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Catechol-O-Methyltransferase (COMT) Val158Met Polymorphism and Eating Disorders: Data From a New Biobank and Meta-Analysis of Previously Published Studies.
Collantoni, Enrico; Solmi, Marco; Gallicchio, Davide; Santonastaso, Paolo; Meneguzzo, Paolo; Carvalho, Andrè F; Stubbs, Brendon; Clementi, Maurizio; Pinato, Claudia; Forzan, Monica; Cassina, Matteo; Fontana, Francesca; Piva, Ivana; Siani, Roberta; Salvo, Pierandrea; Tenconi, Elena; Veronese, Nicola; Correll, Christoph U; Favaro, Angela.
Afiliação
  • Collantoni E; Neuroscience Department, University of Padua, Italy.
  • Solmi M; BIO.VEDA Group (Biobanca Veneta per i Disturbi dell'Alimentazione: Biobank of the Veneto Region Eating Disorders Units), Italy.
  • Gallicchio D; Neuroscience Department, University of Padua, Italy.
  • Santonastaso P; BIO.VEDA Group (Biobanca Veneta per i Disturbi dell'Alimentazione: Biobank of the Veneto Region Eating Disorders Units), Italy.
  • Meneguzzo P; Neuroscience Department, University of Padua, Italy.
  • Carvalho AF; BIO.VEDA Group (Biobanca Veneta per i Disturbi dell'Alimentazione: Biobank of the Veneto Region Eating Disorders Units), Italy.
  • Stubbs B; Neuroscience Department, University of Padua, Italy.
  • Clementi M; BIO.VEDA Group (Biobanca Veneta per i Disturbi dell'Alimentazione: Biobank of the Veneto Region Eating Disorders Units), Italy.
  • Pinato C; Centro Neuroscienze Cognitive (CNC), University of Padua, Italy.
  • Forzan M; Neuroscience Department, University of Padua, Italy.
  • Cassina M; BIO.VEDA Group (Biobanca Veneta per i Disturbi dell'Alimentazione: Biobank of the Veneto Region Eating Disorders Units), Italy.
  • Fontana F; Translational Psychiatry Research Group, Department of Clinical Medicine, Faculty of Medicine, Federal University of Ceará, Brazil.
  • Piva I; Health Service and Population Research Department, Institute of Psychiatry, Psychology and Neuroscience, King's College London, UK.
  • Siani R; Physiotherapy Department, South London and Maudsley NHS Foundation Trust, UK.
  • Salvo P; Faculty of Health, Social Care and Education, Anglia Ruskin University, UK.
  • Tenconi E; Clinical Genetics Unit, Department of Woman and Child Health, University of Padua, Italy.
  • Veronese N; Clinical Genetics Unit, Department of Woman and Child Health, University of Padua, Italy.
  • Correll CU; Clinical Genetics Unit, Department of Woman and Child Health, University of Padua, Italy.
  • Favaro A; Clinical Genetics Unit, Department of Woman and Child Health, University of Padua, Italy.
Eur Eat Disord Rev ; 25(6): 524-532, 2017 11.
Article em En | MEDLINE | ID: mdl-29057600
ABSTRACT

OBJECTIVES:

We investigated whether catechol-O-methyltransferase (COMT) Val158Met polymorphism is associated with eating disorders (EDs).

METHODS:

We conducted a systematic literature search of studies published until 15 January 2017 and added data from the Italian 'Biobanca Veneta per i Disturbi Alimentari' biobank, performing a meta-analysis comparing COMT Val158Met genotype and allele frequencies in EDs and anorexia nervosa (AN) or bulimia nervosa (BN) patients versus controls.

RESULTS:

Ten studies plus Biobanca Veneta per i Disturbi Alimentari (ED n = 920, controls n = 261 controls) with 3541 ED patients (AN = 2388; BN = 233) and 3684 controls were included. 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) 0.96-1.04, p-values 0.46-0.97, I2 = 0%] and when analysing separately patients with AN (ORs 0.94-1.04, p-values 0.31-0.61, I2 = 0%) or BN (ORs 0.80-1.09, p-values 0.28-0.64, I2 = 0-44%).

CONCLUSIONS:

Meta-analysing data results from 11 studies and 7225 subjects show that COMT Val158Met polymorphism is not associated with EDs. Copyright © 2017 John Wiley & Sons, Ltd and Eating Disorders Association.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Catecol O-Metiltransferase / Transtornos da Alimentação e da Ingestão de Alimentos / Polimorfismo de Nucleotídeo Único Tipo de estudo: Observational_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Catecol O-Metiltransferase / Transtornos da Alimentação e da Ingestão de Alimentos / Polimorfismo de Nucleotídeo Único Tipo de estudo: Observational_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article