Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/1242
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dc.contributor.authorTsilidis, Konstantinos K.-
dc.contributor.authorPapatheodorou, Stefania-
dc.contributor.authorIoannidis, John P. A.-
dc.contributor.authorEvangelou, Evangelos-
dc.contributor.otherΤσιλίδης, Κωνσταντίνος-
dc.contributor.otherΠαπαθεοδώρου, Στεφανία-
dc.contributor.otherΙωαννίδης, Ιωάννης-
dc.contributor.otherΕυαγγέλου, Ευάγγελος-
dc.date.accessioned2015-04-02T07:24:49Z-
dc.date.accessioned2015-12-02T09:04:29Z-
dc.date.available2015-04-02T07:24:49Z-
dc.date.available2015-12-02T09:04:29Z-
dc.date.issued2012-10-22-
dc.identifier.citationJournal of the National Cancer Institute, 2012, vol. 104, no. 24, pp. 1867-1878en_US
dc.identifier.issn14602105-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/1242-
dc.description.abstractBackround Numerous biomarkers have been associated with cancer risk. We assessed whether there is evidence for excess statistical significance in results of cancer biomarker studies, suggesting biases. Methods We systematically searched PubMed for meta-analyses of nongenetic biomarkers and cancer risk. The number of observed studies with statistically significant results was compared with the expected number, based on the statistical power of each study under different assumptions for the plausible effect size. We also evaluated small-study effects using asymmetry tests. All statistical tests were two-sided. Results We included 98 meta-analyses with 847 studies. Forty-three meta-analyses (44%) found nominally statistically significant summary effects (random effects). The proportion of meta-analyses with statistically significant effects was highest for infectious agents (86%), inflammatory (67%), and insulin-like growth factor (IGF)/insulin system (52%) biomarkers. Overall, 269 (32%) individual studies observed nominally statistically significant results. A statistically significant excess of the observed over the expected number of studies with statistically significant results was seen in 20 meta-analyses. An excess of observed vs expected was observed in studies of IGF/insulin (P ≤ .04) and inflammation systems (P ≤ .02). Only 12 meta-analyses (12%) had a statistically significant summary effect size, more than 1000 case patients, and no hints of small-study effects or excess statistical significance; only four of them had large effect sizes, three of which pertained to infectious agents (Helicobacter pylori, hepatitis and human papilloma viruses). Conclusions Most well-documented biomarkers of cancer risk without evidence of bias pertain to infectious agents. Conversely, an excess of statistically significant findings was observed in studies of IGF/insulin and inflammation systems, suggesting reporting biases.en_US
dc.formatpdfen_US
dc.language.isoenen_US
dc.relation.ispartofJNCI Journal of the National Cancer Instituteen_US
dc.rights© The Author 2012en_US
dc.subjectCancer risken_US
dc.subjectDietary intakeen_US
dc.subjectEffect sizeen_US
dc.subjectEnvironmental factoren_US
dc.subjectHelicobacter infectionen_US
dc.subjectHepatitisen_US
dc.subjectInflammationen_US
dc.titleEvaluation of Excess Statistical Significance in Meta-analyses of 98 Biomarker Associations with Cancer Risken_US
dc.typeArticleen_US
dc.collaborationUniversity of Ioanninaen_US
dc.collaborationStanford Universityen_US
dc.subject.categoryClinical Medicineen_US
dc.journalsSubscriptionen_US
dc.reviewPeer Revieweden
dc.countryGreeceen_US
dc.countryUSAen_US
dc.subject.fieldMedical and Health Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1093/jnci/djs437en_US
dc.dept.handle123456789/54en
dc.relation.issue24en_US
dc.relation.volume104en_US
cut.common.academicyear2012-2013en_US
dc.identifier.spage1867en_US
dc.identifier.epage1878en_US
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.openairetypearticle-
item.languageiso639-1en-
crisitem.author.deptCyprus International Institute for Environmental and Public Health-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.orcid0000-0002-9451-9094-
crisitem.author.parentorgFaculty of Health Sciences-
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