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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 pub-id-type="doi">10.25557/2073-7998.2018.07.3-10</article-id><article-id custom-type="elpub" pub-id-type="custom">medgen-527</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>НАУЧНЫЕ ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEW</subject></subj-group></article-categories><title-group><article-title>ГЕНЕТИЧЕСКИЕ ОСНОВЫ ОСТЕОПОРОЗА</article-title><trans-title-group xml:lang="en"><trans-title>GENETIC BASIS 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>Миргалиева</surname><given-names>Р. Я.</given-names></name><name name-style="western" xml:lang="en"><surname>Mirgaliyeva</surname><given-names>R. Ya.</given-names></name></name-alternatives><email xlink:type="simple">reginchik55@rambler.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>Хуснутдинова</surname><given-names>Э. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Khusnutdinova</surname><given-names>E. K.</given-names></name></name-alternatives><email xlink:type="simple">reginchik55@rambler.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Хусайнова</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">reginchik55@rambler.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Институт биохимии и генетики — обособленное структурное подразделение Федерального государственного бюджетного научного учреждения Уфимского федерального исследовательского центра Российской академии наук; ГБУЗ Республиканский медико-генетический центр</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Institute of Biochemistry and Genetics — Subdivision of the  Ufa Federal Research Centre of the  Russian Academy of Sciences; Republican Medical Genetic Center</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Институт биохимии и генетики — обособленное структурное подразделение Федерального государственного бюджетного научного учреждения Уфимского федерального исследовательского центра Российской академии наук</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Institute of Biochemistry and Genetics — Subdivision of the  Ufa Federal Research Centre of the  Russian Academy of Sciences</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>08</day><month>10</month><year>2018</year></pub-date><volume>17</volume><issue>7</issue><fpage>3</fpage><lpage>10</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Миргалиева Р.Я., Хуснутдинова Э.К., Хусайнова Р.И., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Миргалиева Р.Я., Хуснутдинова Э.К., Хусайнова Р.И.</copyright-holder><copyright-holder xml:lang="en">Mirgaliyeva R.Y., Khusnutdinova E.K., 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/527">https://www.medgen-journal.ru/jour/article/view/527</self-uri><abstract><p>Остеопороз (ОП) является одним из наиболее распространенных метаболических заболеваний скелета и одной из ведущих причин инвалидности и сокращения продолжительности жизни людей пожилого возраста, что делает его одной из важнейших проблем здравоохранения во всем мире. ОП — многофакторное заболевание, в развитии которого играют роль как генетические, так и средовые факторы риска. В настоящее время наблюдается значительный прогресс в изучении молекулярного патогенеза заболевания, однако исследования генетических основ ОП далеки от завершения. Знание эпидемиологии и понимание патогенеза ОП необходимы для разработки эффективных методов пресимптоматической диагностики, лечения и профилактики заболевания. Обзор посвящен систематизации результатов исследований генетических аспектов ОП и современным тенденциям дальнейшего изучения проблемы.</p></abstract><trans-abstract xml:lang="en"><p>Osteoporosis (OP) is one of the most common metabolic diseases of the skeleton, the frequency of which rises with age. OP is one of the leading causes of disability and a reduction in life expectancy in the elderly, thereby dealing with one of the most important public health problems around the world. A major role in the development of OP play both gender and genetic factors, there are gender and regional differences in the prevalence of the disease. Currently, there has been significant progress in detecting  the molecular pathogenesis of the disease, but studies of the genetic basis of OP are far from completion and there are many issues, which need further study. Understanding the epidemiology and pathogenesis of osteoporosis is necessary for the development of effective methods of presymptomatic diagnostics, treatment and prevention of diseases. The review is devoted to the systematization of the results of studies  on the genetic  aspects of OP and current trends  in further study of the problem.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>остеопороз</kwd><kwd>остеопоретические переломы</kwd><kwd>МПКТ</kwd><kwd>GWAS</kwd><kwd>RANK-RANKL-OPG</kwd><kwd>ПТГ</kwd></kwd-group><kwd-group xml:lang="en"><kwd>osteoporosis</kwd><kwd>osteoporotic fractures</kwd><kwd>BMD</kwd><kwd>GWAS</kwd><kwd>RANK-RANKL-OPG</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">NIH. Osteoporosis. National Institutes of Health Consensus Development Conference Statement. National Institutes of Health Consensus Development Conference Consensus Statement. 1984;5(3):1-6.</mixed-citation><mixed-citation xml:lang="en">NIH. Osteoporosis. National Institutes of Health Consensus Development Conference Statement. 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