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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/omet13204</article-id><article-id custom-type="elpub" pub-id-type="custom">ometendo-13204</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 ИССЛЕДОВАНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL STUDIES</subject></subj-group></article-categories><title-group><article-title>Эффективность лираглутида в комплексной терапии больных псориазом в сочетании с метаболическими нарушениями: метаанализ наблюдательных и контролируемых исследований</article-title><trans-title-group xml:lang="en"><trans-title>Efficacy of liraglutide in combination therapy of patients with psoriasis combined with metabolic disorders: a meta-analysis of observational and controlled studies</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0579-1131</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Коротаева</surname><given-names>Т. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Korotaeva</surname><given-names>T. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Коротаева Татьяна Викторовна - д.м.н.</p><p>Москва</p></bio><bio xml:lang="en"><p>Tatiana V. Korotaeva - MD, PhD, Professor.</p><p>Moscow</p></bio><email xlink:type="simple">tatianakorotaeva@googlemail.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/0000-0002-8520-8702</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Трошина</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Troshina</surname><given-names>E. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Трошина Екатерина Анатольевна - д.м.н., чл.-корр. РАН.</p><p>Москва</p></bio><bio xml:lang="en"><p>Ekaterina A. Troshina - MD, PhD, Professor.</p><p>Moscow</p></bio><email xlink:type="simple">troshina@inbox.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6068-3080</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лила</surname><given-names>А. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Lila</surname><given-names>A. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Лила Александр Михайлович - д.м.н., член-корр. РАН</p><p>Москва</p></bio><bio xml:lang="en"><p>Alexander M. Lila - MD, PhD, Professor.</p><p>Moscow</p></bio><email xlink:type="simple">sokrat@mail.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5290-156X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Паневин</surname><given-names>Т. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Panevin</surname><given-names>T. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Паневин Тарас Сергеевич - к.м.н.</p><p>115522, Москва, Каширское шоссе, 34А</p></bio><bio xml:lang="en"><p>Taras S. Panevin - MD, PhD.</p><p>34A, Kashirskoe shosse, Moscow 115522</p></bio><email xlink:type="simple">tarasel@list.ru</email><xref ref-type="aff" rid="aff-4"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1598-8360</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Насонов</surname><given-names>Е. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Nasonov</surname><given-names>E. L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Насонов Евгений Львович - д.м.н., акад. РАН.</p><p>Москва</p></bio><bio xml:lang="en"><p>Evgeny L. Nasonov - MD, PhD, Professor.</p><p>Moscow</p></bio><email xlink:type="simple">cancelar@irramn.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/0000-0001-5968-2403</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Корсакова</surname><given-names>Ю. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Korsakova</surname><given-names>Yu. L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Юлия Леонидовна Корсакова - к.м.н.</p><p>Москва</p></bio><bio xml:lang="en"><p>Yulia L. Korsakova - MD, PhD.</p><p>Moscow</p></bio><email xlink:type="simple">yulkorsakova@bk.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/0000-0002-4285-0869</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Глухова</surname><given-names>С. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Glukhova</surname><given-names>S. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Глухова Светлана Ивановна - к.ф-м.н.</p><p>Москва</p></bio><bio xml:lang="en"><p>Svetlana I. Gluhova - PhD.</p><p>Moscow</p></bio><email xlink:type="simple">sveglukhova@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>V.A. Nasonova Research Institute of Rheumatology</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБУ «НМИЦ эндокринологии им. академика И.