Diabetes and SGLT2-iss inhibitors in patients with heart failure with preserved or mid-range left ventricular ejection fractions

被引:5
作者
Passantino, Andrea [1 ]
Rizzo, Caterina [1 ]
Scrutinio, Domenico [1 ]
Palazzuoli, Alberto [2 ]
机构
[1] Ist Ricovero E Cura Carattere Sci IRCCS, Ist Clinici Sci Maugeri, Bari, Italy
[2] Univ Siena, Scotte Hosp, Dept Med Sci, Cardiovasc Dis Unit, Siena, Italy
关键词
Diabetes; Heart failure; HFpEF; HFmEF; SGLT2-iss inhibitors; GLYCATION END-PRODUCTS; CARDIOMYOPATHY; OUTCOMES; EMPAGLIFLOZIN; MECHANISMS; TRIAL; CANAGLIFLOZIN; GUIDELINES; MORTALITY; DIAGNOSIS;
D O I
10.1007/s10741-021-10186-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diabetic patients frequently develop heart failure with preserved (HFpEF) or mid-range (HFmEF) cardiac ejection fractions. This condition may be secondary to diabetic cardiomyopathy or one of several relevant comorbidities, mainly hypertension. Several mechanisms link diabetes to HFpEF or HFmEF. Among these, non-enzymatic glycation of interstitial proteins, lipotoxicity, and endothelial dysfunction may promote structural damage and ultimate lead to heart failure. Findings from several large-scale trials indicated that treatment with sodium/glucose cotransporter 2 inhibitors (SGLT2-iss) resulted in significant improvements in cardiovascular outcomes in diabetic patients with high cardiovascular risk. However, there is currently some evidence that suggests a clinical advantage of using SGLT2-iss specifically in cases of HFpEF or HFmEF. Preclinical and clinical studies revealed that SGLT2-iss treatment results in a reduction in left ventricular mass and improved diastolic function. While some of the beneficial effects of SGLT2-iss have already been characterized (e.g., increased natriuresis and diuresis as well as reduced blood pressure, plasma volume, and arterial stiffness, and nephron-protective activities), there is increasing evidence suggesting that SGLT2-iss may have direct actions on the heart. These findings include SGLT2-iss-mediated reductions in the expression of hypertrophic foetal genes and diastolic myofilaments stiffness, increases in global phosphorylation of myofilament regulatory proteins (in HFpEF), inhibition of cardiac late sodium channel current and Na+/H+ exchanger activity, metabolic shifts, and effects on calcium cycling. Preliminary data from previously published studies suggest that SGLT2-iss could be useful for the treatment of HFpEF and HFmEF. Several large ongoing trials, including DELIVER AND EMPEROR -preserved have been designed to evalute the efficacy of SGLT2-iss in improving clinical outcomes in patients diagnosed with HFpEF. The goal of this manuscript is to review the use of SGLT2-iss inhibitors for HFpEF or HFmEF associated with diabetes.
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收藏
页码:683 / 695
页数:13
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