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   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors>
     <author>Ялаев, Б.И.</author>
     <author>Тюрин, А.В.</author>
     <author>Нурлыгаянов, Р.З.</author>
     <author>Хусаинова, Р.И.</author>
     <author></author>
     <author></author>
     <author></author>
     <author></author>
    </authors>
   </contributors>
   <titles>
    <title>РОЛЬ ПОЛИМОРФНЫХ ВАРИАНТОВ ГЕНА ОСТЕОПРОТЕГЕРИНА, РЕЦЕПТОРА ВИТАМИНА D И САЙТОВ СВЯЗЫВАНИЯ МИКРОРНК В РАЗВИТИИ ОСТЕОПОРОЗА</title>
   </titles>
   <dates>
    <year>2020</year>
    <pub-dates>
     <date>2021-01-28</date>
    </pub-dates>
   </dates>
   <doi>10.15643/faaigi-2020-19</doi>
   <abstract>Osteoporosis (OP) is one of the most common multifactorial diseases&#13;
among the elderly population, which is characterized by a high risk of fractures&#13;
and microarchitectural disorders of bone tissue. A comprehensive study of the&#13;
genetic and epigenetic factors of this disease and the specifics of their&#13;
contribution to the structure of OP pathogenesis is relevant [1-2]. The&#13;
development of OP depends on genetic factors that determine 80% of the&#13;
variability in the level of bone mineral density (BMD) and 25% of fractures [3].&#13;
We found an association of rs11540149, rs6854081, rs10098470, rs10793442,&#13;
rs1054204 of microRNA binding sites, rs3134069, rs3102734 and rs7844539 of&#13;
the OPG gene and rs1544410 of the VDR gene with the risk of fractures and the&#13;
formation of low BMD. These data indicate differences in the pathogenesis of&#13;
OP related to sexual differences in the regulation of bone metabolism and the&#13;
different contribution of these loci to the risk of osteoporosis developing</abstract>
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     <url>https://repo.bashgmu.ru/publication/1259</url>
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    <pdf-urls>
     <url>https://repo.bashgmu.ru/files/1429</url>
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