И. Дедова» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>I.I. Dedov National Medical Research Center of Endocrinology</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>ФГБНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой»; ФГБОУ ДПО «Российская медицинская академия непрерывного профессионального образования» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>V.A. Nasonova Research Institute of Rheumatology; Russian Medical Academy of Continuous Professional Education</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-4"><aff xml:lang="ru"><institution>ФГБНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой»; ФГБОУ ВО Дальневосточный государственный медицинский университет Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>V.A. Nasonova Research Institute of Rheumatology; The Far Eastern State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>03</day><month>09</month><year>2025</year></pub-date><volume>22</volume><issue>2</issue><fpage>70</fpage><lpage>76</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Коротаева Т.В., Трошина Е.А., Лила А.М., Паневин Т.С., Насонов Е.Л., Корсакова Ю.Л., Глухова С.И., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Коротаева Т.В., Трошина Е.А., Лила А.М., Паневин Т.С., Насонов Е.Л., Корсакова Ю.Л., Глухова С.И.</copyright-holder><copyright-holder xml:lang="en">Korotaeva T.V., Troshina E.A., Lila A.M., Panevin T.S., Nasonov E.L., Korsakova Y.L., Glukhova S.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://www.omet-endojournals.ru/jour/article/view/13204">https://www.omet-endojournals.ru/jour/article/view/13204</self-uri><abstract><sec><title>Обоснование</title><p>Обоснование. Псориаз характеризуются высокой частотой сопутствующих метаболических нарушений, включая ожирение и сахарный диабет 2 типа (СД2). Имеются ограниченные данные об эффективности агониста рецептора глюкагоноподобного пептида-1 для лечения метаболических нарушений у пациентов с псориазом.</p></sec><sec><title>Цель</title><p>Цель. Анализ эффективности лираглутида в комплексной терапии больных псориазом в сочетании с метаболическими нарушениями.</p></sec><sec><title>Материалы и методы</title><p>Материалы и методы. В базе PubMed проведен поиск исследований по ключевым словам: «psoriasis» и «liraglutide». Найдено 23 публикации, в окончательный анализ вошли 5 исследований с общим размером выборки 52 пациента с псориазом в сочетании с метаболическими нарушениями (СД2 и ожирение). Оценивали влияние лираглутида на распространенность и тяжесть псориаза по динамике индекса площади поражения и тяжести псориаза (PASI), качество жизни по опроснику DLQI и уровень глюкозы плазмы крови натощак, гликированного гемоглобина, индекса массы тела (ИМТ). Результаты представлены в виде средневзвешенной разницы (WMD) и 95% доверительного интервала (ДИ).</p></sec><sec><title>Результаты</title><p>Результаты. Длительность терапии лираглутидом составила от 8 до 16 нед. Доза лираглутида титровалась от 0,6 мг/сут до 3,0 мг/сут. Показана значимая динамика WMD индексов PASI (-6,95 [95% ДИ -11,59; -2,32]) и DLQI (-6,95 [95% ДИ -11,59; -2,32]), а также ИМТ (-2,97 [95% ДИ -3,58; -2,37]) на фоне терапии лираглутидом. Значимой разницы в уровне глюкозы и гликированного гемоглобина выявлено не было.</p></sec><sec><title>Заключение</title><p>Заключение. Результаты метаанализа демонстрируют, что использование лираглутида в комплексной терапии псориаза способствует снижению ИМТ, распространенности и тяжести псориаза, а также улучшению качества жизни больных.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>BACKGROUND</title><p>BACKGROUND: Psoriasis is characterized by a high frequency of comorbid metabolic disorders, including obesity and type 2 diabetes mellitus. There are limited data on the efficacy of glucagon-like peptide-1 receptor agonist for the treatment of metabolic disorders in patients with psoriasis.</p></sec><sec><title>AIM</title><p>AIM: Analysis of the effectiveness of liraglutide in the complex therapy of patients with psoriasis in combination with metabolic disorders.</p></sec><sec><title>MATERIALS AND METHODS</title><p>MATERIALS AND METHODS: The PubMed database was searched for studies using the keywords "psoriasis" and "liraglutide". 