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代谢综合征中心脏不良重构的影像学评估技术。

Imaging techniques for the assessment of adverse cardiac remodeling in metabolic syndrome.

机构信息

Vita-Salute San Raffaele University, Milan, Italy.

First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, 6 viale Benedetto XV, 16132, Genoa, Italy.

出版信息

Heart Fail Rev. 2022 Sep;27(5):1883-1897. doi: 10.1007/s10741-021-10195-6. Epub 2021 Nov 18.

Abstract

Metabolic syndrome (MetS) includes different metabolic conditions (i.e. abdominal obesity, impaired glucose tolerance, hypertriglyceridemia, decreased HDL cholesterol, and/or hypertension) that concour in the development of cardiovascular disease and diabetes. MetS individuals often show adverse cardiac remodeling and myocardial dysfunction even in the absence of overt coronary artery disease or valvular affliction. Diastolic impairment and hypertrophy are hallmarks of MetS-related cardiac remodeling and represent the leading cause of heart failure with preserved ejection fraction (HFpEF). Altered cardiomyocyte function, increased neurohormonal tone, interstitial fibrosis, coronary microvascular dysfunction, and a myriad of metabolic abnormalities have all been implicated in the development and progression of adverse cardiac remodeling related to MetS. However, despite the enormous amount of literature produced on this argument, HF remains a leading cause of morbidity and mortality in such population. The early detection of initial adverse cardiac remodeling would enable the optimal implementation of effective therapies aiming at preventing the progression of the disease to the symptomatic phase. Beyond conventional imaging techniques, such as echocardiography, cardiac tomography, and magnetic resonance, novel post-processing tools and techniques provide information on the biological processes that underlie metabolic heart disease. In this review, we summarize the pathophysiology of MetS-related cardiac remodeling and illustrate the relevance of state-of-the-art multimodality cardiac imaging to identify and quantify the degree of myocardial involvement, prognosticate long-term clinical outcome, and potentially guide therapeutic strategies.

摘要

代谢综合征(MetS)包括不同的代谢异常(即腹部肥胖、葡萄糖耐量受损、高三酰甘油血症、高密度脂蛋白胆固醇降低和/或高血压),这些异常共同导致心血管疾病和糖尿病的发生。即使没有明显的冠状动脉疾病或瓣膜疾病,MetS 患者通常也会出现不良的心脏重构和心肌功能障碍。舒张功能障碍和心肌肥厚是 MetS 相关心脏重构的标志,也是射血分数保留的心力衰竭(HFpEF)的主要原因。心肌细胞功能改变、神经激素张力增加、间质纤维化、冠状动脉微血管功能障碍以及许多代谢异常都与 MetS 相关的不良心脏重构的发生和发展有关。然而,尽管关于这一论点的文献数量巨大,但 HF 仍然是此类人群发病率和死亡率的主要原因。早期发现初始不良心脏重构将能够最佳地实施有效的治疗方法,以防止疾病进展到有症状阶段。除了传统的成像技术,如超声心动图、心脏计算机断层扫描和磁共振成像,新的后处理工具和技术提供了关于代谢性心脏病基础生物学过程的信息。在这篇综述中,我们总结了 MetS 相关心脏重构的病理生理学,并说明了最先进的多模态心脏成像在识别和量化心肌受累程度、预测长期临床结局以及潜在指导治疗策略方面的相关性。

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