• 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

Effect of HMG-CoA reductase inhibitors (statins) on bone mineral density.

作者信息

Funkhouser Holly L, Adera Tilahun, Adler Robert A

机构信息

Endocrinology and Metabolism Section, Medical Service, McGuire Veterans Affairs, Medical Center and Department of Preventive Medicine and Community Health, Virginia Commonwealth University, Richmond, VA 23249, USA.

出版信息

J Clin Densitom. 2002 Summer;5(2):151-8. doi: 10.1385/jcd:5:2:151.

DOI:10.1385/jcd:5:2:151
PMID:12110758
Abstract

Recent studies have suggested that 3-hydroxy-3-methylglutaryl - coenzyme A (HMG-CoA) reductase inhibitors (statins) can increase the bone mineral density (BMD). Our objective was to determine if patients on statin drugs were more likely to have a greater bone mineral density and lower risk of osteoporosis than patients not taking these drugs. A computerized pharmacy system provided complete medication dispensing records for the 983 patients (697 men and 286 women) referred for bone mineral density testing at a single Veterans Affairs Medical Center. In an analysis of covariance model that adjusted for age, body mass index, race, and vitamin use, men using statin drugs were more likely to have a greater BMD of the spine (p < 0.005). The mean difference (effect size) was 0.05 g/cm2 (95% confidence interval of [CL] 0.02-0.09), about 5.3% greater BMD. In women, the association was not significant. The risk of osteoporosis (defined as a T-score < or = -2.5) was determined using logistic regression analysis after adjustment for potential confounding variables. Although not statistically significant, men who received statin drugs for more than 2 yr were approximately half as likely to develop osteoporosis (odds ratio [OR] =.55, 95% CI = 0.28-1.08). A similar effect was observed in women taking statins for any length of time (OR = 0.36, 95% CI = 0.12-1.07). This study suggests that statin drugs may decrease osteoporosis risk, warranting a randomized controlled trial.

摘要

相似文献

1
Effect of HMG-CoA reductase inhibitors (statins) on bone mineral density.
J Clin Densitom. 2002 Summer;5(2):151-8. doi: 10.1385/jcd:5:2:151.
2
Lower femoral neck bone mineral density (BMD) in elderly women not on statins.未服用他汀类药物的老年女性股骨颈骨密度较低。
Women Health. 2019 Sep;59(8):845-853. doi: 10.1080/03630242.2019.1567646. Epub 2019 Feb 5.
3
Efficacy of statins for osteoporosis: a systematic review and meta-analysis.他汀类药物治疗骨质疏松症的疗效:一项系统评价和荟萃分析。
Osteoporos Int. 2017 Jan;28(1):47-57. doi: 10.1007/s00198-016-3844-8. Epub 2016 Nov 25.
4
HMG-CoA reductase inhibitors increase BMD in type 2 diabetes mellitus patients.HMG-CoA还原酶抑制剂可增加2型糖尿病患者的骨密度。
J Clin Endocrinol Metab. 2000 Mar;85(3):1137-42. doi: 10.1210/jcem.85.3.6476.
5
Statin use, bone mineral density, and fracture risk: Geelong Osteoporosis Study.他汀类药物的使用、骨密度与骨折风险:吉朗骨质疏松症研究
Arch Intern Med. 2002 Mar 11;162(5):537-40. doi: 10.1001/archinte.162.5.537.
6
Hydroxymethylglutaryl-coenzyme A reductase inhibitors in osteoporosis management.羟甲基戊二酰辅酶A还原酶抑制剂在骨质疏松症管理中的应用
Ann Pharmacother. 2002 Feb;36(2):326-30. doi: 10.1345/aph.1A071.
7
HMG-CoA reductase inhibitors in osteoporosis: do they reduce the risk of fracture?骨质疏松症中的HMG-CoA还原酶抑制剂:它们能降低骨折风险吗?
Drugs Aging. 2003;20(5):321-36. doi: 10.2165/00002512-200320050-00002.
8
HMG-CoA reductase inhibitors (statins) and bone mineral density: a meta-analysis.HMG-CoA 还原酶抑制剂(他汀类药物)与骨密度:一项荟萃分析。
Bone. 2013 May;54(1):151-6. doi: 10.1016/j.bone.2013.01.044. Epub 2013 Feb 4.
9
Effects of statins vs. non-statin lipid-lowering therapy on bone formation and bone mineral density biomarkers in patients with hyperlipidemia.他汀类药物与非他汀类降脂治疗对高血脂患者骨形成和骨密度生物标志物的影响。
Bone. 2010 Apr;46(4):1011-5. doi: 10.1016/j.bone.2009.12.023. Epub 2010 Jan 4.
10
HMG-CoA reductase inhibitors prevent bone loss in patients with Type 2 diabetes mellitus.HMG-CoA还原酶抑制剂可预防2型糖尿病患者的骨质流失。
Diabet Med. 2004 Sep;21(9):1020-4. doi: 10.1111/j.1464-5491.2004.01292.x.

引用本文的文献

1
Role of Metabolism in Bone Development and Homeostasis.代谢在骨骼发育和稳态中的作用。
Int J Mol Sci. 2020 Nov 26;21(23):8992. doi: 10.3390/ijms21238992.
2
Modified electrospun chitosan membranes for controlled release of simvastatin.改性静电纺丝壳聚糖膜用于辛伐他汀的控制释放。
Int J Pharm. 2020 Jun 30;584:119438. doi: 10.1016/j.ijpharm.2020.119438. Epub 2020 May 17.
3
Efficacy of statins for osteoporosis: a systematic review and meta-analysis.他汀类药物治疗骨质疏松症的疗效:一项系统评价和荟萃分析。
Osteoporos Int. 2017 Jan;28(1):47-57. doi: 10.1007/s00198-016-3844-8. Epub 2016 Nov 25.
4
Novel applications of statins for bone regeneration.他汀类药物在骨再生中的新应用。
Natl Sci Rev. 2015 Mar 1;2(1):85-99. doi: 10.1093/nsr/nwu028. Epub 2014 Aug 16.
5
Simvastatin induces estrogen receptor-alpha expression in bone, restores bone loss, and decreases ERα expression and uterine wet weight in ovariectomized rats.辛伐他汀可诱导骨组织中雌激素受体-α的表达,可恢复骨丢失,并降低去卵巢大鼠的 ERα 表达和子宫湿重。
J Bone Miner Metab. 2011 Jul;29(4):396-403. doi: 10.1007/s00774-010-0231-y. Epub 2010 Nov 10.
6
Local low-dose lovastatin delivery improves the bone-healing defect caused by Nf1 loss of function in osteoblasts.局部低剂量洛伐他汀递送可改善成骨细胞中 NF1 功能丧失引起的骨愈合缺陷。
J Bone Miner Res. 2010 Jul;25(7):1658-67. doi: 10.1002/jbmr.42.
7
The Interleukin-6 inflammation pathway from cholesterol to aging--role of statins, bisphosphonates and plant polyphenols in aging and age-related diseases.从胆固醇到衰老的白细胞介素-6炎症通路——他汀类药物、双膦酸盐和植物多酚在衰老及年龄相关疾病中的作用
Immun Ageing. 2007 Mar 20;4:1. doi: 10.1186/1742-4933-4-1.
8
HMG-CoA reductase inhibitors in osteoporosis: do they reduce the risk of fracture?骨质疏松症中的HMG-CoA还原酶抑制剂:它们能降低骨折风险吗?
Drugs Aging. 2003;20(5):321-36. doi: 10.2165/00002512-200320050-00002.