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糖尿病与心力衰竭:流行病学、病理生理机制及钠-葡萄糖协同转运蛋白2抑制剂的作用

Diabetes Mellitus and Heart Failure: Epidemiology, Pathophysiologic Mechanisms, and the Role of SGLT2 Inhibitors.

作者信息

Theofilis Panagiotis, Oikonomou Evangelos, Tsioufis Konstantinos, Tousoulis Dimitris

机构信息

Department of Cardiology, "Hippokration" General Hospital, University of Athens Medical School, 11527 Athens, Greece.

Department of Cardiology, Thoracic Diseases General Hospital "Sotiria", University of Athens Medical School, 11527 Athens, Greece.

出版信息

Life (Basel). 2023 Feb 10;13(2):497. doi: 10.3390/life13020497.

Abstract

Diabetes mellitus (DM) and heart failure (HF) are frequently encountered afflictions that are linked by a common pathophysiologic background. According to landmark studies, those conditions frequently coexist, and this interaction represents a poor prognostic indicator. Based on mechanistic studies, HF can be propagated by multiple pathophysiologic pathways, such as inflammation, oxidative stress, endothelial dysfunction, fibrosis, cardiac autonomic neuropathy, and alterations in substrate utilization. In this regard, DM may augment myocardial inflammation, fibrosis, autonomic dysfunction, and lipotoxicity. As the interaction between DM and HF appears critical, the new cornerstone in DM and HF treatment, sodium-glucose cotransporter-2 inhibitors (SGLT2i), may be able to revert the pathophysiology of those conditions and lead to beneficial HF outcomes. In this review, we aim to highlight the deleterious pathophysiologic interaction between DM and HF, as well as demonstrate the beneficial role of SGLT2i in this field.

摘要

糖尿病(DM)和心力衰竭(HF)是常见疾病,它们有着共同的病理生理背景。根据具有里程碑意义的研究,这些病症经常共存,且这种相互作用是不良预后指标。基于机制研究,HF可通过多种病理生理途径进展,如炎症、氧化应激、内皮功能障碍、纤维化、心脏自主神经病变以及底物利用改变。在这方面,DM可能会加剧心肌炎症、纤维化、自主神经功能障碍和脂毒性。由于DM与HF之间的相互作用似乎至关重要,DM和HF治疗的新基石——钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i),或许能够逆转这些病症的病理生理过程并带来有益的HF结局。在本综述中,我们旨在强调DM与HF之间有害的病理生理相互作用,并展示SGLT2i在该领域的有益作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c64b/9968235/ea4d705d6e3a/life-13-00497-g001.jpg

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