Suggestive evidence of the genetic association of TMOD1 and PTCSC2 polymorphisms with thyroid carcinoma in the Chinese Han population.

Autor: Tong K; Department of Medical Images, People's Hospital of Wanning, Huanshi three eastern Road, Wancheng Town, Wanning City, Hainan Province, China., Zhang C; Department of Clinical Laboratory, People's Hospital of Wanning, Hainan Province, Wanning, China., Yang T; Department of Medical Images, People's Hospital of Wanning, Huanshi three eastern Road, Wancheng Town, Wanning City, Hainan Province, China., Guo R; Department of Medical Images, People's Hospital of Wanning, Huanshi three eastern Road, Wancheng Town, Wanning City, Hainan Province, China., Wang X; Department of Medical Images, People's Hospital of Wanning, Huanshi three eastern Road, Wancheng Town, Wanning City, Hainan Province, China., Guan R; Department of Medical Images, People's Hospital of Wanning, Huanshi three eastern Road, Wancheng Town, Wanning City, Hainan Province, China. g20212022@163.com., Jin T; Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Northwest University, 710069, Xi'an, Shaanxi, China. jintb@nwu.edu.cn.; Provincial Key Laboratory of Biotechnology of Shaanxi Province, Northwest University, 229 North Taibai Road, 710069, Xi'an, Shaanxi, China. jintb@nwu.edu.cn.
Jazyk: angličtina
Zdroj: BMC endocrine disorders [BMC Endocr Disord] 2022 Oct 31; Vol. 22 (1), pp. 263. Date of Electronic Publication: 2022 Oct 31.
DOI: 10.1186/s12902-022-01177-2
Abstrakt: Background: The purpose of this study was to survey the associations of six single nucleotide polymorphisms (SNPs) in the TMOD1 and PTCSC2 genes with thyroid carcinoma (TC).
Method: Peripheral blood samples were obtained from 510 patients with TC and 509 normal controls. Six SNPs were genotyped by the Agena MassARRAY platform. Logistic regression was used to evaluate the association between SNPs and TC susceptibility by calculating odds ratios (ORs) and 95% confidence intervals (CIs). SNP-SNP interactions were analyzed by multifactor dimensionality reduction (MDR).
Results: Our study showed that rs925489 (OR = 1.45, p = 0.011) and rs965513 (OR = 1.40, p = 0.021) were significantly associated with an increased risk of TC. Rs10982622 decreased TC risk (OR = 0.74, p = 0.025). Further stratification analysis showed that rs10982622 reduced the susceptibility to TC in patients aged ≤ 45 years (OR = 0.69, p = 0.019) and in females (OR = 0.61, p = 0.014). Rs925489 increased TC risk in people aged > 45 years (OR = 1.54, p = 0.044) and in males (OR = 2.34, p = 0.003). In addition, rs965513 was related to an increased risk of TC in males (OR = 2.14, p = 0.007). Additionally, haplotypes in the block (rs925489|rs965513) significantly increased TC risk (p < 0.05). The best predictive model for TC was the combination of rs1052270, rs10982622, rs1475545, rs16924016, and rs925489.
Conclusion: TMOD1 and PTCSC2 polymorphisms were separately correlated with a remarkable decrease and increase in TC risk based on the analysis.
(© 2022. The Author(s).)
Databáze: MEDLINE
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