Therapeutic strategies for primary heart involvement in systemic sclerosis.

Rheumatology and immunology research Pub Date : 2024-07-15 eCollection Date: 2024-06-01 DOI:10.1515/rir-2024-0010
Veronica Batani, Lorenzo Dagna, Giacomo De Luca
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引用次数: 0

Abstract

Primary heart involvement (pHI) is frequent in systemic sclerosis (SSc), even though often underdiagnosed. SSc-pHI has been recently defined as cardiac abnormalities that are predominantly attributable to SSc rather than other causes and/or complications. SSc-pHI represents a major determinant of mortality in SSc, accounting alone for about 12% of disease-related deaths; its early recognition and promptly therapeutic interventions are therefore crucial. Both perfusion defects and myocardial inflammation contribute to the occurrence of myocardial fibrosis that precipitates myocardial remodeling, potentially leading to heart failure and arrhythmic complications. To date, clear evidence and guidelines for effectively managing SSc pHI are not established yet, resulting in a lack of a defined therapeutic algorithm. In this review we summarize the most recent scientific literature on the prevailing therapeutic strategies and interventions to manage SSc-pHI, with particular focus on therapeutic strategies to counteract the 3 major pathogenic events of the disease, i.e. microvascular damage, myocardial inflammation and myocardial fibrosis.

系统性硬化症原发性心脏受累的治疗策略。
原发性心脏受累(pHI)在系统性硬化症(SSc)中很常见,但往往诊断不足。SSc-pHI 最近被定义为主要由 SSc 而非其他原因和/或并发症引起的心脏异常。SSc-pHI是决定SSc患者死亡率的一个主要因素,仅此一项就占疾病相关死亡的12%左右;因此,早期识别SSc-pHI并及时进行治疗干预至关重要。灌注缺损和心肌炎症都会导致心肌纤维化,进而引发心肌重塑,可能导致心力衰竭和心律失常并发症。迄今为止,有效治疗 SSc pHI 的明确证据和指南尚未确立,因此缺乏明确的治疗算法。在这篇综述中,我们总结了有关控制 SSc-pHI 的现行治疗策略和干预措施的最新科学文献,尤其侧重于对抗该疾病三大致病因素(即微血管损伤、心肌炎症和心肌纤维化)的治疗策略。
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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CiteScore
1.40
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