Evidence map›Paper›PMID 41973867›Full record

ReviewThe Journal of clinical endocrinology and metabolism2026

Combination treatment for the management of chronic kidney disease and type 2 diabetes: a review and practical guidance.

Mai Mohsen, Tae Won Yi, Labib Faruque, Calvin Ke, Joseph A Cafazzo, Quynh Pham, Vikas S Sridhar, Adeera Levin, Husam Abdel-Qadir, Frederik Persson and 6 more

Abstract readReview
In one paragraph

Review in The Journal of clinical endocrinology and metabolism, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

16 authors.

Mai MohsenDivision of Nephrology, University Health Network, Toronto, ON M5G 2C4, Canada.
Tae Won YiDivision of Nephrology, University Health Network, Toronto, ON M5G 2C4, Canada.
Labib FaruqueDivision of Nephrology, University Health Network, Toronto, ON M5G 2C4, Canada.
Calvin KeDepartment of Medicine, University of Toronto, Toronto, ON M5S 3H2, Canada.
Joseph A CafazzoCentre for Digital Therapeutics, University Health Network, Toronto, ON M5G 2C4, Canada.
Quynh PhamCentre for Digital Therapeutics, University Health Network, Toronto, ON M5G 2C4, Canada.
Vikas S SridharDivision of Nephrology, University of British Columbia, Vancouver, BC V6Z 1Y6, Canada.
Adeera LevinDivision of Nephrology, University of British Columbia, Vancouver, BC V6Z 1Y6, Canada.
Husam Abdel-QadirInstitute of Health Policy, Management and Evaluation, University of Toronto, Toronto, ON M5T 3M6, Canada.
Frederik PerssonSteno Diabetes Center Copenhagen, Borgmester Ib Juuls Vej 83, Herlev 2730, Denmark.ORCID 0000-0001-6242-6638
Christoph WannerDepartment of Clinical Studies and Epidemiology, Comprehensive Heart Failure Center, University Hospital Würzburg, Würzburg, BY 97078, Germany.ORCID 0000-0001-9507-5301
Peter JüniClinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford OX3 7LF, UK.
Javed ButlerBaylor, Scott & White Research Institute, Dallas, TX 75204, USA.
Nikolaus MarxDepartment of Internal Medicine I - Cardiology, Angiology and Internal Intensive Care Medicine, University Hospital Aachen, Aachen, NRW 52074, Germany.ORCID 0000-0001-6141-634X
David Z I CherneyDivision of Nephrology, University Health Network, Toronto, ON M5G 2C4, Canada.
Ayodele OdutayoDepartment of Nephrology, Sunnybrook Health Sciences Centre, Toronto, ON M4N 3M5, Canada.ORCID 0000-0001-8619-5010

Funding

Allied Health Kidney ScholarshipBanting & Best Diabetes CentreBoehringer IngelheimCanadian Institutes of Health Research (CIHR)Early Career Transition AwardKidney FoundationKidney Foundation of CanadaResearch Excellence, Diversity, and Independence (REDI)University of Toronto
6 · The paper itself

Abstract

contextRenin-angiotensin system inhibitors (RASi), sodium glucose cotransporter-2 inhibitors (SGLT2i), non-steroidal mineralocorticoid receptor antagonists (nsMRA), and glucagon-like peptide-1 receptor agonists (GLP-1RA) are key components of guideline-directed medical treatments (GDMT) for chronic kidney disease (CKD) with type 2 diabetes (T2D). However, the combined use of these medications remains uncommon in clinical practice, in part, due to the absence of specific guidance on implementing combination treatment. Herein, we aim to (1) summarize the evidence supporting combination GDMT in CKD with T2D, (2) propose a practical algorithm to guide the accelerated implementation of quadruple treatment, and (3) discuss strategies to improve the uptake of combination treatment. EVIDENCE ACQUISITION: We searched PubMed from inception to present for English-speaking studies using the search terms: "renin-angiotensin system inhibitor," "sodium glucose cotransporter-2 inhibitor," "nonsteroidal mineralocorticoid receptor antagonist," "glucagon-like peptide-1 receptor agonist," and "diabetes." We focused on clinical guidelines, randomized controlled trials (RCTs), and, if necessary, large observational studies. EVIDENCE SYNTHESIS: SGLT2i, nsMRA, and GLP-1RA confer early cardiovascular and kidney protection through independent mechanisms, allowing them to be combined. RCTs support the use of each agent on top of "standard care," and multiple clinical guidelines endorse combination treatment. However, the optimal order and timing for medication initiation and the approach to managing treatment-related side effects remain uncertain, thereby limiting the uptake of combination treatment.

conclusionCurrent evidence supports the use of combination GDMT in CKD with T2D. We propose a combination treatment algorithm that may combat clinical inertia and achieve greater cardiorenal risk reduction in high-risk patients with CKD and T2D.

Indexed as

Diabetes Mellitus, Type 2Hypoglycemic AgentsPractice Guidelines as TopicRenal Insufficiency, ChronicDrug Therapy, CombinationHumansMineralocorticoid Receptor AntagonistsSodium-Glucose Transporter 2 InhibitorsHypoglycemic AgentsMineralocorticoid Receptor AntagonistsSodium-Glucose Transporter 2 Inhibitorscardiorenal protectioncardiovascular diseasechronic kidney diseasecombination treatmentdiabetesdiabetic kidney disease

Identifiers

PMID41973867
PMCPMC13271800

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.