亲爱的研友该休息了!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,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

Two Years of Denosumab and Teriparatide Administration in Postmenopausal Women With Osteoporosis (The DATA Extension Study): A Randomized Controlled Trial

特立帕肽 德诺苏马布 医学 骨质疏松症 骨矿物 股骨颈 泌尿科 随机对照试验 内科学 外科
作者
Benjamin Z. Leder,Joy N. Tsai,Alexander V. Uihlein,Sherri‐Ann M. Burnett‐Bowie,Yuli Zhu,Katelyn Foley,Hang Lee,Robert M. Neer
出处
期刊:The Journal of Clinical Endocrinology and Metabolism [The Endocrine Society]
卷期号:99 (5): 1694-1700 被引量:258
标识
DOI:10.1210/jc.2013-4440
摘要

Current osteoporosis medications increase bone mineral density (BMD) modestly and reduce, but do not eliminate, fracture risk. Attempts to improve efficacy by administering anabolic agents and bisphosphonates concomitantly have been unsuccessful. Conversely, 12 months of concomitant denosumab and teriparatide therapy increases BMD more than either drug alone.The purpose of this study was to determine whether 24 months of combined denosumab and teriparatide will increase hip and spine BMD more than either individual agent.Preplanned continuation of the Denosumab and Teriparatide Administration (DATA) randomized controlled trial in which postmenopausal osteoporotic women received teriparatide (20 μg daily), denosumab (60 mg every 6 months), or both medications for 24 months.Participants were 94 postmenopausal women with osteoporosis.Lumbar spine, femoral neck, total hip, and distal radius BMD and serum markers of bone turnover were measured.At 24 months, lumbar spine BMD increased more in the combination group (12.9 ± 5.0%) than in either the teriparatide (9.5 ± 5.9%, P = .01) or denosumab (8.3 ± 3.4%, P = .008) groups. Femoral neck BMD also increased more in the combination group (6.8 ± 3.6%) than in either the teriparatide (2.8 ± 3.9%, P = .003) or denosumab (4.1 ± 3.8%, P = .008) groups. Similarly, total hip BMD increased more in the combination group (6.3 ± 2.6%) than in the teriparatide (2.0 ± 3.0%) or denosumab (3.2 ± 2.5%) groups (P < .001 for both). Although spine and hip BMD continued to increase in the second year in all groups, these year 2 increases did not differ among groups. Serum C-telopeptide and N-terminal propeptide of type 1 procollagen were equally suppressed in the denosumab and combination groups, whereas osteocalcin decreased more in the denosumab group than in the combination group, a difference that persisted, but lessened, in the second year of therapy.Two years of concomitant teriparatide and denosumab therapy increases BMD more than therapy with either medication alone and more than has been reported with any current therapy. The combination of these agents may prove to be an important treatment option in patients at high risk of fracture.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

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
李阳完成签到 ,获得积分10
14秒前
脑洞疼应助满意的世界采纳,获得10
15秒前
21秒前
大胆的碧菡完成签到,获得积分10
31秒前
34秒前
NEKO发布了新的文献求助10
39秒前
hhh完成签到 ,获得积分10
51秒前
NEKO发布了新的文献求助100
1分钟前
1分钟前
1分钟前
飞天大南瓜完成签到,获得积分10
1分钟前
高大的清涟完成签到 ,获得积分10
1分钟前
烟花应助忧郁的平安采纳,获得20
1分钟前
1分钟前
1分钟前
调皮的代双完成签到 ,获得积分10
1分钟前
1分钟前
打打应助NEKO采纳,获得10
1分钟前
Su发布了新的文献求助10
1分钟前
2分钟前
2分钟前
So完成签到 ,获得积分10
2分钟前
良辰美景完成签到 ,获得积分10
2分钟前
李爱国应助zakaria采纳,获得10
2分钟前
2分钟前
NEKO发布了新的文献求助10
2分钟前
2分钟前
烤地瓜的z完成签到,获得积分10
2分钟前
2分钟前
江洋大盗发布了新的文献求助10
2分钟前
江洋大盗完成签到,获得积分10
2分钟前
blenx完成签到,获得积分10
3分钟前
小蘑菇应助科研通管家采纳,获得10
3分钟前
LJL完成签到 ,获得积分10
3分钟前
3分钟前
天天快乐应助drirshad采纳,获得10
4分钟前
4分钟前
sulin完成签到 ,获得积分10
4分钟前
Su发布了新的文献求助30
4分钟前
烟花应助NEKO采纳,获得10
4分钟前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Clinical Microbiology Procedures Handbook, Multi-Volume, 5th Edition 临床微生物学程序手册,多卷,第5版 2000
人脑智能与人工智能 1000
King Tyrant 720
Silicon in Organic, Organometallic, and Polymer Chemistry 500
Principles of Plasma Discharges and Materials Processing, 3rd Edition 400
El poder y la palabra: prensa y poder político en las dictaduras : el régimen de Franco ante la prensa y el periodismo 400
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5603300
求助须知:如何正确求助?哪些是违规求助? 4688366
关于积分的说明 14853403
捐赠科研通 4689319
什么是DOI,文献DOI怎么找? 2540601
邀请新用户注册赠送积分活动 1506982
关于科研通互助平台的介绍 1471608