Genetic polymorphisms of antioxidant enzymes (GSTP1/CAT/HMOX1/EPHX1) and childhood asthma risk in Fuzhou

ObjectiveDiscuss the correlation between single nucleotide polymorphisms (SNPs) of the Glutathione s-transferase Pi-1 (GSTP1), Catalase (CAT), Heme oxygenase-1 (HMOX1), and Homo sapiens epoxide hydrolase 1 (EPHX1) genes and the risk of childhood asthma in Fuzhou.MethodsNext generation sequencing (NG...

Full description

Saved in:
Bibliographic Details
Main Authors: Ziling Wu, Qiaobin Chen, CaiChun Lin, HongBiao Huang, Lang Chen
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-05-01
Series:Frontiers in Pediatrics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2025.1524055/full
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850279019705008128
author Ziling Wu
Ziling Wu
Qiaobin Chen
CaiChun Lin
HongBiao Huang
Lang Chen
author_facet Ziling Wu
Ziling Wu
Qiaobin Chen
CaiChun Lin
HongBiao Huang
Lang Chen
author_sort Ziling Wu
collection DOAJ
description ObjectiveDiscuss the correlation between single nucleotide polymorphisms (SNPs) of the Glutathione s-transferase Pi-1 (GSTP1), Catalase (CAT), Heme oxygenase-1 (HMOX1), and Homo sapiens epoxide hydrolase 1 (EPHX1) genes and the risk of childhood asthma in Fuzhou.MethodsNext generation sequencing (NGS) was employed to conduct whole-exome sequencing (WES) on 50 asthmatic children and 50 healthy children. Genetic models for the GSTP1 gene rs1695, rs4891, HMOX1 gene rs2071747, rs17878790, CAT gene rs7943316, rs1049982, rs769217, and EPHX1 gene rs2234922, rs41266231, rs1051740 sites were constructed. Binary logistic regression, linkage disequilibrium analysis, haplotype analysis, and interaction analysis were used to study the correlation between the 10 SNPs of GSTP1, CAT, HMOX1, and EPHX1 genes and the risk of asthma in children in the Fuzhou region.ResultsThe rs1695 A>G variant increased the risk of asthma in the heterozygous, dominant, and allele models. The rs4891 T>C variant increased the risk of asthma in the heterozygous, dominant, and allele models. The rs7943316 A>T variant increased the risk of asthma in the homozygous, recessive, and allele models. The rs769217 C>T variant decreased the risk of asthma in the homozygous, recessive, and allele models. Strong linkage disequilibrium between the GSTP1 gene rs1695 and rs4891, and the CAT gene rs7943316, rs1049982, and rs769217. The GC haplotype composed of GSTP1 gene rs1695 and rs4891 may pose a risk for childhood asthma [P = 0.025, OR = 2.12 (1.09–4.10)], while the AT haplotype may be protective [P = 0.025, OR = 0.47 (0.24–0.92)]. The ATT haplotype composed of CAT gene rs7943316, rs1049982, and rs769217 may be protective against childhood asthma [P = 0.006, OR = 0.45 (0.25–0.79)]. Potential synergistic interaction between the GSTP1 gene rs1695, CAT gene rs7943316, and EPHX1 gene rs41266231. The combination of GSTP1 gene rs1695 and CAT gene rs7943316 formed the best predictive model for assessing the risk of childhood asthma in the Fuzhou region.ConclusionThe genotype GC, composed of GSTP1 gene rs1695 and rs4891, may represent a risk genotype for childhood asthma, whereas genotype AT may represent a protective genotype for childhood asthma. The genotype ATT, composed of CAT gene rs7943316, rs1049982, and rs769217, may represent a protective genotype for childhood asthma. The combination of GSTP1 gene rs1695 and CAT gene rs7943316 constitutes the optimal model for predicting the risk of childhood asthma in the Fuzhou region.
format Article
id doaj-art-22ed31ebfb8a4c529aededbfdbbd9b60
institution OA Journals
issn 2296-2360
language English
publishDate 2025-05-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Pediatrics
spelling doaj-art-22ed31ebfb8a4c529aededbfdbbd9b602025-08-20T01:49:15ZengFrontiers Media S.A.Frontiers in Pediatrics2296-23602025-05-011310.3389/fped.2025.15240551524055Genetic polymorphisms of antioxidant enzymes (GSTP1/CAT/HMOX1/EPHX1) and childhood asthma risk in FuzhouZiling Wu0Ziling Wu1Qiaobin Chen2CaiChun Lin3HongBiao Huang4Lang Chen5Provincial Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, ChinaNingde People's Hospital, Ningde, ChinaProvincial Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, ChinaNingde People's Hospital, Ningde, ChinaProvincial Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, ChinaProvincial Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, ChinaObjectiveDiscuss the correlation