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RESEARCH PRODUCT
Serotonin transporter gene polymorphism in eating disorders: Data from a new biobank and META-analysis of previous studies.
Marco SolmiDavide GallicchioPierandrea SalvoF. FontanaMonica ForzanChristoph U. CorrellPaolo SantonastasoClaudia PinatoMatteo CassinaValeria GiannunzioR. SianiEnrico CollantoniElena TenconiNicola VeroneseI. PivaMaurizio ClementiAngela Favarosubject
medicine.medical_specialtyAnorexia Nervosa5-HTTLPR; anorexia nervosa; binge eating; bulimia nervosa; Eating disorders; Biological Psychiatry; Psychiatry and Mental Health5-HTTLPR03 medical and health sciences0302 clinical medicinebinge eatingGene FrequencymedicineHumansGenetic Predisposition to DiseaseObesityPsychiatryBulimia NervosaBiological PsychiatrySerotonin transporterBiological Specimen BanksSerotonin Plasma Membrane Transport ProteinsPolymorphism GeneticbiologyBinge eatingBulimia nervosaEating disordermedicine.diseaseBiobank030227 psychiatryPsychiatry and Mental healthEating disordersMeta-analysis5-HTTLPREating disordersbiology.proteinGene polymorphismmedicine.symptomPsychology030217 neurology & neurosurgerydescription
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. © 2016 Informa UK Limited, trading as Taylor & Francis Group.
year | journal | country | edition | language |
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2016-01-01 | The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry |