Solmi M, Gallicchio D, Collantoni E, Correll C U, Clementi M, Pinato C, Forzan M, Cassina M, Fontana F, Giannunzio V, Piva I, Siani R, Salvo P, Santonastaso P, Tenconi E, Veronese N, Favaro A
a BIO.VE.D.A. Group (BIObanca VEneta per I Disturbi Dell'alimentazione: Biobank of the Veneto Region Eating Disorders Units) , Veneto Region , Italy ;
g Department of Neuroscience , University of Padova , Italy ;
World J Biol Psychiatry. 2016 Jun;17(4):244-57. doi: 10.3109/15622975.2015.1126675. Epub 2016 Feb 19.
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.
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.
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.
目的 越来越多的人关注5-羟色胺转运体基因启动子区域(5-HTTLPR)多态性与饮食失调(ED)之间的关联,但已发表的研究结果相互矛盾。方法 意大利BIO.VE.D.A.生物样本库提供了976份样本(735例ED患者和241例对照)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。我们进行了一项荟萃分析,纳入了来自BIO.VE.D.A.的数据——比较ED患者与对照组中低功能和高功能基因型及等位基因频率。
结果 提取了21项研究以及BIO.VE.D.A.的数据,提供了来自3736例患者和2707例对照的信息。在双等位基因和三等位基因模型中,ED患者的低功能和高功能基因型频率与对照组均无差异。此外,在双等位基因和三等位基因模型中,ED或神经性贪食症(BN)患者的低功能和高功能等位基因频率与对照组也无差异。敏感性分析后,神经性厌食症(AN)患者与对照组的结果相同。
在研究隐性和显性模型时,结果保持不变。结论 一般而言,5-HTTLPR似乎与ED无关,尤其与AN或BN无关。未来关于ED的研究应探讨种族和精神共病作为可能偏倚来源的作用。