Algarve Biomedical Center Algarve Portugal.
Biomedical and Medical Department Algarve University Algarve Portugal.
J Am Heart Assoc. 2020 Oct 20;9(19):e016614. doi: 10.1161/JAHA.120.016614. Epub 2020 Sep 24.
Background The emergence of specific therapies for transthyretin cardiac amyloidosis (CA) warrants the need for a systematic review of the literature. Methods and Results A systematic review of the literature was conducted according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. A systematic search was performed on MEDLINE, PubMed, and Embase databases on November 29, 2019. Studies were selected based on the following predefined eligibility criteria: English-language randomized controlled trials (RCTs), non-RCTs, or observational studies, which included adult patients with variant/wild-type transthyretin-CA, assessed specific therapies for transthyretin-CA, and reported cardiovascular outcomes. Relevant data were extracted to a predefined template. Quality assessment was based on National Institute for Health and Care Excellence recommendations (RCTs) or a checklist by Downs and Black (non-RCTs). From 1203 records, 24 publications were selected, describing 4 RCTs (6 publications) and 16 non-RCTs (18 publications). Tafamidis was shown to significantly improve all-cause mortality and cardiovascular hospitalizations and reduce worsening in 6-minute walk test, Kansas City Cardiomyopathy Questionnaire-Overall Summary score, and NT-proBNP (N-terminal pro-B-type natriuretic peptide) in variant/wild-type transthyretin-CA. Patisiran showed promising results in a subgroup analysis of patients with variant transthyretin-CA, which have to be confirmed in RCTs. Inotersen showed conflicting results on cardiac imaging parameters. The one study on AG10 had only a 1-month duration and cardiovascular end points were exploratory and limited to cardiac biomarkers. Limited evidence from noncomparative single-arm small non-RCTs existed for diflunisal, epigallocatechin-3-gallate (green tea extract), and doxycycline+tauroursodeoxycholic acid/ursodeoxycholic acid. Conclusions This systematic review of the literature supports the use of tafamidis in wild-type and variant transthyretin-CA. Novel therapeutic targets including transthyretin gene silencers are currently under investigation.
特定疗法在转甲状腺素蛋白心脏淀粉样变(CA)中的出现,需要对文献进行系统回顾。
根据系统评价和荟萃分析的首选报告项目(PRISMA)指南,对文献进行了系统回顾。于 2019 年 11 月 29 日在 MEDLINE、PubMed 和 Embase 数据库中进行了系统搜索。研究入选标准为:英语随机对照试验(RCT)、非 RCT 或观察性研究,纳入成年变异型/野生型转甲状腺素蛋白-CA 患者,评估转甲状腺素蛋白-CA 的特定治疗方法,并报告心血管结局。将相关数据提取到预设模板中。质量评估基于英国国家卫生与保健优化研究所的建议(RCT)或唐斯和布莱克(非 RCT)的检查表。从 1203 条记录中,选择了 24 篇文献,描述了 4 项 RCT(6 篇文献)和 16 项非 RCT(18 篇文献)。塔法米迪在改善所有原因死亡率和心血管住院率以及降低 6 分钟步行试验、堪萨斯城心肌病问卷总概括评分和 N 末端 pro-B 型利钠肽(NT-proBNP)方面显著改善了变异型/野生型转甲状腺素蛋白-CA。帕替沙尼在变异型转甲状腺素蛋白-CA 患者的亚组分析中显示出有希望的结果,但需要在 RCT 中证实。依洛硫酸酯在心脏成像参数方面的结果存在争议。关于 AG10 的一项研究仅持续 1 个月,且心血管终点是探索性的,仅限于心脏生物标志物。非比较性小非 RCT 存在关于双水杨酯、表没食子儿茶素没食子酸酯(绿茶提取物)和多西环素+牛磺熊脱氧胆酸/熊脱氧胆酸的有限证据。
对文献的系统回顾支持在野生型和变异型转甲状腺素蛋白-CA 中使用塔法米迪。目前正在研究新型治疗靶点,包括转甲状腺素蛋白基因沉默剂。