转甲状腺素沉默剂治疗前后转甲状腺素淀粉样变性患者心脏表现的比较研究。

IF 2.3 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Priya Arivalagan, Diego Hernan Delgado
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引用次数: 0

摘要

转甲状腺素淀粉样变性(ATTR)是一种罕见的疾病,由错误折叠的蛋白质淀粉样蛋白沉积在各种器官和组织,通常是心脏和/或神经,导致心肌病(CM)和多神经病变(PN)的发展。虽然这可能是一种无法治愈的疾病,但目前有各种治疗方法可用于ATTR患者,包括转甲状腺素(TTR)沉默剂,如intertersen和patisiran。消音器通过减轻患者出现的心脏和神经症状,帮助减缓疾病进展,改善ATTR患者的生活质量。本研究的目的是比较使用intertersen或patisiran治疗前后混合表型患者99Tc-PYP闪烁成像(PYP扫描)参数所观察到的心脏结果。这项研究包括来自大学健康网络淀粉样变诊所的10名患者。所有患者(平均年龄:63.80±11.70岁,男性60.0%,女性40.0%)均接受intertersen或patisiran治疗。这些患者在治疗前后进行PYP扫描,观察治疗后CM的改善情况。9例(90.0%)患者的CM有所改善,因为根据TTR消音器治疗后的PYP扫描结果,他们的心脏与对侧肺(H/CL)比和/或焦磷酸盐(PYP)等级下降。只有1名患者(10.0%)的结果恶化,因为与治疗前的PYP扫描结果相比,治疗后他们的H/CL比率和PYP分级增加。具有混合表型的ATTR患者应在使用TTR消音器治疗前后进行PYP扫描。通过进行这些扫描,可以通过观察CM体征的改善来确定这种治疗的有效性。H/CL比和/或PYP等级的降低表明TTR消音器在缓解CM的体征和症状方面是有效的,患者应该继续他们的治疗计划。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Study on Cardiac Findings in Patients with Transthyretin Amyloidosis Before and After Treatment with a Transthyretin Silencer.

Transthyretin amyloidosis (ATTR) is a rare disease caused by misfolded proteins, amyloids, that are deposited in various organs and tissues, typically the heart and/or nerves, causing the development of cardiomyopathy (CM) and polyneuropathy (PN). Although this may be an incurable disease, there are various treatments that are currently available for patients with ATTR, including transthyretin (TTR) silencers such as inotersen and patisiran. The silencers help slow down the progression of disease and improve the quality of life of patients with ATTR by alleviating the cardiac and neurological symptoms that patients present. The purpose of this study was to compare the cardiac findings observed in the 99Tc-PYP scintigraphy (PYP scan) parameters of patients with a mixed phenotype before and after treatment with inotersen or patisiran. This study included ten patients from the amyloidosis clinic at the University Health Network. All of the patients (average age: 63.80 ± 11.70; 60.0% males, 40.0% females) received inotersen or patisiran as their treatment. These patients underwent a PYP scan before and after treatment to observe any improvements in terms of their CM post-treatment. Nine (90.0%) patients showed an improvement with their CM, as they showed a decrease in their heart-to-contralateral lung (H/CL) ratio and/or pyrophosphate (PYP) grade based on their results from the PYP scan post-treatment with a TTR silencer. Only one patient (10.0%) had worsening results, as their H/CL ratio and PYP grade increased post-treatment in comparison to the PYP scan results pre-treatment. Patients with ATTR who have a mixed phenotype should undergo a PYP scan before and after treatment with a TTR silencer. By undergoing these scans, the effectiveness of this treatment could be determined by observing any improvements in the signs of CM. A decrease in the H/CL ratio and/or the PYP grade would indicate that the TTR silencer has been effective in alleviating the signs and symptoms of CM, and that the patients should continue with their treatment plan.

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来源期刊
Journal of Cardiovascular Development and Disease
Journal of Cardiovascular Development and Disease CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
2.60
自引率
12.50%
发文量
381
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