Marco Solmi, D. Gallicchio, E. Collantoni, Christoph U. Correll, Maurizio Clementi, C. Pinato, M. Forzan, Matteo Cassina, F. Fontana, Valeria Giannunzio, I. Piva, R. Siani, P. Salvo, P. Santonastaso, E. Tenconi, N. Veronese, A. Favaro
{"title":"Serotonin transporter gene polymorphism in eating disorders: Data from a new biobank and META-analysis of previous studies","authors":"Marco Solmi, D. Gallicchio, E. Collantoni, Christoph U. Correll, Maurizio Clementi, C. Pinato, M. Forzan, Matteo Cassina, F. Fontana, Valeria Giannunzio, I. Piva, R. Siani, P. Salvo, P. Santonastaso, E. Tenconi, N. Veronese, A. Favaro","doi":"10.3109/15622975.2015.1126675","DOIUrl":null,"url":null,"abstract":"Objectives Growing interest focuses on the association between 5-HTTLPR polymorphism and eating disorders (ED), but published findings have been conflicting. Methods The Italian BIO.VE.D.A. biobank provided 976 samples (735 ED patients and 241 controls) for genotyping. We conducted a literature search of studies published up to 1 April 2015, including studies reporting on 5HTTLPR genotype and allele frequencies in obesity and/or ED. We ran a meta-analysis, including data from BIO.VE.D.A. – comparing low and high-functioning genotype and allele frequencies in ED vs. controls. Results Data from 21 studies, plus BIO.VE.D.A., were extracted providing information from 3,736 patients and 2,707 controls. Neither low- nor high-functioning genotype frequencies in ED patients, with both bi- and tri-allelic models, differed from controls. Furthermore, neither low- nor high-functioning allele frequencies in ED or in BN, in both bi- and triallelic models, differed from control groups. After sensitivity analysis, results were the same in AN vs. controls. Results remained unaltered when investigating recessive and dominant models. Conclusions 5HTTLPR does not seem to be associated with ED in general, or with AN or BN in particular. Future studies in ED should explore the role of ethnicity and psychiatric comorbidity as a possible source of bias.","PeriodicalId":22963,"journal":{"name":"The World Journal of Biological Psychiatry","volume":"22 1","pages":"244 - 257"},"PeriodicalIF":0.0000,"publicationDate":"2016-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"22","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The World Journal of Biological Psychiatry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3109/15622975.2015.1126675","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 22
Abstract
Objectives Growing interest focuses on the association between 5-HTTLPR polymorphism and eating disorders (ED), but published findings have been conflicting. Methods The Italian BIO.VE.D.A. biobank provided 976 samples (735 ED patients and 241 controls) for genotyping. We conducted a literature search of studies published up to 1 April 2015, including studies reporting on 5HTTLPR genotype and allele frequencies in obesity and/or ED. We ran a meta-analysis, including data from BIO.VE.D.A. – comparing low and high-functioning genotype and allele frequencies in ED vs. controls. Results Data from 21 studies, plus BIO.VE.D.A., were extracted providing information from 3,736 patients and 2,707 controls. Neither low- nor high-functioning genotype frequencies in ED patients, with both bi- and tri-allelic models, differed from controls. Furthermore, neither low- nor high-functioning allele frequencies in ED or in BN, in both bi- and triallelic models, differed from control groups. After sensitivity analysis, results were the same in AN vs. controls. Results remained unaltered when investigating recessive and dominant models. Conclusions 5HTTLPR does not seem to be associated with ED in general, or with AN or BN in particular. Future studies in ED should explore the role of ethnicity and psychiatric comorbidity as a possible source of bias.
5-HTTLPR多态性与饮食失调(ED)之间的关系越来越受到关注,但已发表的研究结果却相互矛盾。方法意大利BIO.VE.D.A。生物库提供976份样本(735例ED患者和241例对照组)进行基因分型。我们对截至2015年4月1日发表的研究进行了文献检索,包括报告肥胖和/或ED中5HTTLPR基因型和等位基因频率的研究。我们进行了荟萃分析,包括来自BIO.VE.D.A的数据。-比较ED患者与对照组的低功能和高功能基因型和等位基因频率。数据来自21项研究,外加bio . ve . da。,提供了3736名患者和2707名对照者的信息。无论是双等位基因模型还是三等位基因模型,ED患者的低功能基因型频率和高功能基因型频率与对照组都没有差异。此外,在双等位基因和试验等位基因模型中,ED或BN的低功能和高功能等位基因频率与对照组没有差异。经过敏感性分析,AN组与对照组的结果相同。当研究隐性和显性模型时,结果保持不变。结论5HTTLPR似乎与ED无关,特别是与AN或BN无关。未来的ED研究应该探索种族和精神共病作为可能的偏倚来源的作用。