Evidence map›Paper›PMID 27776186›Full record

ArticlePloS one2016

Serum Reactive Oxygen Metabolite Levels Predict Severe Exacerbations of Asthma.

Keitaro Nakamoto, Masato Watanabe, Mitsuru Sada, Toshiya Inui, Masuo Nakamura, Kojiro Honda, Hiroo Wada, Yu Mikami, Hirotaka Matsuzaki, Masafumi Horie and 6 more

Erratum issuedAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Changes in FeNO, d-ROMs, and BHJournal of asthma and allergy · 2024
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Keitaro NakamotoDepartment of Respiratory Medicine, Kyorin University School of Medicine, Tokyo, Japan.
Masato WatanabeDepartment of Respiratory Medicine, Kyorin University School of Medicine, Tokyo, Japan.
Mitsuru SadaDepartment of Respiratory Medicine, Kyorin University School of Medicine, Tokyo, Japan.
Toshiya InuiDepartment of Respiratory Medicine, Kyorin University School of Medicine, Tokyo, Japan.
Masuo NakamuraDepartment of Respiratory Medicine, Kyorin University School of Medicine, Tokyo, Japan.
Kojiro HondaDepartment of Respiratory Medicine, Kyorin University School of Medicine, Tokyo, Japan.
Hiroo WadaDepartment of Respiratory Medicine, Kyorin University School of Medicine, Tokyo, Japan.
Yu MikamiDepartment of Respiratory Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Hirotaka MatsuzakiDepartment of Respiratory Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Masafumi HorieDepartment of Respiratory Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Satoshi NoguchiDepartment of Respiratory Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Yasuhiro YamauchiDepartment of Respiratory Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Hikari KoyamaDepartment of Internal medicine, Teikyo University Mizonokuchi Hospital, Kanagawa, Japan.
Toshiyuki KoganeDepartment of Internal medicine, Teikyo University Mizonokuchi Hospital, Kanagawa, Japan.
Tadashi KohyamaDepartment of Internal medicine, Teikyo University Mizonokuchi Hospital, Kanagawa, Japan.
Hajime TakizawaDepartment of Respiratory Medicine, Kyorin University School of Medicine, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeBronchial asthma (BA) is a chronic airway disease characterized by airway hyperresponsiveness and remodeling, which are intimately linked to chronic airway inflammation. Reactive oxygen species (ROS) such as hydrogen peroxide are generated by inflammatory cells that are involved in the pathogenesis of BA. However, the role of ROS in the management of BA patients is not yet clear. We attempted to determine the role of ROS as a biomarker in the clinical setting of BA. SUBJECTS AND

methodsWe enrolled patients with BA from 2013 through 2015 and studied the degrees of asthma control, anti-asthma treatment, pulmonary function test results, fractional exhaled nitric oxide (FeNO), serum reactive oxygen metabolite (ROM) levels, and serum levels of interleukin (IL)-6 and IL-8.

resultsWe recruited 110 patients with BA. Serum ROM levels correlated with white blood cell (WBC) count (rs = 0.273, p = 0.004), neutrophil count (rs = 0.235, p = 0.014), CRP (rs = 0.403, p < 0.001), and IL-6 (rs = 0.339, p < 0.001). Serum ROM levels and IL-8 and CRP levels negatively correlated with %FEV1 (rs = -0.240, p = 0.012, rs = -0.362, p < 0.001, rs = -0.197, p = 0.039, respectively). Serum ROM levels were significantly higher in patients who experienced severe exacerbation within 3 months than in patients who did not (339 [302-381] vs. 376 [352-414] CARR U, p < 0.025). Receiver-operating characteristics analysis showed that ROM levels correlated significantly with the occurrence of severe exacerbation (area under the curve: 0.699, 95% CI: 0.597-0.801, p = 0.025).

conclusionsSerum levels of ROM were significantly associated with the degrees of airway obstruction, WBC counts, neutrophil counts, IL-6, and severe exacerbations. This biomarker may be useful in predicting severe exacerbations of BA.

Indexed as

AdultAnti-Asthmatic AgentsAsthmaBiomarkersBreath TestsFemaleHumansInterleukin-6Interleukin-8Leukocyte CountMaleMiddle AgedReactive Oxygen SpeciesRespiratory Function TestsROC CurveAnti-Asthmatic AgentsBiomarkersCXCL8 protein, humanIL6 protein, humanInterleukin-6Interleukin-8Reactive Oxygen Species

Identifiers

PMID27776186
PMCPMC5077110

What OpenQuestion holds

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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.