Anti-Diabetic Therapy, Heart Failure and Oxidative Stress: An Update.
Ioanna KoniariDimitrios VelissarisNicholas George KounisEleni-Evangelia KoufouEleni ArtopoulouCesare de GregorioVirginia MplaniThemistoklis ParaskevasGrigorios G TsigkasMing-Yow HungPanagiotis PlotasVaia LambadiariIgnatios IkonomidisPublished in: Journal of clinical medicine (2022)
Diabetes mellitus (DM) and heart failure (HF) are two chronic disorders that affect millions worldwide. Hyperglycemia can induce excessive generation of highly reactive free radicals that promote oxidative stress and further exacerbate diabetes progression and its complications. Vascular dysfunction and damage to cellular proteins, membrane lipids and nucleic acids can stem from overproduction and/or insufficient removal of free radicals. The aim of this article is to review the literature regarding the use of antidiabetic drugs and their role in glycemic control in patients with heart failure and oxidative stress. Metformin exerts a minor benefit to these patients. Thiazolidinediones are not recommended in diabetic patients, as they increase the risk of HF. There is a lack of robust evidence on the use of meglinitides and acarbose. Insulin and dipeptidyl peptidase-4 (DPP-4) inhibitors may have a neutral cardiovascular effect on diabetic patients. The majority of current research focuses on sodium glucose cotransporter 2 (SGLT2) inhibitors and glucagon-like peptide 1 (GLP-1) receptor agonists. SGLT2 inhibitors induce positive cardiovascular effects in diabetic patients, leading to a reduction in cardiovascular mortality and HF hospitalization. GLP-1 receptor agonists may also be used in HF patients, but in the case of chronic kidney disease, SLGT2 inhibitors should be preferred.
Keyphrases
- oxidative stress
- glycemic control
- end stage renal disease
- chronic kidney disease
- type diabetes
- heart failure
- ejection fraction
- newly diagnosed
- acute heart failure
- peritoneal dialysis
- dna damage
- blood glucose
- prognostic factors
- systematic review
- ischemia reperfusion injury
- cardiovascular disease
- stem cells
- mesenchymal stem cells
- risk factors
- adipose tissue
- weight loss
- bone marrow
- weight gain