Evidence map›Paper›PMID 15466390›Full record

ArticleThe American journal of pathology2004

Urinary excretion of fatty acid-binding protein reflects stress overload on the proximal tubules.

Atsuko Kamijo, Takeshi Sugaya, Akihisa Hikawa, Mitsuhiro Okada, Fumikazu Okumura, Masaya Yamanouchi, Akiko Honda, Masaru Okabe, Tomoya Fujino, Yasunobu Hirata and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed, 2 pooled it
3.0field-weighted citation impact, top 10% of its field
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

90 citing papers in PubMed, 2 syntheses or guidelines pooled it, 229 citations in OpenAlex.

  1. Pooled it
  2. Performance of urinary liver-type fatty acid-binding protein in acute kidney injury: a meta-analysis.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2013
    Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Trial
  7. Observational
  8. Article
  9. Article
  10. Article
  11. Statistical consideration in nephrology research.Kidney research and clinical practice · 2025
    Article
  12. Urinary L-FABP: A Novel Biomarker for Evaluating Diabetic Nephropathy Onset and Progression. A Narrative Review.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

30 more citing papers are in PubMed but not listed here.

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

15 authors at 6 institutions in 2 countries.

Atsuko KamijoSt. Marianna University School of Medicine, 2-16-1 Sugao, Miyamae-Ku, Kawasaki 216-8511, Japan.
Takeshi Sugaya
Akihisa Hikawa
Mitsuhiro Okada
Fumikazu Okumura
Masaya Yamanouchi
Akiko Honda
Masaru Okabe
Tomoya Fujino
Yasunobu Hirata
Masao Omata
Ritsuko Kaneko
Hiroshi Fujii
Akiyoshi Fukamizu
Kenjiro Kimura
St. Marianna University School of Medicine · JPTokyo Medical University · JPAlliance University · INNiigata University · JPOsaka University · JPUniversity of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Urinary excretion of human liver-type fatty acid-binding protein (hL-FABP), which is expressed in human proximal tubules and engaged in free fatty acid (FFA) metabolism, was reported to reflect the clinical prognosis of chronic kidney disease. Here we have investigated the pathophysiological significance of hL-FABP in a model of protein overload nephropathy. Because L-FABP is not expressed in the wild-type mice, we generated hL-FABP chromosomal gene transgenic (Tg) mice. Tg mice were intraperitoneally injected with bovine serum albumin (BSA) replete with FFAs (r-BSA group) or FFA-depleted BSA (d-BSA group). The r-BSA group developed significantly more severe tubulointerstitial damage than did the d-BSA group. Renal expression of the hL-FABP gene was more up-regulated, and urinary excretion of hL-FABP was significantly higher, in the r-BSA group than in the d-BSA group. Furthermore, compared with their wild-type littermates injected with r-BSA, the number of infiltrated macrophages was significantly attenuated in Tg mice injected with it on day 28. In patients with kidney disease (n = 50), urinary hL-FABP was correlated with both urinary protein and the severity of tubulointerstitial injury. In conclusion, our experimental model suggests that urinary excretion of hL-FABP reflects stresses, such as urinary protein overload, on the proximal tubules. The clinical observations support this hypothesis.

Indexed as

AnimalsBlotting, NorthernBlotting, WesternCarrier ProteinsDisease Models, AnimalEnzyme-Linked Immunosorbent AssayFatty Acid-Binding ProteinsFemaleGene Expression RegulationHumansImmunohistochemistryKidney DiseasesKidney Tubules, ProximalMaleMiceMice, TransgenicCarrier ProteinsFABP1 protein, humanFabp1 protein, mouseFatty Acid-Binding ProteinsSerum Albumin, Bovine

Identifiers

PMID15466390
PMCPMC1618632
OpenAlexW2055385795

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.