Jin Wenfang, Yao Yu, Lv Yanling
Department of Respiratory and Critical Care Medicine, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine, 1-1 Zhongfu Road, Gulou District, Nanjing, 210003, Jiangsu, China.
Discov Oncol. 2025 May 20;16(1):827. doi: 10.1007/s12672-025-02577-1.
The aim of this study was to investigate the impact of four single nucleotide polymorphisms (SNPs) within the Dectin-1 gene, the interaction between SNPs of the Dectin-1 gene and the low weight on susceptibility to invasive pulmonary aspergillosis (IPA) in patients with lung cancer undergoing surgery. Logistic regression was used to test the relationship between four SNPs of the Dectin-1 gene and IPA susceptibility. The generalized multifactor dimensionality reduction (GMDR) model was used to assess the interaction between SNPs of Dectin-1 gene and low weight. We found that both the rs3901533-TT and the rs3901533-TT or GT genotype were associated with an increased risk of IPA, the adjusted ORs (95% CI) were 1.98 (1.37-2.62) (TT vs. GG) and 1.43 (1.10-1.81) (GT+TT vs. GG), respectively. We also found that rs7309123-GG and rs7309123-GG+CG genotypes were associated with an increased risk of IPA, adjusted OR (95% CI) were 2.06 (1.43-2.71) (GG vs. CC), 1.63 (1.15-2.12) (CG+GG vs. CC), respectively. GMDR model found a statistically significant two-dimensional model combination (including rs3901533 and low weight). The participants with rs3901533-GT or TT genotype and low weight had the highest risk of IPA, compared to participants with rs3901533-GG genotype and without low weight, OR (95% CI) was 3.24 (1.68-4.92) (p < 0.001). In conclusion, rs3901533 and rs7309123 of Dectin-1 gene, the interaction between rs3901533 and low weight were correlated with increased risk of IPA in patients with lung cancer undergoing surgery.
本研究旨在调查Dectin-1基因内4个单核苷酸多态性(SNP)的影响、Dectin-1基因SNP与低体重之间的相互作用对接受手术的肺癌患者侵袭性肺曲霉病(IPA)易感性的影响。采用逻辑回归分析Dectin-1基因的4个SNP与IPA易感性之间的关系。运用广义多因素降维(GMDR)模型评估Dectin-1基因SNP与低体重之间的相互作用。我们发现,rs3901533-TT以及rs3901533-TT或GT基因型均与IPA风险增加相关,校正后的比值比(95%置信区间)分别为1.98(1.37 - 2.62)(TT与GG相比)和1.43(1.10 - 1.81)(GT + TT与GG相比)。我们还发现,rs7309123-GG和rs7309123-GG + CG基因型与IPA风险增加相关,校正后的比值比(95%置信区间)分别为2.06(1.43 - 2.71)(GG与CC相比)、1.63(1.15 - 2.12)(CG + GG与CC相比)。GMDR模型发现了一个具有统计学意义的二维模型组合(包括rs3901533和低体重)。与具有rs3901533-GG基因型且无低体重的参与者相比,具有rs3901533-GT或TT基因型且低体重的参与者患IPA的风险最高,比值比(95%置信区间)为3.24(1.68 - 4.92)(p < 0.001)。总之,Dectin-1基因的rs3901533和rs7309123、rs3901533与低体重之间的相互作用与接受手术的肺癌患者IPA风险增加相关。