исследований терапевтических заболеваний</p><p>630089, г. Новосибирск, ул. Бориса Богаткова 175/1</p></bio><bio xml:lang="en"><p>175/1, Bogatkova Str., Novosibirsk, 630089</p></bio><email xlink:type="simple">elekastanova@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/0000-0002-3538-0280</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Полонская</surname><given-names>Я. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Polonskaya</surname><given-names>Ya. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Полонская Яна Владимировна – д-р биол. наук, ст. науч. сотрудник, лаборатория клинических биохимических и гормональных исследований терапевтических заболеваний</p><p>630089, г. Новосибирск, ул. Бориса Богаткова 175/1</p></bio><bio xml:lang="en"><p>175/1, Bogatkova Str., Novosibirsk, 630089</p></bio><email xlink:type="simple">yana-polonskaya@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/0000-0001-9270-9188</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Щербакова</surname><given-names>Л. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Shcherbakova</surname><given-names>L. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Щербакова Лилия Валерьевна – ст. науч. сотрудник, лаборатория клинико-популяционных и профилактических исследований терапевтических и эндокринных заболеваний</p><p>630089, г. Новосибирск, ул. Бориса Богаткова 175/1</p></bio><bio xml:lang="en"><p>175/1, Bogatkova Str., Novosibirsk, 630089</p></bio><email xlink:type="simple">9584792@mail.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/0000-0002-0436-2549</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шрамко</surname><given-names>В. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Shramko</surname><given-names>V. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Шрамко Виктория Сергеевна – канд. мед. наук, науч. сотрудник, лаборатория клинических биохимических и гормональных исследований терапевтических заболеваний</p><p>630089, г. Новосибирск, ул. Бориса Богаткова 175/1</p></bio><bio xml:lang="en"><p>175/1, Bogatkova Str., Novosibirsk, 630089</p></bio><email xlink:type="simple">nosova@211.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0484-6540</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Стахнёва</surname><given-names>Е. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Stakhneva</surname><given-names>E. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Стахнёва Екатерина Михайловна – канд. биол. наук, ст. науч. сотрудник, лаборатория клинических биохимических и гор- мональных исследований терапевтических заболеваний</p><p>630089, г. Новосибирск, ул. Бориса Богаткова 175/1</p></bio><bio xml:lang="en"><p>175/1, Bogatkova Str., Novosibirsk, 630089</p></bio><email xlink:type="simple">stahneva@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/0000-0001-7875-1566</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Худякова</surname><given-names>А. Д.</given-names></name><name name-style="western" xml:lang="en"><surname>Khudyakova</surname><given-names>A. D.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Худякова Алена Дмитриевна – зав. лабораторией генетических и средовых детерминант жизненного цикла человека</p><p>630089, г. Новосибирск, ул. Бориса Богаткова 175/1</p></bio><bio xml:lang="en"><p>175/1, Bogatkova Str., Novosibirsk, 630089</p></bio><email xlink:type="simple">alene.elene@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7350-534X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Садовский</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Sadovski</surname><given-names>E. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Садовский Евгений Викторович – мл. науч. сотрудник, лаборатория клинических биохимических и гормональных исследований терапевтических заболеваний</p><p>630089, г. Новосибирск, ул. Бориса Богаткова 175/1</p></bio><bio xml:lang="en"><p>175/1, Bogatkova Str., Novosibirsk, 630089</p></bio><email xlink:type="simple">stinger000@mail.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/0000-0002-2470-2133</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Денисова</surname><given-names>Д. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Denisova</surname><given-names>D. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Денисова Диана Вахтанговна – д-р мед. наук, гл. науч. сотрудник, лаборатории профилактической медицины</p><p>630089, г. Новосибирск, ул. Бориса Богаткова 175/1</p></bio><bio xml:lang="en"><p>175/1, Bogatkova Str., Novosibirsk, 630089</p></bio><email xlink:type="simple">denisovadiana@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4936-8362</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Рагино</surname><given-names>Ю. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Ragino</surname><given-names>Yu. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Рагино Юлия Игоревна – д-р мед. наук, член-корр. РАН, руководитель </p><p>630089, г. Новосибирск, ул. Бориса Богаткова 175/1</p></bio><bio xml:lang="en"><p>175/1, Bogatkova Str., Novosibirsk, 630089</p></bio><email xlink:type="simple">ragino@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Научно-исследовательский институт терапии и профилактической медицины (НИИТПМ) – филиал Института цитологии и генетики Сибирского отделения Российской академии наук (ИЦиГ СО РАН)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Research Institute of Internal and Preventive Medicine – Branch of the Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2023</year></pub-date><pub-date pub-type="epub"><day>22</day><month>01</month><year>2024</year></pub-date><volume>22</volume><issue>4</issue><fpage>48</fpage><lpage>56</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Каштанова Е.В., Полонская Я.В., Щербакова Л.В., Шрамко В.С., Стахнёва Е.М., Худякова А.Д., Садовский Е.В., Денисова Д.В., Рагино Ю.И., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Каштанова Е.В., Полонская Я.В., Щербакова Л.В., Шрамко В.С., Стахнёва Е.М., Худякова А.Д., Садовский Е.В., Денисова Д.В., Рагино Ю.И.</copyright-holder><copyright-holder xml:lang="en">Kashtanova E.V., Polonskaya Y.V., Shcherbakova L.V., Shramko V.S., Stakhneva E.M., Khudyakova A.D., Sadovski E.V., Denisova D.V., Ragino Y.I.</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://bulletin.ssmu.ru/jour/article/view/5417">https://bulletin.ssmu.ru/jour/article/view/5417</self-uri><abstract><p>Цель – изучить встречаемость некоторых распространенных терапевтических заболеваний у молодых людей трудоспособного и детородного возраста в зависимости от уровней адипокинов.</p><sec><title>Материалы и методы</title><p>Материалы и методы. В исследование включено 1 340 человек в возрасте 25–44 лет. Методом мультиплексного анализа определены уровни лептина, адипонектина, адипсина, липокалина-2, ингибитора активатора плазминогена-1 (ИАП-1) и резистина. Изучены: гиперхолестеринемия липопротеинов низкой плотности (гиперХС-ЛНП), ишемическая болезнь сердца (ИБС), сахарный диабет 2-го типа (СД2), артериальная гипертензия (АГ), почечная дисфункция (ПД), хронический бронхит (ХБ).</p></sec><sec><title>Результаты</title><p>Результаты. С увеличением уровня адипонектина распространенность определенной ИБС возрастает в 8,6 раз. Самый высокий квартиль уровня адипсина характеризуется увеличением распространенности гиперХС-ЛНП на 12,9%, АГ на 3,9% и ПД на 17,9%. Квартили липолкалина-2 показали более высокую распространенность гиперХС-ЛПН, АГ и ПД в Q4 по сравнению с Q1. Распространенность ХБ ассоциирована со снижением уровня липокалина-2 и выше в Q1 на 35,9%, в сравнении с Q4. В квартилях ИАП-1 встречаемость СД2 и гиперХС-ЛНП в 2 и 1,5 раза соответственно выше, а ПД в 2,5 раза ниже в Q4, чем в Q1. В квартилях резистина на 13–38% увеличивается распространенность гиперХС-ЛНП, АГ, ПД. На 20% снижается распространенность хронического бронхита в Q4 по сравнению с Q1. Встречаемость гиперХС-ЛНП и ПД была выше в Q4 лептина.</p></sec><sec><title>Заключение</title><p>Заключение. Результаты свидетельствуют о необходимости дальнейших исследований, направленных на изучение молекулярных механизмов, лежащих в основе эффектов адипокинов, что позволит найти комбинированный подход, направленный на восстановление нормальных физиологических уровней адипокинов. Это может дать положительный эффект при изученных терапевтических заболеваниях.</p></sec></abstract><trans-abstract xml:lang="en"><p>The aim was to study the prevalence of some common internal diseases in young people of working and childbearing age, depending on the levels of adipokines.</p><sec><title>Materials and methods</title><p>Materials and methods. The study included 1,340 people aged 25–44 years. The levels of leptin, adiponectin, adipsin, lipocalin-2, plasminogen activator inhibitor-1 (PAI-1), and resistin were determined by the multiplex analysis. Low-density lipoprotein hypercholesterolemia (LDL hypercholesterolemia), coronary artery disease (CAD), type 2 diabetes mellitus (T2DM), arterial hypertension (AH), renal dysfunction (RD), and chronic bronchitis (CB) were studied.