Evidence map›Paper›PMID 26071206›Full record

ArticleInflammation2015

Analysis of ADRB2 (Arg16Gly) Gene Variant with Susceptibility, Pharmacogenetic Response and Disease Severity in South Indian Asthmatics.

Srinivas Bandaru, Jyothy Akka, Vijaya Kumar Marri, Mallika Alvala, Deepika Ponnala, Hema Prasad Mundluru

Abstract read
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In one paragraph

Article in Inflammation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. [Research advances in gene polymorphisms in biological pathways of drugs for asthma].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2016
    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

6 authors at 4 institutions in 1 country.

Srinivas BandaruNational Institute of Pharmaceutical Education and Research, Hyderabad, 500 037, India. srinivasgen08@gmail.com.
Jyothy AkkaInstitute of Genetics and Hospital for Genetic Diseases, Osmania University, Hyderabad, 500 016, India.
Vijaya Kumar MarriGovernment General and Chest Hospital, Gandhi Medical College and Osmania Medical College, Hyderabad, 500 038, India.
Mallika AlvalaNational Institute of Pharmaceutical Education and Research, Hyderabad, 500 037, India.
Deepika PonnalaInstitute of Genetics and Hospital for Genetic Diseases, Osmania University, Hyderabad, 500 016, India.
Hema Prasad MundluruInstitute of Genetics and Hospital for Genetic Diseases, Osmania University, Hyderabad, 500 016, India.
Institute of Genetics and Hospital for Genetic Diseases · INNational Institute of Pharmaceutical Education and Research · INOsmania Medical College · INOsmania University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

β2-Adrenergic receptor (β2-AR) plays a crucial role in asthma pathophysiology by regulating, processes of the lung function, and clinical response to bronchodilators. The +46G>A- Gly16Arg polymorphism in the gene encoding β2 adrenergic receptor (ADRB2) has been associated with receptor non-responsiveness after β2-agonist exposure. In the present study, we sought to evaluate the possible association of Gly16Arg polymorphism with asthma susceptibility, pharmacogenetic response to Salbutamol, and varying degrees of disease severity. Three hundred ninety-eight clinically diagnosed patients and 456 healthy controls were enrolled for the study. Patients were classified into severity classes according to Global Initiative for Asthma guidelines. To assess bronchodilator response, spirometry was performed before and 15 min after Salbutamol (200 μg) delivery. Responders to Salbutamol were categorized if percentage reversibility was greater than or equal to 12% in them, while those showing reversibility less than 12% were classified as non-responders. Genotyping was carried out by ARMS-PCR technique. Statistical methods were applied to test for the significance of the results. In the present study, there was lack of significant association of polymorphism with disease susceptibility as well as with bronchodilator response. The polymorphism was not associated with mild and moderate asthma subtypes; however, there was a notable association with severe asthma subtype. In addition, the polymorphism was associated with severe asthma compared to subtypes of mild and moderate asthma combined. In a South Indian population, the ADRB2 Arg/Gly may not form a susceptible variant to develop asthma nor can be a standard predictive marker to bronchodilator response; nevertheless, the patterns in asthma severity can be predicted by analyzing this variant.

Indexed as

Polymorphism, GeneticAdministration, InhalationAdrenergic beta-2 Receptor AgonistsAdultAlbuterolAsthmaBronchodilator AgentsCase-Control StudiesFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseHumansIndiaMaleMiddle AgedADRB2 protein, humanAdrenergic beta-2 Receptor AgonistsAlbuterolBronchodilator AgentsReceptors, Adrenergic, beta-2Arg16Gly variantasthma severityasthma susceptibilitybronchial asthmaSalbutamol response

Identifiers

PMID26071206
OpenAlexW629005627

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.