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A Common Variant in the CDK8 Gene Is Associated with Sporadic Pituitary Adenomas in the Portuguese Population: a Case-Control Study

dc.contributor.authorGaspar, L
dc.contributor.authorGonçalves, C
dc.contributor.authorFonseca, F
dc.contributor.authorCarvalho, D
dc.contributor.authorCortez, L
dc.contributor.authorPalha, A
dc.contributor.authorBarros, I
dc.contributor.authorNobre, E
dc.contributor.authorDuarte, J
dc.contributor.authorAmaral, C
dc.contributor.authorBugalho, MJ
dc.contributor.authorMarques, O
dc.contributor.authorPereira, B
dc.contributor.authorLemos, M
dc.date.accessioned2023-02-13T15:17:54Z
dc.date.available2023-02-13T15:17:54Z
dc.date.issued2022-10
dc.description.abstractThe majority of pituitary adenomas occur in a sporadic context, and in the absence of known genetic predisposition. Three common variants at the NEBL (rs2359536), PCDH15 (rs10763170) and CDK8 (rs17083838) loci were previously associated with sporadic pituitary adenomas in the Han Chinese population, but these findings have not yet been replicated in any other population. The aim of this case-control study was to assess if these variants are associated with susceptibility to sporadic pituitary adenomas in the Portuguese population. Genotype and allele frequencies were determined in 570 cases and in 546 controls. The CDK8 rs17083838 minor allele (A allele) was significantly associated with sporadic pituitary adenomas, under an additive (odds ratio (OR) 1.73, 95% confidence interval (CI) 1.19-2.50, p = 0.004) and dominant (OR 1.82, 95% CI 1.24-2.68, p = 0.002) inheritance model. The NEBL rs2359536 and PCDH15 rs10763170 variants were not associated with the overall risk for the disease, although a borderline significant association was observed between the PCDH15 rs10763170 minor allele (T allele) and somatotrophinomas (dominant model, OR 1.55, 95% CI 1.02-2.35, p = 0.035). These findings suggest that the CDK8 rs17083838 variant, and possibly the PCDH15 rs10763170 variant, may increase susceptibility to sporadic pituitary adenomas in the Portuguese population.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationInt J Mol Sci. 2022 Oct 4;23(19):11749.pt_PT
dc.identifier.doi10.3390/ijms231911749.pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/4404
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherMDPIpt_PT
dc.subjectHCC ENDpt_PT
dc.subjectAdenoma* / geneticspt_PT
dc.subjectHumanspt_PT
dc.subjectPortugalpt_PT
dc.subjectCase-Control Studiespt_PT
dc.subjectCyclin-Dependent Kinase 8* / geneticspt_PT
dc.subjectGenotypept_PT
dc.subjectGenetic Predisposition to Diseasept_PT
dc.subjectPituitary Neoplasms* / geneticspt_PT
dc.subjectPolymorphism, Single Nucleotidept_PT
dc.titleA Common Variant in the CDK8 Gene Is Associated with Sporadic Pituitary Adenomas in the Portuguese Population: a Case-Control Studypt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.startPage11749pt_PT
oaire.citation.titleInternational Journal of Molecular Sciencespt_PT
oaire.citation.volume23pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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