</p></sec><sec><title>Results</title><p>Results. With an increase in the level of adiponectin, the prevalence of CAD increased by 8.6 times. The highest quartile of the adipsin level was characterized by an increase in the prevalence of LDL hypercholesterolemia by 12.9%, AH by 3.9%, and RD by 17.9%. The quartiles of lipolkalin-2 showed higher prevalence of LDL hypercholesterolemia, AH, and RD in Q4 compared to Q1. The prevalence of CB was associated with a decrease in the level of lipocalin-2 and was higher by 35.9% within Q1 compared to Q4. In the quartiles of PAI-1, the prevalence of T2DM and LDL hypercholesterolemia was 2 and 1.5 times higher, respectively, and the prevalence of RD was 2.5 times lower in Q4 than in Q1. In quartiles of resistin, the prevalence of LDL hypercholesterolemia, AH, and RD increased by 13–38%, while the prevalence of CB decreased by 20% in Q4, compared to Q1. The prevalence of LDL hypercholesterolemia and RD was higher within Q4 of leptin.</p></sec><sec><title>Conclusion</title><p>Conclusion. The results indicate the need for further research aimed at studying the molecular mechanisms underlying the effects of adipokines. This will allow to find a combined approach to restoring normal physiological levels of adipokines, which can have a positive effect in the studied internal diseases.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>терапевтические заболевания</kwd><kwd>адипокины</kwd><kwd>адипонектин</kwd><kwd>липокалин-2</kwd><kwd>резистин</kwd></kwd-group><kwd-group xml:lang="en"><kwd>internal diseases</kwd><kwd>adipokines</kwd><kwd>adiponectin</kwd><kwd>lipocalin-2</kwd><kwd>resistin</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Статья подготовлена в рамках государственного задания «Эпидемиологический мониторинг состояния здоровья населения и изучение молекулярно-генетических и молекулярно-биологических механизмов развития распространенных терапевтических заболеваний в Сибири для совершенствования подходов к их диагностике, профилактике и лечению» (№ 122031700094-5_) и при финансовой поддержке гранта Российского научного фонда (№ 21-15-00022)</funding-statement><funding-statement xml:lang="en">The article was written within the state assignment “Epidemiological monitoring of the population’s health and study of molecular genetic and molecular biological mechanisms underlying the development of common internal diseases in Siberia to improve approaches to their diagnosis, prevention, and treatment” (No. 122031700094-5_) and funded by the Russian Science Foundation grant (No. 21-15-00022)</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">Fasshauer M., Blüher M. Adipokines in health and disease. Trends Pharmacol. Sci. 2015;36(7):461–470. DOI: 10.1016/j.tips.2015.04.014.</mixed-citation><mixed-citation xml:lang="en">Fasshauer M., Blüher M. Adipokines in health and disease. Trends Pharmacol. Sci. 2015;36(7):461–470. DOI: 10.1016/j.tips.2015.04.014.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao S., Kusminski C.M., Scherer P.E. Adiponectin, leptin and cardiovascular disorders. Circ. Res. 2021;128(1):136–149. DOI: 10.1161/CIRCRESAHA.120.314458.</mixed-citation><mixed-citation xml:lang="en">Zhao S., Kusminski C.M., Scherer P.E. Adiponectin, leptin and cardiovascular disorders. Circ. Res. 2021;128(1):136–149. DOI: 10.1161/CIRCRESAHA.120.314458.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Bielecka-Dabrowa A., Bartlomiejczyk M.A., Sakowicz A., Maciejewski M., Banach M. The role of adipokines in the development of arterial stiffness and hypertension. Angiology. 2020;71(8):754–761. DOI: 10.1177/0003319720927203.</mixed-citation><mixed-citation xml:lang="en">Bielecka-Dabrowa A., Bartlomiejczyk M.A., Sakowicz A., Maciejewski M., Banach M. The role of adipokines in the development of arterial stiffness and hypertension. Angiology. 2020;71(8):754–761. DOI: 10.1177/0003319720927203.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Mach F., Baigent C., Catapano A.L., Koskinas K.C., Casula M., Badimon L. et al. ESC Scientific Document Group. 2019 ESC/ EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk. European Heart Journal. 2020;1(1):111–188. DOI: 10.1093/eurheartj/ehz455.