23 publications were found, the final analysis included 5 studies with a total sample size of 52 patients with psoriasis combined with metabolic disorders (type 2 diabetes mellitus and obesity). The effect of liraglutide on the prevalence and severity of psoriasis was assessed by the dynamics of the lesion area and psoriasis severity index (PASI), quality of life according to the DLQI questionnaire and the level of fasting plasma glucose, glycated hemoglobin, and body mass index. The results are presented as the weighted mean difference (WMD) and 95% confidence interval (CI).</p></sec><sec><title>RESULTS</title><p>RESULTS: The duration of liraglutide therapy ranged from 8 to 16 weeks. The liraglutide dose was titrated from 0.6 mg/day to 3.0 mg/day. Significant dynamics of the WMD indices PASI (-6.95 [95% CI -11.59; -2.32]) and DLQI (-6.95 [95% CI -11.59; -2.32]), as well as the body mass index (-2.97 [95% CI -3.58; -2.37]) were demonstrated during liraglutide therapy. No significant difference in glucose and glycated hemoglobin levels was found.</p></sec><sec><title>CONCLUSION</title><p>CONCLUSION: The results of the meta-analysis demonstrate that the use of liraglutide in combination therapy for psoriasis helps to reduce BMI, the prevalence and severity of psoriasis, and improve the quality of life of patients.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>псориаз</kwd><kwd>лираглутид</kwd><kwd>ожирение</kwd><kwd>метаанализ</kwd></kwd-group><kwd-group xml:lang="en"><kwd>psoriasis</kwd><kwd>liraglutide</kwd><kwd>obesity</kwd><kwd>metaanalysis</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Источники финансирования. Работа выполнена в рамках фундаментальной научной тематики ФГБНУ НИИР им. В.А. Насоновой №125020501435-8 «Эволюция аксиальных спондилоартритов на основе комплексного динамического изучения молекулярно-биологических, молекулярно-генетических, клинико-визуализационных факторов прогрессирования заболевания, качества жизни, коморбидности и таргетной инновационной терапии»</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">Armstrong AW, Harskamp CT, Armstrong EJ. The association between psoriasis and obesity: a systematic review and meta-analysis of observational studies. Nutr Diabetes. 2012;2(12):e54. doi: https://doi.org/10.1038/nutd.2012.26</mixed-citation><mixed-citation xml:lang="en">Armstrong AW, Harskamp CT, Armstrong EJ. The association between psoriasis and obesity: a systematic review and meta-analysis of observational studies. Nutr Diabetes. 2012;2(12):e54. doi: https://doi.org/10.1038/nutd.2012.26</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Neimann AL, Shin DB, Wang X, Margolis DJ, Troxel AB, Gelfand JM. Prevalence of cardiovascular risk factors in patients with psoriasis. J Am Acad Dermatol. 2006;55(5):829-835. doi: https://doi.org/10.1016/j.jaad.2006.08.040</mixed-citation><mixed-citation xml:lang="en">Neimann AL, Shin DB, Wang X, Margolis DJ, Troxel AB, Gelfand JM. Prevalence of cardiovascular risk factors in patients with psoriasis. J Am Acad Dermatol. 2006;55(5):829-835. doi: https://doi.org/10.1016/j.jaad.2006.08.040</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Snekvik I, Smith CH, Nilsen TIL, et al. Obesity, Waist Circumference, Weight Change, and Risk of Incident Psoriasis: Prospective Data from the HUNT Study. J Invest Dermatol. 2017;137(12):2484-2490. doi: https://doi.org/10.1016/j.jid.2017.07.822</mixed-citation><mixed-citation xml:lang="en">Snekvik I, Smith CH, Nilsen TIL, et al. Obesity, Waist Circumference, Weight Change, and Risk of Incident Psoriasis: Prospective Data from the HUNT Study. J Invest Dermatol. 2017;137(12):2484-2490. doi: https://doi.org/10.1016/j.jid.2017.07.822</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Dal Bello G, Gisondi P, Idolazzi L, Girolomoni G. Psoriatic Arthritis and Diabetes Mellitus: A Narrative Review. Rheumatol Ther. 2020;7(2):271-285. doi: https://doi.org/10.1007/s40744-020-00206-7</mixed-citation><mixed-citation xml:lang="en">Dal Bello G, Gisondi P, Idolazzi L, Girolomoni G. Psoriatic Arthritis and Diabetes Mellitus: A Narrative Review. Rheumatol Ther. 2020;7(2):271-285. doi: https://doi.org/10.1007/s40744-020-00206-7</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Eder L, Chandran V, Cook R, Gladman DD. The Risk of Developing Diabetes Mellitus in Patients with Psoriatic Arthritis: A Cohort Study. J Rheumatol. 2017;44(3):286-291. doi: https://doi.org/10.3899/jrheum.160861</mixed-citation><mixed-citation xml:lang="en">Eder L, Chandran V, Cook R, Gladman DD. The Risk of Developing Diabetes Mellitus in Patients with Psoriatic Arthritis: A Cohort Study. J Rheumatol. 