• 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

依达拉奉治疗弗里德赖希共济失调相关性心肌病:一项为期 6 个月的 III 期研究(IONIA)的结果。

Idebenone in Friedreich ataxia cardiomyopathy-results from a 6-month phase III study (IONIA).

机构信息

Department of Neurology, University of Pennsylvania School of Medicine, Philadelphia, USA.

出版信息

Am Heart J. 2011 Mar;161(3):639-645.e1. doi: 10.1016/j.ahj.2010.10.038. Epub 2011 Jan 31.

DOI:10.1016/j.ahj.2010.10.038
PMID:21392622
Abstract

BACKGROUND

Friedreich ataxia (FRDA) is commonly associated with hypertrophic cardiomyopathy, but little is known about its frequency, severity, or treatment. In this 6-month randomized, double-blind, controlled study, we sought to determine whether idebenone improves cardiac measures in FRDA.

METHODS

Seventy pediatric subjects were treated either with idebenone (450/900 mg/d or 1,350/2,250 mg/d) or with placebo. Electrocardiograms (ECGs) were assessed at each visit, and echocardiograms, at baseline and week 24.

RESULTS

We found ECG abnormalities in 90% of the subjects. On echocardiogram, 81.4% of the total cohort had left ventricular (LV) hypertrophy, as measured by increased LV mass index-Dubois, and the mean ejection fraction (EF) was 56.9%. In linear regression models, longer PR intervals at baseline were marginally associated with longer GAA repeat length (P = .011). Similarly, GAA repeat length did not clearly predict baseline EF (P = .086) and LV mass by M-mode (P = .045). Left ventricular mass index, posterior wall thickness, EF, and ECG parameters were not significantly improved by treatment with idebenone. Some changes in echocardiographic parameters during the treatment phase correlated with baseline status but not with treatment group.

CONCLUSIONS

Idebenone did not decrease LV hypertrophy or improve cardiac function in subjects with FRDA. The present study does not provide evidence of benefit in this cohort over a 6-month treatment period.

摘要

背景

弗里德赖希共济失调(FRDA)通常与肥厚型心肌病相关,但对其发生频率、严重程度或治疗方法知之甚少。在这项为期 6 个月的随机、双盲、对照研究中,我们旨在确定依地苯醌是否能改善 FRDA 的心脏指标。

方法

70 名儿科患者分别接受依地苯醌(450/900mg/d 或 1350/2250mg/d)或安慰剂治疗。每次就诊时评估心电图(ECG),基线和第 24 周评估超声心动图。

结果

我们发现 90%的患者存在心电图异常。在超声心动图上,总队列中有 81.4%的患者存在左心室(LV)肥厚,通过左心室质量指数-Dubois 测量,平均射血分数(EF)为 56.9%。在线性回归模型中,基线时较长的 PR 间期与较长的 GAA 重复长度呈边缘相关(P=0.011)。同样,GAA 重复长度并不能明确预测基线 EF(P=0.086)和 M 模式下的 LV 质量(P=0.045)。依地苯醌治疗并不能显著改善 LV 质量指数、后壁厚度、EF 和心电图参数。治疗阶段的一些超声心动图参数的变化与基线状态相关,但与治疗组无关。

