Evidence mapPaperPMID 41019174Full record

ReviewFood science & nutrition2025

Multi-Target Modulation of Polyphenols in Diabetic Kidney Disease Therapeutics: A Comprehensive Review.

Esienanwan E Efiong, Emmanuel Effa, Esther Peters, Ochuko L Erukainure, Peter U Amadi, Joshua Onyeka Ikebuiro, Sapna Sharma, Christoph Schmaderer, Kathrin Maedler, Emmy Tuenter and 1 more

Abstract readReview
In one paragraph

Review in Food science & nutrition, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
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

11 authors.

Esienanwan E EfiongResearch Unit of Molecular Epidemiology Institute of Epidemiology, Helmholtz Zentrum München Neuherberg Germany.ORCID https://orcid.org/0000-0003-2863-5772
Emmanuel EffaDivision of Nephrology, Department of Internal Medicine, Faculty of Clinical Sciences University of Calabar Calabar Nigeria.
Esther PetersFaculty of Science, Masaryk University Brno Czech Republic.
Ochuko L ErukainureLaser Research Centre, Faculty of Health Sciences University of Johannesburg Doornfontein South Africa.ORCID https://orcid.org/0000-0003-0489-338X
Peter U AmadiDepartment of Pediatrics, Faculty of Medicine and Dentistry University of Alberta Edmonton AB Canada.
Joshua Onyeka IkebuiroHuman and Animal Physiology Group Wageningen University and Research Wageningen the Netherlands.
Sapna SharmaResearch Unit of Molecular Epidemiology Institute of Epidemiology, Helmholtz Zentrum München Neuherberg Germany.
Christoph SchmadererAbteilung für Nephrologie, Klinikum Rechts der Isar der Technischen Universität München München Germany.
Kathrin MaedlerIslet Biology Laboratory Centre for Biomolecular Interactions, University of Bremen Bremen Germany.
Emmy TuenterDepartment of Pharmaceutical Sciences, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences University of Antwerpen Antwerp Belgium.
Harald GrallertResearch Unit of Molecular Epidemiology Institute of Epidemiology, Helmholtz Zentrum München Neuherberg Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic kidney disease (DKD) is a severe complication of diabetes that presents as progressive kidney dysfunction and is the primary cause of end-stage kidney failure. Despite therapeutic advances, including the use of angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, sodium-glucose co-transporter-2 inhibitors, glucagon-like peptide-1 agonists, and non-steroidal mineralocorticoid receptor antagonists, managing DKD remains challenging. Current therapies mainly focus on glycemic control, hypertension management, and albumin reduction to mitigate kidney damage. Nevertheless, these approaches often fail to halt disease progression or restore renal function. There is therefore an urgent need for therapies with safer profiles that can be used singly to target the disease's underlying pathophysiology or integrated into traditional care. Polyphenols possess biological properties capable of addressing these unmet needs by targeting multiple underlying mechanisms involved in DKD pathogenesis. The literature search occurred between September 2024 and April 2025, with most articles sourced from the last 5 years. This review explores polyphenol classes that have demonstrated nephroprotective effects in vitro, in vivo, and in clinical trials. It also highlights the interconnected multi-pathways and molecular mediators potentially regulated by specific polyphenols for kidney function improvement. This multi-target therapeutic approach is especially beneficial for DKD, where several metabolic dysfunctions underlie its pathogenesis. Identifying polyphenols as a therapeutic option could lead to integrative patient care that embraces the strengths of conventional medicine and phytomedicine for better disease management and outcomes. There is therefore a need for more clinical trials to assess polyphenols' safety and efficacy in managing DKD.

Indexed as

diabetes mellitusdiabetic nephropathyend‐stage kidney diseasekidney replacement therapymicrovascular complicationphytochemistry

Identifiers

PMID41019174
PMCPMC12464446

What Socratic holds

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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 Socratic graph.