基质金属蛋白酶-9 启动子基因型对哮喘风险的影响

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL In vivo Pub Date : 2024-09-01 DOI:10.21873/invivo.13677
Kuo-Liang Chiu, Jie-Long He, Guan-Liang Chen, Te-Chun Shen, Li-Hsiou Chen, Jaw-Chyun Chen, 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:已观察到基质金属蛋白酶-9(MMP9)在哮喘患者中过表达,但MMP9基因型在决定哮喘易感性中的作用仍未解决。本研究旨在阐明台湾 MMP9 启动子 rs3918242 基因型对哮喘风险的贡献:研究对象包括453名非哮喘健康对照者和198名哮喘患者,采用聚合酶链式反应-限制性片段长度多态性方法测定MMP9启动子rs3918242基因型:我们的研究结果表明,与野生型CC携带者相比,携带MMP9 rs3918242变异CT或TT基因型的人患哮喘的风险并没有升高(几率比分别为1.28和1.72,95%置信区间分别为0.87-1.87和0.72-4.13;P=0.2417和0.3201)。此外,携带 MMP9 rs3918242 的 T 等位基因的个体患哮喘的风险并不比携带 C 等位基因的个体高(几率比=1.31,95% 置信区间=0.96-1.79,p=0.0869)。有趣的是,在哮喘患者中,MMP9 rs3918242 CT 或 TT 基因型与哮喘症状的严重程度呈正相关(p=0.0035):尽管MMP9 rs3918242的T等位基因与哮喘风险无关,但它可能是哮喘症状严重程度的预测因子。这些发现需要在更大范围和更多样化的人群中进行验证,以进一步阐明 MMP9 在哮喘病因学中的重要性。
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Impacts of Matrix Metalloproteinase-9 Promoter Genotypes on Asthma Risk.

Background/aim: The overexpression of matrix metalloproteinase-9 (MMP9) has been observed in asthmatic patients, yet the role of MMP9 genotype in determining asthma susceptibility remains unresolved. This study aimed to elucidate the contribution of MMP9 promoter rs3918242 genotype to asthma risk in Taiwan.

Materials and methods: A cohort comprising 453 non-asthmatic healthy controls and 198 asthmatic cases was assembled, and the MMP9 rs3918242 genotypes were determined using polymerase chain reaction-restriction fragment length polymorphism methodology.

Results: Our findings indicated that people carrying the variant CT or TT genotype of MMP9 rs3918242 did not demonstrate an elevated risk of asthma compared to wild-type CC carriers (odds ratio=1.28 and 1.72, 95% confidence interval=0.87-1.87 and 0.72-4.13; p=0.2417 and 0.3201, respectively). Furthermore, individuals carrying the T allele at MMP9 rs3918242 did not exhibit a higher risk of asthma than those carrying the C allele (odds ratio=1.31, 95% confidence interval=0.96-1.79, p=0.0869). Interestingly, a positive association was observed between MMP9 rs3918242 CT or TT genotypes and the severity of asthma symptoms among asthmatic patients (p=0.0035).

Conclusion: Although the T allele at MMP9 rs3918242 was not associated with asthma risk, it may serve as a predictor for asthma symptom severity. These findings warrant validation in larger and more diverse populations to further elucidate the significance of MMP9 in asthma etiology.

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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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