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<article article-type="research-article" dtd-version="1.2" xml:lang="ru" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><front><journal-meta><journal-id journal-id-type="issn">2658-6533</journal-id><journal-title-group><journal-title>Research Results in Biomedicine</journal-title></journal-title-group><issn pub-type="epub">2658-6533</issn></journal-meta><article-meta><article-id pub-id-type="doi">10.18413/2658-6533-2022-8-1-0-6</article-id><article-id pub-id-type="publisher-id">2670</article-id><article-categories><subj-group subj-group-type="heading"><subject>Medicine (miscellaneous)</subject></subj-group></article-categories><title-group><article-title>&lt;strong&gt;Association of N-terminal telopeptide-1 with BMD in patients with osteopenia and osteoporosis&lt;/strong&gt;</article-title><trans-title-group xml:lang="en"><trans-title>&lt;strong&gt;Association of N-terminal telopeptide-1 with BMD in patients with osteopenia and osteoporosis&lt;/strong&gt;</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>P.</surname><given-names>Modagan</given-names></name><name xml:lang="en"><surname>P.</surname><given-names>Modagan</given-names></name></name-alternatives><email>pmodagan@gmai.com</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Chand</surname><given-names>Leena</given-names></name><name xml:lang="en"><surname>Chand</surname><given-names>Leena</given-names></name></name-alternatives><email>leenachand@sriramachandra.edu.in</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Menon</surname><given-names>Gopinath</given-names></name><name xml:lang="en"><surname>Menon</surname><given-names>Gopinath</given-names></name></name-alternatives><email>gopimenon2002@yahoo.co.in</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>L. P</surname><given-names>Aruna</given-names></name><name xml:lang="en"><surname>L. P</surname><given-names>Aruna</given-names></name></name-alternatives><email>drarunalatha@gmail.com</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Silambanan</surname><given-names>Santhi</given-names></name><name xml:lang="en"><surname>Silambanan</surname><given-names>Santhi</given-names></name></name-alternatives><email>santhisilambanan@sriramachandra.edu.in</email></contrib></contrib-group><pub-date pub-type="epub"><year>2022</year></pub-date><volume>8</volume><issue>1</issue><fpage>0</fpage><lpage>0</lpage><self-uri content-type="pdf" xlink:href="/media/medicine/2022/1/Биомедицинские_исследования-83-91.pdf" /><abstract xml:lang="ru"><p>Background: Osteoporosis is a common disease of aging population, causing fractures and raising mortality and morbidity. Standard diagnosis usually depends on measuring bone mineral density using a dual energy X-ray absorptiometry. But it does not provide information regarding bone formation or resorption. Bone turnover markers provide information regarding bone formation or resorption before the structural changes in bone occur. The aim of the study: This study was undertaken to investigate the effectiveness of N-terminal telopeptide-1 in the diagnosis of osteopenia and osteoporosis. Materials and methods: The case-control study was conducted in 170 individuals from the Department of Orthopedic Surgery. They were divided into three groups based on bone mineral density; group I with normal BMD (n=57), group II with osteopenia (n=62) and group III with osteoporosis (n=51). Institutional ethics committee approval was obtained. Written informed consent was obtained from all the study participants. Serum N-terminal telopeptide-1 (NTX-1) was analyzed by ELISA. Statistical analysis was performed using the SPSS 16.0 version for Windows. The continuous variables were expressed as mean &amp;plusmn; SD. ANOVA with Tukey&amp;rsquo;s HSD and ROC curve analysis were performed. Odds ratio was analyzed. Pearson correlation coefficient was obtained between BMD and NTX1. P value &amp;lt;.05 was considered statistically significant. Results: There was a significant increase in serum N-terminal telopeptide-1 across the groups. NTX-1 values showed correlation with BMD. The area under the curve during analysis of NTX-1 in patients with normal BMD and osteopenia and osteoporosis were 0.697 and 0.592 respectively. Conclusion: The participants were in the obese as well as over-weight category. Serum N-terminal telopeptide-1 was significantly increased across the groups indicating that bone turnover markers are associated with progression of osteoporosis </p></abstract><trans-abstract xml:lang="en"><p>Background: Osteoporosis is a common disease of aging population, causing fractures and raising mortality and morbidity. Standard diagnosis usually depends on measuring bone mineral density using a dual energy X-ray absorptiometry. But it does not provide information regarding bone formation or resorption. Bone turnover markers provide information regarding bone formation or resorption before the structural changes in bone occur. The aim of the study: This study was undertaken to investigate the effectiveness of N-terminal telopeptide-1 in the diagnosis of osteopenia and osteoporosis. Materials and methods: The case-control study was conducted in 170 individuals from the Department of Orthopedic Surgery. They were divided into three groups based on bone mineral density; group I with normal BMD (n=57), group II with osteopenia (n=62) and group III with osteoporosis (n=51). Institutional ethics committee approval was obtained. Written informed consent was obtained from all the study participants. Serum N-terminal telopeptide-1 (NTX-1) was analyzed by ELISA. Statistical analysis was performed using the SPSS 16.0 version for Windows. The continuous variables were expressed as mean &amp;plusmn; SD. ANOVA with Tukey&amp;rsquo;s HSD and ROC curve analysis were performed. Odds ratio was analyzed. Pearson correlation coefficient was obtained between BMD and NTX1. P value &amp;lt;.05 was considered statistically significant. Results: There was a significant increase in serum N-terminal telopeptide-1 across the groups. NTX-1 values showed correlation with BMD. The area under the curve during analysis of NTX-1 in patients with normal BMD and osteopenia and osteoporosis were 0.697 and 0.592 respectively. Conclusion: The participants were in the obese as well as over-weight category. Serum N-terminal telopeptide-1 was significantly increased across the groups indicating that bone turnover markers are associated with progression of osteoporosis </p></trans-abstract><kwd-group xml:lang="ru"><kwd>osteoporosis</kwd><kwd>osteopenia</kwd><kwd>bone mineral density</kwd><kwd>fractures</kwd><kwd>bone turnover markers</kwd><kwd>NTX-1</kwd></kwd-group><kwd-group xml:lang="en"><kwd>osteoporosis</kwd><kwd>osteopenia</kwd><kwd>bone mineral density</kwd><kwd>fractures</kwd><kwd>bone turnover markers</kwd><kwd>NTX-1</kwd></kwd-group></article-meta></front><back><ack><p>The authors wish to thank the management of Sri Ramachandra Institute of Higher Education and Research for supporting the PhD programme in the form of provision of funds as well as providing necessary infrastructure to conduct the study</p></ack><ref-list><title>Список литературы</title><ref id="B1"><mixed-citation>Inderjeeth C, Nair AP, Chan K, et al. Bone turnover markers in old vs early postmenopausal women. 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