• 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

骨质疏松症的分子机制与新兴治疗策略。

Molecular Mechanisms and Emerging Therapeutics for Osteoporosis.

机构信息

Immunotherapy Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), 125 Gwahak-ro, Yuseong-gu, Daejeon 34141, Korea.

Research Institute of Women's Health, Sookmyung Women's University, 100 Cheongparo47gil, Yongsan-Gu, Seoul 04310, Korea.

出版信息

Int J Mol Sci. 2020 Oct 15;21(20):7623. doi: 10.3390/ijms21207623.

DOI:10.3390/ijms21207623
PMID:33076329
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7589419/
Abstract

Osteoporosis is the most common chronic metabolic bone disease. It has been estimated that more than 10 million people in the United States and 200 million men and women worldwide have osteoporosis. Given that the aging population is rapidly increasing in many countries, osteoporosis could become a global challenge with an impact on the quality of life of the affected individuals. Osteoporosis can be defined as a condition characterized by low bone density and increased risk of fractures due to the deterioration of the bone architecture. Thus, the major goal of treatment is to reduce the risk for fractures. There are several treatment options, mostly medications that can control disease progression in risk groups, such as postmenopausal women and elderly men. Recent studies on the basic molecular mechanisms and clinical implications of osteoporosis have identified novel therapeutic targets. Emerging therapies targeting novel disease mechanisms could provide powerful approaches for osteoporosis management in the future. Here, we review the etiology of osteoporosis and the molecular mechanism of bone remodeling, present current pharmacological options, and discuss emerging therapies targeting novel mechanisms, investigational treatments, and new promising therapeutic approaches.

摘要

骨质疏松症是最常见的慢性代谢性骨病。据估计,美国有超过 1000 万人,全世界有 2 亿男性和女性患有骨质疏松症。鉴于许多国家的人口老龄化速度正在迅速加快,骨质疏松症可能成为一个全球性挑战,影响到受影响个体的生活质量。骨质疏松症可以定义为一种以骨密度低和骨折风险增加为特征的疾病,这是由于骨结构恶化所致。因此,治疗的主要目标是降低骨折风险。有几种治疗选择,主要是药物,可以控制绝经后妇女和老年男性等高危人群的疾病进展。最近对骨质疏松症的基础分子机制和临床意义的研究确定了新的治疗靶点。针对新疾病机制的新兴治疗方法可能为未来的骨质疏松症管理提供有力方法。在这里,我们回顾了骨质疏松症的病因和骨重建的分子机制,介绍了目前的药理学选择,并讨论了针对新机制的新兴治疗方法、正在研究的治疗方法以及新的有前途的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c4f/7589419/89c2cd801a12/ijms-21-07623-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c4f/7589419/dd52cd410f88/ijms-21-07623-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c4f/7589419/89c2cd801a12/ijms-21-07623-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c4f/7589419/dd52cd410f88/ijms-21-07623-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c4f/7589419/89c2cd801a12/ijms-21-07623-g002.jpg

相似文献

1
Molecular Mechanisms and Emerging Therapeutics for Osteoporosis.骨质疏松症的分子机制与新兴治疗策略。
Int J Mol Sci. 2020 Oct 15;21(20):7623. doi: 10.3390/ijms21207623.
2
The Development of Molecular Biology of Osteoporosis.骨质疏松症分子生物学的发展。
Int J Mol Sci. 2021 Jul 30;22(15):8182. doi: 10.3390/ijms22158182.
3
Pharmacological topics of bone metabolism: recent advances in pharmacological management of osteoporosis.骨代谢的药理学主题:骨质疏松症药物治疗的最新进展
J Pharmacol Sci. 2008 Apr;106(4):530-5. doi: 10.1254/jphs.fm0070218.
4
Medical Treatment for Osteoporosis: From Molecular to Clinical Opinions.骨质疏松症的治疗:从分子到临床观点。
Int J Mol Sci. 2019 May 6;20(9):2213. doi: 10.3390/ijms20092213.
5
[Up-to-date treatments for osteoporosis].[骨质疏松症的最新治疗方法]
Orv Hetil. 2006 Feb 19;147(7):301-6.
6
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.
7
Selective estrogen receptor modulators: A possible new treatment of osteoporosis in males.选择性雌激素受体调节剂:男性骨质疏松症的一种可能新疗法。
Med Hypotheses. 2006;67(5):1052-3. doi: 10.1016/j.mehy.2006.04.040. Epub 2006 Jun 21.
8
Advances in osteoporosis from 1970 to 2018.1970 年至 2018 年骨质疏松症的研究进展。
Menopause. 2018 Dec;25(12):1403-1417. doi: 10.1097/GME.0000000000001263.
9
Current and emerging pharmacologic therapies for the management of postmenopausal osteoporosis.用于绝经后骨质疏松症管理的当前和新兴药物治疗。
J Womens Health (Larchmt). 2009 Oct;18(10):1615-26. doi: 10.1089/jwh.2008.1086.
10
New management options for osteoporosis with emphasis on SERMs.以选择性雌激素受体调节剂为重点的骨质疏松症新管理方案。
Climacteric. 2015;18 Suppl 2:56-61. doi: 10.3109/13697137.2015.1104010. Epub 2015 Oct 27.

