METHODS: In a cohort comprising 208 NPC cases and 416 healthy controls, genotyping of MMP-9 rs3918242 was conducted utilizing polymerase chain reaction-restriction fragment length polymorphism methodology.
RESULTS: Individuals harbouring the variant CT or TT genotype of MMP-9 rs3918242 did not demonstrate a discernible alteration in NPC risk when compared to wild-type CC carriers [odds ratio (OR)=0.83 and 0.79, with 95% confidence intervals (95%CI)=0.56-1.24 and 0.27-2.29; p=0.4205 and 0.8675, respectively]. Moreover, the presence of the variant T allele did not confer a modified risk of NPC (OR=0.84, 95%CI=0.60-1.19, p=0.3761). Intriguingly, a protective effect associated with the MMP-9 rs3918242 CT genotype against NPC risk was discerned among individuals abstaining from betel quid chewing behaviour (OR=0.51, 95%CI=0.30-0.87, p=0.0166). Notably, no significant association was established between the MMP-9 rs3918242 CT or TT genotype and NPC risk among individuals with or without smoking or alcohol consumption habits.
CONCLUSIONS: Presence of the variant CT or TT genotype at MMP-9 rs3918242 did not appear to substantially contribute to an elevated risk of NPC. Notably, a protective effect against NPC risk was observed in individuals carrying the CT genotype, particularly in those abstaining from betel quid chewing.
方法:在包括208例NPC和416例健康对照的队列中,采用聚合酶链反应-限制性片段长度多态性方法对MMP-9rs3918242进行基因分型。
结果:与野生型CC携带者相比,携带MMP-9rs3918242的变异CT或TT基因型的个体在NPC风险方面没有明显变化[比值比(OR)=0.83和0.79,95%置信区间(95CI)=0.56-1.24和0.27-2.29;p=0.4205和0.8675]。此外,变异T等位基因的存在并未改变NPC的风险(OR=0.84,95CI=0.60~1.19,p=0.3761).有趣的是,与MMP-9rs3918242CT基因型对NPC风险相关的保护作用在个体中被发现,个体放弃了槟榔咀嚼行为(OR=0.51,95CI=0.30-0.87,p=0.0166).值得注意的是,在有或没有吸烟或饮酒习惯的个体中,MMP-9rs3918242CT或TT基因型与NPC风险之间无显著关联.
结论:在MMP-9rs3918242中存在变异的CT或TT基因型似乎并没有实质上导致NPC风险升高。值得注意的是,在携带CT基因型的个体中观察到对NPC风险的保护作用,尤其是那些放弃嚼槟榔的人。