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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">medsovet</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинский Совет</journal-title><trans-title-group xml:lang="en"><trans-title>Meditsinskiy sovet = Medical Council</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2079-701X</issn><issn pub-type="epub">2658-5790</issn><publisher><publisher-name>REMEDIUM GROUP Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21518/ms2023-310</article-id><article-id custom-type="elpub" pub-id-type="custom">medsovet-7806</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>КОМОРБИДНЫЙ ПАЦИЕНТ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>COMORBID PATIENT</subject></subj-group></article-categories><title-group><article-title>Мочевая кислота как предиктор развития неалкогольной жировой болезни печени у пациентов с артериальной гипертензией</article-title><trans-title-group xml:lang="en"><trans-title>Uric acid as a predictor of the development of non-alcoholic fatty liver disease in patients with arterial hypertension</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3306-0312</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Стаценко</surname><given-names>М. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Statsenko</surname><given-names>M. Е.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Cтаценко Михаил Евгеньевич - доктор медицинских наук, профессор, проректор по научной работе, заведующий кафедрой внутренних болезней.</p><p>400131, Волгоград, площадь Павших Борцов, д. 1</p></bio><bio xml:lang="en"><p>Mikhail Е. Statsenko - Dr. Sci. (Med.), Professor, Vice-Rector for Scientific Work, Head of the Department of Internal Diseases.</p><p>1, Pavshikh Bortsov Square, Volgograd, 400131</p></bio><email xlink:type="simple">mestatsenko@rambler.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/0000-0001-9016-3011</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Стрельцова</surname><given-names>А. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Streltsova</surname><given-names>A. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Стрельцова Анастасия Михайловна - кандидат медицинских наук, ассистент кафедры внутренних болезней.</p><p>400131, Волгоград, площадь Павших Борцов, д. 1</p></bio><bio xml:lang="en"><p>Anastasia М. Streltsova - Cand. Sci. (Med.), Assistant of the Department of Internal Diseases.</p><p>1, Pavshikh Bortsov Square, Volgograd, 400131</p></bio><email xlink:type="simple">nastyc03@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Волгоградский государственный медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Volgograd 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>21</day><month>10</month><year>2023</year></pub-date><volume>0</volume><issue>16</issue><fpage>101</fpage><lpage>107</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Стаценко М.Е., Стрельцова А.М., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Стаценко М.Е., Стрельцова А.М.</copyright-holder><copyright-holder xml:lang="en">Statsenko M.Е., Streltsova A.M.</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.med-sovet.pro/jour/article/view/7806">https://www.med-sovet.pro/jour/article/view/7806</self-uri><abstract><sec><title>Введение</title><p>Введение. В настоящее время повышение уровня мочевой кислоты (МК) рассматривается как независимый фактор риска развития неалкогольной жировой болезни печени. Оксидативный стресс, хроническое системное воспаление, инсулинорезистентность, характерные для неалкогольной жировой болезни печени (НАЖБП), могут представлять собой возможные механизмы связи между развитием гиперурикемии и НАЖБП.</p></sec><sec><title>Цель</title><p>Цель. Уточнить значение и характер связи между увеличением уровня концентрации мочевой кислоты и развитием НАЖБП, а также оценить связь МК и риска сердечно-сосудистых осложнений (ССО) у пациентов с артериальной гипертензией (АГ) и НАЖБП.</p></sec><sec><title>Материалы и методы</title><p>Материалы и методы. Проведено поперечное сравнительное исследование, в котором приняли участие 120 пациентов, в возрасте от 45 до 65 лет с АГ 1–2-й ст., 1–2-й стадии (с НАЖБП (FLI &gt; 60) и без нее). При осмотре осуществляли клиническое обследование: анализ данных анамнеза, антропометрия. Также анализировали липиды, мочевую кислоту в плазме крови. Результаты. В группе коморбидных пациентов было значимо больше больных с превышением референсных значений уровня МК в плазме крови (ОШ = 2,25: 95% ДИ 1,08–4,71). ROC-анализ показал, что при МК, равной 369,5 мкмоль/л, прогнозируется высокий риск развития НАЖБП. Индекс МК/Кр у пациентов с АГ и НАЖБП был статистически значимо выше, чем у пациентов контрольной группы. Увеличение индекса МК/Кр на 1 у.е. увеличивает шансы развития НАЖБП в 1,54 раза (95% ДИ: 1,11–2,13). Также рост концентрации уровня МК на 1 мкмоль/л повышают шансы увеличения 10-летнего риска ССО до 5,0% и более на 0,6%.</p></sec><sec><title>Выводы</title><p>Выводы. При МК, равной 369,5 мкмоль/л, прогнозируется высокий риск развития НАЖБП в изучаемой группе. Рост индекса МК/креатинин на 1 у.е. увеличивает шансы развития НАЖБП в 1,54 раза. Кроме того, увеличение концентрации МК в плазме крови на 1 мкмоль/л повышают шансы роста 10-летнего риска ССО до 5,0% и более на 0,6% у пациентов с АГ и НАЖБП.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Introduction</title><p>Introduction. Currently, increased uric acid (UA) levels are considered an independent risk factor for the development of non-alcoholic fatty liver disease. Oxidative stress, chronic systemic inflammation, and insulin resistance characteristic of non-alcoholic fatty liver disease (NAFLD) may represent possible mechanisms for the association between the development of hyperuricemia and NAFLD.</p></sec><sec><title>Aim</title><p>Aim. To clarify the meaning and nature of the relationship between an increase in the level of UA concentration and the development of NAFLD, as well as to evaluate the relationship between uric acid and the risk of cardiovascular complications in patients with hypertension and NAFLD.</p></sec><sec><title>Materials and methods</title><p>Materials and methods. A cross-sectional comparative study was conducted, which involved 120 patients aged from 45 to 65 with hypertension of 1–2 degrees, 1–2 stages (with and without NAFLD (FLI &gt; 60). During the examination, a clinical examination was carried out: analysis of anamnesis data, anthropometry. Lipids and uric acid in blood plasma were also analyzed.</p></sec><sec><title>Results</title><p>Results. In the group of comorbid patients, there were significantly more patients with excess of the reference values of UA levels in the blood plasma (OR = 2.25: 95% CI 1.08–4.71). ROC analysis showed that with an uric acid level of 369.5 µmol/l, a high risk of developing NAFLD is predicted. The UA/Cr index in patients with hypertension and NAFLD was statistically significantly higher than in patients in the control group. Increase in the MK/Kr index by 1 USD increases the chances of developing NAFLD by 1.54 times (95% CI: 1.11–2.13). Also, an increase in the concentration of sUA level by 1 µmol/l increases the chances of an increase in the 10-year risk of cardiovascular events to 5.0% or more by 0.6%.</p></sec><sec><title>Conclusions</title><p>Conclusions. With an uric acid level of 369.5 µmol/l, a high risk of developing NAFLD in the study group is predicted. Increase in UA/creatinine index by 1 USD increases the chances of developing NAFLD by 1.54 times. In addition, an increase in the concentration of sUA in the blood plasma by 1 µmol/l increases the chances of an increase in the 10-year risk of cardiovascular events to 5.0% or more by 0.6% in patients with hypertension and NAFLD.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>гиперурикемия</kwd><kwd>сердечно-сосудистый риск</kwd><kwd>FLI</kwd><kwd>индекс МК/креатинин</kwd><kwd>метаболический синдром</kwd></kwd-group><kwd-group xml:lang="en"><kwd>hyperuricemia</kwd><kwd>cardiovascular risk</kwd><kwd>FLI</kwd><kwd>UA/creatinine index</kwd><kwd>metabolic syndrome</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа была поддержана грантом молодых ученых ВолгГМУ, приказ 29-КО от 02.06.2020</funding-statement><funding-statement xml:lang="en">The work was supported by the VolSMU Young Scientist Grant, Order 29-KO of June 02, 2020</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">Jichitu A, Bungau S, Stanescu AMA, Vesca CM, Toma MM, Bustea C et al. 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