Marwick Thomas H, Gimelli Alessia, Plein Sven, Bax Jeroen J, Charron Phillippe, Delgado Victoria, Donal Erwan, Lancellotti Patrizio, Levelt Eylem, Maurovich-Horvat Pal, Neubauer Stefan, Pontone Gianluca, Saraste Antti, Cosyns Bernard, Edvardsen Thor, Popescu Bogdan A, Galderisi Maurizio, Derumeaux Genevieve, Bäck Magnus, Bertrand Philippe B, Dweck Marc, Keenan Niall, Magne Julien, Neglia Danilo, Stankovic Ivan
Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne, VIC 3004, Australia.
Fondazione Toscana Gabriele Monasterio, Via Moruzzi, 1, 56124 Pisa, Italy.
Eur Heart J Cardiovasc Imaging. 2022 Jan 24;23(2):e62-e84. doi: 10.1093/ehjci/jeab220.
Heart failure (HF) is among the most important and frequent complications of diabetes mellitus (DM). The detection of subclinical dysfunction is a marker of HF risk and presents a potential target for reducing incident HF in DM. Left ventricular (LV) dysfunction secondary to DM is heterogeneous, with phenotypes including predominantly systolic, predominantly diastolic, and mixed dysfunction. Indeed, the pathogenesis of HF in this setting is heterogeneous. Effective management of this problem will require detailed phenotyping of the contributions of fibrosis, microcirculatory disturbance, abnormal metabolism, and sympathetic innervation, among other mechanisms. For this reason, an imaging strategy for the detection of HF risk needs to not only detect subclinical LV dysfunction (LVD) but also characterize its pathogenesis. At present, it is possible to identify individuals with DM at increased risk HF, and there is evidence that cardioprotection may be of benefit. However, there is insufficient justification for HF screening, because we need stronger evidence of the links between the detection of LVD, treatment, and improved outcome. This review discusses the options for screening for LVD, the potential means of identifying the underlying mechanisms, and the pathways to treatment.
心力衰竭(HF)是糖尿病(DM)最重要且最常见的并发症之一。亚临床功能障碍的检测是HF风险的一个标志物,也是降低DM患者HF发生率的一个潜在靶点。DM继发的左心室(LV)功能障碍具有异质性,其表型包括以收缩功能障碍为主、以舒张功能障碍为主以及混合型功能障碍。实际上,这种情况下HF的发病机制是异质性的。有效解决这个问题需要对纤维化、微循环障碍、代谢异常和交感神经支配等多种机制的作用进行详细的表型分析。因此,用于检测HF风险的成像策略不仅要检测亚临床LV功能障碍(LVD),还要对其发病机制进行特征描述。目前,能够识别出DM患者中发生HF风险增加的个体,并且有证据表明心脏保护可能有益。然而,HF筛查的理由并不充分,因为我们需要更有力的证据来证明LVD检测、治疗与改善预后之间的联系。本综述讨论了LVD筛查的选项、识别潜在机制的可能方法以及治疗途径。