Evidence map›Paper›PMID 36289720›Full record

ReviewBiomedicines2022

SGLT2 Inhibitors in Chronic Kidney Disease: From Mechanisms to Clinical Practice.

Roko Skrabic, Marko Kumric, Josip Vrdoljak, Doris Rusic, Ivna Skrabic, Marino Vilovic, Dinko Martinovic, Vid Duplancic, Tina Ticinovic Kurir, Josko Bozic

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
6.0field-weighted citation impact, top 3% 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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 44 citations in OpenAlex.

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  18. SGLT2 inhibitors: Beyond glycemic control.Journal of clinical & translational endocrinology · 2024
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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

10 authors at 1 institution in 1 country.

Roko SkrabicDepartment of Nephrology, University Hospital of Split, 21000 Split, Croatia.
Marko KumricDepartment of Pathophsiology, University of Split School of Medicine, 21000 Split, Croatia.ORCID 0000-0002-9696-3359
Josip VrdoljakDepartment of Pathophsiology, University of Split School of Medicine, 21000 Split, Croatia.
Doris RusicDepartment of Pharmacy, University of Split School of Medicine, 21000 Split, Croatia.ORCID 0000-0002-7018-4947
Ivna SkrabicDepartment of Pathophsiology, University of Split School of Medicine, 21000 Split, Croatia.
Marino VilovicDepartment of Pathophsiology, University of Split School of Medicine, 21000 Split, Croatia.ORCID 0000-0002-5433-5063
Dinko MartinovicDepartment of Pathophsiology, University of Split School of Medicine, 21000 Split, Croatia.
Vid DuplancicDepartment of Pathophsiology, University of Split School of Medicine, 21000 Split, Croatia.
Tina Ticinovic KurirDepartment of Pathophsiology, University of Split School of Medicine, 21000 Split, Croatia.
Josko BozicDepartment of Pathophsiology, University of Split School of Medicine, 21000 Split, Croatia.ORCID 0000-0003-1634-0635
University of Split · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, sodium-glucose co-transporter 2 inhibitors (SGLT2i) have demonstrated beneficial renoprotective effects, which culminated in the recent approval of their use for patients with chronic kidney disease (CKD), following a similar path to one they had already crossed due to their cardioprotective effects, meaning that SGLT2i represent a cornerstone of heart failure therapy. In the present review, we aimed to discuss the pathophysiological mechanisms operating in CKD that are targeted with SGLT2i, either directly or indirectly. Furthermore, we presented clinical evidence of SGLT2i in CKD with respect to the presence of diabetes mellitus. Despite initial safety concerns with regard to euglycemic diabetic ketoacidosis and transient decline in glomerular filtration rate, the accumulating clinical data are reassuring. In summary, although SGLT2i provide clinicians with an exciting new treatment option for patients with CKD, further research is needed to determine which subgroups of patients with CKD will benefit the most, and which the least, from this therapeutical option.

Indexed as

chronic kidney diseasediabetes mellitusSGLT2 inhibitor

Identifiers

PMID36289720
PMCPMC9598622
OpenAlexW4303613874

What OpenQuestion 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 OpenQuestion graph.