• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
New treatment modalities in osteoporosis.骨质疏松症的新治疗方法。
Endocr Pract. 2010 Sep-Oct;16(5):855-63. doi: 10.4158/EP10048.RA.
2
Novel therapies for osteoporosis.骨质疏松症的新型疗法。
Metabolism. 2015 Oct;64(10):1199-214. doi: 10.1016/j.metabol.2015.07.011. Epub 2015 Jul 21.
3
Potential new drug targets for osteoporosis.骨质疏松症潜在的新药靶点。
Nat Clin Pract Rheumatol. 2009 Jan;5(1):20-7. doi: 10.1038/ncprheum0977.
4
Treatment of post-menopausal osteoporosis: beyond bisphosphonates.绝经后骨质疏松症的治疗:超越双膦酸盐类药物
J Endocrinol Invest. 2015 Jan;38(1):13-29. doi: 10.1007/s40618-014-0152-z. Epub 2014 Sep 7.
5
New therapeutic targets for osteoporosis: beyond denosumab.骨质疏松症的新治疗靶点:超越地舒单抗。
Maturitas. 2012 Nov;73(3):269-72. doi: 10.1016/j.maturitas.2012.08.002. Epub 2012 Aug 24.
6
Pharmacological management of osteogenesis.成骨的药理学管理。
Clinics (Sao Paulo). 2014 Jun;69(6):438-46. doi: 10.6061/clinics/2014(06)12.
7
Management of postmenopausal osteoporosis and the prevention of fractures.绝经后骨质疏松症的管理及骨折预防
Panminerva Med. 2014 Jun;56(2):115-31. Epub 2014 Jun 19.
8
Future therapeutic targets in osteoporosis.骨质疏松症的未来治疗靶点
Curr Opin Rheumatol. 2009 Jul;21(4):380-5. doi: 10.1097/BOR.0b013e32832cbc2a.
9
Targeting the osteoblast: approved and experimental anabolic agents for the treatment of osteoporosis.针对成骨细胞:治疗骨质疏松症的已批准和实验性合成代谢药物。
Hormones (Athens). 2011 Jul-Sep;10(3):174-95. doi: 10.14310/horm.2002.1308.
10
Antiresorptive drugs beyond bisphosphonates and selective oestrogen receptor modulators for the management of postmenopausal osteoporosis.除双膦酸盐和选择性雌激素受体调节剂之外的抗吸收药物用于绝经后骨质疏松症的管理
Drugs Aging. 2014 Jun;31(6):413-24. doi: 10.1007/s40266-014-0179-z.

引用本文的文献

1
Unraveling the Relationship Between Osteoporosis, Treatment Modalities, and Oral Health: A Comprehensive Review.解析骨质疏松症、治疗方式与口腔健康之间的关系:一项综合综述
Cureus. 2023 Nov 25;15(11):e49399. doi: 10.7759/cureus.49399. eCollection 2023 Nov.
2
Network Pharmacological Study on Mechanism of the Therapeutic Effect of Modified Duhuo Jisheng Decoction in Osteoporosis.加味独活寄生汤治疗骨质疏松症疗效机制的网络药理学研究
Front Endocrinol (Lausanne). 2022 Mar 31;13:860649. doi: 10.3389/fendo.2022.860649. eCollection 2022.
3
Investigation of anti-osteoporosis mechanisms of Rehmanniae Radix Preparata based on network pharmacology and experimental verification.基于网络药理学和实验验证的地黄治疗骨质疏松症机制研究。
J Orthop Surg Res. 2021 Oct 14;16(1):599. doi: 10.1186/s13018-021-02751-5.
4
Effects of Rehmannia glutinosa polysaccharides on bone tissue structure and skeletal muscle atrophy in rats with disuse.熟地黄多糖对废用性大鼠骨组织结构和骨骼肌萎缩的影响
Acta Cir Bras. 2021 May 14;36(4):e360403. doi: 10.1590/ACB360403. eCollection 2021.
5
Efficacy and Safety of Denosumab in Osteoporosis or Low Bone Mineral Density Postmenopausal Women.地诺单抗治疗绝经后骨质疏松症或低骨密度女性的疗效与安全性
Front Pharmacol. 2021 Apr 14;12:588095. doi: 10.3389/fphar.2021.588095. eCollection 2021.
6
Osteoblast dysfunctions in bone diseases: from cellular and molecular mechanisms to therapeutic strategies.骨疾病中的成骨细胞功能障碍:从细胞和分子机制到治疗策略
Cell Mol Life Sci. 2015 Apr;72(7):1347-61. doi: 10.1007/s00018-014-1801-2. Epub 2014 Dec 9.
7
Safety of denosumab in postmenopausal women with osteoporosis or low bone mineral density: a meta-analysis.地诺单抗在绝经后骨质疏松症或低骨密度女性中的安全性:一项荟萃分析。
Int J Clin Exp Pathol. 2014 Apr 15;7(5):2113-22. eCollection 2014.
8
The role of midkine in skeletal remodelling.中期因子在骨骼重塑中的作用。
Br J Pharmacol. 2014 Feb;171(4):870-8. doi: 10.1111/bph.12412.
9
Conditional inactivation of noggin in the postnatal skeleton causes osteopenia.条件性敲除出生后骨骼中的noggin 会导致骨质疏松症。
Endocrinology. 2012 Apr;153(4):1616-26. doi: 10.1210/en.2011-1604. Epub 2012 Feb 14.
10
Cathepsin K deficiency in mice induces structural and metabolic changes in the central nervous system that are associated with learning and memory deficits.组织蛋白酶 K 基因敲除小鼠的中枢神经系统发生结构和代谢改变,与学习记忆功能障碍相关。
BMC Neurosci. 2011 Jul 27;12:74. doi: 10.1186/1471-2202-12-74.

