Significant Contributions of Interleukin-13 Genotypes to Asthma Severity.

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
In vivo Pub Date : 2025-09-01 DOI:10.21873/invivo.14057
Te-Chun Shen, Guan-Liang Chen, Li-Hsiou Chen, Yun-Chi Wang, Hou-Yu Shih, Ya-Chen Yang, Chia-Wen Tsai, Wen-Shin Chang, Te-Chun Hsia, DA-Tian Bau
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引用次数: 0

Abstract

Background/aim: Asthma is a complex inflammatory airway disease influenced by genetic and environmental factors. Interleukin-13 (IL-13), particularly its promoter polymorphism rs1800925 and coding variant rs20541, have been implicated in asthma pathogenesis. This study investigated their associations with asthma susceptibility and severity in a Taiwanese population.

Materials and methods: A total of 198 adult patients with asthma and 453 controls without asthma were genotyped for IL-13 rs1800925 and rs20541 using PCR-based assays. Associations with disease risk, age, sex, and asthma severity were analyzed using logistic regression models.

Results: Genotype frequencies of IL-13 rs1800925 and rs20541 conformed to Hardy-Weinberg equilibrium in controls (p =0.1209 and 0.6860). No significant association was found between asthma risk and rs1800925 [CT versus CC: odds ratio (OR)=1.16, 95% confidence interval (CI)=0.80-1.65, p=0.4793; TT versus CC: OR=1.31, 95%CI=0.70-2.45, p=0.5043] or rs20541 (AG versus GG: OR=0.93, 95%CI=0.66-1.33, p=0.7652; AA versus GG: OR=0.84, 95%CI=0.46-1.51, p=0.6577). However, stratified analysis revealed that among individuals aged 25-40, the rs1800925 TT genotype was associated with increased asthma risk (OR=2.16, 95%CI=1.02-4.56, p=0.0637). Notably, rs1800925 CT and TT genotypes were significantly associated with severe asthma symptoms (CT versus CC: OR=2.11, p=0.0287; TT versus CC: OR=4.83, p=0.0057), with carriers of CT+TT genotypes having higher odds of severe asthma (OR=2.46, 95%CI=1.36-4.45, p=0.0041).

Conclusion: While IL-13 rs1800925 and rs20541 polymorphisms were not significantly associated with overall asthma susceptibility, the rs1800925 TT genotype may confer increased risk in younger adults and is significantly linked to more severe asthma severity. IL-13 rs1800925 may serve as a potential genetic biomarker for asthma severity prediction and management in Taiwanese populations.

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白细胞介素-13基因型对哮喘严重程度的重要影响
背景/目的:哮喘是一种受遗传和环境因素影响的复杂气道炎症性疾病。白介素-13 (IL-13),特别是其启动子多态性rs1800925和编码变体rs20541,与哮喘发病有关。本研究探讨其与台湾人群哮喘易感性及严重程度的关系。材料和方法:采用基于pcr的方法,对198例成年哮喘患者和453例非哮喘对照组进行IL-13 rs1800925和rs20541基因分型。使用logistic回归模型分析与疾病风险、年龄、性别和哮喘严重程度的关系。结果:对照组IL-13 rs1800925和rs20541基因型频率符合Hardy-Weinberg平衡(p =0.1209和0.6860)。哮喘风险与rs1800925无显著相关性[CT与CC:优势比(OR)=1.16, 95%可信区间(CI)=0.80-1.65, p=0.4793;TT与CC: OR=1.31, 95%CI=0.70-2.45, p=0.5043]或rs20541 (AG与GG: OR=0.93, 95%CI=0.66-1.33, p=0.7652; AA与GG: OR=0.84, 95%CI=0.46-1.51, p=0.6577)。然而,分层分析显示,在25-40岁的人群中,rs1800925 TT基因型与哮喘风险增加相关(OR=2.16, 95%CI=1.02-4.56, p=0.0637)。值得注意的是,rs1800925 CT和TT基因型与严重哮喘症状显著相关(CT与CC: OR=2.11, p=0.0287; TT与CC: OR=4.83, p=0.0057), CT+TT基因型携带者患严重哮喘的几率更高(OR=2.46, 95%CI=1.36-4.45, p=0.0041)。结论:虽然IL-13 rs1800925和rs20541多态性与整体哮喘易感性无显著相关性,但rs1800925 TT基因型可能会增加年轻人的风险,并与更严重的哮喘严重程度显著相关。IL-13 rs1800925可能作为台湾人群哮喘严重程度预测和管理的潜在遗传生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
In vivo
In vivo 医学-医学:研究与实验
CiteScore
4.20
自引率
4.30%
发文量
330
审稿时长
3-8 weeks
期刊介绍: IN VIVO is an international peer-reviewed journal designed to bring together original high quality works and reviews on experimental and clinical biomedical research within the frames of physiology, pathology and disease management. The topics of IN VIVO include: 1. Experimental development and application of new diagnostic and therapeutic procedures; 2. Pharmacological and toxicological evaluation of new drugs, drug combinations and drug delivery systems; 3. Clinical trials; 4. Development and characterization of models of biomedical research; 5. Cancer diagnosis and treatment; 6. Immunotherapy and vaccines; 7. Radiotherapy, Imaging; 8. Tissue engineering, Regenerative medicine; 9. Carcinogenesis.
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