Evidence map›Paper›PMID 41169443›Full record

ArticleDiabetes, metabolic syndrome and obesity : targets and therapy2025

Aqueous Humor Metabolomics in Different Stages of Diabetic Retinopathy Based on Ultra - Performance Liquid Chromatography - Tandem Mass Spectrometry.

Zetong Nie, Shaofang Pang, Zhaoxiong Wang, Meng Yang, Xiang Zhang, Haoxin Guo, Wenbo Li, Boshi Liu, Weihong Yu, Bojie Hu

Abstract read
In one paragraph

Article in Diabetes, metabolic syndrome and obesity : targets and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Zetong Nie *Tianjin Key Laboratory of Retinal Functions and Diseases, Tianjin Branch of National Clinical Research Center for Ocular Disease, Eye Institute and School of Optometry, Tianjin Medical University Eye Hospital, Tianjin, People' s Republic of China.
Shaofang Pang *Tianjin Key Laboratory of Retinal Functions and Diseases, Tianjin Branch of National Clinical Research Center for Ocular Disease, Eye Institute and School of Optometry, Tianjin Medical University Eye Hospital, Tianjin, People' s Republic of China.
Zhaoxiong Wang *Department of Ophthalmology, Tianjin Baodi Hospital, Tianjin, People' s Republic of China.
Meng YangTianjin Key Laboratory of Retinal Functions and Diseases, Tianjin Branch of National Clinical Research Center for Ocular Disease, Eye Institute and School of Optometry, Tianjin Medical University Eye Hospital, Tianjin, People' s Republic of China.
Xiang ZhangTianjin Key Laboratory of Retinal Functions and Diseases, Tianjin Branch of National Clinical Research Center for Ocular Disease, Eye Institute and School of Optometry, Tianjin Medical University Eye Hospital, Tianjin, People' s Republic of China.
Haoxin GuoTianjin Key Laboratory of Retinal Functions and Diseases, Tianjin Branch of National Clinical Research Center for Ocular Disease, Eye Institute and School of Optometry, Tianjin Medical University Eye Hospital, Tianjin, People' s Republic of China.
Wenbo LiTianjin Key Laboratory of Retinal Functions and Diseases, Tianjin Branch of National Clinical Research Center for Ocular Disease, Eye Institute and School of Optometry, Tianjin Medical University Eye Hospital, Tianjin, People' s Republic of China.
Boshi LiuTianjin Key Laboratory of Retinal Functions and Diseases, Tianjin Branch of National Clinical Research Center for Ocular Disease, Eye Institute and School of Optometry, Tianjin Medical University Eye Hospital, Tianjin, People' s Republic of China.
Weihong YuDepartment of Ophthalmology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences Key Laboratory of Ocular Fundus Diseases, Chinese Academy of Medical Sciences, Beijing, People' s Republic of China.
Bojie HuTianjin Key Laboratory of Retinal Functions and Diseases, Tianjin Branch of National Clinical Research Center for Ocular Disease, Eye Institute and School of Optometry, Tianjin Medical University Eye Hospital, Tianjin, People' s Republic of China.ORCID 0000-0001-7840-8290

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To search for differential metabolites in patients with proliferative diabetic retinopathy (PDR), patients with nonproliferative diabetic retinopathy (NPDR), and control subjects, and to study their potential biomarkers in depth. Patients and Methods: An untargeted metabolomic approach based on ultra-performance liquid chromatography-tandem mass spectrometry was used to study aqueous humor from 63 patients with PDR, 37 patients with NPDR, and 30 non-diabetic controls. Differential metabolites in different periods of diabetic retinopathy (DR) were identified using orthogonal projections to latent structure discriminant analysis and fold-change. Further logistic regression and receiver operating characteristic curve analysis were performed to select and validate potential biomarkers. Results: Compared to the control group, the PDR group had 80 differential metabolites, among which 3-methylhistamine, N-acetyl-L-histidine, and cytosine were identified as potential biomarkers, whereas the NPDR group had 94 differential metabolites, among which and N-acetyl-L-histidine and hypoxanthine were identified as potential biomarkers. Relative to the PDR and NPDR groups, 5-hydroxyindole-3-acetic acid and L-3-hydroxykynurenine may be potential biomarkers suggesting DR developmental stage or progression. Conclusion: The metabolite profiles identified in this study provide insights into the mechanisms of DR onset and progression in future studies and may eventually inform the development of metabolic biomarkers for prognosis and new therapeutic strategies for DR management.

Indexed as

biomarkersdiabetic retinopathymetabolomicsultra-performance liquid chromatography-tandem mass spectrometry

Identifiers

PMID41169443
PMCPMC12570973

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