Evidence map›Paper›PMID 24416365›Full record

ArticlePloS one2014

Cys34-cysteinylated human serum albumin is a sensitive plasma marker in oxidative stress-related chronic diseases.

Kohei Nagumo, Motohiko Tanaka, Victor Tuan Giam Chuang, Hiroko Setoyama, Hiroshi Watanabe, Naoyuki Yamada, Kazuyuki Kubota, Motoko Tanaka, Kazutaka Matsushita, Akira Yoshida and 7 more

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 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
11.5field-weighted citation impact, top 1% 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

85 citing papers in PubMed, 195 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Use of Human Serum Albumin CysAntioxidants (Basel, Switzerland) · 2026
    Review
  6. Chronic Night Shift Is More Detrimental Than Chronic Light at Night on Circadian Rhythmicity and Metabolic Health in a Female Diurnal Rodent.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  7. Article
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  10. Article
  11. Article
  12. Article
  13. Article
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  15. Modulation of Albumin Esterase Activity by Warfarin and Diazepam.International journal of molecular sciences · 2024
    Article
  16. Efficacy of albumin use in decompensated cirrhosis and real-world adoption in Australia.JGH open : an open access journal of gastroenterology and hepatology · 2024
    Review
  17. Article
  18. Article
  19. Article
  20. Article

25 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

17 authors at 6 institutions in 2 countries.

Kohei NagumoDepartment of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, Kumamoto University, Chuo-ku, Kumamoto, Japan.
Motohiko TanakaDepartment of Gastroenterology and Hepatology, Graduate School of Medical Sciences, Kumamoto University, Chuo-ku, Kumamoto, Japan.
Victor Tuan Giam ChuangSchool of Pharmacy, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Perth, Western Australia, Australia.
Hiroko SetoyamaDepartment of Gastroenterology and Hepatology, Graduate School of Medical Sciences, Kumamoto University, Chuo-ku, Kumamoto, Japan.
Hiroshi WatanabeDepartment of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, Kumamoto University, Chuo-ku, Kumamoto, Japan ; Center for Clinical Pharmaceutical Science, Kumamoto University, Chuo-ku, Kumamoto, Japan.
Naoyuki YamadaInstitute of Innovation, Ajinomoto Co., Inc., Kawasaki-ku, Kawasaki, Japan.
Kazuyuki KubotaInstitute of Innovation, Ajinomoto Co., Inc., Kawasaki-ku, Kawasaki, Japan.
Motoko TanakaDepartment of Nephrology, Akebono Clinic, Minami-Ku, Kumamoto, Japan.
Kazutaka MatsushitaDepartment of Nephrology, Akebono Clinic, Minami-Ku, Kumamoto, Japan.
Akira YoshidaJinnouchi Clinic, Diabetes Care Center, Chuo-ku, Kumamoto, Japan.
Hideaki JinnouchiJinnouchi Clinic, Diabetes Care Center, Chuo-ku, Kumamoto, Japan.
Makoto AnrakuFaculty of Pharmaceutical Sciences, Sojo University, Nishi-ku, Kumamoto, Japan.
Daisuke KadowakiDepartment of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, Kumamoto University, Chuo-ku, Kumamoto, Japan ; Center for Clinical Pharmaceutical Science, Kumamoto University, Chuo-ku, Kumamoto, Japan.
Yu IshimaDepartment of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, Kumamoto University, Chuo-ku, Kumamoto, Japan ; Center for Clinical Pharmaceutical Science, Kumamoto University, Chuo-ku, Kumamoto, Japan.
Yutaka SasakiDepartment of Gastroenterology and Hepatology, Graduate School of Medical Sciences, Kumamoto University, Chuo-ku, Kumamoto, Japan.
Masaki OtagiriFaculty of Pharmaceutical Sciences, Sojo University, Nishi-ku, Kumamoto, Japan ; DDS Research Institute, Sojo University, Nishi-ku, Kumamoto, Japan.
Toru MaruyamaDepartment of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, Kumamoto University, Chuo-ku, Kumamoto, Japan ; Center for Clinical Pharmaceutical Science, Kumamoto University, Chuo-ku, Kumamoto, Japan.
Kumamoto University · JPAjinomoto (Japan) · JPSojo University · JPAkebono Clinic · JPAkebono (Japan) · JPCurtin University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The degree of oxidized cysteine (Cys) 34 in human serum albumin (HSA), as determined by high performance liquid chromatography (HPLC), is correlated with oxidative stress related pathological conditions. In order to further characterize the oxidation of Cys34-HSA at the molecular level and to develop a suitable analytical method for a rapid and sensitive clinical laboratory analysis, the use of electrospray ionization time-of-flight mass spectrometer (ESI-TOFMS) was evaluated. A marked increase in the cysteinylation of Cys34 occurs in chronic liver and kidney diseases and diabetes mellitus. A significant positive correlation was observed between the Cys-Cys34-HSA fraction of plasma samples obtained from 229 patients, as determined by ESI-TOFMS, and the degree of oxidized Cys34-HSA determined by HPLC. The Cys-Cys34-HSA fraction was significantly increased with the progression of liver cirrhosis, and was reduced by branched chain amino acids (BCAA) treatment. The changes in the Cys-Cys34-HSA fraction were significantly correlated with the alternations of the plasma levels of advanced oxidized protein products, an oxidative stress marker for proteins. The binding ability of endogenous substances (bilirubin and tryptophan) and drugs (warfarin and diazepam) to HSA purified from chronic liver disease patients were significantly suppressed but significantly improved by BCAA supplementation. Interestingly, the changes in this physiological function of HSA in chronic liver disease were correlated with the Cys-Cys34-HSA fraction. In conclusion, ESI-TOFMS is a suitable high throughput method for the rapid and sensitive quantification of Cys-Cys34-HSA in a large number of samples for evaluating oxidative stress related chronic disease progression or in response to a treatment.

Indexed as

AgedAmino Acids, Branched-ChainBilirubinBiomarkersChronic DiseaseCysteineDiabetes MellitusDiazepamFemaleGlycation End Products, AdvancedHumansLiver CirrhosisMaleMiddle AgedModels, MolecularOxidation-ReductionAmino Acids, Branched-ChainBilirubinBiomarkersCysteineDiazepamGlycation End Products, AdvancedSerum AlbuminTryptophanWarfarin

Identifiers

PMID24416365
PMCPMC3885702
OpenAlexW2031985670

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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.