Evidence map›Paper›PMID 33208131›Full record

ArticleBMC pulmonary medicine2020

Effects of STIP1 and GLCCI1 polymorphisms on the risk of childhood asthma and inhaled corticosteroid response in Chinese asthmatic children.

Juan Huang, Xiaolei Hu, Xiangrong Zheng, Jian Kuang, Chentao Liu, Xia Wang, Yongjun Tang

Open access · goldAbstract read
In one paragraph

Article in BMC pulmonary medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Role of GLCCI1 in inhibiting PI3K-induced NLRP3 inflammasome activation in asthma.Chinese medical journal pulmonary and critical care medicine · 2024
    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

7 authors at 1 institution in 1 country.

Juan HuangDepartment of Pediatric, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Xiaolei HuNational Institution of Drug Clinical Trial, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Xiangrong ZhengDepartment of Pediatric, Xiangya Hospital, Central South University, Changsha, Hunan, China. xrzheng@csu.edu.cn.ORCID http://orcid.org/0000-0001-9864-8646
Jian KuangDepartment of Pediatric, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Chentao LiuDepartment of Pediatric, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Xia WangDepartment of Pediatric, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yongjun TangDepartment of Pediatric, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Central South University · CN

Funding

National Natural Science Foundation of China 81873851Natural Science Foundation of Hunan Province 2018JJ6141
6 · The paper itself

Abstract

backgroundAsthma is a common chronic lung disease in children. We aimed to determine the associations between stress-induced phosphoprotein 1 (STIP1) and glucocorticoid-induced transcript 1 (GLCCI1) polymorphisms and susceptibility of childhood asthma and inhaled corticosteroid (ICS) response in children.

methodsA total of 263 Chinese Han asthmatic children were recruited from the Xiangya Hospital, Central South University. Pulmonary function tests were performed before the treatment and 3 months after the treatment. One hundred fifty non-asthmatic children were recruited. Each participant's DNA was extracted from the peripheral blood and Method of MassARRAY was used to genotype the single-nucleotide polymorphisms (SNPs).

resultsSTIP1 rs2236647 wild-type homozygote (CC) was associated with increased asthma risk of children (OR = 1.858, 95% CI:1.205-2.864), but not associated with the ICS response. GLCCI1 rs37969, rs37972 and rs37973 polymorphisms were not associated with the risk of childhood asthma. However, rs37969 mutant genotypes (TT/GT) were significantly associated with less improvement in PD20 (p = 0.028). We also found significant associations between rs37969, rs37972 and rs37973 mutant genotypes and less improvement in maximal midexpiratory flow (MMEF) after ICS treatment for 3 months (p = 0.036, p = 0.010 and p = 0.003, respectively).

conclusionsSTIP1 rs2236647 was associated with asthma risk of children and GLCCI1 rs37969 mutant genotypes were associated with less improvement in airway hyper-responsiveness. GLCCI1 rs37969, rs37972 and rs37973 polymorphisms might be associated with pulmonary function in childhood asthma patients after ICS treatment.

Indexed as

Administration, InhalationAdrenal Cortex HormonesAsian PeopleAsthmaCase-Control StudiesChildChild, PreschoolDisease SusceptibilityFemaleGenotypeHeat-Shock ProteinsHumansMaleMutationPolymorphism, Single NucleotideReceptors, GlucocorticoidAdrenal Cortex HormonesGLCCI1 protein, humanHeat-Shock ProteinsReceptors, GlucocorticoidSTIP1 protein, humanChildhood asthmaGLCCI1PolymorphismPulmonary functionSTIP1

Identifiers

PMID33208131
PMCPMC7677774
OpenAlexW3100874330

What OpenQuestion holds

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LicenceCC BY
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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.