Evidence map›Paper›PMID 35052792›Full record

ArticleBiomedicines2022

Identification of Druggable Genes for Asthma by Integrated Genomic Network Analysis.

Wirawan Adikusuma, Wan-Hsuan Chou, Min-Rou Lin, Jafit Ting, Lalu Muhammad Irham, Dyah Aryani Perwitasari, Wei-Pin Chang, Wei-Chiao Chang

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Asthma-Genomic Advances Toward Risk Prediction.Clinics in chest medicine · 2024
    Review
  5. Integrated genomic network analysis revealed potential of a druggable target for hemorrhoid treatment.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2023
    Article
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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

8 authors at 4 institutions in 2 countries.

Wirawan AdikusumaDepartment of Clinical Pharmacy, School of Pharmacy, Taipei Medical University, Taipei 11031, Taiwan.ORCID 0000-0001-9165-690X
Wan-Hsuan ChouDepartment of Clinical Pharmacy, School of Pharmacy, Taipei Medical University, Taipei 11031, Taiwan.ORCID 0000-0002-7693-5959
Min-Rou LinDepartment of Clinical Pharmacy, School of Pharmacy, Taipei Medical University, Taipei 11031, Taiwan.ORCID 0000-0003-0247-1984
Jafit TingDepartment of Clinical Pharmacy, School of Pharmacy, Taipei Medical University, Taipei 11031, Taiwan.ORCID 0000-0001-7918-8218
Lalu Muhammad IrhamFaculty of Pharmacy, University of Ahmad Dahlan, Yogyakarta 55164, Indonesia.
Dyah Aryani PerwitasariFaculty of Pharmacy, University of Ahmad Dahlan, Yogyakarta 55164, Indonesia.ORCID 0000-0002-2638-6664
Wei-Pin ChangSchool of Health Care Administration, College of Management, Taipei Medical University, Taipei 11031, Taiwan.
Wei-Chiao ChangDepartment of Clinical Pharmacy, School of Pharmacy, Taipei Medical University, Taipei 11031, Taiwan.
Taipei Medical University · TWUniversitas Ahmad Dahlan · IDWan Fang Hospital · TWUniversity of Muhammadiyah Mataram · ID

Funding

Ministry of Science and Technology MOST108-2314-B-038-027National Health Research Institutes 08A1-MGGP08-037Taipei Medical University 106-5807-001-400
6 · The paper itself

Abstract

Asthma is a common and heterogeneous disease characterized by chronic airway inflammation. Currently, the two main types of asthma medicines are inhaled corticosteroids and long-acting β2-adrenoceptor agonists (LABAs). In addition, biological drugs provide another therapeutic option, especially for patients with severe asthma. However, these drugs were less effective in preventing severe asthma exacerbation, and other drug options are still limited. Herein, we extracted asthma-associated single nucleotide polymorphisms (SNPs) from the genome-wide association studies (GWAS) and phenome-wide association studies (PheWAS) catalog and prioritized candidate genes through five functional annotations. Genes enriched in more than two categories were defined as "biological asthma risk genes." Then, DrugBank was used to match target genes with FDA-approved medications and identify candidate drugs for asthma. We discovered 139 biological asthma risk genes and identified 64 drugs targeting 22 of these genes. Seven of them were approved for asthma, including reslizumab, mepolizumab, theophylline, dyphylline, aminophylline, oxtriphylline, and enprofylline. We also found 17 drugs with clinical or preclinical evidence in treating asthma. In addition, eleven of the 40 candidate drugs were further identified as promising asthma therapy. Noteworthy,

Indexed as

asthmabioinformaticdrug repositioninggenome-wide association studyphenome-wide association study

Identifiers

PMID35052792
PMCPMC8773254
OpenAlexW4205114805

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.