• 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

他法米地用于一名被诊断为转甲状腺素蛋白心脏淀粉样变患者的腹膜透析的经验。

Experience with tafamidis in peritoneal dialysis for a patient diagnosed with transthyretin cardiac amyloidosis.

作者信息

Fazlic Diego López, García Samuel Abrante, Gerard Micaela, Izquierdo Edduin Martín, Bethencourt Alejandro Alonso, Vannini Luca, García Celestino Hernández, Heras Manuel Macía

机构信息

Cardiology Department, Nuestra Señora de la Candelaria University Hospital, Santa Cruz de Tenerife, Tenerife, Spain.

Nephrology Department, Nuestra Señora de la Candelaria University Hospital, Santa Cruz de Tenerife, Tenerife, Spain.

出版信息

Clin Kidney J. 2024 Jul 29;17(8):sfae233. doi: 10.1093/ckj/sfae233. eCollection 2024 Aug.

DOI:10.1093/ckj/sfae233
PMID:39157068
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11328728/
Abstract

Cardiac amyloidosis is a cardiomyopathy resulting from the extracellular deposition of proteins such as transthyretin (TTR). We present the case of a 72-year-old male with hereditary cardiac amyloidosis. After confirming the diagnosis, tafamidis, a TTR stabilizer, was administered. Remarkably, tafamidis, when coupled with peritoneal dialysis for chronic kidney disease, maintained stability in both cardiac and renal functions. Previous studies have demonstrated the efficacy of tafamidis in reducing all-cause mortality and cardiovascular hospitalizations, although its use in severe renal failure lacks specific evaluation. This case suggests a potential application of tafamidis in moderate-severe kidney disease, emphasizing the need for further research in this population.

摘要

心脏淀粉样变性是一种由诸如转甲状腺素蛋白(TTR)等蛋白质在细胞外沉积导致的心肌病。我们报告一例72岁患有遗传性心脏淀粉样变性的男性病例。确诊后,给予TTR稳定剂塔非酰胺进行治疗。值得注意的是,塔非酰胺与慢性肾病的腹膜透析联合使用时,心脏和肾功能均保持稳定。既往研究已证明塔非酰胺在降低全因死亡率和心血管住院率方面的疗效,尽管其在严重肾衰竭中的应用缺乏具体评估。该病例提示塔非酰胺在中重度肾病中具有潜在应用价值,强调了在该人群中进一步研究的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e17/11328728/45396781a37f/sfae233fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e17/11328728/45396781a37f/sfae233fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e17/11328728/45396781a37f/sfae233fig1.jpg

