Evidence map›Paper›PMID 41975298›Full record

ArticleBMC nephrology2026

Cost-utility analysis of sodium-glucose cotransporter-2 inhibitors on chronic kidney disease progression in patients with type 2 diabetes mellitus.

Sukanya Siriyotha, Amarit Tansawet, Oraluck Pattanaprateep, Tanawan Kongmalai, Panu Looareesuwan, Junwei Yang, Suparee W Boonmanunt, Gareth J McKay, John Attia, Ammarin Thakkinstian

Abstract read
In one paragraph

Article in BMC nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

10 authors.

Sukanya SiriyothaDepartment of Clinical Epidemiology and Biostatistics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama VI Road, Pyathai, Bangkok, 10400, Thailand.
Amarit TansawetResearch Affairs, Faculty of Medicine, Chulalongkorn University, 1873, Rama 4 Road, Pathumwan, Bangkok, 10330, Thailand. amarit.t@chula.ac.th.
Oraluck PattanaprateepDepartment of Clinical Epidemiology and Biostatistics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama VI Road, Pyathai, Bangkok, 10400, Thailand. oraluck.pat@mahidol.ac.th.
Tanawan KongmalaiDivision of Endocrinology and Metabolism, Faculty of Medicine Siriraj, Hospital Mahidol University, Bangkok, Thailand.
Panu LooareesuwanDepartment of Clinical Epidemiology and Biostatistics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama VI Road, Pyathai, Bangkok, 10400, Thailand.
Junwei YangDepartment of Clinical Epidemiology and Biostatistics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama VI Road, Pyathai, Bangkok, 10400, Thailand.
Suparee W BoonmanuntDepartment of Clinical Epidemiology and Biostatistics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama VI Road, Pyathai, Bangkok, 10400, Thailand.
Gareth J McKayCentre for Public Health, School of Medicine, Dentistry and Biomedical Sciences, Queen's University Belfast, Belfast, UK.
John AttiaSchool of Medicine and Public Health, Hunter Medical Research Institute, University of Newcastle, New Lambton, NSW, Australia.
Ammarin ThakkinstianDepartment of Clinical Epidemiology and Biostatistics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama VI Road, Pyathai, Bangkok, 10400, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMany trials have highlighted the benefits of sodium-glucose co-transporter 2 inhibitors (SGLT2is) in terms of chronic kidney disease (CKD) progression. However, SGLT2is are high-cost medication, and their cost- effectiveness varies by setting across countries.

methodsThis study aimed to evaluate the cost-effectiveness of sodium-glucose co-transporter 2 inhibitors (SGLT2is) in terms of chronic kidney disease (CKD) progression by utilizing data from the type 2 diabetes mellitus (T2D) cohort collected from 2010 to 2022 to estimate transitional probabilities and costs. Markov models were constructed from the following states: CKD stage 3, 4, 5, and death. Cost and quality-adjusted life year (QALY) were estimated for SGLT2i and non-SGLT2i groups from both hospital and societal perspectives.

resultsFrom a societal perspective, the incremental cost was US$3,485.28 (US$80,245.48 (non-SGLT2i) and US$83,730.76 (SGLT2i)), and US$2,971.00 (US$80,913.73 (non-SGLT2i) and US$83,884.73 (SGLT2i)) in patients with renal replacement therapy (RRT) and without RRT, respectively. The incremental QALY were 2.73 (13.88 (non-SGLT2i) and 16.61 years (SGLT2i)) and 2.79 years (13.78 (non-SGLT2i) and 16.57 years (SGLT2i)) in patients with RRT and without RRT, respectively. ICERs were US$1,276.66 and US$1,064.87 per QALY in patients with and without RRT, respectively. A one-way sensitivity analysis suggested that the admission cost per day had the biggest impact on the ICER. Although SGLT2is are more expensive than alternatives, they remain cost-effective at the Thai willingness to pay threshold of US$4,869 per QALY.

conclusionThis finding was robust in multiple sensitivity analyses, showing consistent net benefit regardless of RRT status. Future research should now focus on differentiating the value of specific drugs within the class. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Cost-Benefit AnalysisDiabetes Mellitus, Type 2Renal Insufficiency, ChronicSodium-Glucose Transporter 2 InhibitorsAgedCost-Effectiveness AnalysisDisease ProgressionFemaleHumansMaleMarkov ChainsMiddle AgedQuality-Adjusted Life YearsSodium-Glucose Transporter 2 InhibitorsChronic kidney diseaseCost-utility analysisSodium-glucose cotransporter-2 inhibitor

Identifiers

PMID41975298
PMCPMC13202843

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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.