Claims of sex differences: an empirical assessment in genetic associations

dc.contributor.authorPatsopoulos, N. A.en
dc.contributor.authorTatsioni, A.en
dc.contributor.authorIoannidis, J. P.en
dc.date.accessioned2015-11-24T19:30:28Z
dc.date.available2015-11-24T19:30:28Z
dc.identifier.issn1538-3598-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/23102
dc.rightsDefault Licence-
dc.subject*Diseaseen
dc.subjectFemaleen
dc.subjectGenetic Diseases, Inbornen
dc.subject*Genetic Variationen
dc.subjectGenotypeen
dc.subjectHumansen
dc.subjectMaleen
dc.subjectPhenotypeen
dc.subjectReproducibility of Resultsen
dc.subjectRisk Factorsen
dc.subject*Sex Characteristicsen
dc.subject*Sex Factorsen
dc.titleClaims of sex differences: an empirical assessment in genetic associationsen
heal.abstractCONTEXT: Many studies try to probe for differences in risks between men and women, and this is a major challenge in the expanding literature of associations between genetic variants and common diseases or traits. OBJECTIVE: To evaluate whether prominently claimed sex differences for genetic effects have sufficient internal and external validity. DATA SOURCES: We searched PubMed through July 6, 2007, for genetic association studies claiming sex-related differences in the articles' titles. Titles and abstracts and, if necessary, the full text of the article were assessed for eligibility. STUDY SELECTION: Two hundred fifteen articles were retrieved by the search. We considered eligible all retrieved association studies that claimed different genetic effects across sexes of 1 or more gene variants for any human disease or phenotype. We considered both biallelic and multiallelic markers (including haplotypes) and both binary and continuous phenotypes and traits. We excluded non-English-language studies; studies evaluating only 1 sex; studies in which sex was treated only as an independent predictor of disease; studies that did not address any association of the investigated genetic variant with a disease or trait; studies not involving humans; and studies in which the authors did not claim any sex difference. DATA EXTRACTION: Two evaluators independently extracted data with a third evaluator arbitrating their discrepancies. Data evaluation included whether analyses were stated to have been specified a priori; whether sex effects were evaluated in the whole study or subgroups thereof; and whether the claims were appropriately documented, insufficiently documented, or spurious. For appropriately and insufficiently documented claims we performed the calculations for gene-sex interaction whenever raw data were available. Finally, we compared the sex-difference claims with the best internal validity against the results of other studies addressing the same interaction. RESULTS: We appraised 432 sex-difference claims in 77 eligible articles. Authors stated that sex comparisons were decided a priori for 286 claims (66.2%), while the entire sample size was used in 210 (48.6%) claims. Appropriate documentation of gene-sex interaction was recorded in 55 claims (12.7%); documentation was insufficient for 303 claims and spurious for the other 74. Data for reanalysis of claims were available for 188 comparisons. Of these, 83 (44.1%) were nominally statistically significant at a P = .05 threshold, and more than half of them (n = 44) had modest P values between .01 and .05. Of 60 claims with seemingly the best internal validity, only 1 was consistently replicated in at least 2 other studies. CONCLUSION: In this sample of highly prominent claims of sex-related differences in genetic associations, most claims were insufficiently documented or spurious, and claims with documented good internal and external validity were uncommon.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primary10.1001/jama.298.8.880-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/17712072-
heal.identifier.secondaryhttp://jama.ama-assn.org/content/298/8/880.full.pdf-
heal.journalNameJAMAen
heal.journalTypepeer-reviewed-
heal.languageen-
heal.publicationDate2007-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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