Congestive heart failure
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Heart failure hospitalization with SGLT-2 inhibitors: a systematic review and meta-analysis of randomized controlled and observational studies.
|
30817235 |
2019 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
Heart Failure Risk Stratification and Efficacy of Sodium-Glucose Cotransporter-2 Inhibitors in Patients With Type 2 Diabetes Mellitus.
|
31474116 |
2019 |
Congestive heart failure
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
SGLT-2 inhibitors were significantly associated with lower rates of HF events (absolute RD, -1.1%; HR, 0.62 [95% CrI, 0.54 to 0.72]) and MI (absolute RD, -0.6%; HR, 0.86 [95% CrI, 0.77 to 0.97]) than were the control groups.
|
29677303 |
2018 |
Congestive heart failure
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
SGLT2 inhibition reduced the risk of cardiovascular death, nonfatal myocardial infarction or nonfatal stroke (RR, 0.81; 95% CI, 0.70-0.94) and heart failure (RR, 0.61; 95% CI, 0.48-0.78), without a clear effect on all-cause mortality (HR, 0.86; 95% CI, 0.73-1.01).
|
30697905 |
2019 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
SGLT2 inhibitors are being actively studied in the treatment of patients with HF, including in those without diabetes mellitus.
|
30704605 |
2019 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
SGLT-2 inhibitors showed significant reduction in hospitalization for heart failure events (RR 0.72; 95% CI 0.6-0.86) compared to placebo.
|
30713085 |
2019 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
Sodium-glucose cotransporter 2 (SGLT2) inhibitors are drugs for diabetes and might prevent heart failure.
|
31105148 |
2019 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
Sodium-glucose cotransporter-2 (SGLT-2) inhibitors have been shown to prevent the development of heart failure and the composite of heart failure and cardiovascular death in patients with T2D without known heart failure who have either established atherosclerotic vascular disease or multiple risk factors.
|
31219877 |
2019 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
Sodium-glucose cotransporter 2 (SGLT2) inhibitors and glucagon-like peptide-1 (GLP-1) agonists are two anti-hyperglycemic classes which have been of special interest after multiple large cardiovascular disease (CVD) outcomes studies have demonstrated superiority of these agents compared to placebo for major adverse CVD events and in some cases, hospitalization for heart failure.
|
31381891 |
2019 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
SGLT-2 inhibitors show clear superiority in reducing cardiovascular and all-cause deaths, hospitalisation for HF, and renal events among new antidiabetic drug classes.
|
31462224 |
2019 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
SGLT2 inhibitors appear to be particularly beneficial in patients with heart failure.
|
31583647 |
2019 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
Sodium-glucose cotransporter 2 (SGLT2) inhibitors have been shown to improve cardiovascular outcomes including hospitalization for heart failure and mortality in people with and without diabetes.<sup>1, 2</sup> The mechanism(s) underlying this benefit remain unclear.
|
31707794 |
2020 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
A growing body of clinical evidence from those trials is now accumulating, and empagliflozin, a sodium-glucose cotransporter 2 (SGLT2) inhibitor, has first demonstrated significant risk reduction, relative to placebo, in CV death, overall mortality, and hospitalization for worsened heart failure in high-risk patients with diabetes mellitus.
|
28043708 |
2017 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
A new class of drugs for heart failure: SGLT2 inhibitors reduce sympathetic overactivity.
|
29415819 |
2018 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
A recent cardiovascular (CV) safety trial, the EMPA-REG OUTCOME trial, showed that empagliflozin, a sodium glucose cotransporter 2 (SGLT2) inhibitor, markedly reduced CV death and all-cause mortality and hospitalization for heart failure in patients with T2DM and established CV disease (CVD).
|
28403850 |
2017 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
Accordingly, SGLT-2 inhibitors could be recommended to prevent HF hospitalisation in patients with T2DM and established cardiovascular disease or with multiple risk factors.
|
31816162 |
2020 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
Accordingly, in this review, we summarize the key pharmacodynamic effects of SGLT2 inhibitors and the clinical evidence that support the rationale for the use of SGLT2 inhibitors in patients with HF who have T2D.
|
29061576 |
2017 |
Congestive heart failure
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Additionally, SGLT2 inhibitors were associated with lower risk of hospitalization because of heart failure compared to both sulfonylureas and DPP-4 inhibitors, as well as lower risk of lower extremity amputation compared to sulfonylureas.
|
30039524 |
2019 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
Although SGLT2-Is are the treatment of choice in patients with T2D and heart failure or uncontrolled hypertension, no consensus was reached regarding the preferential use of SGLT2-Is or GLP1-RAs in patients with established cardiovascular disease.
|
31359366 |
2019 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
Although certain T2D medication use in patients with HF appeared consistent with evidence (less use of thiazolidinediones), others appeared contrary to evidence (less use of metformin and SGLT2 inhibitors).
|
30015065 |
2018 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
Amongst those with type 2 diabetes mellitus who did not have established cardiovascular disease but did present with multiple risk factors, SGLT2 inhibitors lowered the combined endpoint of cardiovascular death or hospitalization for heart failure but had little impact on the occurrence of major adverse cardiac events.
|
31839265 |
2020 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
At the present time, SGLT2 inhibitors are indicated for the treatment of type 2 diabetes; however, the results of ongoing trials in participants with heart failure but without diabetes are eagerly awaited.
|
31400090 |
2019 |
Congestive heart failure
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Based on such evidence, the recent guidelines for the management of type 2 diabetes now suggest that SGLT-2 inhibitors should be preferred among oral agents in combination with metformin, in patients at increased cardiovascular risk, chronic kidney disease or heart failure.
|
31663470 |
2019 |
Congestive heart failure
|
0.100 |
Biomarker
|
disease |
BEFREE |
Based on the available evidence, we conclude that SGLT-2 inhibitors represent an evidence-based therapeutic option for the primary prevention of heart failure hospitalization and secondary prevention of CVD in patients with T2DM, and should be considered early on in the treatment algorithm for patients with multiple risk factors, or those with established CVD.
|
31264765 |
2019 |
Congestive heart failure
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Beneficial effects on kidney disease progression, cardiovascular and all-cause mortality, and hospitalization for heart failure have also been demonstrated with one SGLT2 inhibitor (empagliflozin).
|
28721687 |
2017 |