Evidence map›Paper›PMID 30116501›Full record

ArticleOxidative medicine and cellular longevity2018

Relationship between Xanthine Oxidoreductase Redox and Oxidative Stress among Chronic Kidney Disease Patients.

Hiroyuki Terawaki, Tomoya Hayashi, Takayo Murase, Ryutaro Iijima, Kaito Waki, Yoshihiro Tani, Takashi Nakamura, Kazunobu Yoshimura, Shunya Uchida, Junichiro James Kazama

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Trial
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  11. Impact of renal tubularFrontiers in molecular biosciences · 2023
    Article
  12. Blood Thiol Redox State in Chronic Kidney Disease.International journal of molecular sciences · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
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

10 authors at 4 institutions in 1 country.

Hiroyuki TerawakiDepartment of Internal Medicine, Nephrology, Teikyo University Chiba Medical Center, Chiba, Japan.ORCID 0000-0001-9165-551X
Tomoya HayashiDepartment of Physiology, Meiji University of Integrative Medicine, Kyoto, Japan.
Takayo MuraseRadioisotope and Chemical Analysis Center, Sanwa Kagaku Kenkyusho Co., Ltd., Mie, Japan.
Ryutaro IijimaDepartment of Internal Medicine, Nephrology, Teikyo University Chiba Medical Center, Chiba, Japan.
Kaito WakiDepartment of Internal Medicine, Nephrology, Teikyo University Chiba Medical Center, Chiba, Japan.
Yoshihiro TaniDepartment of Nephrology and Hypertension, Fukushima Medical University, Fukushima, Japan.
Takashi NakamuraPharmacological Study Group, Pharmaceutical Research Laboratories, Sanwa Kagaku Kenkyusho Co., Ltd., Mie, Japan.
Kazunobu YoshimuraDepartment of Internal Medicine, Nephrology, Teikyo University Chiba Medical Center, Chiba, Japan.
Shunya UchidaDepartment of Internal Medicine, Nephrology, Teikyo University School of Medicine, Tokyo, Japan.
Junichiro James KazamaDepartment of Nephrology and Hypertension, Fukushima Medical University, Fukushima, Japan.
Fukushima Medical University · JPTeikyo University Chiba Medical Center · JPMeiji University of Integrative Medicine · JPTeikyo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Xanthine oxidase (XO), an isoform of xanthine oxidoreductase (XOR), is thought to increase the cardiovascular burden among chronic kidney disease (CKD) patients via oxidative radical production. Plasma XOR redox, which is characterized by the ratio of XO to total XOR, changes under different oxidative conditions associated with kidney dysfunction. However, the relationship between plasma XOR redox and oxidative stress (OS) is unclear. Thus, we aimed to clarify whether OS is related to XOR redox. We used the redox state of human serum albumin (HSA) as a marker to investigate the status of OS in CKD patients. HSA is composed of human mercaptoalbumin (HMA), which possesses not oxidized cysteine residues, reversibly oxidized human nonmercaptoalbumin-1 (HNA-1), and strongly oxidized human nonmercaptoalbumin-2 (HNA-2). The subjects included 13 nondialysis patients (7 males and 6 females) with varying degrees of kidney function. We found that ƒ(HMA) was negatively (

Indexed as

FemaleHumansMaleMiddle AgedOxidative StressRenal Insufficiency, ChronicXanthine DehydrogenaseXanthine Dehydrogenase

Identifiers

PMID30116501
PMCPMC6079329
OpenAlexW2813907730

What OpenQuestion holds

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LicenceCC BY
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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.