Xie Tianyue, Tang Zhuqi
Department of Endocrinology, Affiliated Hospital of Nantong University, No.20 Xisi Road, Chongchuan District, Nantong city, 226001, Jiangsu, China.
Diabetol Metab Syndr. 2025 Mar 25;17(1):101. doi: 10.1186/s13098-025-01667-y.
we aimed to evaluate the association of interleukin-1β (IL-1β) gene single nucleotide polymorphisms (SNPs) and its interaction with smoking status on diabetic nephropathy (DN) risk in a Chinese Han population.
The Hardy-Weinberg equilibrium (HWE) was tested by using SNPStats ( https://www.snpstats.net/start.htm ), which was also used for testing the relationship between four SNPs and DN risk and haplotype analysis. The SNP- SNP and gene- smoking interaction were verified by using generalized multifactor dimensionality reduction (GMDR) model.
Logistic regression suggested that the DN risks of participants with rs16944- G allele were significantly higher than those with AA genotype, adjusted OR (95%CI) = 1.62 (1.24-2.01) for AG versus AA, 1.41 (0.75-2.12) for GG versus AA. Additionally, we also found that participants with rs3917356- T allele had an obviously higher DN risk than those with CC genotype, adjusted OR (95%CI) = 1.75 (1.34-2.19) for CT versus CC, 1.87 (1.23-2.54) for TT versus CC. GMDR model found a significant two-locus model (P = 0.011) including rs16944 and smoking. Compared with non- smokers with rs16944- AA genotype, smokers with rs1225404 AG or GG genotype had the highest DN risk after covariates adjustment, OR (95%CI) was 3.04 (1.98-4.12). We also found a haplotype containing rs1143634- T and rs3917356- T was associated with higher DN risk.
we found that the rs16944- G and rs3917356- T allele, interaction between rs16944 and smoking, haplotype containing rs1143634- T and rs3917356- T were all associated with increased DN risk.
我们旨在评估白细胞介素 -1β(IL -1β)基因单核苷酸多态性(SNP)及其与吸烟状态的相互作用对中国汉族人群糖尿病肾病(DN)风险的影响。
使用SNPStats(https://www.snpstats.net/start.htm)检验哈迪 - 温伯格平衡(HWE),其也用于检验4个SNP与DN风险之间的关系及单倍型分析。使用广义多因素降维(GMDR)模型验证SNP - SNP和基因 - 吸烟的相互作用。
逻辑回归表明,携带rs16944 - G等位基因参与者的DN风险显著高于AA基因型者,AG与AA相比,调整后的比值比(95%可信区间)= 1.62(1.24 - 2.01),GG与AA相比为1.41(0.75 - 2.12)。此外,我们还发现携带rs3917356 - T等位基因的参与者DN风险明显高于CC基因型者,CT与CC相比,调整后的比值比(95%可信区间)= 1.75(1.34 - 2.19),TT与CC相比为1.87(1.23 - 2.54)。GMDR模型发现一个显著的两位点模型(P = 0.011),包括rs16944和吸烟。与rs16944 - AA基因型的非吸烟者相比,rs1225404为AG或GG基因型的吸烟者在调整协变量后DN风险最高,比值比(95%可信区间)为3.04(1.98 - 4.12)。我们还发现一个包含rs1143634 - T和rs3917356 - T的单倍型与较高的DN风险相关。
我们发现rs16944 - G和rs3917356 - T等位基因、rs16944与吸烟的相互作用、包含rs1143634 - T和rs3917356 - T的单倍型均与DN风险增加相关。