2017;44(3):286-291. doi: https://doi.org/10.3899/jrheum.160861</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Takahashi H, Honma M, Ishida-Yamamoto A, Iizuka H. Adiponectin and leptin modulate cell proliferation and cytokine secretion of normal human keratinocytes and T lymphocytes. J Dermatol Sci. 2010;59(2):143-145. doi: https://doi.org/10.1016/j.jdermsci.2010.06.004</mixed-citation><mixed-citation xml:lang="en">Takahashi H, Honma M, Ishida-Yamamoto A, Iizuka H. Adiponectin and leptin modulate cell proliferation and cytokine secretion of normal human keratinocytes and T lymphocytes. J Dermatol Sci. 2010;59(2):143-145. doi: https://doi.org/10.1016/j.jdermsci.2010.06.004</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Xue K, Liu H, Jian Q, et al. Leptin induces secretion of pro-inflammatory cytokines by human keratinocytes in vitro--a possible reason for increased severity of psoriasis in patients with a high body mass index. Exp Dermatol. 2013;22(6):406-410. doi: https://doi.org/10.1111/exd.12162</mixed-citation><mixed-citation xml:lang="en">Xue K, Liu H, Jian Q, et al. Leptin induces secretion of pro-inflammatory cytokines by human keratinocytes in vitro--a possible reason for increased severity of psoriasis in patients with a high body mass index. Exp Dermatol. 2013;22(6):406-410. doi: https://doi.org/10.1111/exd.12162</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Dalamaga M, Papadavid E. Can we better strategize our choice of pharmacotherapy for patients with comorbid psoriasis and obesity?. Expert Opin Pharmacother. 2019;20(11):1303-1308. doi: https://doi.org/10.1080/14656566.2019.1603294</mixed-citation><mixed-citation xml:lang="en">Dalamaga M, Papadavid E. Can we better strategize our choice of pharmacotherapy for patients with comorbid psoriasis and obesity?. Expert Opin Pharmacother. 2019;20(11):1303-1308. doi: https://doi.org/10.1080/14656566.2019.1603294</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Gisondi P, Conti A, Galdo G, Piaserico S, De Simone C, Girolomoni G. Ustekinumab does not increase body mass index in patients with chronic plaque psoriasis: a prospective cohort study. Br J Dermatol. 2013;168(5):1124-1127. doi: https://doi.org/10.1111/bjd.12235</mixed-citation><mixed-citation xml:lang="en">Gisondi P, Conti A, Galdo G, Piaserico S, De Simone C, Girolomoni G. Ustekinumab does not increase body mass index in patients with chronic plaque psoriasis: a prospective cohort study. Br J Dermatol. 2013;168(5):1124-1127. doi: https://doi.org/10.1111/bjd.12235</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Chiricozzi A, Gisondi P, Girolomoni G. The pharmacological management of patients with comorbid psoriasis and obesity. Expert Opin Pharmacother. 2019;20(7):863-872. doi: https://doi.org/10.1080/14656566.2019.1583207</mixed-citation><mixed-citation xml:lang="en">Chiricozzi A, Gisondi P, Girolomoni G. The pharmacological management of patients with comorbid psoriasis and obesity. Expert Opin Pharmacother. 2019;20(7):863-872. doi: https://doi.org/10.1080/14656566.2019.1583207</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Di Minno MN, Peluso R, Iervolino S, et al. Weight loss and achievement of minimal disease activity in patients with psoriatic arthritis starting treatment with tumour necrosis factor α blockers. Ann Rheum Dis. 2014;73(6):1157-1162. doi: https://doi.org/10.1136/annrheumdis-2012-202812</mixed-citation><mixed-citation xml:lang="en">Di Minno MN, Peluso R, Iervolino S, et al. Weight loss and achievement of minimal disease activity in patients with psoriatic arthritis starting treatment with tumour necrosis factor α blockers. Ann Rheum Dis. 2014;73(6):1157-1162. doi: https://doi.org/10.1136/annrheumdis-2012-202812</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Klingberg E, Björkman S, Eliasson B, Larsson I, Bilberg A. Weight loss is associated with sustained improvement of disease activity and cardiovascular risk factors in patients with psoriatic arthritis and obesity: a prospective intervention study with two years of follow-up. Arthritis Res Ther. 2020;22(1):254. doi: https://doi.org/10.1186/s13075-020-02350-5</mixed-citation><mixed-citation xml:lang="en">Klingberg E, Björkman S, Eliasson B, Larsson I, Bilberg A. Weight loss is associated with sustained improvement of disease activity and cardiovascular risk factors in patients with psoriatic arthritis and obesity: a prospective intervention study with two years of follow-up. Arthritis Res Ther. 2020;22(1):254. doi: https://doi.org/10.1186/s13075-020-02350-5</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Maglio C, Peltonen M, Rudin A, Carlsson LMS. Bariatric surgery and the incidence of psoriasis and psoriatic arthritis in the Swedish obese subjects study. Obesity (Silver Spring). 