转甲状腺素蛋白心脏淀粉样变的诊断与治疗研究进展

doi:10.13308/j.issn.2095-9354.2024.03.002

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Abstract Transthyretin cardiac amyloidosis (ATTR-CA) has been considered as a rare cardiac dysfunction with occult onset, rapid progression and high mortality, caused by the accumulation of transthyretin fibrils in the myocardium. Recently, with the development of diagnostic techniques, its detection rate has been increasing. The continuous emergence of various small molecule drugs has also changed the previous situation of lacking therapeutic agents, and its mortality has been reduced. This paper mainly summarizes the latest advances in the diagnosis and treatment of ATTR-CA in recent years.

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	WANG Yue
	ZHANG Junfeng

Cite this article:

WANG Yue,ZHANG Junfeng. Research advances in diagnosis and treatment of transthyretin cardiac amyloidosis[J]. JOURNAL OF PRACTICAL ELECTROCARDIOLOGY, 2024, 33(3): 225-231.

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http://zzs.ujs.edu.cn/syxd/EN/ 10.13308/j.issn.2095-9354.2024.03.002 OR http://zzs.ujs.edu.cn/syxd/EN/Y2024/V33/I3/225

[1]	. [J]. JOURNAL OF PRACTICAL ELECTROCARDIOLOGY, 2024, 33(3): 217-224.