Prevention & Lipids
Cardiorenal medicine: chronic kidney disease in heart failure and diabetes, SGLT2 inhibitors, finerenone, and kidney outcome trials.
Also called CKD, cardiorenal syndrome, chronic renal insufficiency
Sources: 5 landmark trials · 12 new papers · 5 key papers · updated Oct 20, 2026
“There is strong evidence suggesting that elevated levels of high-sensitivity C-reaction protein (hs-CRP) are a predictor of increased cardiovascular risk, and quarterly subcutaneous administration of pacibekitug in the TRANQUILITY trial demonstrated large and significant…”
Expert labels are toward TRANQUILITY's result, from named public quotes (n=1). As of Aug 27, 2026.
Unverified · drafted by AI from the sources cited below
Chronic kidney disease involves conditions in which the kidneys perform below the normal level for more than three months.1 Chronic kidney insufficiency is classified by five stages according to the decline in glomerular filtration rate and the degree of kidney damage, as measured by the level of proteinuria.1 The condition is generally characterized by low glomerular filtration rate or albuminuria.2
The most severe form of the condition is end-stage renal disease.1 Estimated glomerular filtration rate is widely utilized as a marker of risk profile in cardiovascular diseases, including heart failure.2 Acute kidney disease, defined as acute kidney injury persisting for 7 to 90 days, represents a window for interventions and is associated with progression to de novo chronic kidney disease.3
Compared with placebo, sodium-glucose cotransporter-2 inhibitors reduced the risk of first heart failure hospitalization or cardiovascular death by 23% in chronic kidney disease based on an analysis of 90,413 patients.1 Finerenone, a selective nonsteroidal mineralocorticoid receptor antagonist, has favorable effects on cardiorenal outcomes in patients with predominantly stage 3 or 4 chronic kidney disease with severely elevated albuminuria and type 2 diabetes.2 In a small subgroup analysis of 5 patients, teriparatide improved bone mineral density at the lumbar spine and femoral neck in stage 4 chronic kidney disease.3
The use of finerenone in patients with type 2 diabetes and a wider range of chronic kidney disease, such as stage 1 or 2, is unclear.1 Additionally, the safety and efficacy of IL-6 inhibition among individuals at high atherosclerotic risk but without a systemic inflammatory disorder is unknown.2
Society guidelines, scientific statements and expert consensus on Chronic kidney disease from the last three months.
This is the first ESC Guideline dedicated to the management of cardiovascular disease (CVD) and chronic kidney disease (CKD), centred around the “STAMP on CKD” framework.
FDA approvals, label changes, device decisions and recalls on Chronic kidney disease from the last three months.
The FDA has noted an original approval for a tablet formulation. However, specific details regarding the drug name and indication were not provided in the announcement.
The FDA has issued a drug approval for an original submission available in a solution formulation. Further details regarding the drug's name and indication were not specified in the release.
Supplementation with <i>Enterococcus lactis</i> (SF68) and its association with biochemical parameters and inflammatory biomarkers related to renal impairment in dogs with chronic kidney disease.
López R — Dec 2026
Risk factors associated with rapid progression of chronic kidney disease. A retrospective cohort study.
Chogtu B — Oct 2026
Primary results of 5 trials behind the evidence on chronic kidney disease, as each trial’s own publication reports them.
Left of the line at 1 favours the intervention; square size tracks trial size.Favours the interventionNo significant differenceFavours the comparator
semaglutide vs placebo · 3,533 patients · N Engl J Med 2024
In patients with type 2 diabetes and chronic kidney disease
Primary outcome: major kidney disease events, a composite of the onset of kidney failure (dialysis, transplantation, or an eGFR of <15 ml per minute per 1.73 m2), at least a 50% reduction in the eGFR from baseline, or death from kidney-related or cardiovascular causes
Cardiovascular Events with Finerenone in Kidney Disease and Type 2 Diabetes
New England Journal of Medicine
1,805 citations · 2021 · among the most cited on Chronic kidney disease
IL-6 inhibition with ziltivekimab in patients at high atherosclerotic risk (RESCUE): a double-blind, randomised, placebo-controlled, phase 2 trial
The Lancet — Ridker P
744 citations · 2021 · among the most cited on Chronic kidney disease
Kidney Function and Outcomes in Patients Hospitalized With Heart Failure
Journal of the American College of Cardiology — Patel R
204 citations · 2021 · among the most cited on Chronic kidney disease
A clinical question appears here only when its condition matches this topic, an outcome and a comparator were extracted from the studies, at least two studies and a patient count are on file, and the certainty is low or higher.
Supports benefit, no benefit shown, and mixed describe the direction of the measured effect. No benefit shown means the evidence does not support a benefit. It is not a finding of harm. Too little evidence means the question did not clear that bar.
Study count, RCT count, and patient count are separate. The patient total adds only studies that are linked into a study family and whose sample size is not flagged as implausible. A reversal is listed only when at least one randomized trial sits on each side of the change.
The overview is drafted from the guideline recommendations, trials, papers, and questions on this page, and every sentence has to cite one of them. It stays unverified until an NPI-verified clinician or a Synapse admin approves it. Approving records that person's name.
Signal Transduction and Targeted Therapy — Ye J — Oct 2026
HR 0.76 (0.66–0.88)
empagliflozin vs placebo · 6,609 patients · N Engl J Med 2023
In patients with chronic kidney disease who were at risk for disease progression
Primary outcome: a composite of progression of kidney disease (defined as end-stage kidney disease, a sustained decrease in eGFR to <10 ml per minute per 1.73 m2, a sustained decrease in eGFR of ≥40% from baseline, or death from renal causes) or death from cardiovascular causes
HR 0.72 (0.64–0.82)
finerenone vs placebo · 7,437 patients · N Engl J Med 2021
In patients with CKD and type 2 diabetes
Primary outcome: a composite of death from cardiovascular causes, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for heart failure
HR 0.87 (0.76–0.98)
dapagliflozin vs placebo · 4,304 patients · N Engl J Med 2020
In patients with chronic kidney disease, regardless of the presence or absence of diabetes
Primary outcome: a composite of a sustained decline in the estimated GFR of at least 50%, end-stage kidney disease, or death from renal or cardiovascular causes
HR 0.61 (0.51–0.72)
finerenone vs placebo · 5,734 patients · N Engl J Med 2020
In patients with CKD and type 2 diabetes
Primary outcome: kidney failure, a sustained decrease of at least 40% in the eGFR from baseline, or death from renal causes
HR 0.82 (0.73–0.93)
Results are quoted from each trial’s primary publication abstract (PubMed); the trial name links to the paper. Ratios below 1 favour the intervention.