基质金属蛋白酶-7启动子基因型与台湾哮喘风险的关系

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
In vivo Pub Date : 2025-09-01 DOI:10.21873/invivo.14056
Kuo-Liang Chiu, Guan-Liang Chen, Chia-Hsiang Li, Jaw-Chyun Chen, Yun-Chi Wang, Hou-Yu Shih, Chia-Wen Tsai, Wen-Shin Chang, Te-Chun Hsia, DA-Tian Bau
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引用次数: 0

摘要

背景/目的:哮喘是一种复杂的慢性气道疾病,具有多因素病因,包括遗传易感性。本研究旨在探讨台湾人群MMP-7启动子多态性-181A>G (rs11568818)与哮喘易感性和严重程度的关系。材料与方法:对198例哮喘患者和453名健康对照者进行PCR-RFLP基因分型分析。结果:虽然基因型与哮喘风险之间没有显著的整体关联[AG与AA:优势比(OR)=1.31, 95%可信区间(CI)=0.82-2.09, p=0.3117;GG与AA: OR=2.42, 95%CI=0.69 ~ 8.46, p=0.2833], G等位基因有显著性差异(OR=1.44, 95%CI=0.96 ~ 2.15, p=0.0950)。在年龄分层分析中,AG基因型显著增加25-40岁人群的哮喘风险(OR=1.86, 95%CI=1.08-3.25, p=0.0365),但在40岁以上人群中无显著增加。性别分层分析显示,男性或女性均无显著相关性。值得注意的是,基因型分布与哮喘严重程度显著相关(p为趋势=0.0040)。AG和GG基因型患者比AA基因型患者更容易出现严重哮喘症状(AG: 24.7% vs. 11.2%, p=0.0144; GG: 5.5% vs. 0.8%, p=0.0418)。优势模型(AG+GG vs. AA)显示,重度组的患病率(30.2%)高于轻度组(12.0%),而GG基因型对重度疾病的OR值较高(OR=7.19 vs. 3.16),接近临界意义。结论:MMP-7-181A>G不是哮喘的主要易感标志物。然而,G等位基因可能作为台湾个体发病较年轻和更严重哮喘表型的潜在生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Associations of Matrix Metalloproteinase-7 Promoter Genotypes With Asthma Risk in Taiwan.

Associations of Matrix Metalloproteinase-7 Promoter Genotypes With Asthma Risk in Taiwan.

Associations of Matrix Metalloproteinase-7 Promoter Genotypes With Asthma Risk in Taiwan.

Associations of Matrix Metalloproteinase-7 Promoter Genotypes With Asthma Risk in Taiwan.

Background/aim: Asthma is a complex chronic airway disease with multifactorial etiologies, including genetic predispositions. This study aimed to investigate the association between the MMP-7 promoter polymorphism -181A>G (rs11568818) and asthma susceptibility and severity in a Taiwanese population.

Materials and methods: PCR-RFLP genotyping analysis was conducted on 198 patients with asthma and 453 healthy controls.

Results: While no significant overall association was observed between genotypes and asthma risk [AG versus AA: odds ratio (OR)=1.31, 95% confidence interval (CI)=0.82-2.09, p=0.3117; GG versus AA: OR=2.42, 95%CI=0.69-8.46, p=0.2833], a borderline significance was found for the G allele (OR=1.44, 95%CI=0.96-2.15, p=0.0950). In age-stratified analysis, the AG genotype significantly increased asthma risk in individuals aged 25-40 years (OR=1.86, 95%CI=1.08-3.25, p=0.0365), but not in those over 40 years. Sex-stratified analyses revealed no significant associations in either males or females. Notably, genotype distribution correlated significantly with asthma severity (p for trend=0.0040). Individuals with AG and GG genotypes were more likely to present severe asthma symptoms compared to those with the AA genotype (AG: 24.7% vs. 11.2%, p=0.0144; GG: 5.5% vs. 0.8%, p=0.0418). The dominant model (AG+GG vs. AA) showed a higher prevalence in the severe group (30.2%) than in the milder group (12.0%), while the GG genotype conferred a high OR for severe disease (OR=7.19 vs. 3.16), approaching borderline significance.

Conclusion: MMP-7-181A>G is not a major susceptibility marker for asthma. However, the G allele may serve as a potential biomarker for younger-onset and more severe asthma phenotypes in Taiwanese individuals.

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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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