Evidence mapPaperPMID 40227261Full record

ArticleAntioxidants (Basel, Switzerland)2025

The Impact of SGLT-2 Inhibitors on Hydroxyl Radical Markers and Diabetic Neuropathy: A Short-Term Clinical Study.

Ágnes Klabuzai, Viktória Bekő, Zsófia Sütő, Marcell Horváth, Zoltán Wágner, Katalin Vágási, Veronika Pfeil, Miklós Süle, György Grosz, István Wittmann and 1 more

Abstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
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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

11 authors.

Ágnes Klabuzai2nd Department of Medicine and Nephrology-Diabetes Centre, University of Pécs Medical School, H-7624 Pécs, Hungary.
Viktória Bekő2nd Department of Medicine and Nephrology-Diabetes Centre, University of Pécs Medical School, H-7624 Pécs, Hungary.
Zsófia Sütő2nd Department of Medicine and Nephrology-Diabetes Centre, University of Pécs Medical School, H-7624 Pécs, Hungary.
Marcell Horváth2nd Department of Medicine and Nephrology-Diabetes Centre, University of Pécs Medical School, H-7624 Pécs, Hungary.
Zoltán WágnerUnified Healthcare Institutions of the City of Pécs, H-7633 Pécs, Hungary.
Katalin VágásiUnified Healthcare Institutions of the City of Pécs, H-7633 Pécs, Hungary.
Veronika PfeilUnified Healthcare Institutions of the City of Pécs, H-7633 Pécs, Hungary.
Miklós SüleMSB-MET Ltd., H-8230 Balatonfüred, Hungary.
György GroszMSB-MET Ltd., H-8230 Balatonfüred, Hungary.
István Wittmann2nd Department of Medicine and Nephrology-Diabetes Centre, University of Pécs Medical School, H-7624 Pécs, Hungary.ORCID 0000-0001-5163-5733
Szilárd Kun2nd Department of Medicine and Nephrology-Diabetes Centre, University of Pécs Medical School, H-7624 Pécs, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Beyond their metabolic effect, sodium-glucose cotransporter-2 (SGLT-2) inhibitors reduce the risk of heart failure and have cardiovascular and nephroprotective effects, yet their exact mechanism of action remains unclear. This prospective study included 40 patients with type 2 diabetes whose physician initiated SGLT-2 inhibitor therapy. Prior to and 4 weeks after the initiation of SGLT-2 inhibitors, in addition to routine clinical and laboratory measurements, hydroxyl free radical and neuropathic evaluations were performed. Body weight, body mass index (BMI), fasting glucose, fructosamine, and albuminuria decreased significantly, whereas red blood cell (RBC) count, hemoglobin, hematocrit, mean corpuscular volume (MCV), and platelet count increased significantly. Urinary o-tyrosine/p-tyrosine and (m-tyrosine+o-tyrosine)/p-tyrosine ratios were significantly reduced, suggesting diminished hydroxyl free radical production. Patients with neuropathy, identified by abnormal baseline current perception threshold (CPT) values, showed significant improvements. Significant correlations between RBCs, platelet parameters, albuminuria, and hydroxyl free radical markers disappeared after SGLT-2 treatment and changes in hydroxyl free radical markers correlated positively with CPT changes. Our results suggest that short-term SGLT-2 inhibition recalibrates metabolic, hematologic, renal, and neuropathic endpoints simultaneously, presumably through attenuating abnormal ortho- and meta-tyrosine incorporation into signaling proteins. Further studies are required to confirm long-term durability and examine whether additional strategies, such as supplementation of the physiological p-tyrosine, could amplify these benefits.

Indexed as

diabetic kidney diseasediabetic neuropathyhydroxyl free radicalmeta-tyrosineortho-tyrosineplateletred blood cellSGLT-2 inhibitor

Identifiers

PMID40227261
PMCPMC11939660

What Socratic holds

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Registered trials

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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.