Evidence map›Paper›PMID 36316666›Full record

ArticleBMC endocrine disorders2022

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

Kaijun Tong, Chang Zhang, Tingting Yang, Rongbiao Guo, Xinyuan Wang, Renyang Guan, Tianbo Jin

Open access · goldAbstract read
In one paragraph

Article in BMC endocrine disorders, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Kaijun Tong *Department of Medical Images, People's Hospital of Wanning, Huanshi three eastern Road, Wancheng Town, Wanning City, Hainan Province, China.
Chang Zhang *Department of Clinical Laboratory, People's Hospital of Wanning, Hainan Province, Wanning, China.
Tingting YangDepartment of Medical Images, People's Hospital of Wanning, Huanshi three eastern Road, Wancheng Town, Wanning City, Hainan Province, China.
Rongbiao GuoDepartment of Medical Images, People's Hospital of Wanning, Huanshi three eastern Road, Wancheng Town, Wanning City, Hainan Province, China.
Xinyuan WangDepartment of Medical Images, People's Hospital of Wanning, Huanshi three eastern Road, Wancheng Town, Wanning City, Hainan Province, China.
Renyang GuanDepartment of Medical Images, People's Hospital of Wanning, Huanshi three eastern Road, Wancheng Town, Wanning City, Hainan Province, China. g20212022@163.com.
Tianbo JinKey Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Northwest University, 710069, Xi'an, Shaanxi, China. jintb@nwu.edu.cn.
First People's Hospital of Nanning · CNNorthwest University · CNWannan Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe 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).

methodPeripheral 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).

resultsOur 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.

conclusionTMOD1 and PTCSC2 polymorphisms were separately correlated with a remarkable decrease and increase in TC risk based on the analysis.

Indexed as

Genetic Predisposition to DiseaseThyroid NeoplasmsTropomodulinAllelesAsian PeopleCase-Control StudiesChinaFemaleGenotypeHaplotypesHumansMalePolymorphism, Single NucleotideTMOD1 protein, humanTropomodulinMultifactor dimensionality reductionPTCSC2Single nucleotide polymorphismsThyroid carcinomaTMOD1

Identifiers

PMID36316666
PMCPMC9620653
OpenAlexW4307887685

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.