Evidence map›Paper›PMID 39993818›Full record

ArticleCMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne2025

Sodium-glucose cotransporter 2 (SGLT2) inhibitors and risk of chronic kidney disease-mineral and bone disorders in patients with type 2 diabetes mellitus and stage 1-3 chronic kidney disease.

Daniel Hsiang-Te Tsai, Albert Tzu-Ming Chuang, Kuan-Hung Liu, Shih-Chieh Shao, Edward Chia-Cheng Lai

Abstract read
In one paragraph

Article in CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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.

Daniel Hsiang-Te TsaiSchool of Pharmacy (Tsai, Chuang, Shao, Lai), Institute of Clinical Pharmacy and Pharmaceutical Sciences (Tsai, Chuang, Shao, Lai), College of Medicine, National Cheng Kung University, Tainan, Taiwan; Population Health Data Center (Tsai, Chuang, Shao, Lai), National Cheng Kung University, Tainan, Taiwan; Institute of Clinical Medicine (Liu), and Division of Nephrology (Liu), Department of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan; Department of Pharmacy (Shao), Keelung Chang Gung Memorial Hospital, Keelung, Taiwan.
Albert Tzu-Ming ChuangSchool of Pharmacy (Tsai, Chuang, Shao, Lai), Institute of Clinical Pharmacy and Pharmaceutical Sciences (Tsai, Chuang, Shao, Lai), College of Medicine, National Cheng Kung University, Tainan, Taiwan; Population Health Data Center (Tsai, Chuang, Shao, Lai), National Cheng Kung University, Tainan, Taiwan; Institute of Clinical Medicine (Liu), and Division of Nephrology (Liu), Department of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan; Department of Pharmacy (Shao), Keelung Chang Gung Memorial Hospital, Keelung, Taiwan.
Kuan-Hung LiuSchool of Pharmacy (Tsai, Chuang, Shao, Lai), Institute of Clinical Pharmacy and Pharmaceutical Sciences (Tsai, Chuang, Shao, Lai), College of Medicine, National Cheng Kung University, Tainan, Taiwan; Population Health Data Center (Tsai, Chuang, Shao, Lai), National Cheng Kung University, Tainan, Taiwan; Institute of Clinical Medicine (Liu), and Division of Nephrology (Liu), Department of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan; Department of Pharmacy (Shao), Keelung Chang Gung Memorial Hospital, Keelung, Taiwan.
Shih-Chieh ShaoSchool of Pharmacy (Tsai, Chuang, Shao, Lai), Institute of Clinical Pharmacy and Pharmaceutical Sciences (Tsai, Chuang, Shao, Lai), College of Medicine, National Cheng Kung University, Tainan, Taiwan; Population Health Data Center (Tsai, Chuang, Shao, Lai), National Cheng Kung University, Tainan, Taiwan; Institute of Clinical Medicine (Liu), and Division of Nephrology (Liu), Department of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan; Department of Pharmacy (Shao), Keelung Chang Gung Memorial Hospital, Keelung, Taiwan. scshao@cgmh.org.tw.
Edward Chia-Cheng LaiSchool of Pharmacy (Tsai, Chuang, Shao, Lai), Institute of Clinical Pharmacy and Pharmaceutical Sciences (Tsai, Chuang, Shao, Lai), College of Medicine, National Cheng Kung University, Tainan, Taiwan; Population Health Data Center (Tsai, Chuang, Shao, Lai), National Cheng Kung University, Tainan, Taiwan; Institute of Clinical Medicine (Liu), and Division of Nephrology (Liu), Department of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan; Department of Pharmacy (Shao), Keelung Chang Gung Memorial Hospital, Keelung, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn patients with type 2 diabetes mellitus and chronic kidney disease (CKD), sodium-glucose cotransporter 2 (SGLT2) inhibitors improve renal outcomes, but may transiently affect biochemical markers of CKD-mineral and bone disorders (CKD-MBD). We sought to evaluate the long-term risk of CKD-MBD associated with use of SGLT2 inhibitors in this patient population.

methodsWe conducted a retrospective cohort study, employing a target trial emulation framework and using electronic medical records of patients from 9 hospitals in Taiwan (2016-2023). We included adults with type 2 diabetes mellitus and stage 1-3 CKD who had newly started either an SGLT2 inhibitor or, as a comparison group, a glucagon-like peptide-1 receptor agonist (GLP-1 RA). The primary outcome was a composite of incident biochemical abnormalities (serum phosphate > 1.5 mmol/L, serum calcium < 2.1 mmol/L, serum intact parathyroid hormone [iPTH] > 6.9 pmol/L, or serum 25-hydroxyvitamin D < 49.9 nmol/L).

resultsThe cohort included 13 379 patients receiving SGLT2 inhibitors (

interpretationUse of SGLT2 inhibitors was associated with a lower incidence of biochemical abnormalities related to CKD-MBD than GLP-1 RAs. These agents may be considered to reduce risk of CKD-MBD in patients with type 2 diabetes mellitus and stage 1-3 CKD.

Indexed as

Chronic Kidney Disease-Mineral and Bone DisorderDiabetes Mellitus, Type 2Renal Insufficiency, ChronicSodium-Glucose Transporter 2 InhibitorsAgedFemaleGlucagon-Like Peptide-1 Receptor AgonistsHumansIncidenceMaleMiddle AgedRetrospective StudiesRisk FactorsTaiwanGlucagon-Like Peptide-1 Receptor AgonistsSodium-Glucose Transporter 2 Inhibitors

Identifiers

PMID39993818
PMCPMC11867598

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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.