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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">zdor</journal-id><journal-title-group><journal-title xml:lang="ru">Проблемы здоровья и экологии</journal-title><trans-title-group xml:lang="en"><trans-title>Health and Ecology Issues</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2220-0967</issn><issn pub-type="epub">2708-6011</issn><publisher><publisher-name>Gomel State Medical University</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.51523/2708-6011.2024-21-4-07</article-id><article-id custom-type="elpub" pub-id-type="custom">zdor-2764</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>КЛИНИЧЕСКАЯ МЕДИЦИНА</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL MEDICINE</subject></subj-group></article-categories><title-group><article-title>Уровень матриксной металлопротеиназы-3 и тканевого ингибитора матриксной металлопротеиназы-1 и металлопротеиназы-3 у пациентов с хронической болезнью почек в стадии С5 и у пациентов с грыжами передней брюшной стенки</article-title><trans-title-group xml:lang="en"><trans-title>Level of matrix metalloproteinase-3 and tissue inhibitor of matrix metalloproteinase-1 and -3 in patients with chronic kidney disease in stage C5 and in patients with anterior abdominal wall hernias</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8269-8075</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Берещенко</surname><given-names>В. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Bereshchenko</surname><given-names>V. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Берещенко Валентин Владимирович, к.м.н., доцент, заведующий кафедрой хирургических болезней № 3</p><p>г. Гомель</p></bio><bio xml:lang="en"><p>Valentin V. Bereshchenko, Candidate of Medical Sciences, Associate Professor, Head of the Department of Surgical Diseases No.3 </p><p>Gomel</p></bio><email xlink:type="simple">val_71@inbox.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/0000-0002-4668-6007</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лызиков</surname><given-names>А. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Nikolaevich</surname><given-names>L. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Лызиков Анатолий Николаевич, д.м.н., профессор, профессор кафедры хирургических болезней № 1 с курсом сердечно-сосудистой хирургии</p><p>г. Гомель</p></bio><bio xml:lang="en"><p>Anatoly N. Lyzikov, Doctor of Medical Sciences, Professor, Professor at the Department of Surgical Diseases No.1 with the course of cardiovascular surgery</p><p>Gomel</p></bio><email xlink:type="simple">Zed-lu@inbox.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Гомельский государственный медицинский университет</institution></aff><aff xml:lang="en"><institution>Gomel State Medical University</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>16</day><month>01</month><year>2025</year></pub-date><volume>21</volume><issue>4</issue><fpage>60</fpage><lpage>67</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Берещенко В.В., Лызиков А.Н., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Берещенко В.В., Лызиков А.Н.</copyright-holder><copyright-holder xml:lang="en">Bereshchenko V.V., Nikolaevich L.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://journal.gsmu.by/jour/article/view/2764">https://journal.gsmu.by/jour/article/view/2764</self-uri><abstract><sec><title>Цель исследования</title><p>Цель исследования. Определить уровни матриксной металлопротеиназы-3 (ММП-3), тканевого ингибитора матриксной металлопротеиназы-1 (ТИМП-1) и тканевого ингибитора матриксной металлопротеиназы-3 (ТИМП-3) в плазме пациентов с хронической болезнью почек (ХБП) в стадии С5 и у пациентов с грыжами передней брюшной стенки.</p></sec><sec><title>Материал и методы</title><p>Материал и методы. Объектом исследования явились пациенты в терминальной стадии хронической болезни почек и пациенты с первичными грыжами передней брюшной стенки. Концентрации ММП-3, ТИМП-1, ТИМП-3 определяли в плазме с помощью иммуноферментного анализа.</p></sec><sec><title>Результаты</title><p>Результаты. В плазме крови у пациентов с ХБП, находящихся на диализной заместительной терапии, отмечается статистически значимое повышение уровня ММП-3, медиана которой составила 185,77 нг/мл, при соотношении с пациентами других анализируемых групп – 45,09 нг/мл и 41,05 нг/мл (р˂ 0,001). Уровень ТИМП-1 (158,85 нг/мл) в плазме статистически был значимо выше у пациентов с ХБП в стадии С5, чем у пациентов с грыжами передней брюшной стенки – 33,16 нг/мл и группой сравнения – 73,46 нг/мл (р ˂ 0,001). В то же время уровень ТИМП-1 определялся также статистически значимо выше в группе сравнения, чем у пациентов с грыжами передней брюшной стенки (р˂0,001). Показатель медианы ТИМП-3 – 35726,43 пг/мл у пациентов с грыжами передней брюшной стенки и у пациентов с ХБП в стадии С5 – 35313,70 пг/мл был статистически значимо выше в сравнении с показателем в группе контроля – 17974,80 пг/мл (р ˂ 0,001).</p></sec><sec><title>Заключение</title><p>Заключение. Выявленные закономерности могут указывать на деструктивные воспалительные изменения и деградацию соединительной ткани у пациентов с ХБП, находящихся на диализной заместительной терапии.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Objectives</title><p>Objectives. To determine the level of matrix metalloproteinase-3 (MMP-3), tissue inhibitor of matrix metalloproteinase-1 (TIMP-1), and tissue inhibitor of matrix metalloproteinase-3 (TIMP-3) in the plasma of patients with chronic kidney disease (CKD) in stage C5, and in patients with anterior abdominal wall hernias.</p></sec><sec><title>Materials and methods</title><p>Materials and methods. The object of the study were patients in the terminal stage of chronic kidney disease and patients with primary anterior abdominal wall hernias. MMP-3, TIMP-1 and TIMP-3 concentrations were determined in plasma by enzyme immunoassay.</p></sec><sec><title>Results</title><p>Results. There was a statistically significant increase in the level of MMP-3, the median of which was 185,77 ng/ml, with the ratio with patients of other analysed groups – 45,09 ng/ml and 41,05 ng/ml (p˂0,001) in plasma of patients with CKD on dialysis replacement therapy. The plasma TIMP-1 level (158,85 ng/ml) was statistically significantly higher in patients with C5 stage CKD than in patients with anterior abdominal wall hernia – 33,16 ng/ml and comparison group – 73,46 ng/ml (p˂0.001). At the same time, the level of TIMP-1 was also statistically significantly higher in the comparison group than in patients with anterior abdominal wall hernias (p˂0,001). The median value of TIMP-3 – 35726,43 pg/ml in patients with anterior abdominal wall hernias and in patients with C5 stage CKD – 35313,70 pg/ml was statistically significantly higher in comparison with the control group – 17974,80 pg/ml (p˂0,001).</p></sec><sec><title>Conclusion</title><p>Conclusion. The obtained patterns may indicate pronounced inflammatory processes and connective tissue degradation in patients with chronic kidney disease undergoing dialysis replacement therapy.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>матриксная металлопротеиназа-3</kwd><kwd>тканевый ингибитор матриксной металлопротеиназы-1</kwd><kwd>тканевый ингибитор матриксной металлопротеиназы-3</kwd><kwd>хроническая болезнь почек</kwd><kwd>грыжи передней брюшной стенки</kwd></kwd-group><kwd-group xml:lang="en"><kwd>matrix metalloproteinase-3</kwd><kwd>tissue inhibitor of matrix metalloproteinase-1</kwd><kwd>tissue inhibitor of matrix metalloproteinase-3</kwd><kwd>chronic kidney disease</kwd><kwd>anterior abdominal wall hernia</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Исследование проведено в рамках выполнения НИОК(Т)Р «Разработать методы диагностики и патогенетического лечения хронических прогрессирующих заболеваний паренхиматозных органов и связанных с ними состояний, сопровождающихся нарушением процессов регенерации», номер госрегистрации 20190387 от 29.03.2019.</funding-statement><funding-statement xml:lang="en">The study was carried out within the Research, Development, Experimental and Technological Work “To develop methods for the diagnosis and pathogenetic treatment of chronic progressive diseases of the parenchymal organs and related conditions accompanied by a violation of the regeneration processes”, number of State registration 20190387 dated 03.29.2019.</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">Wan J, Zhang G, Li X, et al. 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