{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T05:29:30Z","timestamp":1787030970525,"version":"build-2736575974"},"reference-count":28,"publisher":"Scientific Scholar","issue":"4&5","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2022,10]]},"abstract":"<jats:sec>\n                    <jats:title>Background &amp; objectives:<\/jats:title>\n                    <jats:p>Osteoporosis is a systemic skeletal disease, characterized by a low bone mass leading to increased bone fragility and hence, a greater susceptibility to the risk of fracture. Since age-related oxidative stress is one of the factors that has been implicated in developing low bone mineral density (BMD), leading to osteoporosis, this study wanted to explore the expression of antioxidant enzymes in individuals with osteoporosis. The present study focused on mapping polymorphism in an important antioxidant enzyme glutathione peroxidase 1 (GPx1) among osteoporosis and healthy Asian Indians.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods:<\/jats:title>\n                    <jats:p>Dual-energy X-ray absorptiometry was used to assess BMD of individuals and was classified into normal (n=96) and osteoporotic (n=88) groups. Biochemical parameters such as vitamin D, total oxidant status (TOS), and GPx1 enzyme activity were estimated from plasma samples of recruited individuals. Quantitative real-time qRT-PCR was carried out using GAPDH as an endogenous control. Genomic DNA was isolated from whole blood, and polymorphisms were evaluated by sequencing.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results:<\/jats:title>\n                    <jats:p>\n                      The BMD was lower in osteoporotic individuals, and further analysis of biochemical parameters indicated significantly low 25-hydroxy vitamin D and GPx1 with higher TOS levels in osteoporotic as compared to healthy individuals. Furthermore, qRT-PCR revealed low expression of\n                      <jats:italic toggle=\"yes\">GPX1<\/jats:italic>\n                      in osteoporotic individuals.\n                      <jats:italic toggle=\"yes\">GPX1<\/jats:italic>\n                      sequence analysis of the promoter and two exons revealed the lower frequency of five alanine repeats in the osteoporotic individuals.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Interpretation &amp; conclusions:<\/jats:title>\n                    <jats:p>\n                      In this study, the\n                      <jats:italic toggle=\"yes\">in silico<\/jats:italic>\n                      analysis revealed the lower frequency of five alanine repeats in exon 1 of\n                      <jats:italic toggle=\"yes\">GPX1<\/jats:italic>\n                      and high TOS to be associated with osteoporosis. However, no polymorphism was found in exon 2 of\n                      <jats:italic toggle=\"yes\">GPX1<\/jats:italic>\n                      among the two study groups.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.4103\/ijmr.ijmr_208_20","type":"journal-article","created":{"date-parts":[[2024,4,16]],"date-time":"2024-04-16T03:04:33Z","timestamp":1713236673000},"page":"640-647","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":3,"title":["Polyalanine polymorphism in the signal peptide of Glutathione peroxidase 1 (GPX1) gene &amp; its association with osteoporosis"],"prefix":"10.25259","volume":"156","author":[{"given":"Soni Ghumnani","family":"Ahuja","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Arjun","family":"Shahu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Subrata","family":"Rath","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Neeraj","family":"Adkar","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yogesh","family":"Shouche","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Saroj","family":"Ghaskadbi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Richa","family":"Ashma","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"10894","reference":[{"key":"R1-12-20241212","doi-asserted-by":"crossref","first-page":"3318","DOI":"10.1172\/JCI27071","article-title":"Pathogenesis 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