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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">diaendo</journal-id><journal-title-group><journal-title xml:lang="ru">Сахарный диабет</journal-title><trans-title-group xml:lang="en"><trans-title>Diabetes mellitus</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2072-0351</issn><issn pub-type="epub">2072-0378</issn><publisher><publisher-name>Endocrinology research centre</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14341/DM13088</article-id><article-id custom-type="elpub" pub-id-type="custom">diaendo-13088</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>Эндотелиальная дисфункция у лиц с ожирением при наличии и отсутствии сахарного диабета 2 типа: оценка специфических маркеров</article-title><trans-title-group xml:lang="en"><trans-title>Endothelial dysfunction in patients with obesity and type 2 diabetes mellitus or normoglycemia: assessment of specific markers</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5268-430X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Покровская</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Pokrovskaya</surname><given-names>E. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Покровская Елена Владиславовна – научный сотрудник.</p><p>117036, Москва, ул. Дм. Ульянова, д. 11</p></bio><bio xml:lang="en"><p>Elena V. Pokrovskaya - research associate.</p><p>11 Dm. Ulyanova street, 117036 Moscow</p></bio><email xlink:type="simple">pokrovskaya.93@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/0000-0001-6612-6851</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шестакова</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Shestakova</surname><given-names>E. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Шестакова Екатерина Алексеевна - доктор медицинских наук, ведущий научный сотрудник.</p><p>Москва</p></bio><bio xml:lang="en"><p>Ekaterina A. Shestakova - MD, PhD, leading research associate.</p><p>Moscow</p></bio><email xlink:type="simple">katiashestakova@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/0000-0002-5057-127X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шестакова</surname><given-names>М. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Shestakova</surname><given-names>M. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Шестакова Марина Владимировна – доктор медицинских наук, профессор, академик РАН.</p><p>Москва</p></bio><bio xml:lang="en"><p>Marina V. Shestakova - MD, PhD, Professor.</p><p>Moscow</p></bio><email xlink:type="simple">nephro@endocrincentr.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ГНЦ РФ ФГБУ «Национальный медицинский исследовательский центр эндокринологии»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Endocrinology Research Centre</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>10</month><year>2023</year></pub-date><volume>26</volume><issue>5</issue><fpage>439</fpage><lpage>445</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Покровская Е.В., Шестакова Е.А., Шестакова М.В., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Покровская Е.В., Шестакова Е.А., Шестакова М.В.</copyright-holder><copyright-holder xml:lang="en">Pokrovskaya E.V., Shestakova E.A., Shestakova M.V.</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.dia-endojournals.ru/jour/article/view/13088">https://www.dia-endojournals.ru/jour/article/view/13088</self-uri><abstract><sec><title>ОБОСНОВАНИЕ</title><p>ОБОСНОВАНИЕ. Одной из важнейших функций эндотелия является поддержание гомеостаза организма человека. На сегодняшний день сформулирована концепция, согласно которой, эндотелиальная дисфункция является центральным звеном в патогенезе сердечно-сосудистых заболеваний (ССЗ). Наличие сахарного диабета (СД) значимо увеличивает риски ССЗ. Часто СД 2 типа (СД2) наблюдается при избыточной массе тела, однако существует популяция лиц с ожирением, у которых в течение длительного времени не развивается СД2.</p></sec><sec><title>ЦЕЛЬ</title><p>ЦЕЛЬ. Сравнить уровень маркеров эндотелиальной дисфункции в двух группах лиц c ожирением (без СД2 и с СД2), а также оценить влияние приема антидиабетических кардиопротективных препаратов (агонистов рецепторов глюкагоноподобного пептида 1 (арГПП-1) и ингибиторов натрий-глюкозного транспортера 2 (иНГЛТ-2)) на данные маркеры.