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慢性查加斯心脏病的发病机制。

Pathogenesis of chronic Chagas heart disease.

作者信息

Marin-Neto Jose Antonio, Cunha-Neto Edécio, Maciel Benedito C, Simões Marcus V

机构信息

Cardiology Division, Department of Internal Medicine, Medical School of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.

出版信息

Circulation. 2007 Mar 6;115(9):1109-23. doi: 10.1161/CIRCULATIONAHA.106.624296.

Abstract

BACKGROUND

Chagas disease remains a significant public health issue and a major cause of morbidity and mortality in Latin America. Despite nearly 1 century of research, the pathogenesis of chronic Chagas cardiomyopathy is incompletely understood, the most intriguing challenge of which is the complex host-parasite interaction.

METHODS AND RESULTS

A systematic review of the literature found in MEDLINE, EMBASE, BIREME, LILACS, and SCIELO was performed to search for relevant references on pathogenesis and pathophysiology of Chagas disease. Evidence from studies in animal models and in anima nobile points to 4 main pathogenetic mechanisms to explain the development of chronic Chagas heart disease: autonomic nervous system derangements, microvascular disturbances, parasite-dependent myocardial aggression, and immune-mediated myocardial injury. Despite its prominent peculiarities, the role of autonomic derangements and microcirculatory disturbances is probably ancillary among causes of chronic myocardial damage. The pathogenesis of chronic Chagas heart disease is dependent on a low-grade but incessant systemic infection with documented immune-adverse reaction. Parasite persistence and immunological mechanisms are inextricably related in the myocardial aggression in the chronic phase of Chagas heart disease.

CONCLUSIONS

Most clinical studies have been performed in very small number of patients. Future research should explore the clinical potential implications and therapeutic opportunities of these 2 fundamental underlying pathogenetic mechanisms.

摘要

背景

恰加斯病仍然是一个重大的公共卫生问题,也是拉丁美洲发病和死亡的主要原因。尽管经过了近一个世纪的研究,但慢性恰加斯心肌病的发病机制仍未完全明了,其中最具挑战性的是复杂的宿主-寄生虫相互作用。

方法与结果

对MEDLINE、EMBASE、BIREME、LILACS和SCIELO数据库中的文献进行系统综述,以查找有关恰加斯病发病机制和病理生理学的相关参考文献。动物模型和人体研究的证据指向4种主要的发病机制来解释慢性恰加斯心脏病的发展:自主神经系统紊乱、微血管紊乱、寄生虫依赖性心肌侵袭和免疫介导的心肌损伤。尽管自主神经紊乱和微循环紊乱有其突出的特点,但它们在慢性心肌损伤原因中可能起辅助作用。慢性恰加斯心脏病的发病机制取决于低度但持续的全身感染以及已证实的免疫不良反应。在恰加斯心脏病的慢性期,寄生虫的持续存在和免疫机制在心肌侵袭中有着千丝万缕的联系。

结论

大多数临床研究仅在极少数患者中进行。未来的研究应探索这两种基本发病机制的临床潜在影响和治疗机会。

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