结论

依地苯醌不能减少 FRDA 患者的 LV 肥厚或改善心脏功能。本研究在 6 个月的治疗期间并未为这一队列提供获益证据。

相似文献

1
Idebenone in Friedreich ataxia cardiomyopathy-results from a 6-month phase III study (IONIA).依达拉奉治疗弗里德赖希共济失调相关性心肌病:一项为期 6 个月的 III 期研究(IONIA)的结果。
Am Heart J. 2011 Mar;161(3):639-645.e1. doi: 10.1016/j.ahj.2010.10.038. Epub 2011 Jan 31.
2
[Successful idebenone therapy of hypertrophic cardiomyopathy in Friedreich ataxia].
Orv Hetil. 2003 Jun 22;144(25):1241-4.
3
Heart hypertrophy and function are improved by idebenone in Friedreich's ataxia.艾地苯醌可改善弗里德赖希共济失调患者的心脏肥大及功能。
Free Radic Res. 2002 Apr;36(4):467-9. doi: 10.1080/10715760290021333.
4
Assessment of neurological efficacy of idebenone in pediatric patients with Friedreich's ataxia: data from a 6-month controlled study followed by a 12-month open-label extension study.评价依地酸二钠治疗小儿弗里德里希共济失调的神经功效:一项为期 6 个月的对照研究和一项为期 12 个月的开放性扩展研究的数据。
J Neurol. 2012 Feb;259(2):284-91. doi: 10.1007/s00415-011-6174-y. Epub 2011 Jul 22.
5
Exercise capacity and idebenone intervention in children and adolescents with Friedreich ataxia.运动能力和依地酸二钠钙干预弗里德里希共济失调儿童和青少年。
Arch Phys Med Rehabil. 2010 Jul;91(7):1044-50. doi: 10.1016/j.apmr.2010.04.007.
6
Antioxidants and other pharmacological treatments for Friedreich ataxia.用于弗里德赖希共济失调的抗氧化剂及其他药物治疗
Cochrane Database Syst Rev. 2012 Apr 18(4):CD007791. doi: 10.1002/14651858.CD007791.pub3.
7
A phase 3, double-blind, placebo-controlled trial of idebenone in friedreich ataxia.艾地苯醌治疗弗里德赖希共济失调的一项3期、双盲、安慰剂对照试验。
Arch Neurol. 2010 Aug;67(8):941-7. doi: 10.1001/archneurol.2010.168.
8
Idebenone: an emerging therapy for Friedreich ataxia.艾地苯醌:一种用于弗里德赖希共济失调的新兴疗法。
J Neurol. 2009 Mar;256 Suppl 1:25-30. doi: 10.1007/s00415-009-1005-0.
9
Low-dose idebenone treatment in Friedreich's ataxia with and without cardiac hypertrophy.低剂量艾地苯醌治疗伴或不伴心脏肥大的弗里德赖希共济失调。
J Neurol. 2009 Sep;256(9):1434-7. doi: 10.1007/s00415-009-5130-6. Epub 2009 Apr 12.
10
Idebenone treatment in Friedreich patients: one-year-long randomized placebo-controlled trial.艾地苯醌治疗弗里德赖希共济失调患者:为期一年的随机安慰剂对照试验。
Neurology. 2003 May 27;60(10):1676-9. doi: 10.1212/01.wnl.0000055872.50364.fc.

引用本文的文献

1
Efficacy and Safety of Coenzyme Q10 Supplementation in Neonates, Infants and Children: An Overview.辅酶Q10补充剂在新生儿、婴儿和儿童中的疗效与安全性:综述
Antioxidants (Basel). 2024 Apr 26;13(5):530. doi: 10.3390/antiox13050530.
2
Emerging antioxidant therapies in Friedreich's ataxia.弗里德赖希共济失调的新兴抗氧化治疗方法。
Front Pharmacol. 2024 Feb 6;15:1359618. doi: 10.3389/fphar.2024.1359618. eCollection 2024.
3
Neurodegenerative Diseases: New Hopes and Perspectives.神经退行性疾病:新的希望和展望。
Curr Mol Med. 2024;24(8):1004-1032. doi: 10.2174/1566524023666230907093451.
4
Apparent Opportunities and Hidden Pitfalls: The Conflicting Results of Restoring NRF2-Regulated Redox Metabolism in Friedreich's Ataxia Pre-Clinical Models and Clinical Trials.明显的机遇与潜在的陷阱:在弗里德赖希共济失调临床前模型和临床试验中恢复NRF2调节的氧化还原代谢的矛盾结果。
Biomedicines. 2023 Apr 27;11(5):1293. doi: 10.3390/biomedicines11051293.
5
Adenosine Improves Mitochondrial Function and Biogenesis in Friedreich's Ataxia Fibroblasts Following L-Buthionine Sulfoximine-Induced Oxidative Stress.在L-丁硫氨酸亚砜亚胺诱导的氧化应激后,腺苷可改善弗里德赖希共济失调成纤维细胞的线粒体功能和生物发生。
Biology (Basel). 2023 Apr 6;12(4):559. doi: 10.3390/biology12040559.
6
Skin fibroblast metabolomic profiling reveals that lipid dysfunction predicts the severity of Friedreich's ataxia.皮肤成纤维细胞代谢组学分析显示脂代谢功能障碍可预测弗里德赖希共济失调的严重程度。
J Lipid Res. 2022 Sep;63(9):100255. doi: 10.1016/j.jlr.2022.100255. Epub 2022 Jul 16.
7
Friedreich ataxia: clinical features and new developments.弗里德赖希共济失调:临床特征和新进展。
Neurodegener Dis Manag. 2022 Oct;12(5):267-283. doi: 10.2217/nmt-2022-0011. Epub 2022 Jun 29.
8
Discovery of Therapeutics Targeting Oxidative Stress in Autosomal Recessive Cerebellar Ataxia: A Systematic Review.常染色体隐性遗传性小脑共济失调中靶向氧化应激的治疗方法的发现:一项系统评价
Pharmaceuticals (Basel). 2022 Jun 19;15(6):764. doi: 10.3390/ph15060764.
9
Current Drug Repurposing Strategies for Rare Neurodegenerative Disorders.罕见神经退行性疾病的当前药物再利用策略
Front Pharmacol. 2021 Dec 21;12:768023. doi: 10.3389/fphar.2021.768023. eCollection 2021.
10
Mitochondrial Dysfunction in Atrial Fibrillation-Mechanisms and Pharmacological Interventions.心房颤动中的线粒体功能障碍——机制与药物干预
J Clin Med. 2021 May 28;10(11):2385. doi: 10.3390/jcm10112385.