清晨好,您是今天最早来到科研通的研友!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您科研之路漫漫前行!

Comparison of the efficacy between sequential therapy with teriparatide and denosumab and denosumab monotherapy in suppressing fragility fracture risk

德诺苏马布 特立帕肽 医学 骨质疏松症 骨矿物 泌尿科 内科学 外科
作者
Jae‐Won Shin,Quen He,Yong June Suk,Sang-Ho Kim,Hak-Sun Kim
出处
期刊:Osteoporosis International [Springer Science+Business Media]
卷期号:33 (11): 2409-2416 被引量:3
标识
DOI:10.1007/s00198-022-06495-8
摘要

SummaryIn this retrospective study, the effectiveness of short-term teriparatide with denosumab in reducing fragility fracture risk was determined in comparison with denosumab monotherapy. Administration of sequential teriparatide with denosumab showed excellent outcomes in suppressing the risk for fragility fractures compared with denosumab monotherapy.IntroductionTo determine the effectiveness of short-term teriparatide with denosumab in reducing the risk of fragility fractures in comparison to denosumab monotherapy. MethodsThe data of postmenopausal patients treated with denosumab for > 2 years between August 2015 and October 2020 were retrospectively analyzed. One hundred sixty four postmenopausal women of a total 615 were excluded, since they did not undergo > 2 bone mineral density (BMD) tests, were lost to follow-up, or received long-term teriparatide therapy. Total 320 patients received denosumab monotherapy and 131 patients received teriparatide for ≥ 3 months followed by denosumab. The number of osteoporotic fractures, presence of back pain before and after treatment, and annual BMD during treatment were comparatively assessed using t-test, Chi-square test, and linear mixed model analysis. ResultsBefore treatment, the denosumab monotherapy group had fewer osteoporotic fractures (mean ± standard deviation; 0.459 ± 0.689) than the sequential therapy group had (1.037 ± 0.871; p < 0.001). After treatment, the sequential therapy group had fewer osteoporotic fractures than the denosumab monotherapy group had (0.119 ± 0.348 versus 0.144 ± 0.385; p < 0.001). At 1 and 2 years after treatment, the increase in lumbar spine BMD was greater in the sequential therapy group than in the denosumab monotherapy group (p = 0.08, group × time). The difference between post and pre-treatment back pain visual analog scale score was significantly lower in the sequential therapy group than in the monotherapy group (3.246 ± 3.426 versus 1.734 ± 3.049; p < 0.001). ConclusionShort-term teriparatide use before denosumab showed excellent outcomes in suppressing the risk of fragility fractures compared with denosumab monotherapy.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
humorlife完成签到,获得积分10
10秒前
现代的冰海完成签到,获得积分10
11秒前
zyyicu完成签到,获得积分10
12秒前
25秒前
CRUSADER发布了新的文献求助50
36秒前
糟糕的翅膀完成签到,获得积分10
44秒前
齐天小圣完成签到 ,获得积分10
1分钟前
flyingpig完成签到,获得积分10
1分钟前
星辰大海应助一一采纳,获得10
1分钟前
无花果应助科研通管家采纳,获得10
1分钟前
2分钟前
一一发布了新的文献求助10
2分钟前
英俊的铭应助CRUSADER采纳,获得50
2分钟前
ffff完成签到 ,获得积分10
2分钟前
drsaidu完成签到,获得积分10
2分钟前
3分钟前
虚幻的岩完成签到,获得积分10
3分钟前
CRUSADER发布了新的文献求助50
3分钟前
HFH应助科研通管家采纳,获得30
3分钟前
HFH应助科研通管家采纳,获得30
3分钟前
halide完成签到,获得积分10
3分钟前
飞天大南瓜完成签到,获得积分10
3分钟前
潜行者完成签到 ,获得积分10
3分钟前
老戎完成签到 ,获得积分10
4分钟前
4分钟前
DR_MING发布了新的文献求助10
4分钟前
英姑应助DR_MING采纳,获得10
5分钟前
酷波er应助一一采纳,获得10
5分钟前
李爱国应助xfcy采纳,获得10
5分钟前
5分钟前
白华苍松发布了新的文献求助10
5分钟前
朱志伟完成签到,获得积分10
5分钟前
美满尔蓝完成签到,获得积分10
6分钟前
7分钟前
xfcy发布了新的文献求助10
7分钟前
7分钟前
7分钟前
7分钟前
一一发布了新的文献求助10
7分钟前
xfcy完成签到,获得积分10
7分钟前
高分求助中
Adhesion Science: Principles & Practice 1234
Cold War Transcended: Australia's China Policy, 1949-1990 998
Signals, Systems, and Signal Processing 610
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 600
Testimonial Injustice and Trust 510
Burger's Medicinal Chemistry and Drug Discovery 400
Fundamentals of Body MRI 3rd Edition 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6635983
求助须知:如何正确求助?哪些是违规求助? 8394885
关于积分的说明 17952580
捐赠科研通 5820145
什么是DOI,文献DOI怎么找? 2966406
邀请新用户注册赠送积分活动 1941499
关于科研通互助平台的介绍 1855124