<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>24(1)</volume><submitter>Iwamoto N</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>This exploratory study compared the inhibition of bone erosion progression in rheumatoid arthritis (RA) patients treated with a conventional synthetic disease-modifying anti-rheumatic drug (csDMARD) plus denosumab versus csDMARD therapy alone and investigated the effects of denosumab on bone micro-architecture and other bone-related parameters using high-resolution peripheral quantitative computed tomography (HR-pQCT).&lt;h4>Methods&lt;/h4>In this open-label, randomized, parallel-group study, patients with RA undergoing treatment with a csDMARD were randomly assigned (1:1) to continue csDMARD therapy alone or to continue csDMARDs with denosumab (60-mg subcutaneous injection once every 6 months) for 12 months. The primary endpoint was the change from baseline in the depth of bo</pubmed_abstract><journal>Arthritis research &amp; therapy</journal><pagination>264</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9727996</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Inhibition of bone erosion, determined by high-resolution peripheral quantitative computed tomography (HR-pQCT), in rheumatoid arthritis patients receiving a conventional synthetic disease-modifying anti-rheumatic drug (csDMARD) plus denosumab vs csDMARD therapy alone: an open-label, randomized, parallel-group study.</pubmed_title><pmcid>PMC9727996</pmcid><pubmed_authors>Iwamoto N</pubmed_authors><pubmed_authors>Chiba K</pubmed_authors><pubmed_authors>Furuyama M</pubmed_authors><pubmed_authors>Saito K</pubmed_authors><pubmed_authors>Kawakami A</pubmed_authors><pubmed_authors>Tamai M</pubmed_authors><pubmed_authors>Okada A</pubmed_authors><pubmed_authors>Kawashiri SY</pubmed_authors><pubmed_authors>Kobayashi M</pubmed_authors><pubmed_authors>Oki N</pubmed_authors><pubmed_authors>Uetani M</pubmed_authors><pubmed_authors>Hosogaya N</pubmed_authors><pubmed_authors>Sato S</pubmed_authors><pubmed_authors>Koga T</pubmed_authors><pubmed_authors>Okubo N</pubmed_authors><pubmed_authors>Watanabe K</pubmed_authors><pubmed_authors>Osaki M</pubmed_authors><pubmed_authors>Shiraishi K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Inhibition of bone erosion, determined by high-resolution peripheral quantitative computed tomography (HR-pQCT), in rheumatoid arthritis patients receiving a conventional synthetic disease-modifying anti-rheumatic drug (csDMARD) plus denosumab vs csDMARD therapy alone: an open-label, randomized, parallel-group study.</name><description>&lt;h4>Background&lt;/h4>This exploratory study compared the inhibition of bone erosion progression in rheumatoid arthritis (RA) patients treated with a conventional synthetic disease-modifying anti-rheumatic drug (csDMARD) plus denosumab versus csDMARD therapy alone and investigated the effects of denosumab on bone micro-architecture and other bone-related parameters using high-resolution peripheral quantitative computed tomography (HR-pQCT).&lt;h4>Methods&lt;/h4>In this open-label, randomized, parallel-group study, patients with RA undergoing treatment with a csDMARD were randomly assigned (1:1) to continue csDMARD therapy alone or to continue csDMARDs with denosumab (60-mg subcutaneous injection once every 6 months) for 12 months. The primary endpoint was the change from baseline in the depth of bo</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-22T05:39:33.93Z</modification><creation>2025-04-05T21:23:54.248Z</creation></dates><accession>S-EPMC9727996</accession><cross_references><pubmed>36476479</pubmed><doi>10.1186/s13075-022-02957-w</doi></cross_references></HashMap>