淀粉样变性
心脏淀粉样变性
医学
转甲状腺素
淀粉样蛋白(真菌学)
淀粉样变性
疾病
心力衰竭
病理
生物信息学
内科学
免疫球蛋白轻链
免疫学
抗体
生物
作者
Gnana Deepthi Medarametla,Ravi S. Kahlon,Lampimukhi Mahitha,Sanobar Shariff,Naga Praneeth Vakkalagadda,Hitesh Chopra,Mohammad Amjad Kamal,Neil Patel,Yashendra Sethi,Nirja Kaka
出处
期刊:PubMed
日期:2023-01-01
卷期号:22: 781-808
标识
DOI:10.17179/excli2023-6284
摘要
Amyloidosis is a protein deposition disorder in which insoluble fibril structures accumulate in the bodily tissues damaging the organ function. Cardiac amyloidosis is a severe but under-reported medical condition characterized by the accumulation of amyloid in the extracellular area of the myocardium, which results in thickening and stiffening of ventricular walls. Cardiac amyloidosis has recently gained much attention with its slowly surging incidence. With this study, we seek to comprehensively compile the pathophysiology and clinical picture of cardiac amyloidosis subtypes, extending a clinically oriented, up-to-date clinical approach to diagnosis and therapy. Cardiac amyloidosis can be caused by rare genetic mutations which may be inherited or acquired. The growing incidence can be attributed to advancements in imaging methods and other diagnostic modalities. Most occurrences of cardiac amyloidosis result from two forms of precursor protein: transthyretin [TTR] amyloid and immunoglobulin-derived light-chain amyloid. Prompt identification of cardiac amyloidosis can facilitate the implementation of evolving therapeutic interventions to enhance the outcomes. The modalities for the management of CA have evolved significantly in the last ten years. Apart from therapies for modifying disease and heart failure, a myriad of novel therapeutic approaches that target specific aspects of the disease, including gene therapies, are being researched. These aim at impeding its progression and improving clinical outcomes. See also Figure 1(Fig. 1).
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