引用本文的文献

1
Mechanism of action of curculigoside ameliorating osteoporosis: an analysis based on network pharmacology and experimental validation.仙茅苷改善骨质疏松症的作用机制:基于网络药理学和实验验证的分析
Front Endocrinol (Lausanne). 2025 Aug 21;16:1549471. doi: 10.3389/fendo.2025.1549471. eCollection 2025.
2
Identification and validation of the cellular senescence-associated molecular pattern and diagnostic markers for osteoporosis.骨质疏松症细胞衰老相关分子模式及诊断标志物的鉴定与验证
BMC Med Genomics. 2025 Sep 2;18(1):140. doi: 10.1186/s12920-025-02205-5.
3
Erythrocyte Membrane-Cloaked and Alendronate-Loaded Hollow Prussian Blue Nanoparticles for Synergistic Osteoporosis Therapy via Antioxidant and Targeted Delivery Mechanisms.

本文引用的文献

1
Prospect of Stem Cell Therapy and Regenerative Medicine in Osteoporosis.干细胞治疗与骨质疏松症再生医学的前景。
Front Endocrinol (Lausanne). 2020 Jul 3;11:430. doi: 10.3389/fendo.2020.00430. eCollection 2020.
2
Pros and Cons of Denosumab Treatment for Osteoporosis and Implication for RANKL Aptamer Therapy.地诺单抗治疗骨质疏松症的利弊及RANKL适体疗法的意义
Front Cell Dev Biol. 2020 May 14;8:325. doi: 10.3389/fcell.2020.00325. eCollection 2020.
3
The Unraveling: Cardiac and Musculoskeletal Defects and Their Role in Common Alzheimer Disease Morbidity and Mortality.
红细胞膜包覆且负载阿仑膦酸盐的中空普鲁士蓝纳米颗粒通过抗氧化和靶向递送机制协同治疗骨质疏松症
ACS Omega. 2025 Aug 5;10(32):36068-36081. doi: 10.1021/acsomega.5c03693. eCollection 2025 Aug 19.
4
Nrf2 signaling pathway: focus on oxidative stress in osteoporosis.核因子E2相关因子2(Nrf2)信号通路:聚焦于骨质疏松症中的氧化应激
Osteoporos Int. 2025 Jul 15. doi: 10.1007/s00198-025-07592-0.
5
Beyond Bone Loss: A Biology Perspective on Osteoporosis Pathogenesis, Multi-Omics Approaches, and Interconnected Mechanisms.超越骨质流失:骨质疏松症发病机制、多组学方法及相互关联机制的生物学视角
Biomedicines. 2025 Jun 12;13(6):1443. doi: 10.3390/biomedicines13061443.
6
Mettl7a alleviated bone loss in osteoporosis mice by targeting the O-GlcNAcylation of Bsp via m6A methylation.Mettl7a通过m6A甲基化靶向Bsp的O-连接N-乙酰葡糖胺化,从而减轻骨质疏松症小鼠的骨质流失。
Stem Cells Transl Med. 2025 Jun 25;14(7). doi: 10.1093/stcltm/szaf024.
7
Unlocking the potential of stem cell-derived extracellular vesicles in osteoporosis therapy: a systematic review and meta-analysis of preclinical studies.解锁干细胞衍生细胞外囊泡在骨质疏松症治疗中的潜力:一项临床前研究的系统评价和荟萃分析
J Transl Med. 2025 Jun 18;23(1):683. doi: 10.1186/s12967-025-06654-5.
8
