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Effect of romosozumab on bone mineral density and trabecular bone score in premenopausal women with low bone mass

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dc.contributor.author이유미-
dc.contributor.author홍남기-
dc.contributor.author신성재-
dc.contributor.author이승현-
dc.contributor.author조성준-
dc.date.accessioned2025-05-02T00:15:01Z-
dc.date.available2025-05-02T00:15:01Z-
dc.date.issued2025-02-
dc.identifier.issn0937-941X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/205326-
dc.description.abstractWe investigated the efficacy of romosozumab in premenopausal women with low bone mass. Romosozumab substantially increased bone mineral density and trabecular bone score in these women, aligning with its proven therapeutic benefits for postmenopausal osteoporosis. Purpose: Romosozumab, an anti-sclerostin antibody, is a promising anabolic agent that increases bone formation and decreases bone resorption. However, its efficacy in premenopausal women with low bone mass remains understudied. Methods: We retrospectively reviewed premenopausal women with low bone mass treated with romosozumab (ROMO group) or drug-naïve patients (control group). Patients in the ROMO group were classified into the glucocorticoid-induced osteoporosis (GIOP), idiopathic osteoporosis (IOP), and pregnancy and lactation-induced osteoporosis (PLO) subgroups. Bone mineral density (BMD) and trabecular bone score (TBS) were measured before and after one year of romosozumab treatment. Results: Twenty-five patients in the ROMO group and five in the control group were included in the study. Among patients in the ROMO group, 12 were in the GIOP, 9 in the IOP, and 4 in the PLO subgroups. The mean age was 37.0 years [32.0-42.0], and the median body mass index was 18.8 kg/m2 [17.5-21.3]. After romosozumab treatment, lumbar spine (LS), femur neck (FN) BMD, and TBS increased from baseline (LSBMD, 12.8% [8.2-19.3], p < 0.001; FNBMD, 4.6% [- 0.6-10.7], p = 0.016; TBS, 4.1% ± 3.8, p < 0.001) in the ROMO group. Patients in both the GIOP and IOP subgroups showed a significant increase in LSBMD, while those in the IOP subgroup demonstrated significant increases in FNBMD. Conclusion: We demonstrated romosozumab's efficacy in BMD increment in premenopausal women. Romosozumab may be a potential treatment option for premenopausal women with low bone mass, regardless of etiologies, although further research on fracture risk reduction is warranted.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherSpringer International-
dc.relation.isPartOfOSTEOPOROSIS INTERNATIONAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAbsorptiometry, Photon / methods-
dc.subject.MESHAdult-
dc.subject.MESHAntibodies, Monoclonal* / pharmacology-
dc.subject.MESHAntibodies, Monoclonal* / therapeutic use-
dc.subject.MESHBone Density Conservation Agents* / pharmacology-
dc.subject.MESHBone Density Conservation Agents* / therapeutic use-
dc.subject.MESHBone Density* / drug effects-
dc.subject.MESHBone Density* / physiology-
dc.subject.MESHCancellous Bone* / diagnostic imaging-
dc.subject.MESHCancellous Bone* / drug effects-
dc.subject.MESHCancellous Bone* / physiopathology-
dc.subject.MESHFemale-
dc.subject.MESHFemur Neck / physiopathology-
dc.subject.MESHGlucocorticoids / adverse effects-
dc.subject.MESHGlucocorticoids / pharmacology-
dc.subject.MESHGlucocorticoids / therapeutic use-
dc.subject.MESHHumans-
dc.subject.MESHLumbar Vertebrae* / physiopathology-
dc.subject.MESHMiddle Aged-
dc.subject.MESHOsteoporosis / chemically induced-
dc.subject.MESHOsteoporosis / drug therapy-
dc.subject.MESHOsteoporosis / physiopathology-
dc.subject.MESHPregnancy-
dc.subject.MESHPregnancy Complications / drug therapy-
dc.subject.MESHPregnancy Complications / physiopathology-
dc.subject.MESHPremenopause* / physiology-
dc.subject.MESHRetrospective Studies-
dc.titleEffect of romosozumab on bone mineral density and trabecular bone score in premenopausal women with low bone mass-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Microbiology (미생물학교실)-
dc.contributor.googleauthorSeunghyun Lee-
dc.contributor.googleauthorNamki Hong-
dc.contributor.googleauthorSung Joon Cho-
dc.contributor.googleauthorSungjae Shin-
dc.contributor.googleauthorYumie Rhee-
dc.identifier.doi10.1007/s00198-024-07336-6-
dc.contributor.localIdA02114-
dc.contributor.localIdA03012-
dc.contributor.localIdA04388-
dc.relation.journalcodeJ02451-
dc.identifier.eissn1433-2965-
dc.identifier.pmid39812671-
dc.identifier.urlhttps://link.springer.com/article/10.1007/s00198-024-07336-6-
dc.subject.keywordBone mineral density-
dc.subject.keywordLow bone mass-
dc.subject.keywordPremenopausal women-
dc.subject.keywordRomosozumab-
dc.subject.keywordTrabecular bone score-
dc.contributor.affiliatedAuthor이유미-
dc.contributor.affiliatedAuthor홍남기-
dc.citation.volume36-
dc.citation.number2-
dc.citation.startPage323-
dc.citation.endPage331-
dc.identifier.bibliographicCitationOSTEOPOROSIS INTERNATIONAL, Vol.36(2) : 323-331, 2025-02-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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