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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/omet12843</article-id><article-id custom-type="elpub" pub-id-type="custom">ometendo-12843</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>Ассоциация носительства полиморфизма rs4646994 гена АСЕ с ожирением и андрогенным дефицитом у мужчин</article-title><trans-title-group xml:lang="en"><trans-title>Association of сarriage of the rs4646994 polymorphism of the ACE gene with obesity and androgen deficiency in men</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8968-3968</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Мосалев</surname><given-names>К. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Mosalev</surname><given-names>K. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Мосалев Кирилл Игоревич, клинический ординатор</p><p>630117, Новосибирск, ул. Тимакова, д. 2 </p><p>eLibrary SPIN: 7500-8330</p></bio><bio xml:lang="en"><p>Kirill I. Mosalev</p><p>2 Timakova street, 630117 Novosibirsk</p><p>eLibrary SPIN: 7500-8330</p></bio><email xlink:type="simple">mosalevkir@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/0000-0001-8486-3185</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Янковская</surname><given-names>С. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Yankovskaya</surname><given-names>S. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Янковская Светлана Валерьевна, аспирант</p><p>Новосибирск</p><p>eLibrary SPIN: 6478-6922</p></bio><bio xml:lang="en"><p>Svetlana V. Yankovskaya</p><p>Novosibirsk</p><p>eLibrary SPIN: 6478-6922</p></bio><email xlink:type="simple">svetlanaiankovskaia@gmail.com</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4942-1987</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Иванов</surname><given-names>И. Д.</given-names></name><name name-style="western" xml:lang="en"><surname>Ivanov</surname><given-names>I. D.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Иванов Игорь Диадорович, кандидат биологических наук</p><p>Новосибирск</p><p>eLibrary SPIN: 2427-3279;</p><p>Scopus Author ID: 125626</p></bio><bio xml:lang="en"><p>Igor D. Ivanov, PhD in biology</p><p>Novosibirsk</p><p>eLibrary SPIN: 2427-3279;</p><p>Scopus Author ID: 125626</p></bio><email xlink:type="simple">diadoryh@mail.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/0000-0002-4579-425X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Пинхасов</surname><given-names>Б. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Pinkhasov</surname><given-names>B. B.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Пинхасов Борис Борисович, доктор медицинских наук </p><p>Новосибирск</p><p>eLibrary SPIN: 4848-4370</p></bio><bio xml:lang="en"><p>Boris B. Pinkhasov, MD, PhD</p><p>Novosibirsk</p><p>eLibrary SPIN: 4848-4370</p></bio><email xlink:type="simple">pin@centercem.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/0000-0003-4534-7289</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Селятицкая</surname><given-names>В. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Selyatitskaya</surname><given-names>V. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Селятицкая Вера Георгиевна, доктор биологических наук, профессор </p><p>Новосибирск</p><p>Researcher ID: ААМ-4242-2021;</p><p>Scopus Author ID: 6602668364;</p><p>eLibrary SPIN: 9992-0023</p></bio><bio xml:lang="en"><p>Vera G. Selyatitskaya, PhD in biology, Professor</p><p>Novosibirsk</p><p>Researcher ID: ААМ-4242-2021;</p><p>Scopus Author ID: 6602668364;</p><p>eLibrary SPIN: 9992-0023</p></bio><email xlink:type="simple">ccem@centercem.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Федеральный исследовательский центр фундаментальной и трансляционной медицины;&#13;
Новосибирский государственный университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Federal Research Center for Fundamental and Translational Medicine;&#13;
Novosibirsk State University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Федеральный исследовательский центр фундаментальной и трансляционной медицины</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Federal Research Center for Fundamental and Translational Medicine</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>28</day><month>10</month><year>2022</year></pub-date><volume>19</volume><issue>3</issue><fpage>271</fpage><lpage>279</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Мосалев К.И., Янковская С.В., Иванов И.Д., Пинхасов Б.Б., Селятицкая В.Г., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Мосалев К.И., Янковская С.В., Иванов И.Д., Пинхасов Б.Б., Селятицкая В.Г.</copyright-holder><copyright-holder xml:lang="en">Mosalev K.I., Yankovskaya S.V., Ivanov I.D., Pinkhasov B.B., Selyatitskaya V.G.</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/12843">https://www.omet-endojournals.ru/jour/article/view/12843</self-uri><abstract><sec><title>Обоснование</title><p>Обоснование. Ожирение и андрогенный дефицит (АнД) характеризуются схожими нарушениями параметров метаболизма, наличием признаков инсулинорезистентности, метаболического синдрома, риском развития сердечнососудистых заболеваний (ССЗ) и сосудистых осложнений. Эти факты указывают на возможность наличия общих механизмов, определяющих предрасположенность к развитию ожирения и АнД, к которым могут относиться генетические факторы, в частности, полиморфизм rs4646994 гена ACE, который, по последним данным, ассоциирован с риском развития ССЗ, гипертонической болезни и ожирения.