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http://purl.uniprot.org/citations/36316666http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/36316666http://www.w3.org/2000/01/rdf-schema#comment"

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."xsd:string
http://purl.uniprot.org/citations/36316666http://purl.org/dc/terms/identifier"doi:10.1186/s12902-022-01177-2"xsd:string
http://purl.uniprot.org/citations/36316666http://purl.uniprot.org/core/author"Guo R."xsd:string
http://purl.uniprot.org/citations/36316666http://purl.uniprot.org/core/author"Wang X."xsd:string
http://purl.uniprot.org/citations/36316666http://purl.uniprot.org/core/author"Zhang C."xsd:string
http://purl.uniprot.org/citations/36316666http://purl.uniprot.org/core/author"Yang T."xsd:string
http://purl.uniprot.org/citations/36316666http://purl.uniprot.org/core/author"Jin T."xsd:string
http://purl.uniprot.org/citations/36316666http://purl.uniprot.org/core/author"Guan R."xsd:string
http://purl.uniprot.org/citations/36316666http://purl.uniprot.org/core/author"Tong K."xsd:string
http://purl.uniprot.org/citations/36316666http://purl.uniprot.org/core/date"2022"xsd:gYear
http://purl.uniprot.org/citations/36316666http://purl.uniprot.org/core/name"BMC Endocr Disord"xsd:string
http://purl.uniprot.org/citations/36316666http://purl.uniprot.org/core/pages"263"xsd:string
http://purl.uniprot.org/citations/36316666http://purl.uniprot.org/core/title"Suggestive evidence of the genetic association of TMOD1 and PTCSC2 polymorphisms with thyroid carcinoma in the Chinese Han population."xsd:string
http://purl.uniprot.org/citations/36316666http://purl.uniprot.org/core/volume"22"xsd:string
http://purl.uniprot.org/citations/36316666http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/36316666
http://purl.uniprot.org/citations/36316666http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/36316666
http://purl.uniprot.org/uniprot/#_P28289-mappedCitation-36316666http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/36316666
http://purl.uniprot.org/uniprot/P28289http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/36316666