</p></sec><sec><title>МАТЕРИАЛЫ И МЕТОДЫ</title><p>МАТЕРИАЛЫ И МЕТОДЫ. В данное исследование были включены 2 группы пациентов с ожирением, одна из которых не имела нарушений углеводного обмена, вторая страдала СД2. Оценивались маркеры эндотелиальной дисфункции: фактор фон Виллебранда, сосудистый эндотелиальный фактор роста А, растворимый Е-селектин (sE-selectin), растворимая молекула межклеточной адгезии-1.</p></sec><sec><title>РЕЗУЛЬТАТЫ</title><p>РЕЗУЛЬТАТЫ. Получено значимое повышение уровня sЕ-Selectin в группе пациентов с ожирением и СД2 по сравнению с лицами без нарушений углеводного обмена (46,65 [36,23; 66,66] vs 33,05 [22,1; 53,31] нг/мл). Различий по уровням маркеров эндотелиальной дисфункции в подгруппах пациентов с СД2 с уровнем гликированного гемоглобина &lt;8% и &gt;8% обнаружено не было. Также не отмечено влияние назначения кардиопротективных препаратов (иНГЛТ-2 и/или арГПП-1) на исследуемые показатели функции эндотелия у лиц с СД2, по результатам значимых корреляций маркеров эндотелиальной дисфункции не получено.</p></sec><sec><title>ЗАКЛЮЧЕНИЕ</title><p>ЗАКЛЮЧЕНИЕ. Мы предполагаем, что повышение уровня sE-selectin может являться ранним маркером эндотелиальной дисфункции у лиц с ожирением и СД2.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>BACKGROUND</title><p>BACKGROUND: One of the function of the endothelium is the maintenance of body's homeostasis. Endothelial dysfunction is known to be profoundly implicated in the pathogenesis of cardiovascular diseases (CVD). The presence of diabetes mellitus significantly increases the risks of CVD. Type 2 diabetes mellitus (T2DM) is often observed in obesity, however, there is a population of people with obesity, who do not develop T2DM for a long time.</p></sec><sec><title>AIM</title><p>AIM: To compare the level of markers of endothelial dysfunction in two groups of individuals (without T2DM and with T2DM), as well as to evaluate the impact of cardioprotective medication (GPP-1 and SGLT-2) on these markers.</p></sec><sec><title>MATERIALS AND METHODS</title><p>MATERIALS AND METHODS: We recruited 2 groups of patients with obesity into this study: the 1st group with no carbohydrate metabolism disorders, the 2nd with T2DM. Several markers of endothelial dysfunction were evaluated: human von Willebrand factor (VWF), vascular endothelial growth factor A (VEGF-A), soluble form E-selectin (sE-selectin), soluble intercellular adhesion molecule-1 (sICAM1).</p></sec><sec><title>RESULTS</title><p>RESULTS: A significant increase in sE-Selectin was seen in the group of patients with obesity and T2DM compared with those without carbohydrate metabolism disorders (46.65 [36.23; 66.66] vs 33.05 [22.1;53.31] ng/ml). There were no differences in the level of markers of endothelial dysfunction in the subgroups of patients with T2DM with HbA1c &lt; 8% and &gt;8%. There was also no effect of cardioprotective drugs (SGLT-2 and / or GPP-1) on any of endothelial dysfunction markers in individuals with T2DM.</p></sec><sec><title>CONCLUSION</title><p>CONCLUSION: We suggest that an increase in sE-selectin may be an early marker of endothelial dysfunction in obese individuals and T2DM.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>эндотелиальная дисфункция</kwd><kwd>сахарный диабет 2 типа</kwd><kwd>ожирение</kwd><kwd>метаболически здоровое ожирение</kwd><kwd>фактор фон Виллебранда (VWF)</kwd><kwd>сосудистый эндотелиальный фактор роста А (VEGF-A)</kwd><kwd>растворимый Е-селектин (sE-selectin)</kwd><kwd>растворимая молекула межклеточной адгезии-1 (sICAM1)</kwd></kwd-group><kwd-group xml:lang="en"><kwd>endothelial dysfunction</kwd><kwd>type 2 diabetes mellitus</kwd><kwd>obesity</kwd><kwd>metabolically healthy obesity</kwd><kwd>human von Willebrand factor (VWF)</kwd><kwd>vascular endothelial growth factor A (VEGF-A)</kwd><kwd>soluble form E-selectin (sE-selectin)</kwd><kwd>soluble intercellular adhesion molecule-1 (sICAM1)</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Исследование выполнено за счет гранта Российского научного фонда № 19-15-00361, https://rscf.ru/project/19-15-00361/.</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">Lin X, Li H. 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