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Bone Bridge Effect for the Treatment of Acute Osteoporotic Vertebral Compression Fractures: A Multistrategic Approach Using an Anabolic Agent

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dc.contributor.authorYoon, Ja-Yeong-
dc.contributor.authorKim, Sung-Min-
dc.contributor.authorMoon, Seong-Hwan-
dc.contributor.authorKim, Hak-Sun-
dc.contributor.authorSuk, Kyung-Soo-
dc.contributor.authorPark, Si-Young-
dc.contributor.authorKwon, Ji-Won-
dc.contributor.authorLee, Byung Ho-
dc.date.accessioned2026-06-12T07:45:48Z-
dc.date.available2026-06-12T07:45:48Z-
dc.date.created2026-06-05-
dc.date.issued2026-06-
dc.identifier.issn0513-5796-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/212604-
dc.description.abstractPurpose: To determine the bone bridge effect (BBE) and compare treatment outcomes of different osteoporosis medications in patients with lumbar osteoporotic vertebral compression fractures (OVCF). Materials and Methods: This study followed 264 patients with lumbar OVCFs undergoing conservative treatment for more than 12 months. Patients were divided into four groups based on medication: denosumab monotherapy (group D), teriparatide and denosumab combination (group TDco), sequential romosozumab followed by denosumab (group RDse), and bisphosphonate mono-therapy (group B). Changes in bone mineral density (BMD), radiological parameters including BBE, and visual analog scale (VAS) scores were compared from injury to 1 year post-injury. Results: The 1-year BBE incidence was highest in groups treated with anabolic agents: group RDse (56.3%) and group TDco (51.8%). These rates were significantly higher than in group D (28.6%) and group B (21.1%). The annual BMD increase was significantly greater in group TDco (1.04) compared to the other groups (RDse: 0.63; D: 0.55; B: 0.35). VAS scores decreased significantly by the 3-month mark in anabolic agent groups and in patients with confirmed BBE, indicating rapid pain relief. Multivariate logistic regression analysis confirmed that anabolic agent groups (TDco and RDse) were significant independent predictors of BBE formation (odds ratio 2.717 and 3.472, respectively), even after adjusting for confounding variables such as initial BMD. Conclusion: Anabolic agents appeared to be associated with more BBE formation, greater BMD gains, and faster pain reduction compared to anti-resorptive agents. Therefore, treatment strategies using anabolic agents, such as those in groups TDco and RDse, maybe important considerations for treating patients with OVCFs.-
dc.languageEnglish-
dc.publisherYonsei University-
dc.relation.isPartOfYONSEI MEDICAL JOURNAL-
dc.relation.isPartOfYONSEI MEDICAL JOURNAL-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHAnabolic Agents* / therapeutic use-
dc.subject.MESHBone Density / drug effects-
dc.subject.MESHBone Density Conservation Agents* / therapeutic use-
dc.subject.MESHDenosumab / therapeutic use-
dc.subject.MESHFemale-
dc.subject.MESHFractures, Compression* / drug therapy-
dc.subject.MESHHumans-
dc.subject.MESHLumbar Vertebrae-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHOsteoporotic Fractures* / drug therapy-
dc.subject.MESHSpinal Fractures* / drug therapy-
dc.subject.MESHTeriparatide / therapeutic use-
dc.subject.MESHTreatment Outcome-
dc.titleBone Bridge Effect for the Treatment of Acute Osteoporotic Vertebral Compression Fractures: A Multistrategic Approach Using an Anabolic Agent-
dc.typeArticle-
dc.contributor.googleauthorYoon, Ja-Yeong-
dc.contributor.googleauthorKim, Sung-Min-
dc.contributor.googleauthorMoon, Seong-Hwan-
dc.contributor.googleauthorKim, Hak-Sun-
dc.contributor.googleauthorSuk, Kyung-Soo-
dc.contributor.googleauthorPark, Si-Young-
dc.contributor.googleauthorKwon, Ji-Won-
dc.contributor.googleauthorLee, Byung Ho-
dc.identifier.doi10.3349/ymj.2025.0325-
dc.relation.journalcodeJ02813-
dc.identifier.eissn1976-2437-
dc.identifier.pmid42198860-
dc.subject.keywordOsteoporosis-
dc.subject.keywordosteoporotic vertebral compression fractures-
dc.subject.keywordtreatment strategy-
dc.subject.keywordanabolic agents-
dc.subject.keywordbone bridge effect-
dc.contributor.affiliatedAuthorMoon, Seong-Hwan-
dc.contributor.affiliatedAuthorKim, Hak-Sun-
dc.contributor.affiliatedAuthorSuk, Kyung-Soo-
dc.contributor.affiliatedAuthorPark, Si-Young-
dc.contributor.affiliatedAuthorKwon, Ji-Won-
dc.contributor.affiliatedAuthorLee, Byung Ho-
dc.identifier.scopusid2-s2.0-105038904047-
dc.identifier.wosid001769260400006-
dc.citation.volume67-
dc.citation.number6-
dc.citation.startPage492-
dc.citation.endPage501-
dc.identifier.bibliographicCitationYONSEI MEDICAL JOURNAL, Vol.67(6) : 492-501, 2026-06-
dc.identifier.rimsid93231-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorOsteoporosis-
dc.subject.keywordAuthorosteoporotic vertebral compression fractures-
dc.subject.keywordAuthortreatment strategy-
dc.subject.keywordAuthoranabolic agents-
dc.subject.keywordAuthorbone bridge effect-
dc.subject.keywordPlusTHORACOLUMBAR BURST FRACTURE-
dc.subject.keywordPlusPOSTMENOPAUSAL WOMEN-
dc.subject.keywordPlusTERIPARATIDE-
dc.subject.keywordPlusROMOSOZUMAB-
dc.subject.keywordPlusDENOSUMAB-
dc.subject.keywordPlusVERTEBROPLASTY-
dc.subject.keywordPlusALENDRONATE-
dc.subject.keywordPlusPREVENTION-
dc.subject.keywordPlusMANAGEMENT-
dc.subject.keywordPlusEXTENSION-
dc.type.docTypeArticle-
dc.identifier.kciidART003338167-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Orthopedic Surgery (정형외과학교실) > 1. Journal Papers

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