Evidence map›Paper›PMID 31999731›Full record

ArticlePloS one2020

Role of GSTM1 and GSTT1 genotypes in differentiated thyroid cancer and interaction with lifestyle factors: Results from case-control studies in France and New Caledonia.

Catherine Tcheandjieu, Emilie Cordina-Duverger, Claire Mulot, Dominique Baron-Dubourdieu, Anne-Valérie Guizard, Claire Schvartz, Pierre Laurent-Puig, Pascal Guénel, Thérèse Truong

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. 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
0.7field-weighted citation impact, top 34% 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, 10 citations in OpenAlex.

  1. Powerful quantifiers for cancer transcriptomics.World journal of clinical oncology · 2020
    Review
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

9 authors at 4 institutions in 2 countries.

Catherine TcheandjieuUniversité Paris-Saclay, UVSQ, INSERM, CESP, Villejuif, France.
Emilie Cordina-DuvergerUniversité Paris-Saclay, UVSQ, INSERM, CESP, Villejuif, France.
Claire MulotCentre de Recherche des Cordeliers, INSERM, Sorbonne Université, USPC, Université Paris Descartes, Université Paris Diderot, EPIGENETEC, Paris, France.
Dominique Baron-DubourdieuLaboratory of Anatomy and Cytopathology, Noumea, New Caledonia, France.
Anne-Valérie GuizardRegistre Général des Tumeurs du Calvados, Centre François Baclesse, Caen, France.
Claire SchvartzRegistre spécialisé des Cancers de la Thyroide Marne-Ardennes Institut GODINOT, Reims, France.
Pierre Laurent-PuigCentre de Recherche des Cordeliers, INSERM, Sorbonne Université, USPC, Université Paris Descartes, Université Paris Diderot, EPIGENETEC, Paris, France.
Pascal GuénelUniversité Paris-Saclay, UVSQ, INSERM, CESP, Villejuif, France.
Thérèse TruongUniversité Paris-Saclay, UVSQ, INSERM, CESP, Villejuif, France.ORCID 0000-0002-2943-6786
Inserm · FRDélégation Paris 5 · FRInstitut Jean Godinot · FRUniversity of New Caledonia · NC

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGSTM1 and GSTT1 are involved in detoxification of xenobiotics, products of oxidative stress and in steroid hormones metabolism. We investigated whether GSTM1 and GSTT1 gene deletion was associated with DTC risk and explored interaction with non-genetic risk factors of DTC.

methodsThe study included 661 DTC cases and 736 controls from two case-control studies conducted in France and New Caledonia. Odds ratios (OR) and their confidence interval (CI) for DTC associated with GST genotypes, alcohol drinking, tobacco smoking, body mass index and hormonal factors were calculated using logistic regression models.

resultsResults are presented for Europeans and Melanesians combined, as no heterogeneity between groups was detected. We found that DTC risk increased with obesity and decrease with alcohol drinking. After stratification by gene deletion status, the OR for obesity was 5.75, (95%CI 2.25-14.7) among individuals with GSTT1 and GSTM1-deleted genotype, and 1.26, (95%CI 0.89-1.77) in carriers of both genes (p-interaction = 0.02). The OR for drinking ≥1 glass/week was 0.33 (95%CI 0.15-0.74) in GSTT1-null individuals while it was 1.01 (95%CI 0.67-1.52) in non-null carriers of the gene (p-interaction = 0.01). No interaction between GST genotypes and other non-genetic risk factors was detected.

conclusionGSTM1 and GSTT1 genotypes may modulate the DTC risk associated with BMI and alcohol consumption.

Indexed as

Life StyleAlcohol DrinkingBody Mass IndexCase-Control StudiesFemaleGene DeletionGenotypeGlutathione TransferaseGonadal Steroid HormonesHealth Risk BehaviorsHumansMaleMiddle AgedNew CaledoniaObesityThyroid Neoplasmsglutathione S-transferase T1Glutathione TransferaseGonadal Steroid Hormones

Identifiers

PMID31999731
PMCPMC6992216
OpenAlexW3003196284

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.