Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/133093
Title: A systematic review and secondary data analysis of the interactions between the serotonin transporter 5-HTTLPR polymorphism and environmental and psychological factors in eating disorders
Author: Rozenblat, Vanja
Ong, Deborah
Fuller-Tyszkiewicz, Matthew
Akkermann, Kirsti
Collier, David
Engels, Rutger C. M. E.
Fernández Aranda, Fernando
Harro, Jaanus
Homberg, Judith R.
Karwautz, Andreas
Kiive, Evelyn
Klump, Kelly L.
Larson, Christine L.
Racine, Sarah E.
Richardson, Jodie
Steiger, Howard
Stoltenberg, Scott F.
Van Strien, Tatjana
Wagner, Gudrun
Treasure, Janet
Krug, Isabel
Keywords: Bulímia
Trastorns de la conducta alimentària
Metaanàlisi
Ressenyes sistemàtiques (Investigació mèdica)
Bulimia
Eating disorders
Meta-analysis
Systematic reviews (Medical research)
Issue Date: Jan-2017
Publisher: Elsevier Ltd
Abstract: Objectives: to summarize and synthesize the growing gene x environment (GxE) research investigating the promoter region of the serotonin transporter gene (5-HTTLPR) in the eating disorders (ED) field, and overcome the common limitation of low sample size, by undertaking a systematic review followed by a secondary data meta-analysis of studies identified by the review. Method: a systematic review of articles using PsycINFO, PubMed, and EMBASE was undertaken to identify studies investigating the interaction between 5-HTTLPR and an environmental or psychological factor, with an ED-related outcome variable. Seven studies were identified by the systematic review, with complete data sets of five community (n = 1750, 64.5% female) and two clinical (n = 426,100% female) samples combined to perform four secondary-data analyses: 5-I-M1PR x Traumatic Life Events to predict ED status (n = 909), 5-HTTLPR x Sexual and Physical Abuse to predict bulimic symptoms (n = 1097), 5-HTTLPR x Depression to predict bulimic symptoms (n = 1256), and 5-HTTLPRx Impulsiveness to predict disordered eating (n = 1149). Results: under a multiplicative model, the low function (s) allele of 5-HTTLPR interacted with traumatic life events and experiencing both sexual and physical abuse (but not only one) to predict increased likelihood of an ED and bulimic symptoms, respectively. However, under an additive model there was also an interaction between sexual and physical abuse considered independently and 5-HTTLPR, and no interaction with traumatic life events. No other GxE interactions were significant. Conclusion: early promising results should be followed-up with continued cross-institutional collaboration in order to achieve the large sample sizes necessary for genetic research.
Note: Versió postprint del document publicat a: https://doi.org/10.1016/j.jpsychires.2016.09.023
It is part of: Journal of Psychiatric Research, 2017, vol. 84, p. 62-72
URI: http://hdl.handle.net/2445/133093
Related resource: https://doi.org/10.1016/j.jpsychires.2016.09.023
ISSN: 0022-3956
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Articles publicats en revistes (Ciències Clíniques)

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