</p></sec><sec><title>Цель</title><p>Цель. Изучить ассоциацию носительства полиморфных вариантов локуса rs4646994 гена АСЕ с особенностями антропометрического и андрогенного статусов у мужчин.</p></sec><sec><title>Материалы и методы</title><p>Материалы и методы. В период с апреля 2020 по октябрь 2021 г. были обследованы пациенты мужского пола в возрасте 18–75 лет, планово госпитализированные в терапевтический стационар с коморбидной соматической патологией (гипертоническая болезнь, ишемическая болезнь сердца, дорсопатия, вегетососудистая дистония, гастроэзофагеальная рефлюксная болезнь, другая соматическая патология). Были проведены антропометрия, исследование содержания гормонов репродуктивной системы в сыворотке крови с использованием иммуноферментного анализа, а также генетическое исследование на предмет носительства полиморфных вариантов локуса rs4646994 гена АСЕ методом полимеразной цепной реакции (ПЦР) с последующим электрофорезом продуктов ПЦР. Результаты. В исследовании приняло участие 82 пациента. По результатам генетического анализа в группу гомозигот по дикому типу (I/I, Г1) были отнесены 17 человек, в группу гетерозигот (I/D, Г2) — 41 человек, в группу гомозигот по мутантному аллелю (D/D, Г3) — 24 человека. Показатели массы тела, окружностей груди, талии и бедер, величина индекса массы тела у пациентов — носителей аллеля D полиморфизма rs4646994 были статистически значимо выше, чем у гомозигот I/I. Статистически значимыми оказались и различия в гормональном статусе: пациенты из Г1 по сравнению с Г2 и Г3 имели более высокий уровень общего тестостерона; из Г1 по сравнению с Г3 — более высокий уровень свободного тестостерона.</p></sec><sec><title>Заключение</title><p>Заключение. Выявлена ассоциация носительства аллеля D полиморфного локуса rs4646994 гена АСЕ с избыточной массой тела и АнД.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>BACKGROUND</title><p>BACKGROUND: Obesity and androgen deficiency (AnD) are characterized by similar disturbances in metabolic parameters, the presence of signs of insulin resistance, metabolic syndrome, the risk of developing cardiovascular diseases (CVD) and vascular complications. These facts indicate the possibility of the presence of common mechanisms that determine the predisposition to the development of obesity and AnD, which may include genetic factors, in particular, the rs4646994 polymorphism of the ACE gene, which, according to recent data, is associated with the risk of developing CVD, hypertension, and obesity.</p></sec><sec><title>AIM</title><p>AIM: To study the association of the carriage of polymorphic variants of the rs4646994 locus of the ACE gene with the features of anthropometric and androgenic status in men.</p></sec><sec><title>MATERIALS AND METHODS</title><p>MATERIALS AND METHODS: In the period from April 2020 to October 2021 there were observed male patients aged 18–75 years old, who were hospitalized in a therapeutic hospital because of comorbid somatic pathology (hypertension, coronary heart disease, dorsopathy, vegetative-vascular dystonia, gastroesophageal reflux disease, and others). Anthropometry, a study of the content of hormones of the reproductive system in the blood serum using enzyme-linked immunosorbent assay (ELISA), as well as a genetic study for the carriage of polymorphic variants of the rs4646994 locus of the ACE gene by the polymerase chain reaction (PCR) method, followed by electrophoresis of PCR products, were carried out. </p></sec><sec><title>RESULTS</title><p>RESULTS: 82 patients took part in research. According to the results of genetic analysis, 17 people were assigned to the group of homozygotes for the wild type (I/I, G1), 41 people were assigned to the group of heterozygotes (I/D, G2), and 41 people were assigned to the group of homozygotes for the mutant allele (D/D, G3) 24 people. Body weight, chest circumference, waist and hips, body mass index in patients carrying the D allele of the rs4646994 polymorphism were statistically significantly higher than in I/I homozygotes. Differences in hormonal status also turned out to be statistically significant: patients from G1 compared with G2 and G3 had higher levels of total testosterone; from G1 compared to G3 — a higher level of free testosterone.</p></sec><sec><title>CONCLUSION</title><p>CONCLUSION: An association of the carriage of the D allele of the rs4646994 polymorphic locus of the ACE gene with overweight and ADI was revealed.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>ожирение</kwd><kwd>андрогенный дефицит</kwd><kwd>полиморфизм rs4646994 гена АСЕ</kwd></kwd-group><kwd-group xml:lang="en"><kwd>оbesity</kwd><kwd>androgen deficiency</kwd><kwd>polymorphism rs4646994 of the ACE gene</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа выполнена с использованием оборудования ЦКП «Протеомный анализ», поддержанного финансированием Минобрнауки России (соглашение № 075-15-2021-691)</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">Nyberg ST, Batty GD, Pentti J, et al. 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