Evidence map›Paper›PMID 36210442›Full record

ReviewBMC medicine2022

New strategies to improve clinical outcomes for diabetic kidney disease.

Thomas Forst, Chantal Mathieu, Francesco Giorgino, David C Wheeler, Nikolaos Papanas, Roland E Schmieder, Atef Halabi, Oliver Schnell, Marina Streckbein, Katherine R Tuttle

Abstract readReview
In one paragraph

Review in BMC medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing 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

51 citing papers in PubMed.

  1. Article
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  4. The gut as a central hub for multi-organ crosstalk in aging.Cellular and molecular life sciences : CMLS · 2026
    Review
  5. Article
  6. Article
  7. Article
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  12. Mechanisms of Xuefu Zhuyu decoction in treating diabetic kidney disease-induced renal fibrosis: UPLC-Q/TOF-MS, network pharmacology, and experimental validation.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2025
    Article
  13. Article
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  17. Review
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  19. Observational
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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.

Thomas ForstClinical Research Services, Mannheim GmbH, Grenadierstrasse 1, D-68167, Mannheim, Germany. Thomas.Forst@crs-group.de.
Chantal MathieuDepartment of Endocrinology, UZ Gasthuisberg, Katholieke Universiteit, Leuven, Belgium.
Francesco GiorginoDepartment of Emergency and Organ Transplantation Section of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, University of Bari Aldo Moro, Bari, Italy.
David C WheelerDepartment of Renal Medicine, University College London, London, UK.
Nikolaos PapanasDiabetes Centre, Second Department of Internal Medicine, Democritus University of Thrace, Alexandroupolis, Greece.
Roland E SchmiederDepartment of Nephrology and Hypertension, University Hospital Erlangen, Erlangen, Germany.
Atef HalabiClinical Research Services, Kiel, Germany.
Oliver SchnellForschergruppe Diabetes e.V., Munich, Germany.
Marina StreckbeinClinical Research Services, Mannheim GmbH, Grenadierstrasse 1, D-68167, Mannheim, Germany.
Katherine R TuttleDivision of Nephrology, Institute of Translational Health Sciences, University of Washington, Seattle, WA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiabetic kidney disease (DKD), the most common cause of kidney failure and end-stage kidney disease worldwide, will develop in almost half of all people with type 2 diabetes. With the incidence of type 2 diabetes continuing to increase, early detection and management of DKD is of great clinical importance. MAIN BODY: This review provides a comprehensive clinical update for DKD in people with type 2 diabetes, with a special focus on new treatment modalities. The traditional strategies for prevention and treatment of DKD, i.e., glycemic control and blood pressure management, have only modest effects on minimizing glomerular filtration rate decline or progression to end-stage kidney disease. While cardiovascular outcome trials of SGLT-2i show a positive effect of SGLT-2i on several kidney disease-related endpoints, the effect of GLP-1 RA on kidney-disease endpoints other than reduced albuminuria remain to be established. Non-steroidal mineralocorticoid receptor antagonists also evoke cardiovascular and kidney protective effects.

conclusionWith these new agents and the promise of additional agents under clinical development, clinicians will be more able to personalize treatment of DKD in patients with type 2 diabetes.

Indexed as

Diabetes Mellitus, Type 2Diabetic NephropathiesKidney Failure, ChronicGlucagon-Like Peptide 1HumansMineralocorticoid Receptor AntagonistsGlucagon-Like Peptide 1Mineralocorticoid Receptor AntagonistsDiabetic kidney diseaseKidney protective agentsType 2 diabetes

Identifiers

PMID36210442
PMCPMC9548386

What OpenQuestion holds

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LicenceCC BY
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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.