The Effect of Denosumab in Elderly Patients Regarding Bone Density and Fracture Risk.

Q2 Medicine
Journal of Bone Metabolism Pub Date : 2023-08-01 Epub Date: 2023-08-31 DOI:10.11005/jbm.2023.30.3.275
Sung-Hyun Yoon, Karam Kim, Ki-Choul Kim
{"title":"The Effect of Denosumab in Elderly Patients Regarding Bone Density and Fracture Risk.","authors":"Sung-Hyun Yoon,&nbsp;Karam Kim,&nbsp;Ki-Choul Kim","doi":"10.11005/jbm.2023.30.3.275","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>With an aging population, the importance of treating and diagnosing osteoporosis is increasing. Osteoporosis, previously known as a resorptive change primarily related to endocrinological mechanisms, is also being approached as a phenomenon of senile change. Denosumab is gaining popularity among osteoporosis medications due to its ability to increase bone mineral density (BMD) and the economic benefit arising from the 6-month cycle. In line with previous literature, this study aimed to examine the BMD-augmenting effect of denosumab through which it reduces fracture risk in individuals aged over 80 years.</p><p><strong>Methods: </strong>We reviewed patients who received denosumab between 2018 and 2022 with a minimum clinical observation period of 12 months. BMD was measured every 12 months, and patients were classified per their period of denosumab use. Fracture risk was evaluated using the fracture risk assessment tool (FRAX) and fracture incidence during the observation period were assessed.</p><p><strong>Results: </strong>Among 155 patients, a significant increase in BMD was observed at 3 sites: the lumbar spine, femoral neck, and total hip (p<0.001, p<0.001, and p=0.001, respectively). The patients were divided according to the length of clinical follow-up they received, and similar results were found in all subgroups. Fracture risk assessment was performed using FRAX and the incidence of fracture events during follow-up. FRAX significantly decreased in all subgroups except those who received 24 months of follow-up (p=0.003, p=0.41, p=0.001 in the 12, 24, and ≥36 months groups, respectively).</p><p><strong>Conclusions: </strong>Denosumab use resulted in long-term BMD increase and reduced fracture risk in individuals aged 80 and above.</p>","PeriodicalId":15070,"journal":{"name":"Journal of Bone Metabolism","volume":"30 3","pages":"275-282"},"PeriodicalIF":0.0000,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/d2/70/jbm-2023-30-3-275.PMC10509027.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Bone Metabolism","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.11005/jbm.2023.30.3.275","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/8/31 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Background: With an aging population, the importance of treating and diagnosing osteoporosis is increasing. Osteoporosis, previously known as a resorptive change primarily related to endocrinological mechanisms, is also being approached as a phenomenon of senile change. Denosumab is gaining popularity among osteoporosis medications due to its ability to increase bone mineral density (BMD) and the economic benefit arising from the 6-month cycle. In line with previous literature, this study aimed to examine the BMD-augmenting effect of denosumab through which it reduces fracture risk in individuals aged over 80 years.

Methods: We reviewed patients who received denosumab between 2018 and 2022 with a minimum clinical observation period of 12 months. BMD was measured every 12 months, and patients were classified per their period of denosumab use. Fracture risk was evaluated using the fracture risk assessment tool (FRAX) and fracture incidence during the observation period were assessed.

Results: Among 155 patients, a significant increase in BMD was observed at 3 sites: the lumbar spine, femoral neck, and total hip (p<0.001, p<0.001, and p=0.001, respectively). The patients were divided according to the length of clinical follow-up they received, and similar results were found in all subgroups. Fracture risk assessment was performed using FRAX and the incidence of fracture events during follow-up. FRAX significantly decreased in all subgroups except those who received 24 months of follow-up (p=0.003, p=0.41, p=0.001 in the 12, 24, and ≥36 months groups, respectively).

Conclusions: Denosumab use resulted in long-term BMD increase and reduced fracture risk in individuals aged 80 and above.

Abstract Image

Abstract Image

Abstract Image

Denosumab对老年患者骨密度和骨折风险的影响。
背景:随着人口老龄化,骨质疏松症的治疗和诊断越来越重要。骨质疏松症,以前被称为一种主要与内分泌机制有关的吸收性变化,也被认为是一种老年变化现象。Denosumab在骨质疏松症药物中越来越受欢迎,因为它能够增加骨密度(BMD),并在6个月的周期中产生经济效益。与先前的文献一致,本研究旨在检验狄诺沙单抗的骨密度增强作用,通过该作用降低80岁以上人群的骨折风险。方法:我们回顾了2018年至2022年间接受狄诺沙单抗治疗的患者,其最短临床观察期为12个月。每12个月测量一次BMD,并根据患者使用狄诺沙单抗的时间对患者进行分类。使用骨折风险评估工具(FRAX)评估骨折风险,并评估观察期内的骨折发生率。结果:在155名患者中,在腰椎、股骨颈和全髋关节3个部位观察到BMD显著增加(P结论:Denosumab的使用导致80岁及以上个体的长期BMD增加和骨折风险降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Bone Metabolism
Journal of Bone Metabolism Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
3.70
自引率
0.00%
发文量
23
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信