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Comparative Proteomic Analysis of Whole Kidney, Medulla, and Cortical Tubules in Diabetic Pathogenesis of Kidney Injury in Mice
Published on: May 2, 2025
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Epidemiological and transcriptome data identify potential key genes involved in inflammatory response for diabetic
Shan He1, Yiwei Chen2, Jian Ye1
1Department of Nephrology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China.
Scientific Reports
|December 6, 2025
Summary
The neutrophil percentage-to-albumin ratio (NPAR) is a significant indicator for diabetic nephropathy (DN) risk. Novel insights into DN
Area of Science:
- Nephrology
- Immunology
- Genetics
Background:
- Diabetic nephropathy (DN) is a significant complication of diabetes, linked to inflammatory processes.
- The neutrophil percentage-to-albumin ratio (NPAR) is an emerging inflammatory marker.
Purpose of the Study:
- To investigate the association between NPAR and DN risk.
- To explore the underlying molecular mechanisms and potential therapeutic targets in DN development.
Main Methods:
- Analysis of National Health and Nutrition Examination Survey (NHANES) data (2009-2018) for epidemiological association.
- Bioinformatic analysis of Gene Expression Omnibus (GEO) transcriptomic data to identify hub genes and pathways.
- Multivariate linear regression and subgroup analyses to assess NPAR's association with DN.
Main Results:
- A significant positive association was found between NPAR and the risk of DN (OR 1.62-2.06).
- This association was consistent across various demographic and clinical subgroups.
- Bioinformatics identified 49 hub genes, including DUSP1, CXCR1, and SKIL, with the p38MAPK pathway playing a central role in DN.
- Resveratrol, curcumin, and genistein showed strong interactions with key genes (DUSP1, CXCR1, SKIL), suggesting therapeutic potential.
Conclusions:
- NPAR is a reliable diagnostic indicator for DN.
- Inflammatory response significantly influences DN development and progression.
- Resveratrol, curcumin, and genistein hold promise as potential therapeutic agents for DN.
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