Evidence map›Paper›PMID 42121049›Full record

ArticleBMC nephrology2026

Serum pentosidine levels are associated with reduced eGFR, including in individuals with preserved renal function: a cross-sectional analysis from the Fukuoka Epidemiological Study of Atherosclerosis.

Kenji Ito, Koji Takahashi, Kazuhiro Tada, Toshiki Maeda, Yukiko Shinohara, Yori Inoue, Atsushi Satoh, Makiko Abe, Tetsuhiko Yasuno, Hisatomi Arima and 1 more

Abstract read
In one paragraph

Article in BMC 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.

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

11 authors.

Kenji ItoDivision of Nephrology and Rheumatology, Department of Internal Medicine, Faculty of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180, Japan. kito@fukuoka-u.ac.jp.
Koji TakahashiDivision of Nephrology and Rheumatology, Department of Internal Medicine, Faculty of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180, Japan.
Kazuhiro TadaDivision of Nephrology and Rheumatology, Department of Internal Medicine, Faculty of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180, Japan.
Toshiki MaedaDepartment of Preventive Medicine and Public Health, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Yukiko ShinoharaDepartment of Preventive Medicine and Public Health, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Yori InoueDivision of Nephrology and Rheumatology, Department of Internal Medicine, Faculty of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180, Japan.
Atsushi SatohLaboratory of Epidemiology and Prevention, Kobe Pharmaceutical University, Kobe, Japan.
Makiko AbeDepartment of Preventive Medicine and Public Health, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Tetsuhiko YasunoDivision of Nephrology and Rheumatology, Department of Internal Medicine, Faculty of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180, Japan.
Hisatomi ArimaDepartment of Preventive Medicine and Public Health, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Kosuke MasutaniDivision of Nephrology and Rheumatology, Department of Internal Medicine, Faculty of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180, Japan.

Funding

Japan Society for the Promotion of Science 20K10487
6 · The paper itself

Abstract

backgroundAdvanced glycation end products, particularly pentosidine, are implicated in age-related diseases and are influenced by renal function and glycemic status. Although elevated pentosidine levels are well documented in individuals with chronic kidney disease (CKD) stage G3b or higher, their association with early reductions in estimated glomerular filtration rate (eGFR), including in individuals with preserved renal function, remains incompletely understood.

methodsWe conducted a cross-sectional analysis of 813 Japanese adults from the Fukuoka Epidemiological Study of Atherosclerosis who underwent routine health checkups. Serum pentosidine and Nε-(carboxymethyl)lysine (CML) levels were measured and analyzed in relation to eGFR categories and glycemic markers.

resultsSerum pentosidine levels were significantly associated with early reductions in eGFR, even among individuals with values including individuals with preserved renal function (P for trend < 0.01), whereas serum CML levels remained largely unchanged. In multivariable logistic regression analysis, lower eGFR category was significantly associated with elevated serum pentosidine levels (odds ratio, 1.94; 95% confidence interval, 1.40-2.70) after adjustment for covariates. In contrast, no significant association was observed between HbA1c-defined glycemic status and serum pentosidine levels. Triglycerides, high-sensitivity C-reactive protein (hs-CRP), and obesity (body mass index ≥ 25 kg/m²) were inversely associated with serum pentosidine levels.

conclusionsLower eGFR, including in individuals with preserved renal function, was associated with higher serum pentosidine levels in this general population. These findings suggest that subtle reductions in renal function, even in individuals with preserved renal function, are associated with higher serum pentosidine levels, which may reflect a combination of cumulative oxidative stress and altered renal handling.

Indexed as

ArginineAtherosclerosisGlomerular Filtration RateLysineAgedBiomarkersCross-Sectional StudiesFemaleGlycation End Products, AdvancedHumansJapanMaleMiddle AgedArginineBiomarkersGlycation End Products, AdvancedLysineN(6)-carboxymethyllysinepentosidineAdvanced glycation end productsChronic kidney diseasePentosidine

Identifiers

PMID42121049
PMCPMC13343869

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.