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心脏淀粉样变性——诊断和治疗的多学科方法。

Cardiac amyloidosis-interdisciplinary approach to diagnosis and therapy.

机构信息

Department of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.

Amyloidosezentrum Niedersachsen, Hannover Medical School, Hannover, Germany.

出版信息

Herz. 2022 Aug;47(4):324-331. doi: 10.1007/s00059-022-05122-w. Epub 2022 Jun 8.

Abstract

The vast majority of cardiac amyloidosis (CA) cases are caused by light chain (AL) or transthyretin (ATTR) amyloidosis. The latter is divided into hereditary (ATTRv) and wild-type forms (ATTRwt). The incidence of ATTRwt amyloidosis has significantly increased, particularly due to the improved diagnosis of cardiac manifestations, with relevant proportions in patient populations with heart failure (HF) and preserved ejection fraction (HFpEF). Cardiac amyloidosis should be suspected in HF with indicative clinical scenarios/"red flags" with typical signs of CA in echocardiography. Further noninvasive imaging (cardiovascular magnetic resonance imaging, scintigraphy) and specific laboratory diagnostics are important for the diagnosis and typing of CA into the underlying main forms of ATTR and AL amyloidosis. The histopathologic analysis of an endomyocardial biopsy is necessary if noninvasive diagnostic methods do not enable reliable typing of CA. This is crucial for initiating specific therapy. Therapy of HF in CA is largely limited to the use of diuretics in the absence of evidence on the benefit of classic HF therapy with neurohormonal modulators. Innovative therapies have been developed for amyloidosis with improvement in organ protection, prognosis, and quality of life. These include specific cytoreductive therapies for monoclonal light-chain disease in AL amyloidosis and pharmacologic stabilization or inhibition of transthyretin expression in ATTR amyloidosis. Since the CA underlying amyloidosis is a systemic disease also affecting other organ systems, close interdisciplinary cooperation is crucial for rapid and effective diagnosis and therapy.

摘要

绝大多数心脏淀粉样变性(CA)是由轻链(AL)或转甲状腺素(ATTR)淀粉样变性引起的。后者分为遗传性(ATTRv)和野生型(ATTRwt)。ATTRwt 淀粉样变性的发病率显著增加,尤其是由于心脏表现诊断的改善,心力衰竭(HF)和射血分数保留(HFpEF)患者人群中的相关比例增加。如果超声心动图有提示性临床情况/“红旗”且有 CA 的典型迹象,应怀疑 HF 合并 CA。进一步的非侵入性成像(心血管磁共振成像、闪烁扫描)和特定的实验室诊断对于 CA 的诊断和分型为 ATTR 和 AL 淀粉样变性的主要形式非常重要。如果非侵入性诊断方法不能可靠地对 CA 进行分型,则需要进行心内膜心肌活检的组织病理学分析。这对于启动特定的治疗至关重要。CA 合并 HF 的治疗在很大程度上仅限于利尿剂的使用,因为没有经典 HF 治疗中神经激素调节剂获益的证据。已经开发出针对淀粉样变性的创新疗法,这些疗法可改善器官保护、预后和生活质量。这些疗法包括 AL 淀粉样变性中单克隆轻链疾病的特异性细胞减少疗法以及 ATTR 淀粉样变性中转甲状腺素表达的药理学稳定或抑制。由于 CA 合并淀粉样变性是一种影响其他器官系统的全身性疾病,因此快速、有效的诊断和治疗需要密切的跨学科合作。

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