本文引用的文献

1
Skeletal actions of insulin-like growth factors.胰岛素样生长因子的骨骼作用。
Expert Rev Endocrinol Metab. 2006 Jan;1(1):47-56. doi: 10.1586/17446651.1.1.47.
2
Odanacatib, a cathepsin-K inhibitor for osteoporosis: a two-year study in postmenopausal women with low bone density.odanacatib,一种用于骨质疏松症的组织蛋白酶 K 抑制剂:一项为期两年的绝经后低骨密度女性研究。
J Bone Miner Res. 2010 May;25(5):937-47. doi: 10.1359/jbmr.091035.
3
Effect of transdermal teriparatide administration on bone mineral density in postmenopausal women.经皮特立帕肽给药对绝经后妇女骨密度的影响。
J Clin Endocrinol Metab. 2010 Jan;95(1):151-8. doi: 10.1210/jc.2009-0358. Epub 2009 Oct 26.
4
Treatment with a soluble receptor for activin improves bone mass and structure in the axial and appendicular skeleton of female cynomolgus macaques (Macaca fascicularis).可溶性激活素受体治疗可改善雌性食蟹猴(Macaca fascicularis)轴性和附肢骨骼的骨量和结构。
Bone. 2010 Jan;46(1):64-71. doi: 10.1016/j.bone.2009.09.018. Epub 2009 Sep 23.
5
Effects of the Src kinase inhibitor saracatinib (AZD0530) on bone turnover in healthy men: a randomized, double-blind, placebo-controlled, multiple-ascending-dose phase I trial.Src 激酶抑制剂 saracatinib(AZD0530)对健康男性骨转换的影响:一项随机、双盲、安慰剂对照、多剂量递增 I 期临床试验。
J Bone Miner Res. 2010 Mar;25(3):463-71. doi: 10.1359/jbmr.090830.
6
Denosumab for prevention of fractures in postmenopausal women with osteoporosis.地诺单抗预防绝经后骨质疏松症女性骨折
N Engl J Med. 2009 Aug 20;361(8):756-65. doi: 10.1056/NEJMoa0809493. Epub 2009 Aug 11.
7
Increasing options for the treatment of osteoporosis.骨质疏松症治疗选择的增加。
N Engl J Med. 2009 Aug 20;361(8):818-20. doi: 10.1056/NEJMe0905480. Epub 2009 Aug 11.
8
Bazedoxifene, a selective estrogen receptor modulator: effects on the endometrium, ovaries, and breast from a randomized controlled trial in osteoporotic postmenopausal women.巴泽多昔芬,一种选择性雌激素受体调节剂:一项骨质疏松绝经后妇女随机对照试验中对子宫内膜、卵巢和乳房的影响。
Menopause. 2009 Nov-Dec;16(6):1109-15. doi: 10.1097/gme.0b013e3181a818db.
9
Cathepsin K inhibitors for osteoporosis and potential off-target effects.组织蛋白酶 K 抑制剂治疗骨质疏松症及其潜在的非靶标作用。
Expert Opin Investig Drugs. 2009 May;18(5):585-600. doi: 10.1517/13543780902832661.
10
Wnt inhibitory factor 1 is epigenetically silenced in human osteosarcoma, and targeted disruption accelerates osteosarcomagenesis in mice.Wnt抑制因子1在人类骨肉瘤中发生表观遗传沉默,其靶向破坏会加速小鼠骨肉瘤的发生。
J Clin Invest. 2009 Apr;119(4):837-51. doi: 10.1172/JCI37175. Epub 2009 Mar 23.