</mixed-citation><mixed-citation xml:lang="en">Mach F., Baigent C., Catapano A.L., Koskinas K.C., Casula M., Badimon L. et al. ESC Scientific Document Group. 2019 ESC/ EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk. European Heart Journal. 2020;1(1):111–188. DOI: 10.1093/eurheartj/ehz455.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Rydén L., Grant P.J., Anker S.D., Berne C., Cosentino F., Danchin N. et al. Guidelines on diabetes, pre-diabetes, and cardiovascular diseases developed in collaboration with the EASD: The Task Force on diabetes, pre-diabetes, and cardiovascular diseases of the European Society of Cardiology (ESC) and developed in collaboration with the European Association for the Study of Diabetes (EASD). European Heart Journal. 2013;34(39):3035–3087. DOI: 10.1093/eurheartj/eht108.</mixed-citation><mixed-citation xml:lang="en">Rydén L., Grant P.J., Anker S.D., Berne C., Cosentino F., Danchin N. et al. Guidelines on diabetes, pre-diabetes, and cardiovascular diseases developed in collaboration with the EASD: The Task Force on diabetes, pre-diabetes, and cardiovascular diseases of the European Society of Cardiology (ESC) and developed in collaboration with the European Association for the Study of Diabetes (EASD). European Heart Journal. 2013;34(39):3035–3087. DOI: 10.1093/eurheartj/eht108.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Артериальная гипертензия у взрослых. Клинические рекомендации 2020. Российский кардиологический журнал. 2020;25(3):3786. DOI: 10.15829/1560-4071-2020-3-3786.</mixed-citation><mixed-citation xml:lang="en">Артериальная гипертензия у взрослых. Клинические рекомендации 2020. Российский кардиологический журнал. 2020;25(3):3786. DOI: 10.15829/1560-4071-2020-3-3786.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Кокосов А.Н. Хронический необструктивный бронхит. Клиническая медицина. 1999;1:11–16.</mixed-citation><mixed-citation xml:lang="en">Кокосов А.Н. Хронический необструктивный бронхит. Клиническая медицина. 1999;1:11–16.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Achari A.E., Jain S.K. Adiponectin, a therapeutic target for obesity, diabetes, and endothelial dysfunction. Int. J. Mol. Sci. 2017;18:1321. DOI: 10.3390/ijms18061321.</mixed-citation><mixed-citation xml:lang="en">Achari A.E., Jain S.K. Adiponectin, a therapeutic target for obesity, diabetes, and endothelial dysfunction. Int. J. Mol. Sci. 2017;18:1321. DOI: 10.3390/ijms18061321.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Gariballa S., Alkaabi J., Yasin J., Al Essa A. Total adiponectin in overweight and obese subjects and its response to visceral fat loss. BMC Endocr. Disord. 2019;19(1):55. DOI: 10.1186/s12902-019-0386-z.</mixed-citation><mixed-citation xml:lang="en">Gariballa S., Alkaabi J., Yasin J., Al Essa A. Total adiponectin in overweight and obese subjects and its response to visceral fat loss. BMC Endocr. Disord. 2019;19(1):55. DOI: 10.1186/s12902-019-0386-z.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Liu C., Feng X., Li Q., Wang Y., Li Q., Hua M. Adiponectin, TNF-α and inflammatory cytokines and risk of type 2 diabetes: A systematic review and meta-analysis. Cytokine. 2016;86:100–109. DOI: 10.1016/j.cyto.2016.06.028.</mixed-citation><mixed-citation xml:lang="en">Liu C., Feng X., Li Q., Wang Y., Li Q., Hua M. Adiponectin, TNF-α and inflammatory cytokines and risk of type 2 diabetes: A systematic review and meta-analysis. Cytokine. 2016;86:100–109. DOI: 10.1016/j.cyto.2016.06.028.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Lindberg S., Jensen J.S., Pedersen S.H., Galatius S., Frystyk J., Flyvbjerg A. et al. Low adiponectin levels and increased risk of type 2 diabetes in patients with myocardial infarction. Diabetes Care. 2014;37:3003–3008.</mixed-citation><mixed-citation xml:lang="en">Lindberg S., Jensen J.S., Pedersen S.H., Galatius S., Frystyk J., Flyvbjerg A. et al. Low adiponectin levels and increased risk of type 2 diabetes in patients with myocardial infarction. Diabetes Care. 2014;37:3003–3008.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Kou H., Deng J., Gao D., Song A., Han Z., Wei J. et al. Relationship among adiponectin, insulin resistance and atherosclerosis in non-diabetic hypertensive patients and healthy adults. Clin. Exp. Hypertens. 2018;40(7):656–663. DOI: 10.1080/10641963.2018.1425414.