Evidence map›Paper›PMID 40721549›Full record

ArticleInternational urology and nephrology2026

Uncovering hidden risks: metabolic and inflammatory insights in normoalbuminuric chronic kidney disease.

Lijuan Zhang, Jiang Bai, Meng Di, Zehui Liu, Letian He, Junnan Guo

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Article in International urology and nephrology, 2026. 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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6 authors.

Lijuan Zhang *Department of Nephrology, Shanxi Provincial People's Hospital (Fifth Hospital) of Shanxi Medical University, Taiyuan, Shanxi, China.
Jiang Bai *Department of Nephrology, Shanxi Provincial People's Hospital (Fifth Hospital) of Shanxi Medical University, Taiyuan, Shanxi, China. bai_jianghean@163.com.
Meng DiSchool of Stomatology, Shanxi Medical University, Taiyuan, Shanxi, China.
Zehui LiuThe First Clinical Medical College, Shanxi Medical University, Taiyuan, Shanxi, China.
Letian HeThe First Clinical Medical College, Shanxi Medical University, Taiyuan, Shanxi, China.
Junnan GuoDepartment of Nephrology, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.

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No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWhile elevated levels of albuminuria beyond 30 mg/g are linked to adverse outcomes, recent studies have revealed an increased risk of chronic kidney disease (CKD) progression and cardiovascular events within the normoalbuminuric range (urinary albumin-to-creatinine ratio, UACR < 30 mg/g). This study aims to examine metabolite levels and inflammatory markers among CKD patients in the normal albuminuria groups.

methodsWe recruited 24 patients diagnosed with CKD exhibiting normoalbuminuria from The Kidney Precision Medicine Project (KPMP). The patients were divided into two groups based on their UACR levels: 0-15 mg/g and 15-30 mg/g. Differential metabolites were identified through Ultrahigh Performance Liquid Chromatography-Tandem Mass Spectrometry (UPLC-MS/MS).

resultsThe results indicated that patients with CKD and a UACR of 15-30 mg/g exhibited significant pathology, including a higher percentage of tubular atrophy and elevated levels of metabolites. These metabolites were classified into Lipids (60.0%), Amino Acids and Peptides (6.6%), Cofactors and Vitamins (6.6%), and Nucleotides (3.3%), associated with porphyrin metabolism, arginine biosynthesis, lysine degradation, and fatty acid metabolism, contrasting with CKD patients having a UACR of 0-15 mg/g. Noteworthy positive correlations were observed between caprate levels and IL-12p70, gamma-glutamylleucine and IL-10, as well as taurolithocholate and IL-10.

conclusionIn patients with CKD and normal albuminuria, there exist metabolic variances compared to those with high levels of albuminuria, and these metabolites are linked to inflammatory status. This offers a foundation for early detection and proactive measures before reaching the normal threshold in CKD.

Indexed as

AlbuminuriaInflammationRenal Insufficiency, ChronicAdultAgedBiomarkersFemaleHumansMaleMiddle AgedBiomarkersAlbuminuriaChronic kidney diseaseInflammationMetabolites

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