Evidence map›Paper›PMID 35327323›Full record

ArticleBiomedicines2022

The Effect of SGLT2 Inhibition on Diabetic Kidney Disease in a Model of Diabetic Retinopathy.

Jennifer Rose Matthews, Markus P Schlaich, Elizabeth Piroska Rakoczy, Vance Bruce Matthews, Lakshini Yasaswi Herat

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Comparative Effects of Monascin and Monascinol Produced byJournal of fungi (Basel, Switzerland) · 2024
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  5. Review
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  7. Tubular deficiency of ABCA1 augments cholesterol- and NaAmerican journal of physiology. Renal physiology · 2024
    Article
  8. Review
  9. Article
  10. 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 at 1 institution in 1 country.

Jennifer Rose MatthewsDobney Hypertension Centre, School of Biomedical Sciences-Royal Perth Hospital Unit, University of Western Australia, Crawley, WA 6009, Australia.
Markus P SchlaichDobney Hypertension Centre, Medical School-Royal Perth Hospital Unit, University of Western Australia, Crawley, WA 6009, Australia.ORCID 0000-0002-1765-0195
Elizabeth Piroska RakoczyDepartment of Molecular Ophthalmology, University of Western Australia, Crawley, WA 6009, Australia.
Vance Bruce MatthewsDobney Hypertension Centre, School of Biomedical Sciences-Royal Perth Hospital Unit, University of Western Australia, Crawley, WA 6009, Australia.ORCID 0000-0001-9804-9344
Lakshini Yasaswi HeratDobney Hypertension Centre, School of Biomedical Sciences-Royal Perth Hospital Unit, University of Western Australia, Crawley, WA 6009, Australia.ORCID 0000-0001-9818-006X
The University of Western Australia · AU

Funding

Diabetes Australia Research Program DARP-VMatthews2019Diabetes Research Western Australia DRWA-LHerat-2019Raine Medical Research Foundation Raine- LHerat-2019Royal Perth Hospital Research Foundation RPHRF-VMatthews-2017
6 · The paper itself

Abstract

Diabetic kidney disease (DKD) is a chronic disorder characterized by elevated urine albumin excretion, reduced glomerular filtration rate, or both. At present, angiotensin-converting enzyme inhibitors or angiotensin receptor blockers are the standard care for the treatment of DKD, resulting in improved outcomes. However, alternative treatments may be required because although the standard treatments have been found to slow the progression of DKD, they have not been found to halt the disease. In the past decade, sodium glucose co-transporter 2 (SGLT2) inhibitors have been widely researched in the area of cardiovascular disease and diabetes and have been shown to improve cardiovascular outcomes. SGLT2 inhibitors including canagliflozin and dapagliflozin have been shown to slow the progression of kidney disease. There is currently an omission of literature where three SGLT2 inhibitors have been simultaneously compared in a rodent diabetic model. After diabetic Akimba mice were treated with SGLT2 inhibitors for 8 weeks, there was not only a beneficial impact on the pancreas, signified by an increase in the islet mass and increased plasma insulin levels, but also on the kidneys, signified by a reduction in average kidney to body weight ratio and improvement in renal histology. These findings suggest that SGLT2 inhibition promotes improvement in both pancreatic and kidney health.

Indexed as

Akimbacanagliflozindapagliflozindiabetic kidneyempagliflozinKimbamouse modelsodium glucose co-transporter 2 inhibition

Identifiers

PMID35327323
PMCPMC8944990
OpenAlexW4212853654

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.