</mixed-citation><mixed-citation xml:lang="en">Kou H., Deng J., Gao D., Song A., Han Z., Wei J. et al. Relationship among adiponectin, insulin resistance and atherosclerosis in non-diabetic hypertensive patients and healthy adults. Clin. Exp. Hypertens. 2018;40(7):656–663. DOI: 10.1080/10641963.2018.1425414.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Kim D.H., Kim C., Ding E.L., Townsend M.K., Lipsitz L.A. Adiponectin levels and the risk of hypertension: a systematic review and meta-analysis. Hypertension. 2013;62(1):27–32. DOI: 10.1161/HYPERTENSIONAHA.113.01453.</mixed-citation><mixed-citation xml:lang="en">Kim D.H., Kim C., Ding E.L., Townsend M.K., Lipsitz L.A. Adiponectin levels and the risk of hypertension: a systematic review and meta-analysis. Hypertension. 2013;62(1):27–32. DOI: 10.1161/HYPERTENSIONAHA.113.01453.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Doumatey A.P., Bentley A.R., Zhou J., Huang H., Adeyemo A., Rotimi C.N. Paradoxical hyperadiponectinemia is associated with the metabolically healthy obese (MHO) phenotype in African Americans. J. Endocrinol. Metab. 2012;2(2):51–65. DOI: 10.4021/jem95W.</mixed-citation><mixed-citation xml:lang="en">Doumatey A.P., Bentley A.R., Zhou J., Huang H., Adeyemo A., Rotimi C.N. Paradoxical hyperadiponectinemia is associated with the metabolically healthy obese (MHO) phenotype in African Americans. J. Endocrinol. Metab. 2012;2(2):51–65. DOI: 10.4021/jem95W.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Kobayashi H., Ouchi N., Kihara S., Walsh K., Kumada M., Abe Y. et al. Selective suppression of endothelial cell apoptosis by the high molecular weight form of adiponectin. Circ. Res. 2004;94(4):27–31. DOI: 10.1161/01.RES.0000119921.86460.37.</mixed-citation><mixed-citation xml:lang="en">Kobayashi H., Ouchi N., Kihara S., Walsh K., Kumada M., Abe Y. et al. Selective suppression of endothelial cell apoptosis by the high molecular weight form of adiponectin. Circ. Res. 2004;94(4):27–31. DOI: 10.1161/01.RES.0000119921.86460.37.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Woodward L., Akoumianakis I., Antoniades C. Unravelling the adiponectin paradox: Novel roles of adiponectin in the regulation of cardiovascular disease. Br. J. Pharmacol. 2017;174:4007–4020. DOI: 10.1111/bph.13619.</mixed-citation><mixed-citation xml:lang="en">Woodward L., Akoumianakis I., Antoniades C. Unravelling the adiponectin paradox: Novel roles of adiponectin in the regulation of cardiovascular disease. Br. J. Pharmacol. 2017;174:4007–4020. DOI: 10.1111/bph.13619.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Wannamethee S.G., Whincup P., Lennon L., Sattar N. Circulating adiponectin levels and mortality in elderly men with and without cardiovascular disease and heart failure. Arch. Intern. Med. 2007;167:1510–1517. DOI: 10.1001/archinte.167.14.1510.</mixed-citation><mixed-citation xml:lang="en">Wannamethee S.G., Whincup P., Lennon L., Sattar N. Circulating adiponectin levels and mortality in elderly men with and without cardiovascular disease and heart failure. Arch. Intern. Med. 2007;167:1510–1517. DOI: 10.1001/archinte.167.14.1510.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">McEntegart M.B., Awede B., Petrie M.C., Sattar N., Dunn F.G., Macfarlane N.G. et al. Increase in serum adiponectin concentration in patients with heart failure and cachexia: Relationship with leptin, other cytokines, and B-type natriuretic peptide. Eur. Heart J. 2007;28:829–835. DOI: 10.1093/eurheartj/ehm033.</mixed-citation><mixed-citation xml:lang="en">McEntegart M.B., Awede B., Petrie M.C., Sattar N., Dunn F.G., Macfarlane N.G. et al. Increase in serum adiponectin concentration in patients with heart failure and cachexia: Relationship with leptin, other cytokines, and B-type natriuretic peptide. Eur. Heart J. 2007;28:829–835. DOI: 10.1093/eurheartj/ehm033.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Dornbush S., Aeddula N.R. Physiology, leptin. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing, 2021.</mixed-citation><mixed-citation xml:lang="en">Dornbush S., Aeddula N.R. Physiology, leptin. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing, 2021.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Khazaei M., Tahergorabi Z. Leptin and its cardiovascular effects: Focus on angiogenesis. Advanced Biomedical Research. 2015;4(1):79. DOI: 10.4103/2277-9175.156526.</mixed-citation><mixed-citation xml:lang="en">Khazaei M., Tahergorabi Z. Leptin and its cardiovascular effects: Focus on angiogenesis. Advanced Biomedical Research. 