骨质疏松症的新治疗方法。

New treatment modalities in osteoporosis.

机构信息

Department of Research, Saint Francis Hospital and Medical Center, Hartford, Connecticut 06105-1299 , USA.

出版信息

Endocr Pract. 2010 Sep-Oct;16(5):855-63. doi: 10.4158/EP10048.RA.

DOI:10.4158/EP10048.RA
PMID:20350910
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3278773/
Abstract

OBJECTIVE

To describe recently discovered agents for the management of osteoporosis.

METHODS

A literature review (PubMed search) was conducted to identify agents at various stages of development for osteoporosis treatment. Agents under study or review for approval were included.

RESULTS

In menopause, bone remodeling is increased, and agents that suppress bone resorption can stabilize bone mass. In contrast, agents that target the osteoblast can increase bone formation and bone mass. Novel antiresorptive agents can target the formation or the activity of osteoclasts. They include denosumab, an antibody to receptor activated nuclear factor κB; new selective estrogen receptor modulators, such as bazedoxifene; and cathepsin K inhibitors, such as odanacatib. Src kinase inhibitors are in the early phases of development. Parathyroid hormone is the only approved anabolic agent for the treatment of osteoporosis. Novel anabolic therapies for osteoporosis may include the use of factors with anabolic properties for bone or the neutralization of growth factor antagonists. Recent discoveries have demonstrated that the Wnt/β-catenin signaling pathway has a central role in osteoblastic cell differentiation. Antibodies to Wnt antagonists, such as sclerostin, are under development as new therapeutic approaches for osteoporosis. Anabolic therapies have the potential to enhance bone mass, but their long-term safety must be proven.

CONCLUSIONS

New developments in the treatment of osteoporosis include novel antiresorptive and anabolic agents. Their success will depend on their long-term effectiveness and safety profile.

摘要

目的

描述最近发现的用于骨质疏松症治疗的药物。

方法

对骨质疏松症治疗的各个阶段的药物进行了文献回顾(PubMed 搜索)。研究或审查中的药物包括在内。

结果

在绝经期间,骨重塑增加,抑制骨吸收的药物可以稳定骨量。相比之下,针对成骨细胞的药物可以增加骨形成和骨量。新型抗吸收药物可以靶向破骨细胞的形成或活性。它们包括针对核因子 κB 受体激活的抗酒石酸酸性磷酸酶 4(Denosumab)的抗体;新的选择性雌激素受体调节剂,如 bazedoxifene;和组织蛋白酶 K 抑制剂,如odanacatib。Src 激酶抑制剂处于早期开发阶段。甲状旁腺激素是治疗骨质疏松症的唯一批准的合成代谢药物。用于骨质疏松症的新型合成代谢疗法可能包括使用具有成骨特性的因子或中和生长因子拮抗剂。最近的发现表明 Wnt/β-连环蛋白信号通路在成骨细胞分化中具有核心作用。针对 Wnt 拮抗剂(如硬化素)的抗体正在开发中,作为骨质疏松症的新治疗方法。合成代谢疗法有增强骨量的潜力,但必须证明其长期安全性。

结论

骨质疏松症治疗的新进展包括新型抗吸收和合成代谢药物。它们的成功将取决于其长期有效性和安全性。