Healthcare disparities in heart failure patients (with and without type 2 diabetes) and use of sodium glucose co-transport inhibitors (SGLT2-i)

Endocrine ◽  
2021 ◽  
Author(s):  
Shivank Madan ◽  
Muhammad Farooq ◽  
Karim Diab ◽  
Angelos A. Melainis ◽  
Katherine E. DiPalo ◽  
...  
2012 ◽  
Vol 18 (10) ◽  
pp. S188
Author(s):  
Toshio Naka ◽  
Takafumi Akagami ◽  
Takashi Doi ◽  
Tohru Masuyama ◽  
Mitsumasa Ohyanagi

2020 ◽  
Vol 15 (SP1) ◽  
pp. 14-21
Author(s):  
Phyllis Sin ◽  
Rohan Sanjanwala ◽  
Shelley Zieroth

Heart failure increases in prevalence with age and is usually associated with various cardiac and non-cardiac comorbidities.  For common coexisting conditions such as renal dysfunction, anemia and type 2 diabetes mellitus, important pathophysiologic links have been implicated between cardiac dysfunction and the underlying condition.  Indeed, the number and severity of comorbidities in the setting of heart failure is an important driver of prognosis.  By targeting the management of coexisting diseases, it may be possible to improve functional capacity, quality of life and perhaps even overall mortality in heart failure patients.  Recent clinical trial data has provided insights into cardio-renal interactions in acute heart failure, the impact of iron replacement therapy in iron deficient heart failure patients, and the role of pharmacologic therapies to prevent heart failure related events in high risk patients with type 2 diabetes. 


2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Chengcong Chen ◽  
Ying Huang ◽  
Yongmei Zeng ◽  
Xiyan Lu ◽  
Guoqing Dong

Abstract Background The most significant manifestation of heart failure is exercise intolerance. This systematic review and meta-analysis was performed to investigate whether dipeptidyl peptidase-4 (DPP-4) inhibitors or glucagon-like peptide 1 receptor agonists (GLP-1 RAs), widely used anti-diabetic drugs, could improve exercise tolerance in heart failure patients with or without type 2 diabetes mellitus. Methods An electronic search of PubMed, EMBASE and the Cochrane Library was carried out through March 8th, 2019, for eligible trials. Only randomized controlled studies were included. The primary outcome was exercise tolerance [6-min walk test (6MWT) and peak O2 consumption], and the secondary outcomes included quality of life (QoL), adverse events (AEs) and all-cause death. Result After the literature was screened by two reviewers independently, four trials (659 patients) conducted with heart failure patients with or without type 2 diabetes met the eligibility criteria. The results suggested that targeting the DPP-4-GLP-1 pathway can improve exercise tolerance in heart failure patients [MD 24.88 (95% CI 5.45, 44.31), P = 0.01] without decreasing QoL [SMD -0.51 (95% CI -1.13, 0.10), P = 0.10]; additionally, targeting the DPP-4-GLP-1 pathway did not show signs of increasing the incidence of serious AEs or mortality. Conclusion Our results suggest that DPP-4 inhibitors or GLP-1 RAs improve exercise tolerance in heart failure patients. Although the use of these drugs for heart failure has not been approved by any organization, they may be a better choice for type 2 diabetes mellitus patients with heart failure. Furthermore, as this pathway contributes to the improvement of exercise tolerance, it may be worth further investigation in exercise-intolerant patients with other diseases.


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