2015;4(1):79. DOI: 10.4103/2277-9175.156526.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Fried S.K., Ricci M.R., Russell C.D., Laferrère B. Regulation of leptin production in humans. J. Nutr. 2000;130(12):3127S–3131S. DOI: 10.1093/jn/130.12.3127S.</mixed-citation><mixed-citation xml:lang="en">Fried S.K., Ricci M.R., Russell C.D., Laferrère B. Regulation of leptin production in humans. J. Nutr. 2000;130(12):3127S–3131S. DOI: 10.1093/jn/130.12.3127S.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Katsiki N., Mikhailidis D.P., Banach M. Leptin, cardiovascular diseases and type 2 diabetes mellitus review-article. Acta Pharmacol. Sin. 2018;39:1176–1188. DOI: 10.1038/aps.2018.40.</mixed-citation><mixed-citation xml:lang="en">Katsiki N., Mikhailidis D.P., Banach M. Leptin, cardiovascular diseases and type 2 diabetes mellitus review-article. Acta Pharmacol. Sin. 2018;39:1176–1188. DOI: 10.1038/aps.2018.40.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Marchelek-Mysliwiec M., Wisniewska M., Nowosiad-Magda M., Safranow K., Kwiatkowska E., Banach B. et al. Association between plasma concentration of klotho protein, osteocalcin, leptin, adiponectin, and bone mineral density in patients with chronic kidney disease. Horm. Metab. Res. 2018;50:816–821. DOI: 10.1055/a-0752-4615.</mixed-citation><mixed-citation xml:lang="en">Marchelek-Mysliwiec M., Wisniewska M., Nowosiad-Magda M., Safranow K., Kwiatkowska E., Banach B. et al. Association between plasma concentration of klotho protein, osteocalcin, leptin, adiponectin, and bone mineral density in patients with chronic kidney disease. Horm. Metab. Res. 2018;50:816–821. DOI: 10.1055/a-0752-4615.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Wang J.S., Lee W.J., Lee I.T., Lin S.Y., Lee W.L., Liang K.W. et al. Association between serum adipsin levels and insulin resistance in subjects with various degrees of glucose intolerance. J. Endocr. Soc. 2018;3(2):403–410. DOI: 10.1210/js.2018-00359.</mixed-citation><mixed-citation xml:lang="en">Wang J.S., Lee W.J., Lee I.T., Lin S.Y., Lee W.L., Liang K.W. et al. Association between serum adipsin levels and insulin resistance in subjects with various degrees of glucose intolerance. J. Endocr. Soc. 2018;3(2):403–410. DOI: 10.1210/js.2018-00359.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Василенко М.А., Кириенкова Е.В., Скуратовская Д.А., Затолокин П.А., Миронюк Н.И., Литвинова Л.С. Роль продукции адипсина и лептина в формировании инсулинорезистентности у больных абдоминальным ожирением. Доклады Академии наук. 2017;475(3):336–341. DOI: 10.7868/S0869565217210228.</mixed-citation><mixed-citation xml:lang="en">Василенко М.А., Кириенкова Е.В., Скуратовская Д.А., Затолокин П.А., Миронюк Н.И., Литвинова Л.С. Роль продукции адипсина и лептина в формировании инсулинорезистентности у больных абдоминальным ожирением. Доклады Академии наук. 2017;475(3):336–341. DOI: 10.7868/S0869565217210228.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Hertle E., Arts I.C., van der Kallen C.J., Feskens E.J., Schalkwijk C.G., Stehouwer C.D. et al. The alternative complement pathway is longitudinally associated with adverse cardiovascular outcomes. Thromb. Haemost. 2016;115(2):446–457. DOI: 10.1160/TH15-05-0439.</mixed-citation><mixed-citation xml:lang="en">Hertle E., Arts I.C., van der Kallen C.J., Feskens E.J., Schalkwijk C.G., Stehouwer C.D. et al. The alternative complement pathway is longitudinally associated with adverse cardiovascular outcomes. Thromb. Haemost. 2016;115(2):446–457. DOI: 10.1160/TH15-05-0439.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Song N.J., Kim S., Jang B.H., Chang S.H., Yun U.J., Park K.M. et al. Molecule-induced complement factor D (adipsin) promotes lipid accumulation and adipocyte differentiation. PLoS One. 2016;11(9):e0162228. DOI: 10.1371/journal.pone.0162228.</mixed-citation><mixed-citation xml:lang="en">Song N.J., Kim S., Jang B.H., Chang S.H., Yun U.J., Park K.M. et al. Molecule-induced complement factor D (adipsin) promotes lipid accumulation and adipocyte differentiation. PLoS One. 2016;11(9):e0162228. DOI: 10.1371/journal.pone.0162228.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Jalal D., Renner B., Laskowski J., Stites E., Cooper J., Valente K. et al. Endothelial microparticles and systemic complement activation in patients with chronic kidney disease. J. Am. Heart Assoc. 