Evidence map›Paper›PMID 36482455›Full record

ArticleJournal of translational medicine2022

Genetically predicted testosterone and cancers risk in men: a two-sample Mendelian randomization study.

Junke Chang, Yongming Wu, Sicheng Zhou, Ye Tian, Yan Wang, Jie Tian, Wenpeng Song, Yinxian Dong, Jue Li, Ziyi Zhao and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
3.6field-weighted citation impact, top 6% 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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

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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

11 authors at 1 institution in 1 country.

Junke ChangDepartment of Thoracic Surgery, West China Hospital, Sichuan University, Chengdu, China.
Yongming WuDepartment of Thoracic Surgery, West China Hospital, Sichuan University, Chengdu, China.
Sicheng ZhouDepartment of Thoracic Surgery, West China Hospital, Sichuan University, Chengdu, China.
Ye TianHealthy Food Evaluation Research Center, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, China.
Yan WangDepartment of Thoracic Surgery, West China Hospital, Sichuan University, Chengdu, China.
Jie TianDepartment of Thoracic Surgery, West China Hospital, Sichuan University, Chengdu, China.
Wenpeng SongDepartment of Thoracic Surgery, West China Hospital, Sichuan University, Chengdu, China.
Yinxian DongDepartment of Thoracic Surgery, West China Hospital, Sichuan University, Chengdu, China.
Jue LiDepartment of Thoracic Surgery, West China Hospital, Sichuan University, Chengdu, China.
Ziyi ZhaoDepartment of Thoracic Surgery, West China Hospital, Sichuan University, Chengdu, China.
Guowei CheDepartment of Lung Cancer Center, West China Hospital, Sichuan University, Chengdu, China. cheguoweixw@126.com.ORCID 0000-0001-6196-8355
Sichuan University · CN

Funding

Medical Research Council MC_PC_17228
6 · The paper itself

Abstract

objectiveIn observational studies, testosterone has been reported to be associated with some types of cancers. However, the direction and magnitude of the causal association between testosterone and different types of cancer remain unclear. This Mendelian randomization study assessed the causal associations of total testosterone (TT) and bioavailable testosterone (BT) with cancer risk in men.

methodsWe performed two-sample Mendelian randomization using publicly available GWAS summary statistics to investigate the genetically causal association between testosterone and the risk of 22 kinds of cancers in men. Causal estimates were calculated by the inverse variance weighted method. We also performed additional sensitivity tests to evaluate the validity of the casualty.

resultsGenetically predicted BT level were significantly associated with an increased risk of prostate cancer [odds ratio (OR) = 1.17 95% confidence interval (CI): 1.09-1.26, P = 2.51E

conclusionThis study investigated the role of testosterone in the development of prostate cancer, stomach cancer, pancreatic cancer, and small intestine cancer but found no strong association with the other cancers in men.

Indexed as

Pancreatic NeoplasmsProstatic NeoplasmsStomach NeoplasmsHumansMaleTestosteroneTestosteroneBioavailable testosteroneCancerMendelian randomizationTestosterone

Identifiers

PMID36482455
PMCPMC9730605
OpenAlexW4311079890

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.