Zhang Xin, Gu Yulu, Li Yong, Cui Heran, Liu Xiaoli, Sun Hui, Yu Qiong, Yu Yaqin, Liu Yawen, Zhan Siyan, Cheng Yi
Department of Epidemiology and Biostatistics, School of Public Health, Jilin University, Changchun 130021, China.
Department of Pharmacy, The First Hospital of Jilin University, Changchun 130021, China.
Int J Endocrinol. 2020 Feb 11;2020:4539747. doi: 10.1155/2020/4539747. eCollection 2020.
In this study, we aimed to investigate the associations of three single-nucleotide polymorphisms (SNPs) on TITF1/TITF2 (rs944289, rs965513, and rs1443434) with susceptibility to papillary thyroid carcinoma (PTC) and with nodular goiter (NG) in northern Chinese Han populations.
We performed a case-control study comprising 861 PTC patients, 562 NG patients, and 896 normal controls (NCs). One TITF1 SNP (rs944289) and two TITF2 SNPs (rs965513 and rs1443434) were genotyped. Departures from Hardy-Weinberg equilibrium (HWE) in the control group were evaluated using chi-square test. Associations of the SNPs with PTC and with NG were assessed by unconditional logistic regression using the online SNPStats program. Bonferroni correction was performed for multiple tests in genotype analyses. Data analysis was performed by SPSS24.0 unless otherwise specified.
For rs944289, T allele was associated with increased risks for both PTC (OR = 1.23, 95% CI: 1.08-1.41, =0.002) and NG (OR = 1.28, 95% CI: 1.10-1.50, =0.002) and NG (OR = 1.28, 95% CI: 1.10-1.50, =0.002) and NG (OR = 1.28, 95% CI: 1.10-1.50, =0.002) and NG (OR = 1.28, 95% CI: 1.10-1.50, =0.002) and NG (OR = 1.28, 95% CI: 1.10-1.50, =0.002) and NG (OR = 1.28, 95% CI: 1.10-1.50, =0.002) and NG (OR = 1.28, 95% CI: 1.10-1.50, =0.002) and NG (OR = 1.28, 95% CI: 1.10-1.50.
There are associations of rs944289 and rs1443434 polymorphisms with PTC risk and association of rs944289 polymorphism with NG risk. Haplotypes T-G-G and T-G-T are risk haplotypes of PTC and NG, respectively.
在本研究中,我们旨在调查中国北方汉族人群中TITF1/TITF2基因上的三个单核苷酸多态性(SNP,即rs944289、rs965513和rs1443434)与乳头状甲状腺癌(PTC)易感性以及结节性甲状腺肿(NG)的相关性。
我们进行了一项病例对照研究,包括861例PTC患者、562例NG患者和896例正常对照(NC)。对一个TITF1 SNP(rs944289)和两个TITF2 SNP(rs965513和rs1443434)进行基因分型。使用卡方检验评估对照组中偏离哈迪-温伯格平衡(HWE)的情况。使用在线SNPStats程序通过无条件逻辑回归评估SNP与PTC和NG的相关性。在基因型分析中对多重检验进行Bonferroni校正。除非另有说明,数据分析使用SPSS24.0进行。
对于rs944289,T等位基因与PTC(OR = 1.23,95% CI:1.08 - 1.41,P = 0.002)和NG(OR = 1.28,95% CI:1.10 - 1.50,P = 0.002)的风险增加相关。
rs944289和rs1443434多态性与PTC风险相关,rs944289多态性与NG风险相关。单倍型T - G - G和T - G - T分别是PTC和NG的风险单倍型。