Evidence map›Paper›PMID 41130867›Full record

ReviewEuropean journal of internal medicine2026

Contemporary management of advanced chronic kidney disease: An evidence-based review.

Lyle W Baker, Cene Ovincy, Levon Souvalian, LaTonya J Hickson, Fouad T Chebib

Abstract readReview
In one paragraph

Review in European journal of internal medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

  1. [Rehmanniae radix preparata alleviates chronic kidney disease in mice through a multi-target mechanism].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
    Article
  2. Review
  3. Review
  4. Article
  5. Article
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

5 authors.

Lyle W BakerDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Jacksonville, FL, USA.
Cene OvincyDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Jacksonville, FL, USA.
Levon SouvalianDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Jacksonville, FL, USA; Mayo Clinic Florida PKD Center of Excellence, Jacksonville, FL, USA.
LaTonya J HicksonDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Jacksonville, FL, USA.
Fouad T ChebibDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Jacksonville, FL, USA; Mayo Clinic Florida PKD Center of Excellence, Jacksonville, FL, USA. Electronic address: Chebib.fouad@mayo.edu.

Funding

Novel role of urinary urate in renal cystogenesis and water regulationR01DK142878 · NIDDK · MAYO CLINIC JACKSONVILLE · PI CHEBIB, FOUAD T · 2025 to 2025
$3.0M
Resource Development CoreU54DK144863 · NIDDK · MAYO CLINIC ROCHESTER · PI Neera Kanhouwa Dahl · 2025 to 2026
$822k
NIDDK NIH HHS R01 DK142878NIDDK NIH HHS U54 DK144863
6 · The paper itself

Abstract

Chronic kidney disease (CKD) is a major contributor to global morbidity and mortality, traditionally managed through renin-angiotensin system (RAS) inhibition and supportive care. Recent therapeutic advances have transformed this landscape, offering targeted interventions that modify disease progression and improve cardiovascular and renal outcomes. This review summarizes emerging treatments across key domains of CKD management. Sodium-glucose cotransporter 2 (SGLT2) inhibitors and glucagon-like peptide-1 (GLP-1) receptor agonists have demonstrated robust cardiorenal benefits, particularly in patients with type 2 diabetes mellitus (T2DM). SGLT2 inhibitors are now widely used in CKD and heart failure, including among non-diabetic populations. GLP-1 receptor agonists are approved for T2DM and cardiovascular risk reduction, with recent expansion to CKD in T2DM. Nonsteroidal mineralocorticoid receptor antagonists (nsMRAs), particularly finerenone, provide additional cardiorenal protection with a lower risk of hyperkalemia than traditional steroidal agents. In autosomal dominant polycystic kidney disease (ADPKD), tolvaptan remains the only approved disease-modifying therapy, with clinical trials and real-world data supporting its efficacy across a range of disease stages. Emerging regenerative strategies, including mesenchymal stem cell (MSC) therapy and xenotransplantation using genetically modified pig kidneys, have shown early promise in preclinical models and limited human studies. While further research is needed to optimize patient selection and long-term outcomes, these approaches represent important future directions in nephrology. Together, these developments mark a shift toward mechanism-based, precision therapies in CKD care. Internal medicine clinicians are pivotal in identifying appropriate candidates for these treatments and integrating evolving evidence into practice to improve patient outcomes.

Indexed as

Renal Insufficiency, ChronicSodium-Glucose Transporter 2 InhibitorsDiabetes Mellitus, Type 2Glucagon-Like Peptide-1 Receptor AgonistsHumansMineralocorticoid Receptor AntagonistsPolycystic Kidney, Autosomal DominantTolvaptanGlucagon-Like Peptide-1 Receptor AgonistsMineralocorticoid Receptor AntagonistsSodium-Glucose Transporter 2 InhibitorsTolvaptanADPKDAutosomal dominant polycystic kidney diseaseChronic kidney diseaseCKDDisease modifying treatmentEnd stage kidney diseaseESKDMesenchymal stem cellMSCNonsteroidal mineralocorticoid receptor antagonistsnsMRAsSGLT2iSodium-glucose cotransporter-2 inhibitorsVaptansXenotransplant

Identifiers

PMID41130867
PMCPMC12560998

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.