Evidence map›Paper›PMID 32823491›Full record

ReviewJournal of clinical medicine2020

Virus-Induced Asthma Exacerbations: SIRT1 Targeted Approach.

Yosuke Fukuda, Kaho Akimoto, Tetsuya Homma, Jonathan R Baker, Kazuhiro Ito, Peter J Barnes, Hironori Sagara

Open access · goldAbstract readReview
In one paragraph

Review in Journal of clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Senotherapy for chronic lung disease.Pharmacological reviews · 2025
    Review
  5. Article
  6. Review
  7. The sirtuin family in health and disease.Signal transduction and targeted therapy · 2022
    Review
  8. Roles of sirtuins in asthma.Respiratory research · 2022
    Review
  9. Review
  10. Review
  11. Article
  12. 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

7 authors at 2 institutions in 2 countries.

Yosuke FukudaDepartment of Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Shinagawa-ku, Tokyo 142-8555, Japan.ORCID 0000-0002-7087-1595
Kaho AkimotoDepartment of Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Shinagawa-ku, Tokyo 142-8555, Japan.
Tetsuya HommaDepartment of Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Shinagawa-ku, Tokyo 142-8555, Japan.
Jonathan R BakerAirway Disease, National Heart and Lung Institute, Imperial College, London SW3 6LY, UK.
Kazuhiro ItoAirway Disease, National Heart and Lung Institute, Imperial College, London SW3 6LY, UK.
Peter J BarnesAirway Disease, National Heart and Lung Institute, Imperial College, London SW3 6LY, UK.ORCID 0000-0002-5122-4018
Hironori SagaraDepartment of Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Shinagawa-ku, Tokyo 142-8555, Japan.
Showa University · JPImperial College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prevalence of asthma has increased worldwide. Asthma exacerbations triggered by upper respiratory tract viral infections remain a major clinical problem and account for hospital admissions and time lost from work. Virus-induced asthma exacerbations cause airway inflammation, resulting in worsening asthma and deterioration in the patients' quality of life, which may require systemic corticosteroid therapy. Despite recent advances in understanding the cellular and molecular mechanisms underlying asthma exacerbations, current therapeutic modalities are inadequate for complete prevention and treatment of these episodes. The pathological role of cellular senescence, especially that involving the silent information regulator 2 homolog sirtuin (SIRT) protein family, has recently been demonstrated in stable and exacerbated chronic respiratory disease states. This review discusses the role of SIRT1 in the pathogenesis of bronchial asthma. It also discusses the role of SIRT1 in inflammatory cells that play an important role in virus-induced asthma exacerbations. Recent studies have hypothesized that SIRT1 is one of major contributors to cellular senescence. SIRT1 levels decrease in Th2 and non-Th2-related airway inflammation, indicating the role of SIRT1 in several endotypes and phenotypes of asthma. Moreover, several models have demonstrated relationships between viral infection and SIRT1. Therefore, targeting SIRT1 is a novel strategy that may be effective for treating virus-induced asthma exacerbations in the future.

Indexed as

asthmacellular senescenceexacerbationsSIRT1virus infection

Identifiers

PMID32823491
PMCPMC7464235
OpenAlexW3048677986

What OpenQuestion holds

Textmetadata
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.