Evidence map›Paper›PMID 42884034›Full record

ReviewInternational journal of molecular sciences2026

The Role of Glycolysis in Diabetic Kidney Disease.

Yifan Wang, Xin Jiang, Liwen Cui, Yongke You, Wenjuan Zhu, Chongfei Jiang, Zhouning Liao, Jianbo Guo, Hao Lu, Baoyi Shao and 3 more

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Yifan WangDivision of Nephrology, Department of Medicine, The University of Hong Kong-Shenzhen Hospital, Shenzhen 518053, China.ORCID 0000-0002-7887-9719
Xin JiangSchool of Chinese Medicine, The University of Hong Kong, Hong Kong 999000, China.ORCID 0009-0004-7950-3897
Liwen CuiDivision of Nephrology, Department of Medicine, The University of Hong Kong-Shenzhen Hospital, Shenzhen 518053, China.
Yongke YouDepartment of Nephrology, Shenzhen University General Hospital, Shenzhen University, Shenzhen 518055, China.
Wenjuan ZhuDivision of Nephrology, Department of Medicine, The University of Hong Kong-Shenzhen Hospital, Shenzhen 518053, China.ORCID 0000-0003-0922-4054
Chongfei JiangDivision of Nephrology, Department of Medicine, The University of Hong Kong-Shenzhen Hospital, Shenzhen 518053, China.
Zhouning LiaoDivision of Nephrology, Department of Medicine, The University of Hong Kong-Shenzhen Hospital, Shenzhen 518053, China.
Jianbo GuoSchool of Chinese Medicine, The University of Hong Kong, Hong Kong 999000, China.
Hao LuSchool of Chinese Medicine, The University of Hong Kong, Hong Kong 999000, China.
Baoyi ShaoSchool of Chinese Medicine, The University of Hong Kong, Hong Kong 999000, China.
Xiaozhou LuoState Key Laboratory of Quantitative Synthetic Biology, Center for Synthetic Biochemistry, Shenzhen Institute of Synthetic Biology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.
Pearl PaiDivision of Nephrology, Department of Medicine, The University of Hong Kong-Shenzhen Hospital, Shenzhen 518053, China.ORCID 0000-0002-2493-1606
Haiyong ChenSchool of Chinese Medicine, The University of Hong Kong, Hong Kong 999000, China.ORCID 0000-0002-4889-2752

Funding

HKU Seed Funds 2502251990, and 2402101703Hong Kong Research Grants Council 17125323, 17125524, and 17125925
6 · The paper itself

Abstract

Diabetic kidney disease (DKD) is a leading cause of end-stage kidney disease worldwide and remains associated with high morbidity and mortality. In DKD, glycolytic reprogramming is triggered by hyperglycemia, hypoxia, oxidative stress, and inflammatory activation, which converge to drive metabolic imbalance. These stimuli promote excessive glycolytic flux, lactate accumulation, and diverse post-translational modifications, thereby reinforcing pathological reactions such as epithelial-mesenchymal transition, inflammation, and renal fibrosis. Accumulating evidence indicates that glycolytic alterations in DKD are highly cell type-specific. In podocytes, impaired glycolysis disrupts actin cytoskeletal integrity, promotes foot process fusion/effacement, and compromises the glomerular filtration barrier, ultimately leading to proteinuria. In tubular epithelial cells, glycolysis drives mesenchymal transformation and fibrogenesis, and engages in crosstalk with macrophages. In mesangial cells, glycolysis promotes mesangial cell hypertrophy and contributes to mesangial expansion. Mechanistically, central regulators including HIF-1α and PKM2, are modulated through glycolysis associated mechanisms, linking glycolysis to mitochondrial dysfunction, pathological cellular phenotypes, and DKD progression. Therapeutically, SGLT2 inhibitors have been clinically applied for DKD and kidney protection. Clinical studies further show that they can suppress maladaptive glycolytic activation in human metabolic analysis. Collectively, current evidence highlights glycolysis as a key driver of DKD and therapeutic targets for DKD management.

Indexed as

Diabetic NephropathiesGlycolysisAnimalsEpithelial-Mesenchymal TransitionHumansHypoxia-Inducible Factor 1, alpha SubunitMetabolic ReprogrammingPodocytesHypoxia-Inducible Factor 1, alpha Subunitdiabetic kidney diseaseepithelial–mesenchymal transitionglycolysisHIF-1αmetabolic reprogrammingPKM2podocytepost-translational modificationSGLT2

Identifiers

PMID42884034
PMCPMC13664804

What OpenQuestion 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 OpenQuestion graph.