Prostate cancer genetic propensity risk score may modify the association between this tumour and type 2 diabetes mellitus (MCC-Spain study).

dc.contributor.authorBarrios-Rodríguez, Rocío
dc.contributor.authorGarcía-Esquinas, Esther
dc.contributor.authorPérez-Gómez, Beatriz
dc.contributor.authorCastaño-Vinyals, Gemma
dc.contributor.authorLlorca, Javier
dc.contributor.authorde Larrea-Baz, Nerea Fernández
dc.contributor.authorOlmedo-Requena, Rocío
dc.contributor.authorVanaclocha-Espi, Mercedes
dc.contributor.authorAlguacil, Juan
dc.contributor.authorFernández-Tardón, Guillermo
dc.contributor.authorFernández-Navarro, Pablo
dc.contributor.authorCecchini, Lluís
dc.contributor.authorLope, Virginia
dc.contributor.authorGómez-Acebo, Inés
dc.contributor.authorAragonés, Nuria
dc.contributor.authorKogevinas, Manolis
dc.contributor.authorPollán, Marina
dc.contributor.authorJiménez-Moleón, José Juan
dc.date.accessioned2025-01-07T14:11:21Z
dc.date.available2025-01-07T14:11:21Z
dc.date.issued2021-10-02
dc.description.abstractSome studies have reported an inverse association between type 2 diabetes mellitus (T2DM) and prostate cancer (PCa), but results on this issue are still inconsistent. In this study, we evaluate whether this heterogeneity might be related to differences in this relationship by tumour or by individual genetic susceptibility to PCa. We studied 1047 incident PCa cases and 1379 randomly selected controls, recruited in 7 Spanish provinces for the population-based MCC-Spain case-control. Tumour were classified by aggressiveness according to the International Society of Urological Pathology (ISUP), and we constructed a PCa polygenic risk score (PRS) as proxy for genetic susceptibility. The epidemiological questionnaire collected detailed self-reported data on T2DM diagnosis and treatment. The association between T2DM status and PCa was studied by fitting mixed logistic regression models, and, for its association by aggressiveness of PCa, with multinomial logistic regression models. To evaluate the possible modulator role of PRS in this relationship, we included the corresponding interaction term in the model, and repeated the analysis stratified by PRS tertiles. Globally, our results showed an inverse association between T2DM and overall PCa limited to grade 1 tumours (ORISUP = 1: 0.72; 95% CI: 0.53-0.98), which could be compatible with a detection bias. However, PCa risk also varied with duration of diabetes treatment -inversely to metformin and positively with insulin-, without differences by aggressiveness. When we considered genetic susceptibility, T2DM was more strongly associated with lower PCa risk in those with lower PRS (ORtertile 1: 0.31; 95% CI: 0.11-0.87), independently of ISUP grade. Our findings reinforce the need to include aggressiveness and susceptibility of PCa, and T2DM treatments in the study of the relationship between both diseases.
dc.identifier.doi10.1038/s41391-021-00446-w
dc.identifier.essn1476-5608
dc.identifier.pmid34601492
dc.identifier.unpaywallURLhttp://repositori.upf.edu/bitstream/10230/53679/1/barrios-ppc-pros.pdf
dc.identifier.urihttps://hdl.handle.net/10668/26204
dc.issue.number4
dc.journal.titleProstate cancer and prostatic diseases
dc.journal.titleabbreviationProstate Cancer Prostatic Dis
dc.language.isoen
dc.organizationSAS - Hospital Universitario San Cecilio
dc.organizationSAS - Hospital Universitario Virgen de las Nieves
dc.organizationSAS - Hospital Universitario San Cecilio
dc.organizationInstituto de Investigación Biosanitaria de Granada (ibs.GRANADA)
dc.page.number694-699
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rights.accessRightsopen access
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshDiabetes Mellitus, Type 2
dc.subject.meshGenetic Predisposition to Disease
dc.subject.meshProstatic Neoplasms
dc.subject.meshRisk Factors
dc.subject.meshSpain
dc.subject.meshCase-Control Studies
dc.titleProstate cancer genetic propensity risk score may modify the association between this tumour and type 2 diabetes mellitus (MCC-Spain study).
dc.typeresearch article
dc.type.hasVersionAM
dc.volume.number25

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