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Accelerated fusion dynamics by recombinant human bone morphogenetic protein-2 following transforaminal lumbar interbody fusion, particularly in osteoporotic conditions

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dc.contributor.author김학선-
dc.contributor.author문성환-
dc.contributor.author박시영-
dc.contributor.author석경수-
dc.contributor.author권지원-
dc.contributor.author이병호-
dc.contributor.author김상호-
dc.contributor.author신재원-
dc.date.accessioned2025-02-03T08:13:02Z-
dc.date.available2025-02-03T08:13:02Z-
dc.date.issued2024-11-
dc.identifier.issn1529-9430-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/201598-
dc.description.abstractBackground context: Early fusion is crucial in interbody procedures to minimize mechanical complications resulting from delayed union, especially for patients with osteoporosis. Bone morphogenetic proteins (BMPs) are used in spinal fusion procedures; however, limited evaluation exists regarding time-to-fusion for BMP use, particularly in patients with osteoporosis. Purpose: To evaluate the difference in time-to-fusion after single-level transforaminal lumbar interbody fusion (TLIF) surgery between recombinant human bone morphogenetic protein-2 (rhBMP-2) usage and nonusage groups according to bone density. Study design: Retrospective single-center cohort study. Patient sample: This study enrolled 132 patients (mean age, 65.25±8.66; male patients, 40.9%) who underwent single-level TLIF for degenerative disorders between February 2012 and December 2021, with pre- and postoperative computed tomography (CT). Outcome measure: The interbody fusion mass and bone graft status on postoperative CT scans was obtained annually, and time-to-fusion was recorded for each patient. Methods: The patients were divided into 2 groups based on rhBMP-2 use during the interbody fusion procedure. Patients were further divided into osteoporosis, osteopenia, and normal groups based on preoperative L1 vertebral body attenuation values, using cutoffs of 90 and 120 Hounsfield units. It was strictly defined that fusion is considered complete when a trabecular bone bridge was formed, and therefore, the time-to-fusion was measured in years. Time-to-fusion was statistically compared between BMP group and non-BMP groups, followed by further comparison according to bone density. Results: The time-to-fusion differed significantly between BMP and non-BMP groups, with half of the patients achieving fusion within 2.5 years in the BMP group compared with 4 years in the non-BMP group (p<.001). The fusion rate varied based on bone density, with the maximum difference observed in the osteoporosis group, when half of the patients achieved fusion within 3 years in the BMP group compared to 5 years in the non-BMP group (p<.001). Subgroup analysis was conducted, revealing no significant associations between time-to-fusion and factors known to influence the fusion process, including age, gender, medical history, smoking and alcohol use, and medication history, except for rh-BMP2 use and bone density. Conclusions: RhBMP-2 usage significantly reduced time-to-fusion in single-level TLIF, especially in patients with osteoporosis. Level of evidence: Level III.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherElsevier Science Inc.-
dc.relation.isPartOfSPINE JOURNAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAged-
dc.subject.MESHBone Density / drug effects-
dc.subject.MESHBone Morphogenetic Protein 2* / adverse effects-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHLumbar Vertebrae* / surgery-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHOsteoporosis* / surgery-
dc.subject.MESHRecombinant Proteins* / administration & dosage-
dc.subject.MESHRecombinant Proteins* / therapeutic use-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHSpinal Fusion* / adverse effects-
dc.subject.MESHSpinal Fusion* / methods-
dc.subject.MESHTransforming Growth Factor beta / adverse effects-
dc.subject.MESHTransforming Growth Factor beta / therapeutic use-
dc.titleAccelerated fusion dynamics by recombinant human bone morphogenetic protein-2 following transforaminal lumbar interbody fusion, particularly in osteoporotic conditions-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Orthopedic Surgery (정형외과학교실)-
dc.contributor.googleauthorSang-Ho Kim-
dc.contributor.googleauthorYung Park-
dc.contributor.googleauthorJae-Won Shin-
dc.contributor.googleauthorJoong-Won Ha-
dc.contributor.googleauthorHee-Min Choi-
dc.contributor.googleauthorHak-Sun Kim-
dc.contributor.googleauthorSeong-Hwan Moon-
dc.contributor.googleauthorKyung-Soo Suk-
dc.contributor.googleauthorSi-Young Park-
dc.contributor.googleauthorByung-Ho Lee-
dc.contributor.googleauthorJi-Won Kwon-
dc.identifier.doi10.1016/j.spinee.2024.06.010-
dc.contributor.localIdA01093-
dc.contributor.localIdA01365-
dc.contributor.localIdA01554-
dc.contributor.localIdA01926-
dc.contributor.localIdA06027-
dc.contributor.localIdA02801-
dc.relation.journalcodeJ02675-
dc.identifier.eissn1878-1632-
dc.identifier.pmid38909911-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S1529943024003024-
dc.subject.keywordAttenuation rate-
dc.subject.keywordBone mineral density-
dc.subject.keywordBone morphogenetic protein-
dc.subject.keywordOsteoporosis-
dc.subject.keywordTime-to-fusion-
dc.subject.keywordTransforaminal lumbar interbody fusion-
dc.contributor.alternativeNameKim, Hak Sun-
dc.contributor.affiliatedAuthor김학선-
dc.contributor.affiliatedAuthor문성환-
dc.contributor.affiliatedAuthor박시영-
dc.contributor.affiliatedAuthor석경수-
dc.contributor.affiliatedAuthor권지원-
dc.contributor.affiliatedAuthor이병호-
dc.citation.volume24-
dc.citation.number11-
dc.citation.startPage2078-
dc.citation.endPage2085-
dc.identifier.bibliographicCitationSPINE JOURNAL, Vol.24(11) : 2078-2085, 2024-11-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Orthopedic Surgery (정형외과학교실) > 1. Journal Papers

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