Evidence map›Paper›PMID 41301440›Full record

ReviewBiomolecules2025

The Emerging Role of Sialic Acids in Obesity and Diabetes: Molecular Mechanisms and Therapeutic Perspectives.

Xinyi Peng, Haojun Li, Qingwen Wang, Peng George Wang, Yang Ji

Abstract readReview
In one paragraph

Review in Biomolecules, 2025. 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

5 authors.

Xinyi PengDepartment of Pharmacology, School of Medicine, Southern University of Science and Technology, Shenzhen 518055, China.
Haojun LiDepartment of Pharmacology, School of Medicine, Southern University of Science and Technology, Shenzhen 518055, China.
Qingwen WangDepartment of Rheumatism and Immunology, Peking University Shenzhen Hospital, Shenzhen 518036, China.
Peng George WangDepartment of Pharmacology, School of Medicine, Southern University of Science and Technology, Shenzhen 518055, China.ORCID 0000-0003-3335-6794
Yang JiDepartment of Pharmacology, School of Medicine, Southern University of Science and Technology, Shenzhen 518055, China.ORCID 0000-0002-7409-7824

Funding

Key-Area Research and Development Program of Guangdong Province 2022B1111050001National Natural Science Foundation of China 32200770National Natural Science Foundation of China 82273841Science, Technology and Innovation Commission of Shenzhen Municipality KQTD20200909113758004Shenzhen Key Laboratory of Inflammatory and Immunology Diseases ZDSYS20200811143756018Shenzhen Natural Science Foundation JCYJ20230807095115030Shenzhen Natural Science Foundation JCYJ20240813100420027
6 · The paper itself

Abstract

Sialic acids are terminal monosaccharides that cap glycans on glycoconjugates. Accumulating clinical and experimental evidence shows that obesity, insulin resistance, and diabetes are accompanied by changes in sialic-acid levels. In these conditions, the sialic-acid axis is also broadly remodeled: writers (sialyltransferases), erasers (neuraminidases), and readers (Siglecs) are dysregulated across adipose tissue, liver, pancreas, endothelium, and blood, shifting insulin signaling and inflammatory tone. This review summarizes relevant studies from the perspectives of disease clinical indicators, molecular mechanisms, and interventions targeting sialic acid. Taken together, these results confirm that sialic acids and related molecules play important roles in multiple metabolic diseases; however, controversies remain due to differences in glycan structure, isoforms, and tissue specificity, particularly regarding the precise roles of neuraminidases. Future studies should build on advanced, standardized glycomic and glycoproteomic measures to define molecule- and tissue-specific roles of sialic acids in metabolic disease, enabling reliable biomarkers and guiding targeted therapy.

Indexed as

Diabetes MellitusObesitySialic AcidsAnimalsHumansInsulin ResistanceSialyltransferasesSialic AcidsSialyltransferasesdiabetesGM3 gangliosideIgG glycosylationinsulin resistanceneuraminidaseobesitysialic acidssialyltransferaseSiglec

Identifiers

PMID41301440
PMCPMC12650102

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.