2017;25(12):2068-2073. doi: https://doi.org/10.1002/oby.21955</mixed-citation><mixed-citation xml:lang="en">Maglio C, Peltonen M, Rudin A, Carlsson LMS. Bariatric surgery and the incidence of psoriasis and psoriatic arthritis in the Swedish obese subjects study. Obesity (Silver Spring). 2017;25(12):2068-2073. doi: https://doi.org/10.1002/oby.21955</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Egeberg A, Sørensen JA, Gislason GH, et al. Incidence and prognosis of psoriasis and psoriatic arthritis in patients undergoing bariatric surgery [published correction appears in JAMA Surg. 2018;153(7):692]. JAMA Surg. 2017;152(4):344-349. doi: https://doi.org/10.1001/jamasurg.2016.4610</mixed-citation><mixed-citation xml:lang="en">Egeberg A, Sørensen JA, Gislason GH, et al. Incidence and prognosis of psoriasis and psoriatic arthritis in patients undergoing bariatric surgery [published correction appears in JAMA Surg. 2018;153(7):692]. JAMA Surg. 2017;152(4):344-349. doi: https://doi.org/10.1001/jamasurg.2016.4610</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Насонов Е.Л., Паневин Т.С., Трошина Е.А. Агонисты рецепторов глюкагоноподобного пептида-1: перспективы применения в ревматологии. // Научно-практическая ревматология. — 2024. — Т.62. — №2. — С.135–144 doi: https://doi.org/10.47360/1995-4484-2024-135-144</mixed-citation><mixed-citation xml:lang="en">Nasonov EL, Panevin TS, Troshina EA. Glucagon-like peptide-1 receptor agonists: Prospects for use in rheumatology. Nauchno-Prakticheskaya Revmatologia = Rheumatology Science and Practice. 2024;62(2):135–144 (In Russ.) doi: https://doi.org/10.47360/1995-4484-2024-135-144</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Chang G, Chen B, Zhang L. Efficacy of GLP-1rA, liraglutide, in plaque psoriasis treatment with type 2 diabetes: a systematic review and meta-analysis of prospective cohort and before-after studies. J Dermatolog Treat. 2022;33(3):1299-1305. doi: https://doi.org/10.1080/09546634.2021.1882658</mixed-citation><mixed-citation xml:lang="en">Chang G, Chen B, Zhang L. Efficacy of GLP-1rA, liraglutide, in plaque psoriasis treatment with type 2 diabetes: a systematic review and meta-analysis of prospective cohort and before-after studies. J Dermatolog Treat. 2022;33(3):1299-1305. doi: https://doi.org/10.1080/09546634.2021.1882658</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Ahern T, Tobin AM, Corrigan M, et al. Glucagon-like peptide-1 analogue therapy for psoriasis patients with obesity and type 2 diabetes: a prospective cohort study. J Eur Acad Dermatol Venereol. 2013;27(11):1440-1443. doi: https://doi.org/10.1111/j.1468-3083.2012.04609.x</mixed-citation><mixed-citation xml:lang="en">Ahern T, Tobin AM, Corrigan M, et al. Glucagon-like peptide-1 analogue therapy for psoriasis patients with obesity and type 2 diabetes: a prospective cohort study. J Eur Acad Dermatol Venereol. 2013;27(11):1440-1443. doi: https://doi.org/10.1111/j.1468-3083.2012.04609.x</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Buysschaert M, Baeck M, Preumont V, et al. Improvement of psoriasis during glucagon-like peptide-1 analogue therapy in type 2 diabetes is associated with decreasing dermal γδ T-cell number: a prospective case-series study. Br J Dermatol. 2014;171(1):155-161. doi: https://doi.org/10.1111/bjd.12886</mixed-citation><mixed-citation xml:lang="en">Buysschaert M, Baeck M, Preumont V, et al. Improvement of psoriasis during glucagon-like peptide-1 analogue therapy in type 2 diabetes is associated with decreasing dermal γδ T-cell number: a prospective case-series study. Br J Dermatol. 2014;171(1):155-161. doi: https://doi.org/10.1111/bjd.12886</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Faurschou A, Gyldenløve M, Rohde U, et al. Lack of effect of the glucagon-like peptide-1 receptor agonist liraglutide on psoriasis in glucose-tolerant patients--a randomized placebo-controlled trial. J Eur Acad Dermatol Venereol. 