Evidence map›Paper›PMID 33106255›Full record

ReviewDiabetes2021

SGLT2 Inhibition for CKD and Cardiovascular Disease in Type 2 Diabetes: Report of a Scientific Workshop Sponsored by the National Kidney Foundation.

Katherine R Tuttle, Frank C Brosius, Matthew A Cavender, Paola Fioretto, Kevin J Fowler, Hiddo J L Heerspink, Tom Manley, Darren K McGuire, Mark E Molitch, Amy K Mottl and 7 more

Open access · bronzeAbstract readReview
In one paragraph

Review in Diabetes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
10.6field-weighted citation impact, top 1% of its field
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

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 118 citations in OpenAlex.

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  20. Polymorphic and Expressional Analysis of GenesInternational journal of hypertension · 2025
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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

17 authors at 16 institutions in 7 countries.

Katherine R TuttleProvidence Health Care and University of Washington School of Medicine, Spokane, WA katherine.tuttle@providence.org.
Frank C BrosiusUniversity of Arizona College of Medicine, Tucson, AZ.ORCID 0000-0002-4244-8335
Matthew A CavenderUniversity of North Carolina School of Medicine, Chapel Hill, NC.
Paola FiorettoDepartment of Medicine, University of Padua, Padua, Italy.
Kevin J FowlerThe Voice of the Patient, Inc, Elmhurst, IL.
Hiddo J L HeerspinkUniversity of Groningen, Groningen, the Netherlands.
Tom ManleyNational Kidney Foundation, New York, NY.
Darren K McGuireUniversity of Texas Southwestern Medical Center, Dallas, TX.
Mark E MolitchDivision of Endocrinology, Metabolism and Molecular Medicine, Northwestern, University Feinberg School of Medicine, Chicago, IL.
Amy K MottlUniversity of North Carolina School of Medicine, Chapel Hill, NC.
Leigh PerreaultUniversity of Colorado Anschutz Medical Campus, Aurora, CO.
Sylvia E RosasJoslin Diabetes Center and Harvard Medical School, Boston, MA.
Peter RossingSteno Diabetes Center Copenhagen, Gentofte, Denmark.
Laura SolaUniversity of the Republic, Montevideo, Uruguay.
Volker VallonUniversity of California-San Diego, La Jolla, CA.
Christoph WannerDivision of Nephrology, University Hospital Würzburg, Würzburg, Germany.
Vlado PerkovicGeorge Institute for Global Health, UNSW Sydney, Australia.
University of North Carolina at Chapel Hill · USJoslin Diabetes Center · USNational Kidney Foundation · USNorthwestern University · USThe University of Texas Southwestern Medical Center · USUniversidad de la República de Uruguay · UYUniversitätsklinikum Würzburg · DEUniversity of Arizona · USUniversity of California San Diego · USUniversity of Colorado Anschutz Medical Campus · USUniversity of Copenhagen · DKUniversity of Groningen · NLUniversity of Padua · ITUniversity of Washington · USUNSW Sydney · AUVoice of America (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetes is the most frequent cause of chronic kidney disease (CKD), leading to nearly half of all cases of kidney failure requiring replacement therapy. The principal cause of death among patients with diabetes and CKD is cardiovascular disease (CVD). Sodium/glucose cotransporter 2 (SGLT2) inhibitors were developed to lower blood glucose levels by inhibiting glucose reabsorption in the proximal tubule. In clinical trials designed to demonstrate the CVD safety of SGLT2 inhibitors in type 2 diabetes mellitus (T2DM), consistent reductions in risks for secondary kidney disease end points (albuminuria and a composite of serum creatinine doubling or 40% estimated glomerular filtration rate decline, kidney failure, or death), along with reductions in CVD events, were observed. In patients with CKD, the kidney and CVD benefits of canagliflozin were established by the CREDENCE (Canagliflozin and Renal Events in Diabetes With Established Nephropathy Clinical Evaluation) trial in patients with T2DM, urinary albumin-creatinine ratio >300 mg/g, and estimated glomerular filtration rate of 30 to <90 mL/min/1.73 m

Indexed as

Cardiovascular DiseasesDiabetes Mellitus, Type 2Diabetic NephropathiesEducationHumansRenal Insufficiency, ChronicSodium-Glucose Transporter 2 InhibitorsSodium-Glucose Transporter 2 Inhibitors

Identifiers

PMID33106255
PMCPMC8162454
OpenAlexW3093635194

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.