2018;7(14):e007818. DOI: 10.1161/JAHA.117.007818.</mixed-citation><mixed-citation xml:lang="en">Jalal D., Renner B., Laskowski J., Stites E., Cooper J., Valente K. et al. Endothelial microparticles and systemic complement activation in patients with chronic kidney disease. J. Am. Heart Assoc. 2018;7(14):e007818. DOI: 10.1161/JAHA.117.007818.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Buonafine M., Martinez-Martinez E., Jaisser F. More than a simple biomarker: the role of NGAL in cardiovascular and renal diseases. Clin. Sci. (London). 2018;132(9):909–923. DOI: 10.1042/CS20171592.</mixed-citation><mixed-citation xml:lang="en">Buonafine M., Martinez-Martinez E., Jaisser F. More than a simple biomarker: the role of NGAL in cardiovascular and renal diseases. Clin. Sci. (London). 2018;132(9):909–923. DOI: 10.1042/CS20171592.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Cabedo Martinez A.I., Weinhäupl K., Lee W.K., Wolff N.A., Storch B., Żerko S. et al. Biochemical and structural characterization of the interaction between the siderocalin NGAL/ LCN2 (neutrophil gelatinase-associated lipocalin/lipocalin 2) and the N-terminal domain of its endocytic receptor SLC22A17. J. Biol. Chem. 2016;291(6):2917–2930. DOI: 10.1074/jbc.M115.685644.</mixed-citation><mixed-citation xml:lang="en">Cabedo Martinez A.I., Weinhäupl K., Lee W.K., Wolff N.A., Storch B., Żerko S. et al. Biochemical and structural characterization of the interaction between the siderocalin NGAL/ LCN2 (neutrophil gelatinase-associated lipocalin/lipocalin 2) and the N-terminal domain of its endocytic receptor SLC22A17. J. Biol. Chem. 2016;291(6):2917–2930. DOI: 10.1074/jbc.M115.685644.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Chella Krishnan K., Sabir S., Shum M., Meng Y., Acín-Pérez R., Lang J.M. et al. Sex-specific metabolic functions of adipose lipocalin-2. Mol. Metab. 2019;30:30–47. DOI: 10.1016/j.molmet.2019.09.009.</mixed-citation><mixed-citation xml:lang="en">Chella Krishnan K., Sabir S., Shum M., Meng Y., Acín-Pérez R., Lang J.M. et al. Sex-specific metabolic functions of adipose lipocalin-2. Mol. Metab. 2019;30:30–47. DOI: 10.1016/j.molmet.2019.09.009.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Chong J.J.H., Prince R.L., Thompson P.L., Thavapalachandran S., Ooi E., Devine A. et al. Association between plasma neutrophil gelatinase-associated lipocalin and cardiac disease hospitalizations and deaths in older women. J. Am. Heart Assoc. 2019;8(1):e011028. DOI: 10.1161/JAHA.118.011028.</mixed-citation><mixed-citation xml:lang="en">Chong J.J.H., Prince R.L., Thompson P.L., Thavapalachandran S., Ooi E., Devine A. et al. Association between plasma neutrophil gelatinase-associated lipocalin and cardiac disease hospitalizations and deaths in older women. J. Am. Heart Assoc. 2019;8(1):e011028. DOI: 10.1161/JAHA.118.011028.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Cruz D.N., Gaiao S., Maisel A., Ronco C., Devarajan P. Neutrophil Gelatinase-Associated Lipocalin as a Biomarker of Cardiovascular Disease: A Systematic Review. Clin. Chem. Lab. Med. 2012;50:1533–1545. DOI: 10.1515/cclm-2012-0307.</mixed-citation><mixed-citation xml:lang="en">Cruz D.N., Gaiao S., Maisel A., Ronco C., Devarajan P. Neutrophil Gelatinase-Associated Lipocalin as a Biomarker of Cardiovascular Disease: A Systematic Review. Clin. Chem. Lab. Med. 2012;50:1533–1545. DOI: 10.1515/cclm-2012-0307.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Wang L.K., Wang H., Wu X.L., Shi L., Yang R.M., Wang Y.C. Relationships among resistin, adiponectin, and leptin and microvascular complications in patients with type 2 diabetes mellitus. J. Int. Med. Res. 2020;48(4):300060519870407. DOI: 10.1177/0300060519870407.</mixed-citation><mixed-citation xml:lang="en">Wang L.K., Wang H., Wu X.L., Shi L., Yang R.M., Wang Y.C. Relationships among resistin, adiponectin, and leptin and microvascular complications in patients with type 2 diabetes mellitus. J. Int. Med. Res. 2020;48(4):300060519870407. DOI: 10.1177/0300060519870407.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Niaz S., Latif J., Hussain S. Serum resistin: A possible link between inflammation, hypertension and coronary artery disease. Pak. J. Med. Sci. 2019;35(3):641–646. DOI: 10.12669/pjms.35.3.274.</mixed-citation><mixed-citation xml:lang="en">Niaz S., Latif J., Hussain S. Serum resistin: A possible link between inflammation, hypertension and coronary artery disease. Pak. J. Med. Sci. 2019;35(3):641–646. DOI: 10.12669/pjms.35.3.274.