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There were no significant group differences in COMT Val158Met alleles and genotype frequencies between patients and controls, for all EDs pooled together [range of odds ratios (ORs): 0.96\u20131.04, <jats:italic>p<\/jats:italic>\u2010values: 0.46\u20130.97, <jats:italic>I<\/jats:italic><jats:sup>2<\/jats:sup>\u2009=\u20090%] and when analysing separately patients with AN (ORs: 0.94\u20131.04, <jats:italic>p<\/jats:italic>\u2010values: 0.31\u20130.61, <jats:italic>I<\/jats:italic><jats:sup>2<\/jats:sup>\u2009=\u20090%) or BN (ORs: 0.80\u20131.09, <jats:italic>p<\/jats:italic>\u2010values: 0.28\u20130.64, <jats:italic>I<\/jats:italic><jats:sup>2<\/jats:sup>\u2009=\u20090\u201344%).<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>Meta\u2010analysing data results from 11 studies and 7225 subjects show that COMT Val158Met polymorphism is not associated with EDs. Copyright \u00a9 2017 John Wiley &amp; Sons, Ltd and Eating Disorders Association.<\/jats:p><\/jats:sec>","DOI":"10.1002\/erv.2555","type":"journal-article","created":{"date-parts":[[2017,10,23]],"date-time":"2017-10-23T04:30:10Z","timestamp":1508733010000},"page":"524-532","source":"Crossref","is-referenced-by-count":6,"title":["Catechol\u2010<i>O<\/i>\u2010Methyltransferase (COMT) Val158Met Polymorphism and Eating Disorders: Data From a New Biobank and Meta\u2010Analysis of Previously Published Studies"],"prefix":"10.1002","volume":"25","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-6730-1778","authenticated-orcid":false,"given":"Enrico","family":"Collantoni","sequence":"first","affiliation":[{"name":"Neuroscience Department University of Padua  Italy"},{"name":"BIO.VEDA Group (Biobanca Veneta per i Disturbi dell'Alimentazione: Biobank of the Veneto Region Eating Disorders Units)  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