2015;29(3):555-559. doi: https://doi.org/10.1111/jdv.12629</mixed-citation><mixed-citation xml:lang="en">Faurschou A, Gyldenløve M, Rohde U, et al. Lack of effect of the glucagon-like peptide-1 receptor agonist liraglutide on psoriasis in glucose-tolerant patients--a randomized placebo-controlled trial. J Eur Acad Dermatol Venereol. 2015;29(3):555-559. doi: https://doi.org/10.1111/jdv.12629</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Xu X, Lin L, Chen P, et al. Treatment with liraglutide, a glucagon-like peptide-1 analogue, improves effectively the skin lesions of psoriasis patients with type 2 diabetes: A prospective cohort study. Diabetes Res Clin Pract. 2019;150:167-173. doi: https://doi.org/10.1016/j.diabres.2019.03.002</mixed-citation><mixed-citation xml:lang="en">Xu X, Lin L, Chen P, et al. Treatment with liraglutide, a glucagon-like peptide-1 analogue, improves effectively the skin lesions of psoriasis patients with type 2 diabetes: A prospective cohort study. Diabetes Res Clin Pract. 2019;150:167-173. doi: https://doi.org/10.1016/j.diabres.2019.03.002</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Nicolau J, Nadal A, Sanchís P, Pujol A, Nadal C, Masmiquel L. Effects of liraglutide among patients living with psoriasis and obesity. Med Clin (Barc). 2023;161(7):293-296. doi: https://doi.org/10.1016/j.medcli.2023.05.021</mixed-citation><mixed-citation xml:lang="en">Nicolau J, Nadal A, Sanchís P, Pujol A, Nadal C, Masmiquel L. Effects of liraglutide among patients living with psoriasis and obesity. Med Clin (Barc). 2023;161(7):293-296. doi: https://doi.org/10.1016/j.medcli.2023.05.021</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Mehdi SF, Pusapati S, Anwar MS, et al. Glucagon-like peptide-1: a multi-faceted anti-inflammatory agent. Front Immunol. 2023;14:1148209. doi: https://doi.org/10.3389/fimmu.2023.1148209</mixed-citation><mixed-citation xml:lang="en">Mehdi SF, Pusapati S, Anwar MS, et al. Glucagon-like peptide-1: a multi-faceted anti-inflammatory agent. Front Immunol. 2023;14:1148209. doi: https://doi.org/10.3389/fimmu.2023.1148209</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Kim W, Egan JM. The role of incretins in glucose homeostasis and diabetes treatment. Pharmacol Rev. 2008;60(4):470-512. doi: https://doi.org/10.1124/pr.108.000604</mixed-citation><mixed-citation xml:lang="en">Kim W, Egan JM. The role of incretins in glucose homeostasis and diabetes treatment. Pharmacol Rev. 2008;60(4):470-512. doi: https://doi.org/10.1124/pr.108.000604</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Faurschou A, Pedersen J, Gyldenløve M, et al. Increased expression of glucagon-like peptide-1 receptors in psoriasis plaques. Exp Dermatol. 2013;22(2):150-152. doi: https://doi.org/10.1111/exd.12081</mixed-citation><mixed-citation xml:lang="en">Faurschou A, Pedersen J, Gyldenløve M, et al. Increased expression of glucagon-like peptide-1 receptors in psoriasis plaques. Exp Dermatol. 2013;22(2):150-152. doi: https://doi.org/10.1111/exd.12081</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Costanzo G, Curatolo S, Busà B, Belfiore A, Gullo D. Two birds one stone: semaglutide is highly effective against severe psoriasis in a type 2 diabetic patient. Endocrinol Diabetes Metab Case. doi: https://doi.org/10.1530/EDM-21-0007</mixed-citation><mixed-citation xml:lang="en">Costanzo G, Curatolo S, Busà B, Belfiore A, Gullo D. Two birds one stone: semaglutide is highly effective against severe psoriasis in a type 2 diabetic patient. Endocrinol Diabetes Metab Case. doi: https://doi.org/10.1530/EDM-21-0007</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Malavazos AE, Meregalli C, Sorrentino F, et al. Semaglutide therapy decreases epicardial fat inflammation and improves psoriasis severity in patients affected by abdominal obesity and type-2 diabetes. Endocrinol Diabetes Metab Case Rep. 2023;2023(3):23-0017. doi: https://doi.org/10.1530/EDM-23-0017</mixed-citation><mixed-citation xml:lang="en">Malavazos AE, Meregalli C, Sorrentino F, et al. Semaglutide therapy decreases epicardial fat inflammation and improves psoriasis severity in patients affected by abdominal obesity and type-2 diabetes. Endocrinol Diabetes Metab Case Rep. 2023;2023(3):23-0017. doi: https://doi.org/10.1530/EDM-23-0017</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>
