Evidence mapPaperPMID 40434618Full record

ReviewAdvances in therapy2025

Guideline-Recommended Disease-Modifying Therapies for Patients with Cardiorenal Disease: A Call-to-Action Narrative Review.

Christoph Wanner, Ming-Hui Zhao, Alpesh N Amin, Luca De Nicola, Andrew J Sauer, Alaster M Allum, Unai Aranda, You-Seon Nam, Javed Butler

Abstract readReview
In one paragraph

Review in Advances in therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Article
  6. Addressing Unmet Needs in the Management of Chronic Kidney Disease.International journal of general medicine · 2026
    Review
  7. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Christoph WannerDepartment of Clinical Research and Epidemiology, Comprehensive Heart Failure Center, University Hospital of Würzburg, Am Schwarzenberg 15, 97078, Würzburg, Germany. wanner_c@ukw.de.
Ming-Hui ZhaoRenal Division, Peking University First Hospital, Peking, China.
Alpesh N AminDepartment of Medicine, Division of Hospital Medicine & Palliative Medicine, University of California, Irvine, CA, USA.
Luca De NicolaDepartment of Advanced Medical and Surgical Sciences, University of Campania L. Vanvitelli, Naples, Italy.
Andrew J SauerDepartment of Cardiology, Saint Luke's Mid America Heart Institute, Kansas City, MO, USA.
Alaster M AllumGlobal Medical Affairs, Renal Medicine, AstraZeneca, Cambridge, UK.
Unai ArandaGlobal Medical Affairs, BioPharmaceuticals Medical, AstraZeneca, Gaithersburg, MD, USA.
You-Seon NamGlobal Medical Affairs, BioPharmaceuticals Medical, AstraZeneca, Gaithersburg, MD, USA.
Javed ButlerBaylor Scott & White Research Institute, Dallas, TX, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Substantial gaps exist between recommendations for guideline-directed medical therapy (GDMT) for chronic kidney disease (CKD) and its use in real-world clinical practice. This includes suboptimal dosing of renin-angiotensin system inhibitors (RASi), low uptake of sodium-glucose co-transporter 2 inhibitors (SGLT2i) for CKD, and low uptake and/or transient use of potassium binders to manage RASi-induced hyperkalemia. Suboptimal RASi therapy deprives patients of the full cardiorenal benefits associated with RASi, and increases the risk of cardiorenal adverse events and mortality. Hyperkalemia can be managed and optimal RASi dosing can be continued by using novel potassium binders, such as sodium zirconium cyclosilicate or patiromer. Similarly, low uptake of SGLT2i might be associated with the concern of an accelerated decline in estimated glomerular filtration rate and, therefore, disease progression when initiating SGLT2i. Numerous clinical trials have demonstrated that adding SGLT2i to RASi therapy can improve clinical outcomes and prolong patient survival in CKD. The recently published Kidney Disease: Improving Global Outcomes (KDIGO) 2024 clinical practice guideline for the evaluation and management of CKD extends the recommendation of SGLT2i to individuals with CKD without diabetes, reinforces the cardiorenal benefits of optimized RASi, recommends the addition of newer drug classes in suitable patients with CKD, and notes the use of novel potassium binders to manage hyperkalemia and enable optimal use of GDMT. In doing so, the guideline targets achievement of the "quadruple aim" of GDMT in CKD, i.e., enabling optimal use of RASi and SGLT2i in most patients, along with nonsteroidal mineralocorticoid receptor antagonists, and glucagon-like peptide-1 receptor agonists in diabetic kidney disease. This manuscript constitutes a call to action to raise awareness of the growing clinical and economic burdens of CKD and to promote a united approach to the early detection and optimal treatment of CKD through stricter adherence to GDMT.

Indexed as

Cardio-Renal SyndromeRenal Insufficiency, ChronicSodium-Glucose Transporter 2 InhibitorsAngiotensin-Converting Enzyme InhibitorsHumansHyperkalemiaPractice Guidelines as TopicRenin-Angiotensin SystemAngiotensin-Converting Enzyme InhibitorsSodium-Glucose Transporter 2 InhibitorsChronic kidney diseaseGlucagon-like peptide-1 receptor agonistGuideline-directed medical therapyHyperkalemiaKDIGONon-steroidal mineralocorticoid receptor antagonistRenin-angiotensin system inhibitorSodium-glucose co-transporter 2 inhibitorSodium zirconium cyclosilicateType 2 diabetes

Identifiers

PMID40434618
PMCPMC12182529

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.