相似文献

1
Experience with tafamidis in peritoneal dialysis for a patient diagnosed with transthyretin cardiac amyloidosis.他法米地用于一名被诊断为转甲状腺素蛋白心脏淀粉样变患者的腹膜透析的经验。
Clin Kidney J. 2024 Jul 29;17(8):sfae233. doi: 10.1093/ckj/sfae233. eCollection 2024 Aug.
2
Tafamidis: a selective transthyretin stabilizer to treat wild-type ATTR amyloidosis and hereditary ATTR amyloidosis with cardiomyopathy.塔非酰胺:一种用于治疗野生型转甲状腺素蛋白淀粉样变性和遗传性转甲状腺素蛋白淀粉样变性心肌病的选择性转甲状腺素蛋白稳定剂。
Drugs Today (Barc). 2019 Dec;55(12):727-734. doi: 10.1358/dot.2019.55.12.3078389.
3
Monitoring treatment response to tafamidis by serial native T1 and extracellular volume in transthyretin amyloid cardiomyopathy.监测转甲状腺素蛋白淀粉样变心肌病中 Tafamidis 治疗反应的系列天然 T1 和细胞外容积。
ESC Heart Fail. 2019 Feb;6(1):232-236. doi: 10.1002/ehf2.12382. Epub 2018 Nov 27.
4
Updated Evaluation of the Safety, Efficacy and Tolerability of Tafamidis in the Treatment of Hereditary Transthyretin Amyloid Polyneuropathy.塔非酰胺治疗遗传性转甲状腺素蛋白淀粉样多神经病的安全性、有效性和耐受性的最新评估
Drug Healthc Patient Saf. 2023 Feb 17;15:51-62. doi: 10.2147/DHPS.S338577. eCollection 2023.
5
Failure of Tafamidis to Halt Progression of Ala36Pro TTR Oculomeningovascular Amyloidosis.塔非酰胺未能阻止Ala36Pro转甲状腺素蛋白眼脑脊髓血管淀粉样变性的进展。
J Stroke Cerebrovasc Dis. 2018 Sep;27(9):e212-e214. doi: 10.1016/j.jstrokecerebrovasdis.2018.04.033. Epub 2018 May 18.
6
Tafamidis decreased cardiac amyloidosis deposition in patients with Ala97Ser hereditary transthyretin cardiomyopathy: a 12-month follow-up cohort study.他法米替尼可降低 Ala97Ser 遗传性转甲状腺素蛋白心肌病患者的心脏淀粉样变性沉积:一项为期 12 个月的随访队列研究。
Orphanet J Rare Dis. 2023 Sep 13;18(1):289. doi: 10.1186/s13023-023-02824-0.
7
Cardiac Amyloidosis Due to Transthyretin Protein: A Review.心肌淀粉样变:转甲状腺素蛋白相关性心肌淀粉样变综述。
JAMA. 2024 Mar 5;331(9):778-791. doi: 10.1001/jama.2024.0442.
8
Tafamidis in transthyretin amyloid cardiomyopathy: effects on transthyretin stabilization and clinical outcomes.塔非酰胺在转甲状腺素蛋白淀粉样心肌病中的作用:对转甲状腺素蛋白稳定性及临床结局的影响
Circ Heart Fail. 2015 May;8(3):519-26. doi: 10.1161/CIRCHEARTFAILURE.113.000890. Epub 2015 Apr 14.
9
Treatment With Tafamidis Slows Disease Progression in Early-Stage Transthyretin Cardiomyopathy.用塔非酰胺治疗可减缓早期转甲状腺素蛋白心肌病的疾病进展。
Clin Med Insights Cardiol. 2017 Sep 18;11:1179546817730322. doi: 10.1177/1179546817730322. eCollection 2017.
10
Relationship of binding-site occupancy, transthyretin stabilisation and disease modification in patients with tafamidis-treated transthyretin amyloid cardiomyopathy.在接受塔法米替治疗的转甲状腺素淀粉样变心肌病患者中,结合部位占有率、转甲状腺素蛋白稳定化与疾病改善的关系。
Amyloid. 2023 Jun;30(2):208-219. doi: 10.1080/13506129.2022.2145876. Epub 2022 Nov 18.

本文引用的文献

1
Real-World Efficacy of Tafamidis in Patients With Transthyretin Amyloidosis and Heart Failure.他法米地对转甲状腺素蛋白淀粉样变和心力衰竭患者的真实世界疗效
Curr Probl Cardiol. 2023 Jun;48(6):101667. doi: 10.1016/j.cpcardiol.2023.101667. Epub 2023 Feb 23.
2
Long-Term Survival With Tafamidis in Patients With Transthyretin Amyloid Cardiomyopathy.用塔法米迪治疗转甲状腺素蛋白淀粉样心肌病患者的长期生存。
Circ Heart Fail. 2022 Jan;15(1):e008193. doi: 10.1161/CIRCHEARTFAILURE.120.008193. Epub 2021 Dec 20.
3
Efficacy and safety of tafamidis doses in the Tafamidis in Transthyretin Cardiomyopathy Clinical Trial (ATTR-ACT) and long-term extension study.
在转甲状腺素蛋白心肌病临床试验(ATTR-ACT)和长期扩展研究中,他司美替尼剂量的疗效和安全性。
Eur J Heart Fail. 2021 Feb;23(2):277-285. doi: 10.1002/ejhf.2027. Epub 2020 Nov 12.
4
Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy.特发性甲状腺素运载蛋白淀粉样变心肌病患者的塔法米迪治疗。
N Engl J Med. 2018 Sep 13;379(11):1007-1016. doi: 10.1056/NEJMoa1805689. Epub 2018 Aug 27.
5
Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis.用于遗传性转甲状腺素蛋白淀粉样变性的 RNAi 治疗药物 Patisiran
N Engl J Med. 2018 Jul 5;379(1):11-21. doi: 10.1056/NEJMoa1716153.