Evidence map›Paper›PMID 30381539›Full record

ArticleThe Indian journal of medical research2018

Association of increased risk of asthma with elevated arginase & interleukin-13 levels in serum & rs2781666 G/T genotype of arginase I.

Suhasini Donthi, Venkata Sanjeev Kumar Neela, Sumanlatha Gaddam, Hidayath Hussain Mohammed, Soheb Sadath Ansari, Vijaya Lakshmi Valluri, Krovvidi S R Sivasai

Open access · diamondAbstract read
In one paragraph

Article in The Indian journal of medical research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 32% 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, 6 citations in OpenAlex.

  1. IL-9R/Arg1 pathway promotes polyamine metabolism in human airway macrophages.The Journal of allergy and clinical immunology · 2026
    Article
  2. Effect ofJournal of asthma and allergy · 2025
    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

7 authors at 1 institution in 1 country.

Suhasini DonthiDepartment of Biotechnology, Sreenidhi Institute of Science & Technology; Immunology & Molecular Biology Division, LEPRA Society Blue Peter Public Health & Research Centre, Hyderabad, India.
Venkata Sanjeev Kumar NeelaImmunology & Molecular Biology Division, LEPRA Society Blue Peter Public Health & Research Centre, Hyderabad, India.
Sumanlatha GaddamAllergy & Pulmonology Clinic, Bhagwan Mahavir Hospital & Research Centre, Hyderabad, India.
Hidayath Hussain MohammedDepartment of Pulmonology, Shadan Institute of Medical Sciences, Hyderabad, India.
Soheb Sadath AnsariAllergy & Pulmonology Clinic, Bhagwan Mahavir Hospital & Research Centre, Hyderabad, India.
Vijaya Lakshmi ValluriImmunology & Molecular Biology Division, LEPRA Society Blue Peter Public Health & Research Centre, Hyderabad, India.
Krovvidi S R SivasaiDepartment of Biotechnology, Sreenidhi Institute of Science & Technology, Hyderabad, India.
Shadan Hospital and Institute of Medical Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

objectivesHigh expression of arginase gene and its elevated level in serum and bronchial lavage reported in animal models indicated an association with the pathogenesis of asthma. This study was undertaken to assess the serum arginase activity in symptomatic asthma patients and healthy controls and to correlate it with cytokine levels [interleukin (IL)-4 and IL-13] and arginase I (ARG1) gene polymorphism.

methodsAsthma was confirmed by lung function test according to the GINA guidelines in patients attending Allergy and Pulmonology Clinic, Bhagwan Mahavir Hospital and Research Centre, Hyderabad, India, a tertiary care centre, during 2013-2015. Serum arginase was analyzed using a biochemical assay, total IgE and cytokine levels by enzyme-linked immunosorbent assay and genotyping of ARG1 for single-nucleotide polymorphisms (SNPs) rs2781666 and rs60389358 using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method.

resultsThere was a significant two-fold elevation in the arginase activity in asthmatics as compared to healthy controls which correlated with disease severity. Non-atopic asthmatics showed elevated activity of arginase compared to atopics, indicating its possible role in intrinsic asthma. Levels of serum IL-13 and IL-4 were significantly high in asthma group which correlated with disease severity that was assessed by spirometry. A positive correlation was observed between arginase activity and IL-13 concentration. Genetic analysis of ARG1 SNPs revealed that rs2781666 G/T genotype, T allele and C-T haplotype (rs60389358 and rs2781666) were associated with susceptibility to asthma. INTERPRETATION &

conclusionsThis study indicated that high arginase activity and IL-13 concentration in the serum and ARG1 rs2781666 G/T genotype might increase the risk of asthma in susceptible population. Further studies need to be done with a large sample to confirm these findings.

Indexed as

Genetic Predisposition to DiseaseAdolescentAdultArginaseAsthmaFemaleGenetic Association StudiesGenotypeHaplotypesHumansInterleukin-13MaleMiddle AgedPolymorphism, Single NucleotideRisk FactorsYoung AdultARG1 protein, humanArginaseInterleukin-13Atopiccytokinesgenetic polymorphismhaplotypenon-atopicseverity

Identifiers

PMID30381539
PMCPMC6206777
OpenAlexW2895898237

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.