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One-year bone mineral density gains with anti-osteoporotic medications and clinical factors associated with non-BMD gainers

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dc.contributor.authorJang, Seol A.-
dc.contributor.authorHeo, Seok-Jae-
dc.contributor.authorKwon, Su Jin-
dc.contributor.authorKim, Chul Sik-
dc.contributor.authorPark, Seok Won-
dc.contributor.authorKim, Kyoung Min-
dc.contributor.author장슬아-
dc.date.accessioned2026-01-19T02:14:12Z-
dc.date.available2026-01-19T02:14:12Z-
dc.date.created2026-01-02-
dc.date.issued2025-11-
dc.identifier.issn0914-8779-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/209913-
dc.description.abstractIntroduction Despite the increasing number of anti-osteoporotic medications for improving bone mineral density (BMD) and reducing fracture risk, some patients show unsatisfactory responses. Materials and methods We retrospectively analyzed 2134 patients who received anti-osteoporotic medications between March 2020 and October 2024. BMD percentage changes at the lumbar spine, femoral neck, and total hip were assessed after 1 year. Patients were categorized as "non-BMD gainers" (<3% increase at all sites) or "BMD gainers" (>= 3% increase at any site). Multivariable logistic regression was used to evaluate associations with non-BMD gainer status, including age, body mass index, baseline T-score, and medication class. Results 578 patients (27.1%) were classified as non-BMD gainers. The observed rates of non-BMD gainer varied across medication classes in this real-world cohort, with selective estrogen receptor modulators (SERMs) showing the highest non-BMD gain rate (46.0%), followed by bisphosphonates (32.2%), teriparatide (35.1%), denosumab (19.5%), and romosozumab (5.6%). Non-BMD gainers had high baseline BMD and low bone turnover markers, and were more likely to have a history of osteoporosis treatment. In multivariable logistic regression analysis, older age (>= 75 years), SERM use, and high baseline BMD T-scores were independently associated with increased risk of non-BMD gainer status. Conversely, low T-scores (<=-3.0) were associated with a significantly reduced likelihood of being a non-BMD gainer. Conclusion Approximately 25% of patients did not achieve BMD gain after 1 year of treatment. Older age, higher baseline BMD T-scores, and SERM use were associated with an increased probability of non-BMD gainer status in this observational study.-
dc.languageEnglish-
dc.publisherJapanese Society of Bone and Mineral Metabolism-
dc.relation.isPartOfJOURNAL OF BONE AND MINERAL METABOLISM-
dc.relation.isPartOfJOURNAL OF BONE AND MINERAL METABOLISM-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHBone Density Conservation Agents* / pharmacology-
dc.subject.MESHBone Density Conservation Agents* / therapeutic use-
dc.subject.MESHBone Density* / drug effects-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHLumbar Vertebrae / drug effects-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHOsteoporosis* / drug therapy-
dc.subject.MESHRetrospective Studies-
dc.titleOne-year bone mineral density gains with anti-osteoporotic medications and clinical factors associated with non-BMD gainers-
dc.typeArticle-
dc.contributor.googleauthorJang, Seol A.-
dc.contributor.googleauthorHeo, Seok-Jae-
dc.contributor.googleauthorKwon, Su Jin-
dc.contributor.googleauthorKim, Chul Sik-
dc.contributor.googleauthorPark, Seok Won-
dc.contributor.googleauthorKim, Kyoung Min-
dc.identifier.doi10.1007/s00774-025-01641-8-
dc.relation.journalcodeJ01277-
dc.identifier.eissn1435-5604-
dc.identifier.pmid41044438-
dc.identifier.urlhttps://link.springer.com/article/10.1007/s00774-025-01641-8-
dc.subject.keywordOsteoporosis-
dc.subject.keywordBone mineral density-
dc.subject.keywordAnti-osteoporotic drugs-
dc.subject.keywordTreatment response-
dc.contributor.affiliatedAuthorJang, Seol A.-
dc.contributor.affiliatedAuthorHeo, Seok-Jae-
dc.contributor.affiliatedAuthorKwon, Su Jin-
dc.contributor.affiliatedAuthorKim, Chul Sik-
dc.contributor.affiliatedAuthorPark, Seok Won-
dc.contributor.affiliatedAuthorKim, Kyoung Min-
dc.identifier.scopusid2-s2.0-105017865417-
dc.identifier.wosid001587362600001-
dc.citation.volume43-
dc.citation.number6-
dc.citation.startPage662-
dc.citation.endPage671-
dc.identifier.bibliographicCitationJOURNAL OF BONE AND MINERAL METABOLISM, Vol.43(6) : 662-671, 2025-11-
dc.identifier.rimsid90623-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorOsteoporosis-
dc.subject.keywordAuthorBone mineral density-
dc.subject.keywordAuthorAnti-osteoporotic drugs-
dc.subject.keywordAuthorTreatment response-
dc.subject.keywordPlusPOSTMENOPAUSAL WOMEN-
dc.subject.keywordPlusRETROSPECTIVE ANALYSIS-
dc.subject.keywordPlusTERIPARATIDE-
dc.subject.keywordPlusDENOSUMAB-
dc.subject.keywordPlusROMOSOZUMAB-
dc.subject.keywordPlusNONRESPONSE-
dc.subject.keywordPlusPREVENTION-
dc.subject.keywordPlusMANAGEMENT-
dc.subject.keywordPlusFRACTURES-
dc.subject.keywordPlusTHERAPY-
dc.type.docTypeArticle; Early Access-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryEndocrinology & Metabolism-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalResearchAreaEndocrinology & Metabolism-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Biomedical Systems Informatics (의생명시스템정보학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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