Evidence map›Paper›PMID 24465563›Full record

ArticlePloS one2014

1H NMR-based metabolite profiling of plasma in a rat model of chronic kidney disease.

Ju-Ae Kim, Hyo-Jung Choi, Yong-Kook Kwon, Do Hyun Ryu, Tae-Hwan Kwon, Geum-Sook Hwang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.8field-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

20 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Methods and protocols · 2025
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  4. Review
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  16. Article
  17. Frontiers in pharmacology · 2017
    Article
  18. Metabonomic biomarkers for risk factors of chronic kidney disease.International urology and nephrology · 2016
    Review
  19. Article
  20. Metabolomics and renal disease.Current opinion in nephrology and hypertension · 2015 · on this map
    Review
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

6 authors at 3 institutions in 1 country.

Ju-Ae KimIntegrated Metabolomics Research Group, Seoul Center, Korea Basic Science Institute, Seoul, Korea ; Department of Chemistry, Sungkyunkwan University, Suwon, Korea.
Hyo-Jung ChoiDepartment of Biochemistry and Cell Biology, School of Medicine, Kyungpook National University, Taegu, Korea.
Yong-Kook KwonIntegrated Metabolomics Research Group, Seoul Center, Korea Basic Science Institute, Seoul, Korea ; Graduate School of Analytical Science and Technology, Chungnam University, Daejeon, Korea.
Do Hyun RyuDepartment of Chemistry, Sungkyunkwan University, Suwon, Korea.
Tae-Hwan KwonDepartment of Biochemistry and Cell Biology, School of Medicine, Kyungpook National University, Taegu, Korea.
Geum-Sook HwangIntegrated Metabolomics Research Group, Seoul Center, Korea Basic Science Institute, Seoul, Korea ; Graduate School of Analytical Science and Technology, Chungnam University, Daejeon, Korea.
Chungnam National University · KRKyungpook National University · KRSungkyunkwan University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic kidney disease (CKD) is characterized by the gradual loss of the kidney function to excrete wastes and fluids from the blood. (1)H NMR-based metabolomics was exploited to investigate the altered metabolic pattern in rats with CKD induced by surgical reduction of the renal mass (i.e., 5/6 nephrectomy (5/6 Nx)), particularly for identifying specific metabolic biomarkers associated with early of CKD. Plasma metabolite profiling was performed in CKD rats (at 4- or 8-weeks after 5/6 Nx) compared to sham-operated rats. Principle components analysis (PCA), partial least squares-discriminant analysis (PLS-DA) and orthogonal partial least squares-discriminant analysis (OPLS-DA) score plots showed a significant separation between the groups. The resulting metabolic profiles demonstrated significantly increased plasma levels of organic anions, including citrate, β-hydroxybutyrate, lactate, acetate, acetoacetate, and formate in CKD. Moreover, levels of alanine, glutamine, and glutamate were significantly higher. These changes were likely to be associated with complicated metabolic acidosis in CKD for counteracting systemic metabolic acidosis or increased protein catabolism from muscle. In contrast, levels of VLDL/LDL (CH2)n and N-acetylglycoproteins were decreased. Taken together, the observed changes of plasma metabolite profiles in CKD rats provide insights into the disturbed metabolism in early phase of CKD, in particular for the altered metabolism of acid-base and/or amino acids.

Indexed as

AnimalsKidneyMagnetic Resonance SpectroscopyMaleMetabolomeRatsRats, Sprague-DawleyRenal Insufficiency, ChronicTranscriptome

Identifiers

PMID24465563
PMCPMC3896356
OpenAlexW2021581517

What OpenQuestion holds

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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.