Division of Chest Medicine, Department of Internal Medicine, Taichung Tzu Chi Hospital, Taichung, Taiwan, R.O.C.
Department of Post-Baccalaureate Veterinary Medicine, Asia University, Taichung, Taiwan, R.O.C.
In Vivo. 2024 Sep-Oct;38(5):2144-2151. doi: 10.21873/invivo.13677.
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.
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.
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).
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.
背景/目的:基质金属蛋白酶-9(MMP9)的过表达已在哮喘患者中观察到,但 MMP9 基因型在决定哮喘易感性方面的作用仍未解决。本研究旨在阐明 MMP9 启动子 rs3918242 基因型对台湾地区哮喘风险的贡献。
我们组建了一个包含 453 名非哮喘健康对照者和 198 例哮喘病例的队列,并使用聚合酶链反应-限制性片段长度多态性方法确定 MMP9 rs3918242 的基因型。
我们的研究结果表明,与野生型 CC 携带者相比,携带 MMP9 rs3918242 的 CT 或 TT 变异型基因型的人并未增加哮喘的风险(比值比=1.28 和 1.72,95%置信区间=0.87-1.87 和 0.72-4.13;p=0.2417 和 0.3201)。此外,携带 MMP9 rs3918242 的 T 等位基因的个体并未比携带 C 等位基因的个体表现出更高的哮喘风险(比值比=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之间存在正相关(p=0.0035)。
尽管 MMP9 rs3918242 的 T 等位基因与哮喘风险无关,但它可能作为哮喘症状严重程度的预测因子。这些发现需要在更大和更多样化的人群中进行验证,以进一步阐明 MMP9 在哮喘发病机制中的意义。