• 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

与二丙酸倍氯米松不同,丙酸氟替卡松不影响骨代谢。

Fluticasone propionate does not influence bone metabolism in contrast to beclomethasone dipropionate.

作者信息

Bootsma G P, Dekhuijzen P N, Festen J, Mulder P G, Swinkels L M, van Herwaarden C L

机构信息

Department of Pulmonary Diseases, University Hospital, Nijmegen, the Netherlands.

出版信息

Am J Respir Crit Care Med. 1996 Mar;153(3):924-30. doi: 10.1164/ajrccm.153.3.8630574.

DOI:10.1164/ajrccm.153.3.8630574
PMID:8630574
Abstract

Inhaled corticosteroids (ICS) in dosages above 1,000 micrograms/d may influence parameters of bone metabolism. Fluticasone propionate (FP) is a new ICS with a higher clinical potency than beclomethasone dipropionate (BDP) combined with negligible oral bioavailability. The aim of this study was to evaluate the effects of FP and BDP in clinically equipotent dosages on indices of bone metabolism and morning cortisol. FP 750 micrograms/d and BDP 1,500 micrograms/d were compared in a randomized, double-blind, crossover study consisting of two 6-wk treatment periods, each preceded by a 3-wk single-blind placebo period. Twenty-one nonsmoking asthmatic completed the study. FP had the same effect on FEV1 and peak expiratory flow as the double dose of BDP. Both treatments did not change morning cortisol. BDP decreased both osteocalcin and procollagen type 1 carboxyterminal propeptide, indices of bone formation, significantly by 18.5 and 21.9%, respectively. In contrast, FP did not change any variable of bone formation. FP and BDP did not increase type 1 collagen carboxyterminal telopeptide and deoxypyridinoline crosslinks, both markers of bone resorption. In changes in parameters of bone metabolism indicate adverse effects on bone quality in the long term, FP may offer an advantage over BDP.

摘要

剂量超过1000微克/天的吸入性糖皮质激素(ICS)可能会影响骨代谢参数。丙酸氟替卡松(FP)是一种新型ICS,其临床效力高于二丙酸倍氯米松(BDP),且口服生物利用度可忽略不计。本研究的目的是评估临床等效剂量的FP和BDP对骨代谢指标和早晨皮质醇的影响。在一项随机、双盲、交叉研究中,比较了750微克/天的FP和1500微克/天的BDP,该研究包括两个6周的治疗期,每个治疗期之前都有一个3周的单盲安慰剂期。21名不吸烟的哮喘患者完成了该研究。FP对第一秒用力呼气容积(FEV1)和呼气峰值流速的作用与双倍剂量的BDP相同。两种治疗均未改变早晨皮质醇水平。BDP使骨钙素和I型前胶原羧基末端前肽(骨形成指标)分别显著降低18.5%和21.9%。相比之下,FP未改变任何骨形成变量。FP和BDP均未增加I型胶原羧基末端肽和脱氧吡啶啉交联物(两者均为骨吸收标志物)。如果骨代谢参数的变化表明长期对骨质量有不良影响,那么FP可能比BDP具有优势。

相似文献

1
Fluticasone propionate does not influence bone metabolism in contrast to beclomethasone dipropionate.与二丙酸倍氯米松不同,丙酸氟替卡松不影响骨代谢。
Am J Respir Crit Care Med. 1996 Mar;153(3):924-30. doi: 10.1164/ajrccm.153.3.8630574.
2
Safety and efficacy of fluticasone and beclomethasone in moderate to severe asthma. Belgian Multicenter Study Group.氟替卡松和倍氯米松治疗中重度哮喘的安全性和有效性。比利时多中心研究组。
Am J Respir Crit Care Med. 1998 Mar;157(3 Pt 1):827-32. doi: 10.1164/ajrccm.157.3.9610009.
3
A randomized, double-blind comparison of beclomethasone dipropionate extrafine aerosol and fluticasone propionate.丙酸倍氯米松超细气雾剂与丙酸氟替卡松的随机双盲对照研究。
Ann Allergy Asthma Immunol. 2001 May;86(5):575-82. doi: 10.1016/S1081-1206(10)62907-9.
4
Skin bruising, adrenal function and markers of bone metabolism in asthmatics using inhaled beclomethasone and fluticasone.使用吸入性倍氯米松和氟替卡松的哮喘患者的皮肤瘀斑、肾上腺功能及骨代谢标志物
Eur Respir J. 1999 May;13(5):993-8. doi: 10.1034/j.1399-3003.1999.13e11.x.
5
A comparison of fluticasone propionate, 1 mg daily, with beclomethasone dipropionate, 2 mg daily, in the treatment of severe asthma. International Study Group.每日1毫克丙酸氟替卡松与每日2毫克二丙酸倍氯米松治疗重度哮喘的比较。国际研究小组。
Eur Respir J. 1993 Jun;6(6):877-85.
6
Fluticasone propionate and budesonide do not influence bone metabolism in the long term treatment of asthma.丙酸氟替卡松和布地奈德在哮喘的长期治疗中不影响骨代谢。
Allergol Immunopathol (Madr). 2001 Jan-Feb;29(1):22-7. doi: 10.1016/s0301-0546(01)79011-8.
7
Fluticasone propionate 1 mg daily and beclomethasone dipropionate 2 mg daily: a comparison over 1 yr.丙酸氟替卡松每日1毫克与二丙酸倍氯米松每日2毫克:1年的比较
Respir Med. 1996 Nov;90(10):609-17. doi: 10.1016/s0954-6111(96)90019-0.
8
Clinical experience with fluticasone propionate in asthma: a meta-analysis of efficacy and systemic activity compared with budesonide and beclomethasone dipropionate at half the microgram dose or less.丙酸氟替卡松治疗哮喘的临床经验:与布地奈德和二丙酸倍氯米松在半微克剂量或更低剂量下的疗效和全身活性的荟萃分析。
Respir Med. 1998 Jan;92(1):95-104. doi: 10.1016/s0954-6111(98)90039-7.
9
A randomized, double-blind study comparing the effects of beclomethasone and fluticasone on bone density over two years.一项为期两年的随机双盲研究,比较倍氯米松和氟替卡松对骨密度的影响。
Eur Respir J. 1999 Jun;13(6):1267-75.
10
Comparison of fluticasone propionate and beclomethasone dipropionate on direct and indirect measurements of bronchial hyperresponsiveness in patients with stable asthma.丙酸氟替卡松与二丙酸倍氯米松对稳定期哮喘患者支气管高反应性直接和间接测量的比较
Thorax. 1995 Oct;50(10):1044-50. doi: 10.1136/thx.50.10.1044.

引用本文的文献

1
Fluticasone versus beclomethasone or budesonide for chronic asthma in adults and children.氟替卡松与倍氯米松或布地奈德用于成人和儿童慢性哮喘的比较。
Cochrane Database Syst Rev. 2007 Oct 17;2007(4):CD002310. doi: 10.1002/14651858.CD002310.pub4.
2
Biochemical markers of bone metabolism and calciuria with inhaled budesonide therapy.吸入布地奈德治疗对骨代谢生化标志物及尿钙的影响
Pediatr Nephrol. 2004 May;19(5):511-5. doi: 10.1007/s00467-004-1418-z. Epub 2004 Mar 9.
3
Inhaled corticosteroid effects on bone metabolism in asthma and mild chronic obstructive pulmonary disease.
吸入性皮质类固醇对哮喘和轻度慢性阻塞性肺疾病骨代谢的影响。
Cochrane Database Syst Rev. 2002;2002(1):CD003537. doi: 10.1002/14651858.CD003537.
4
Effect of one year treatment with inhaled fluticasone propionate or beclomethasone dipropionate on bone density and bone metabolism: a randomised parallel group study in adult asthmatic subjects.吸入丙酸氟替卡松或二丙酸倍氯米松治疗一年对骨密度和骨代谢的影响:一项针对成年哮喘患者的随机平行组研究。
Thorax. 2000 May;55(5):375-82. doi: 10.1136/thorax.55.5.375.
5
Measures for detecting systemic bioactivity with inhaled and intranasal corticosteroids.吸入性和鼻内用糖皮质激素全身生物活性检测方法
Thorax. 1997 May;52(5):476-82. doi: 10.1136/thx.52.5.476.