between single nucleotide polymorphisms (SNPs) of the Glutathione s-transferase Pi-1 (GSTP1), Catalase (CAT), Heme oxygenase-1 (HMOX1), and Homo sapiens epoxide hydrolase 1 (EPHX1) genes and the risk of childhood asthma in Fuzhou.MethodsNext generation sequencing (NGS) was employed to conduct whole-exome sequencing (WES) on 50 asthmatic children and 50 healthy children. Genetic models for the GSTP1 gene rs1695, rs4891, HMOX1 gene rs2071747, rs17878790, CAT gene rs7943316, rs1049982, rs769217, and EPHX1 gene rs2234922, rs41266231, rs1051740 sites were constructed. Binary logistic regression, linkage disequilibrium analysis, haplotype analysis, and interaction analysis were used to study the correlation between the 10 SNPs of GSTP1, CAT, HMOX1, and EPHX1 genes and the risk of asthma in children in the Fuzhou region.ResultsThe rs1695 A>G variant increased the risk of asthma in the heterozygous, dominant, and allele models. The rs4891 T>C variant increased the risk of asthma in the heterozygous, dominant, and allele models. The rs7943316 A>T variant increased the risk of asthma in the homozygous, recessive, and allele models. The rs769217 C>T variant decreased the risk of asthma in the homozygous, recessive, and allele models. Strong linkage disequilibrium between the GSTP1 gene rs1695 and rs4891, and the CAT gene rs7943316, rs1049982, and rs769217. The GC haplotype composed of GSTP1 gene rs1695 and rs4891 may pose a risk for childhood asthma [P = 0.025, OR = 2.12 (1.09–4.10)], while the AT haplotype may be protective [P = 0.025, OR = 0.47 (0.24–0.92)]. The ATT haplotype composed of CAT gene rs7943316, rs1049982, and rs769217 may be protective against childhood asthma [P = 0.006, OR = 0.45 (0.25–0.79)]. Potential synergistic interaction between the GSTP1 gene rs1695, CAT gene rs7943316, and EPHX1 gene rs41266231. The combination of GSTP1 gene rs1695 and CAT gene rs7943316 formed the best predictive model for assessing the risk of childhood asthma in the Fuzhou region.ConclusionThe genotype GC, composed of GSTP1 gene rs1695 and rs4891, may represent a risk genotype for childhood asthma, whereas genotype AT may represent a protective genotype for childhood asthma. The genotype ATT, composed of CAT gene rs7943316, rs1049982, and rs769217, may represent a protective genotype for childhood asthma. The combination of GSTP1 gene rs1695 and CAT gene rs7943316 constitutes the optimal model for predicting the risk of childhood asthma in the Fuzhou region.https://www.frontiersin.org/articles/10.3389/fped.2025.1524055/fullbronchial asthmasingle nucleotide polymorphismsantioxidant enzymesGSTP1CATHMOX1
spellingShingle Ziling Wu
Ziling Wu
Qiaobin Chen
CaiChun Lin
HongBiao Huang
Lang Chen
Genetic polymorphisms of antioxidant enzymes (GSTP1/CAT/HMOX1/EPHX1) and childhood asthma risk in Fuzhou
Frontiers in Pediatrics
bronchial asthma
single nucleotide polymorphisms
antioxidant enzymes
GSTP1
CAT
HMOX1
title Genetic polymorphisms of antioxidant enzymes (GSTP1/CAT/HMOX1/EPHX1) and childhood asthma risk in Fuzhou
title_full Genetic polymorphisms of antioxidant enzymes (GSTP1/CAT/HMOX1/EPHX1) and childhood asthma risk in Fuzhou
title_fullStr Genetic polymorphisms of antioxidant enzymes (GSTP1/CAT/HMOX1/EPHX1) and childhood asthma risk in Fuzhou
title_full_unstemmed Genetic polymorphisms of antioxidant enzymes (GSTP1/CAT/HMOX1/EPHX1) and childhood asthma risk in Fuzhou
title_short Genetic polymorphisms of antioxidant enzymes (GSTP1/CAT/HMOX1/EPHX1) and childhood asthma risk in Fuzhou
title_sort genetic polymorphisms of antioxidant enzymes gstp1 cat hmox1 ephx1 and childhood asthma risk in fuzhou
topic bronchial asthma
single nucleotide polymorphisms
antioxidant enzymes
GSTP1
CAT
HMOX1
url https://www.frontiersin.org/articles/10.3389/fped.2025.1524055/full
work_keys_str_mv AT zilingwu geneticpolymorphismsofantioxidantenzymesgstp1cathmox1ephx1andchildhoodasthmariskinfuzhou
AT zilingwu geneticpolymorphismsofantioxidantenzymesgstp1cathmox1ephx1andchildhoodasthmariskinfuzhou
AT qiaobinchen geneticpolymorphismsofantioxidantenzymesgstp1cathmox1ephx1andchildhoodasthmariskinfuzhou
AT caichunlin geneticpolymorphismsofantioxidantenzymesgstp1cathmox1ephx1andchildhoodasthmariskinfuzhou
AT hongbiaohuang geneticpolymorphismsofantioxidantenzymesgstp1cathmox1ephx1andchildhoodasthmariskinfuzhou
AT langchen geneticpolymorphismsofantioxidantenzymesgstp1cathmox1ephx1andchildhoodasthmariskinfuzhou