• 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

绝经后骨质疏松症的发病机制。

Pathogenesis of postmenopausal osteoporosis.

作者信息

Lindsay R

机构信息

Columbia University College of Physicians and Surgeons, New York, NY.

出版信息

Baillieres Clin Rheumatol. 1993 Oct;7(3):499-513. doi: 10.1016/s0950-3579(05)80075-5.

DOI:10.1016/s0950-3579(05)80075-5
PMID:8293486
Abstract

Osteoporosis is a disorder of ageing that shares with other disorders of ageing a multifactorial pathogenesis. The important factors for osteoporosis include the diet, life-style and intercurrent factors such as disease. However, it is clear that loss of ovarian function is an important determinant of bone loss, and oestrogen appears to be the key factor involved. Thus, not only does loss of ovarian function result in bone loss, it can be stopped by adequate oestrogen intervention. Numerous techniques are available to measure bone mass non-invasively and to estimate the risk of future fracture. Thus, for the postmenopausal woman who is concerned about osteoporosis, and who is willing to accept intervention to prevent the disease, bone mass measurement allows the clinician to determine the risk of future osteoporotic fracture and to provide intervention if required. Future studies may elucidate whether determination of skeletal remodelling using biochemistry adds significantly to risk determination. This may be required when considering agents other than oestrogen for intervention among asymptomatic women, as these agents primarily affect the skeleton, while the effects of oestrogen are wide ranging in the body.

摘要

骨质疏松症是一种衰老性疾病,与其他衰老性疾病一样具有多因素发病机制。骨质疏松症的重要因素包括饮食、生活方式以及诸如疾病等并发因素。然而,卵巢功能丧失显然是骨质流失的一个重要决定因素,雌激素似乎是其中的关键因素。因此,卵巢功能丧失不仅会导致骨质流失,通过适当的雌激素干预还可以阻止这种情况。有多种技术可用于非侵入性地测量骨量并估计未来骨折的风险。因此,对于担心患骨质疏松症且愿意接受干预以预防该疾病的绝经后女性,骨量测量使临床医生能够确定未来发生骨质疏松性骨折的风险,并在需要时提供干预措施。未来的研究可能会阐明,使用生物化学方法测定骨骼重塑是否能显著提高风险判定的准确性。在考虑对无症状女性使用雌激素以外的药物进行干预时,这可能是必要的,因为这些药物主要影响骨骼,而雌激素对身体的影响范围广泛。

相似文献

1
Pathogenesis of postmenopausal osteoporosis.绝经后骨质疏松症的发病机制。
Baillieres Clin Rheumatol. 1993 Oct;7(3):499-513. doi: 10.1016/s0950-3579(05)80075-5.
2
Bone loss, contraception and lactation.骨质流失、避孕与哺乳。
Acta Obstet Gynecol Scand. 1993 Apr;72(3):148-56. doi: 10.3109/00016349309013363.
3
Bone mass and the risk of breast cancer: the influence of cumulative exposure to oestrogen and reproductive correlates. Results of the Marburg breast cancer and osteoporosis trial (MABOT).骨量与乳腺癌风险:雌激素累积暴露及生殖相关因素的影响。马尔堡乳腺癌与骨质疏松症试验(MABOT)结果
Maturitas. 2007 Mar 20;56(3):312-21. doi: 10.1016/j.maturitas.2006.09.005. Epub 2006 Oct 17.
4
An in silico approach to elucidate the pathways leading to primary osteoporosis: age-related vs. postmenopausal.一种阐明导致原发性骨质疏松症的途径的计算方法:与年龄相关的与绝经后相关的。
Biomech Model Mechanobiol. 2024 Aug;23(4):1393-1409. doi: 10.1007/s10237-024-01846-2. Epub 2024 May 3.
5
Randomised controlled study of effect of parathyroid hormone on vertebral-bone mass and fracture incidence among postmenopausal women on oestrogen with osteoporosis.甲状旁腺激素对接受雌激素治疗的绝经后骨质疏松症女性椎体骨量及骨折发生率影响的随机对照研究。
Lancet. 1997 Aug 23;350(9077):550-5. doi: 10.1016/S0140-6736(97)02342-8.
6
[Osteoporosis--pathogenesis and prophylaxis].[骨质疏松症——发病机制与预防]
Wiad Lek. 2004;57 Suppl 1:295-300.
7
Pathogenesis of osteoporosis.
Bone. 1995 Aug;17(2 Suppl):19S-22S. doi: 10.1016/8756-3282(95)00202-o.
8
[Differential osteoporosis diagnosis in the woman].
Ther Umsch. 1998 Nov;55(11):685-95.
9
[Screening techniques].[筛查技术]
Presse Med. 2002 Apr 20;31(15):694-8.
10
A theoretical analysis of the relative influences of peak BMD, age-related bone loss and menopause on the development of osteoporosis.对峰值骨密度、年龄相关性骨质流失和绝经对骨质疏松症发展的相对影响的理论分析。
Osteoporos Int. 2003 Oct;14(10):843-7. doi: 10.1007/s00198-003-1454-8. Epub 2003 Aug 7.

引用本文的文献

1
Comparison of the therapeutic effects of mesenchymal stem cells derived from human dental pulp (DP), adipose tissue (AD), placental amniotic membrane (PM), and umbilical cord (UC) on postmenopausal osteoporosis.人牙髓(DP)、脂肪组织(AD)、胎盘羊膜(PM)和脐带(UC)来源的间充质干细胞对绝经后骨质疏松症治疗效果的比较
Front Pharmacol. 2024 Mar 27;15:1349199. doi: 10.3389/fphar.2024.1349199. eCollection 2024.
2
Therapeutic effect of icariin combined with stem cells on postmenopausal osteoporosis in rats.淫羊藿苷联合干细胞对大鼠绝经后骨质疏松症的治疗作用
J Bone Miner Metab. 2018 Mar;36(2):180-188. doi: 10.1007/s00774-017-0831-x. Epub 2017 Jul 5.
3
Prevention of disuse osteoporosis in rats by Cordyceps sinensis extract.
蛹虫草提取物预防大鼠废用性骨质疏松症。
Osteoporos Int. 2012 Sep;23(9):2347-57. doi: 10.1007/s00198-011-1842-4. Epub 2011 Dec 13.
4
Risk factors for low bone mineral density among a large group of Norwegian women with fractures.一大群挪威骨折女性中骨密度低的风险因素。
Eur J Epidemiol. 2000 Mar;16(3):223-9. doi: 10.1023/a:1007672331628.
5
Genetic and environmental factors affecting bone mineral density in large families.大家庭中影响骨密度的遗传和环境因素。
Postgrad Med J. 1998 Jun;74(872):349-54. doi: 10.1136/pgmj.74.872.349.