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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">avk</journal-id><journal-title-group><journal-title xml:lang="ru">Архивъ внутренней медицины</journal-title><trans-title-group xml:lang="en"><trans-title>The Russian Archives of Internal Medicine</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2226-6704</issn><issn pub-type="epub">2411-6564</issn><publisher><publisher-name>“SINAPS” LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.20514/2226-6704-2023-13-3-213-223</article-id><article-id custom-type="edn" pub-id-type="custom">PKZRCJ</article-id><article-id custom-type="elpub" pub-id-type="custom">avk-1616</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 ARTICLE</subject></subj-group></article-categories><title-group><article-title>АНАЛИЗ БИОМАРКЕРОВ ВОСПАЛЕНИЯ В КОНДЕНСАТЕ ВЫДЫХАЕМОГО ВОЗДУХА У ПАЦИЕНТОВ С ХОБЛ В СОЧЕТАНИИ С ОБЛИТЕРИРУЮЩИМ АТЕРОСКЛЕРОЗОМ АРТЕРИЙ НИЖНИХ КОНЕЧНОСТЕЙ</article-title><trans-title-group xml:lang="en"><trans-title>Analysis of Inflammation Biomarkers in Exhaled Breath Condensate in Patients with COPD Combined with Peripheral Arterial Disease</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Котляров</surname><given-names>С. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Kotlyarov</surname><given-names>S. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Рязань</p></bio><bio xml:lang="en"><p>Ryazan </p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сучков</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Suchkov</surname><given-names>I. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Рязань</p></bio><bio xml:lang="en"><p>Ryazan </p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Урясьев</surname><given-names>О. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Uryasev</surname><given-names>O. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Рязань</p></bio><bio xml:lang="en"><p>Ryazan </p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Котлярова</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kotlyarova</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Рязань</p></bio><bio xml:lang="en"><p>Ryazan </p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Рязанский государственный медицинский университет им. акад. И.П. Павлова</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Ryazan State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2023</year></pub-date><pub-date pub-type="epub"><day>07</day><month>06</month><year>2023</year></pub-date><volume>13</volume><issue>3</issue><fpage>213</fpage><lpage>223</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Котляров С.Н., Сучков И.А., Урясьев О.М., Котлярова А.А., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Котляров С.Н., Сучков И.А., Урясьев О.М., Котлярова А.А.</copyright-holder><copyright-holder xml:lang="en">Kotlyarov S.N., Suchkov I.A., Uryasev O.M., Kotlyarova A.A.</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.medarhive.ru/jour/article/view/1616">https://www.medarhive.ru/jour/article/view/1616</self-uri><abstract><p>Актуальность. Хроническая обструктивная болезнь легких (ХОБЛ) является одной из наиболее значимых респираторных патологий, что связано с ее высокой распространенностью и влиянием на прогноз. Частота обострений и коморбидность — важные факторы, влияющие на течение ХОБЛ. Считается, что локальное и системное воспаление могут лежать в основе гетерогенного течения ХОБЛ. В этой связи оценка активности локального воспаления в дыхательных путях может быть полезна для оценки течения ХОБЛ. Цель. Изучить молекулярные механизмы ХОБЛ и оценить биомаркеры воспаления в конденсате выдыхаемого воздуха у пациентов с ХОБЛ с частыми обострениями в сочетании с периферическим атеросклерозом. Материалы и методы. Проведен биоинформационный анализ данных из Gene Expression Omnibus (GEO) с целью изучения генной онтологии дифференциально экспрессируемых генов при ХОБЛ. Далее проведено исследование провоспалительных цитокинов интерлейкина — 1 бета (interleukin (IL)-1β) и фактора некроза опухоли альфа (tumor necrosis factor alpha (TNFα)) в конденсате выдыхаемого воздуха (КВВ) у пациентов с ХОБЛ с частыми обострениями без сопутствующих атеросклеротических сердечно-сосудистых заболеваний (АССЗ) и у пациентов с ХОБЛ с частыми обострениями и облитерирующим атеросклерозом артерий нижних конечностей (ОААНК) в сравнении со здоровым контролем. Результаты. Дифференциально экспрессируемые гены вовлечены в биологические процессы и сигнальные пути по Киотской энциклопедии генов и геномов (Kyoto Encyclopedia of Genes and Genomes, KEGG пути), связанные с иммунным ответом, которые могут связывать развитие и прогрессирование ХОБЛ и атеросклероза. У пациентов с ХОБЛ в сочетании с атеросклерозом наблюдались более высокие значения IL-1β и TNFα в КВВ, по сравнению с контролем (p &lt;0,001). У пациентов с ХОБЛ с частыми обострениями и ОААНК были обнаружены наиболее высокие уровни IL-1β и TNFα в КВВ в сравнении с пациентами без АССЗ (р=0,0038 и p=0,0005 соответственно). Вывод. У пациентов с ХОБЛ с частыми обострениями и ОААНК повышены уровни TNFα и IL1β в КВВ, что может свидетельствовать о наличии локального воспаления в дыхательных путях, выраженность которого связана с клиническим течением ХОБЛ. </p></abstract><trans-abstract xml:lang="en"><p>Background. Chronic obstructive pulmonary disease (COPD) is one of the most signiﬁcant diseases due to its high prevalence and impact on prog- nosis. The frequency of exacerbations and comorbidity are important factors inﬂuencing the course of COPD. It is believed that local and systemic inﬂammation may underlie this heterogeneous course of COPD. In this regard, assessment of local inﬂammation activity in the respiratory tract may be useful to assess the course of COPD. Aim. To study molecular mechanisms of COPD and assess inﬂammation biomarkers in the exhaled breath condensate (EBC) in patients with COPD with the phenotype of frequent exacerbations combined with peripheral atherosclerosis. Materials and Methods. Bioinformatic analysis of data from Gene Expression Omnibus (GEO) was performed to examine gene ontology of differentially expressed genes in COPD. Proinﬂammatory cytokines interleukin-1 beta (IL-1β) and tumor necrosis factor alpha (TNFα) in EBC in COPD patients without concomitant atherosclerotic cardiovascular disease (ASCVD) in the stable course phase, in patients with COPD with the phenotype of frequent ex- acerbations and peripheral artery disease (PAD) compared with healthy controls were examined. Results. Differentially expressed genes are involved in biological processes and signaling pathways according to the Kyoto Encyclopedia of Genes and Genomes (KEGG pathway) associated with the immune response that may link the development and progression of COPD and atherosclerosis. Patients with COPD combined with atherosclerosis had higher values of IL-1β and TNFα in EBC compared with controls (p &lt;0.001). COPD patients with frequent exacerbations and PAD had the highest levels of IL-1β and TNFα in EBC compared with patients without ASCVD (p=0.0038 and p=0.0005, respectively). Conclusion. TNFα and IL1-β levels in EBC are elevated in COPD patients with frequent exacerbations and PAD, which may indicate the presence of local inﬂammation in the airways, the severity of which is associated with the clinical course of COPD.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>ХОБЛ</kwd><kwd>воспаление</kwd><kwd>конденсат выдыхаемого воздуха</kwd><kwd>иммунная система</kwd><kwd>цитокины</kwd></kwd-group><kwd-group xml:lang="en"><kwd>COPD</kwd><kwd>inflammation</kwd><kwd>exhaled breath condensate</kwd><kwd>immune system</kwd><kwd>cytokines</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">Aursulesei Onofrei V., Ceasovschih A., Marcu DTM. et al. 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