Palm Tocotrienol Preserves Trabecular Osteocyte Indices and Modulates the Expression of Osteocyte Markers in Ovariectomized Rats.棕榈生育三烯酚可维持去卵巢大鼠的小梁骨细胞指数并调节骨细胞标志物的表达。
Biomedicines. 2025 May 18;13(5):1220. doi: 10.3390/biomedicines13051220.
9
Mechanosignaling in Osteoporosis: When Cells Feel the Force.骨质疏松症中的机械信号转导:当细胞感知到力时。
Int J Mol Sci. 2025 Apr 24;26(9):4007. doi: 10.3390/ijms26094007.
10
Plastrum Testudinis Stimulates Bone Formation through Wnt/β-catenin Signaling Pathway Regulated by miR-214.龟甲通过miR-214调控的Wnt/β-连环蛋白信号通路刺激骨形成。
Chin J Integr Med. 2025 May 13. doi: 10.1007/s11655-025-4012-9.
《 unraveling :心脏和肌肉骨骼缺陷及其在常见阿尔茨海默病发病和死亡中的作用》。
Am J Pathol. 2020 Aug;190(8):1609-1621. doi: 10.1016/j.ajpath.2020.04.013. Epub 2020 May 11.
4
Pathogenesis of glucocorticoid-induced osteoporosis and options for treatment.糖皮质激素性骨质疏松症的发病机制与治疗选择。
Nat Rev Endocrinol. 2020 Aug;16(8):437-447. doi: 10.1038/s41574-020-0341-0. Epub 2020 Apr 14.
5
At the Crossroads of the Adipocyte and Osteoclast Differentiation Programs: Future Therapeutic Perspectives.在脂肪细胞和破骨细胞分化程序的十字路口:未来的治疗前景。
Int J Mol Sci. 2020 Mar 26;21(7):2277. doi: 10.3390/ijms21072277.
6
Glucosylceramide synthase regulates adipo-osteogenic differentiation through synergistic activation of PPARγ with GlcCer.葡萄糖神经酰胺合酶通过协同激活 PPARγ与 GlcCer 调节脂肪成骨分化。
FASEB J. 2020 Jan;34(1):1270-1287. doi: 10.1096/fj.201901437R. Epub 2019 Nov 29.
7
A road map for understanding molecular and genetic determinants of osteoporosis.骨质疏松症分子和遗传决定因素的理解路线图。
Nat Rev Endocrinol. 2020 Feb;16(2):91-103. doi: 10.1038/s41574-019-0282-7. Epub 2019 Dec 2.
8
Stem cells in Osteoporosis: From Biology to New Therapeutic Approaches.骨质疏松症中的干细胞:从生物学到新的治疗方法
Stem Cells Int. 2019 Jun 2;2019:1730978. doi: 10.1155/2019/1730978. eCollection 2019.
9
Petunidin, a B-ring 5'--Methylated Derivative of Delphinidin, Stimulates Osteoblastogenesis and Reduces sRANKL-Induced Bone Loss.矢车菊素-3-O-葡萄糖苷,天竺葵素的 B 环 5'-甲基化衍生物,可刺激成骨细胞分化,减少 sRANKL 诱导的骨丢失。
Int J Mol Sci. 2019 Jun 7;20(11):2795. doi: 10.3390/ijms20112795.
10
Anti-Osteoporotic Effects of Kukoamine B Isolated from Cortex Extract on Osteoblast and Osteoclast Cells and Ovariectomized Osteoporosis Model Mice.从桑白皮提取物中分离得到的桑根酮 B 对成骨细胞和破骨细胞及去卵巢骨质疏松症模型小鼠的抗骨质疏松作用。
Int J Mol Sci. 2019 Jun 6;20(11):2784. doi: 10.3390/ijms20112784.