Evidence mapPaperPMID 42391213Full record

ArticlePloS one2026

Association of urinary post-translationally modified fetuin-A fragments with diabetic kidney disease risk stratification in Japanese patients with type 2 diabetes.

Toshiko Mori, Hiroyuki Ito, Taiki Kozasa, Chizuko Yukawa, Suzuko Matsumoto, Hideyuki Inoue, Shinichi Antoku

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Article in PloS one, 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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7 authors.

Toshiko MoriDepartment of Diabetes, Metabolism and Kidney Disease, Edogawa Hospital, Tokyo, Japan.ORCID https://orcid.org/0009-0003-2104-3990
Hiroyuki ItoDepartment of Diabetes, Metabolism and Kidney Disease, Edogawa Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-8143-0082
Taiki KozasaClinical Test Management Division, PreMedica Inc., Tokyo, Japan.
Chizuko YukawaLaboratory Department, Edogawa Hospital, Tokyo, Japan.
Suzuko MatsumotoDepartment of Diabetes, Metabolism and Kidney Disease, Edogawa Hospital, Tokyo, Japan.
Hideyuki InoueDepartment of Diabetes, Metabolism and Kidney Disease, Edogawa Hospital, Tokyo, Japan.
Shinichi AntokuDepartment of Diabetes, Metabolism and Kidney Disease, Edogawa Hospital, Tokyo, Japan.

Funding

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6 · The paper itself

Abstract

aimsConventional biomarkers such as estimated glomerular filtration rate (eGFR) and urinary albumin-to-creatinine ratio (uACR) primarily reflect glomerular damage and often fail to detect early tubular injury. Consequently, patients with "non-albuminuric diabetic kidney disease (DKD)" may be overlooked. This study evaluated the independent association between urinary post-translationally modified fetuin-A fragments (uPTM-FetA) and DKD risk stratification in Japanese patients with type 2 diabetes.

methodsWe conducted a cross-sectional study of 219 outpatients with type 2 diabetes between November 2023 and February 2024 at Edogawa Hospital. First-morning urine samples were analyzed for uPTM-FetA and urinary liver-type fatty acid-binding protein (uL-FABP) using enzyme-linked immunosorbent assays. DKD risk was classified into four categories based on the KDIGO guidelines. The association between uPTM-FetA and higher DKD-risk (categories 2 + 3 + 4) was assessed using multiple logistic regression and restricted cubic spline (RCS) analyses, validated by bootstrapping.

resultsThe optimal cutoff value for uPTM-FetA was determined to be 11.76 ng/mgCr. Multivariable analysis adjusted for potential confounders revealed that high uPTM-FetA levels were significantly and independently associated with DKD-risk categories 2 + 3 + 4 (adjusted odds ratio: 3.88; 95% CI: 2.02-7.45; P < 0.01). RCS analysis indicated a significant non-linear association (P = 0.04). Notably, high uPTM-FetA was detected in 38.8% of patients with normoalbuminuria and 42.0% of those with preserved eGFR. A striking discrepancy was observed compared to uL-FABP: while high uL-FABP was completely absent (0.0%) in patients within the low-to-moderate risk categories (categories 1 and 2), high uPTM-FetA was observed in 34.0% and 60.8% of these patients, respectively.

conclusionsuPTM-FetA is independently associated with DKD severity and is elevated in a substantial proportion of patients with early-stage disease where conventional markers remain normal. Unlike uL-FABP, which increases predominantly in advanced stages, uPTM-FetA appears to identify tubular stress earlier. Thus, uPTM-FetA serves as a valuable complementary biomarker to uACR for refining DKD risk stratification.

Indexed as

alpha-2-HS-GlycoproteinDiabetes Mellitus, Type 2Diabetic NephropathiesAgedBiomarkersCross-Sectional StudiesEast Asian PeopleFatty Acid-Binding ProteinsFemaleGlomerular Filtration RateHumansJapanMaleMiddle AgedProtein Processing, Post-TranslationalRisk Assessmentalpha-2-HS-GlycoproteinBiomarkersFatty Acid-Binding Proteins

Identifiers

PMID42391213
PMCPMC13327179

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