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Jiang Y., Lu L., Hu Y., Li Q., An C., Yu X. et al. Resistin induces hypertension and insulin resistance in mice via a TLR4-dependent pathway. Sci. Rep. 2016;6:22193. DOI: 10.1038/srep22193.</mixed-citation><mixed-citation xml:lang="en">Jiang Y., Lu L., Hu Y., Li Q., An C., Yu X. et al. Resistin induces hypertension and insulin resistance in mice via a TLR4-dependent pathway. Sci. Rep. 2016;6:22193. DOI: 10.1038/srep22193.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Chen C., Jiang J., Lü J.M., Chai H., Wang X., Lin P.H. et al. Resistin decreases expression of endothelial nitric oxide synthase through oxidative stress in human coronary artery endothelial cells. Am. J. Physiol. Heart Circ. Physiol. 2010;299(1):H193–201. DOI: 10.1152/ajpheart.00431.2009.</mixed-citation><mixed-citation xml:lang="en">Chen C., Jiang J., Lü J.M., Chai H., Wang X., Lin P.H. et al. Resistin decreases expression of endothelial nitric oxide synthase through oxidative stress in human coronary artery endothelial cells. Am. J. Physiol. Heart Circ. Physiol. 2010;299(1):H193–201. DOI: 10.1152/ajpheart.00431.2009.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Axelsson J., Bergsten A., Qureshi A.R., Heimbürger O., Bárány P., Lönnqvist F. et al. Elevated resistin levels in chronic kidney disease are associated with decreased glomerular filtration rate and inflammation, but not with insulin resistance. Kidney Int. 2006;69(3):596–604. DOI: 10.1038/sj.ki.5000089.</mixed-citation><mixed-citation xml:lang="en">Axelsson J., Bergsten A., Qureshi A.R., Heimbürger O., Bárány P., Lönnqvist F. et al. Elevated resistin levels in chronic kidney disease are associated with decreased glomerular filtration rate and inflammation, but not with insulin resistance. Kidney Int. 2006;69(3):596–604. DOI: 10.1038/sj.ki.5000089.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Dan S., Aditya P., Banerjee P., Bal C., Roy H., Banerjee I. Effect of chronic kidney disease on serum resistin level. Niger J. Clin. Pract. 2014;17(6):735–738. DOI: 10.4103/1119-3077.144387.</mixed-citation><mixed-citation xml:lang="en">Dan S., Aditya P., Banerjee P., Bal C., Roy H., Banerjee I. Effect of chronic kidney disease on serum resistin level. Niger J. Clin. Pract. 2014;17(6):735–738. DOI: 10.4103/1119-3077.144387.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Liu G., Deng Y., Sun L., Ye X., Yao P., Hu Y. et al. Elevated plasma tumor necrosis factor-α receptor 2 and resistin are associated with increased incidence of kidney function decline in Chinese adults. Endocrine. 2016;52(3):541–549. DOI: 10.1007/s12020-015-0807-3.</mixed-citation><mixed-citation xml:lang="en">Liu G., Deng Y., Sun L., Ye X., Yao P., Hu Y. et al. Elevated plasma tumor necrosis factor-α receptor 2 and resistin are associated with increased incidence of kidney function decline in Chinese adults. Endocrine. 2016;52(3):541–549. DOI: 10.1007/s12020-015-0807-3.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Pérez-Bautista O., Montaño M., Pérez-Padilla R., Zúñiga-Ramos J., Camacho-Priego M., Barrientos-Gutiérrez T. et al. Women with COPD by biomass show different serum profile of adipokines, incretins, and peptide hormones than smokers. Respir. Res. 2018;19(1):239. DOI: 10.1186/s12931-018-0943-4.</mixed-citation><mixed-citation xml:lang="en">Pérez-Bautista O., Montaño M., Pérez-Padilla R., Zúñiga-Ramos J., Camacho-Priego M., Barrientos-Gutiérrez T. et al. Women with COPD by biomass show different serum profile of adipokines, incretins, and peptide hormones than smokers. Respir. Res. 2018;19(1):239. DOI: 10.1186/s12931-018-0943-4.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Vecchiola A., García K., González-Gómez L.M., Tapia-Castillo A., Artigas R., Baudrand R. et al. Plasminogen activator inhibitor-1 and adiponectin are associated with metabolic syndrome components. Am. J. Hypertens. 2022;35(4):311–318. DOI: 10.1093/ajh/hpab138.</mixed-citation><mixed-citation xml:lang="en">Vecchiola A., García K., González-Gómez L.M., Tapia-Castillo A., Artigas R., Baudrand R. et al. Plasminogen activator inhibitor-1 and adiponectin are associated with metabolic syndrome components. Am. J. Hypertens. 2022;35(4):311–318. DOI: 10.1093/ajh/hpab138.</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>
