Central nervous system involvement in cardiac amyloidosis: Redefining the heart-brain axis.

IF 3.6 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Domenico Mario Giamundo, Giuliano Cassataro, Stefano Ministrini, Simon F Stämpfli
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引用次数: 0

Abstract

Background: Amyloidosis is characterised by the extracellular accumulation of misfolded proteins forming amorphous aggregates called amyloid. Cardiac amyloidosis results from myocardial involvement in systemic amyloidosis, leading to impaired heart function. Besides myocardial involvement, cardiac amyloidosis may also directly and indirectly affect the central nervous system.

Methods: This narrative review summarises current evidence about on central nervous system involvement in cardiac amyloidosis and the pathophysiological mechanisms linking heart and brain in the context of this systemic disease.

Results: Although the pathophysiological relationship between cardiac amyloidosis and cognitive decline remains poorly understood, central nervous system involvement likely results from the complex interplay of direct amyloid deposition, cerebrovascular changes, and cardiac dysfunction.

Conclusion: The growing awareness of cognitive impairment in patients with cardiac amyloidosis highlights the need for further research and supports a multidisciplinary approach in the assessment and management of affected individuals.

心脏淀粉样变涉及中枢神经系统:重新定义心脑轴。
背景:淀粉样变性的特征是细胞外积聚错误折叠的蛋白质,形成无定形的聚集体,称为淀粉样蛋白。心脏淀粉样变性是由心肌累及全身淀粉样变性引起的,导致心功能受损。除心肌受累外,心肌淀粉样变还可直接或间接影响中枢神经系统。方法:本文综述了目前关于中枢神经系统参与心脏淀粉样变的证据,以及在这种全身性疾病背景下心脏和大脑联系的病理生理机制。结果:尽管心脏淀粉样变性和认知能力下降之间的病理生理关系尚不清楚,但中枢神经系统的受累可能是淀粉样蛋白直接沉积、脑血管改变和心功能障碍的复杂相互作用的结果。结论:对心脏淀粉样变性患者认知功能障碍的认识日益提高,表明需要进一步研究,并支持对受影响个体进行多学科评估和管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.50
自引率
3.60%
发文量
192
审稿时长
1 months
期刊介绍: EJCI considers any original contribution from the most sophisticated basic molecular sciences to applied clinical and translational research and evidence-based medicine across a broad range of subspecialties. The EJCI publishes reports of high-quality research that pertain to the genetic, molecular, cellular, or physiological basis of human biology and disease, as well as research that addresses prevalence, diagnosis, course, treatment, and prevention of disease. We are primarily interested in studies directly pertinent to humans, but submission of robust in vitro and animal work is also encouraged. Interdisciplinary work and research using innovative methods and combinations of laboratory, clinical, and epidemiological methodologies and techniques is of great interest to the journal. Several categories of manuscripts (for detailed description see below) are considered: editorials, original articles (also including randomized clinical trials, systematic reviews and meta-analyses), reviews (narrative reviews), opinion articles (including debates, perspectives and commentaries); and letters to the Editor.
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