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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">medgen</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинская генетика</journal-title><trans-title-group xml:lang="en"><trans-title>Medical Genetics</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2073-7998</issn><publisher><publisher-name>Publishing House «Genius Media» LLC</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">medgen-1685</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>КРАТКИЕ СООБЩЕНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>BRIEF REPORT</subject></subj-group></article-categories><title-group><article-title>Исследование генетических и эпигенетических факторов развития остеопороза</article-title><trans-title-group xml:lang="en"><trans-title>The study of genetic and epigenetic factors in the development of osteoporosis</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>Ялаев</surname><given-names>Б. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Yalaev</surname><given-names>B. I.</given-names></name></name-alternatives><email xlink:type="simple">yalaev.bulat@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Хусаинова</surname><given-names>Р. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Khusainova</surname><given-names>R. I.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Институт биохимии и генетики - обособленное структурное подразделение ФГБНУ Уфимского федерального исследовательского центра Российской академии наук</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Institute of Biochemistry and Genetics of the Ufa Federal Research Centre RAS</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2020</year></pub-date><pub-date pub-type="epub"><day>26</day><month>11</month><year>2020</year></pub-date><volume>19</volume><issue>8</issue><fpage>65</fpage><lpage>66</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Ялаев Б.И., Хусаинова Р.И., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Ялаев Б.И., Хусаинова Р.И.</copyright-holder><copyright-holder xml:lang="en">Yalaev B.I., Khusainova R.I.</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.medgen-journal.ru/jour/article/view/1685">https://www.medgen-journal.ru/jour/article/view/1685</self-uri><abstract><p>Актуальным представляется комплексное исследование генетических и эпигенетических факторов и специфики их вклада в структуру патогенеза остеопороза. Обнаружена значимость полиморфных вариантов rs11540149, rs6854081, rs10098470, rs10793442, rs1054204 сайтов связывания микроРНК и rs3134069, rs3102734 и rs7844539 гена OPG в увеличении риска переломов и формировании низкого уровня минеральной плотности костной ткани.</p></abstract><trans-abstract xml:lang="en"><p>Osteoporosis is one of the most common multifactorial diseases, which is characterized by a high risk of fractures and microarchitectural disorders of bone tissue. The study of genetic and epigenetic factors of this disease and their contribution to pathogenesis is relevant. We found the significance of the polymorphic variants rs11540149, rs6854081, rs10098470, rs10793442, rs1054204, rs3134069, rs3102734 and rs7844539 in increasing the risk of fractures and forming a low level of bone mineral density.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>остеопороз</kwd><kwd>микроРНК</kwd><kwd>остеопротегерин</kwd><kwd>эпигенетика</kwd></kwd-group><kwd-group xml:lang="en"><kwd>osteoporosis</kwd><kwd>microRNA</kwd><kwd>osteoprotegerin</kwd><kwd>epigenetics</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
