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Psychiatric disorders and SLC6A4 gene variants: possible effects on alcohol dependence and alzheimer's disease.
Calabrò, Marco; Mandelli, Laura; Crisafulli, Concetta; Porcelli, Stefano; Albani, Diego; Politis, Antonis; Papadimitriou, George N; Di Nicola, Marco; Janiri, Luigi; Colombo, Roberto; Martinotti, Giovanni; Bellomo, Antonello; Vieta, Eduard; Bonassi, Stefano; Frustaci, Alessandra; Ducci, Giuseppe; Landi, Stefano; Boccia, Stefania; Serretti, Alessandro.
Afiliação
  • Calabrò M; Department of Biomedical and Dental Sciences and Morphofunctional Imaging, University of Messina, Messina, Italy.
  • Mandelli L; Department of Biomedical and NeuroMotor Sciences, University of Bologna, Viale Carlo Pepoli 5, 40123, Bologna, Italy.
  • Crisafulli C; Department of Biomedical and Dental Sciences and Morphofunctional Imaging, University of Messina, Messina, Italy.
  • Porcelli S; Department of Biomedical and NeuroMotor Sciences, University of Bologna, Viale Carlo Pepoli 5, 40123, Bologna, Italy.
  • Albani D; Laboratory of Biology of Neurodegenerative Disorders, Neuroscience Department, Istituto di Ricerche Farmacologiche Mario Negri IRCSS, Milan, Italy.
  • Politis A; Department of Psychiatry, University of Athens Medical School, Eginition Hospital, Athens, Greece.
  • Papadimitriou GN; Department of Psychiatry, University of Athens Medical School, Eginition Hospital, Athens, Greece.
  • Di Nicola M; Fondazione Policlinico Universitario "A. Gemelli" - IRCCS, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Janiri L; Fondazione Policlinico Universitario "A. Gemelli" - IRCCS, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Colombo R; Fondazione Policlinico Universitario "A. Gemelli" - IRCCS, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Martinotti G; Department of Neuroscience, Imaging and Clinical Sciences, University "G. d'Annunzio" of Chieti, Chieti, Italy.
  • Bellomo A; Psychiatry Unit, Department of Medical Sciences, University of Foggia, Foggia, Italy.
  • Vieta E; Bipolar Disorders Unit, Institute of Neuroscience, Hospital Clínic, University of Barcelona, IDIBAPS, CIBERSAM, Barcelona, Catalonia, Spain.
  • Bonassi S; Unit of Clinical and Molecular Epidemiology, IRCCS San Raffaele Pisana, Rome, Italy, and Department of Human Sciences and Quality of Life Promotion, San Raffaele University, Rome, Italy.
  • Frustaci A; Barnet, Enfield and Haringey Mental Health NHS Trust, St.Ann's Hospital, St.Ann's Road, London, N15 3 TH, UK.
  • Ducci G; Mental Health Department, ASL Roma 1, Rome, Italy.
  • Landi S; Dipartimento di Biologia, Università di Pisa, Pisa, Italy.
  • Boccia S; Section of Hygiene, Institute of Public Health, Universita' Cattolica del Sacro Cuore, Fondazione Policlinico "Agostino Gemelli" IRCCS, Rome, Italy.
  • Serretti A; Department of Biomedical and NeuroMotor Sciences, University of Bologna, Viale Carlo Pepoli 5, 40123, Bologna, Italy. alessandro.serretti@unibo.it.
Mol Biol Rep ; 47(1): 191-200, 2020 Jan.
Article em En | MEDLINE | ID: mdl-31595439
ABSTRACT
Serotoninergic system is one of the most important neurotransmission systems investigated in the field of psychiatry. Extensive evidence reveals how alterations of this system, and especially of the SLC6A4 gene, may be associated with psychiatric disorders. In this study we aimed to evaluate the pleiotropic nature of SLC6A4 alterations and their association with the overall risk of brain diseases rather than disorder-specific. SLC6A4 variants, namely 5HTTLPR, STin2, rs2066713, rs25531, rs4251417, rs6354 and rs7224199 were investigated in 4 independent cohorts of subjects with specific psychiatric disorders, including Alcohol dependence disorder (ALC), Alzheimer disease (ALZ), Schizophrenia (SCZ) and Bipolar disorder (BPD). Other variables (biochemical parameters and Psychiatric scales scores) were also tested for association. SLC6A4 polymorphisms are not associated with the risk of developing major psychiatric disorders (SCZ and BPD); however some signals were detected in ALC (HTTLPR pd = 9.25 × 10-03, pr = 7.24 × 10-03; rs2066713 pd = 6.35 × 10-08; rs25531 pd = 2.95 × 10-02; rs4251417 pd = 2.46 × 10-03), and ALZ (rs6354 pr = 1.22 × 10-02; rs7224199 pd = 1.00 × 10-08, pr = 2.65 × 10-02) cohorts. Some associations were also observed on exploratory analyses. Our findings did not reveal any major influence on SCZ and BPD development; On the other hand, some alteration of the SLC6A4 sequence were associated with an increased risk of ALC and ALZ disorders, suggesting common pathways. The results of this study should be carefully interpreted since it suffers of some inherent limitations (e.g. cohort size, slight ethnic heterogeneity). Further analyses may provide better detail on the molecular processes behind SLC6A4 alterations.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Alcoolismo / Proteínas da Membrana Plasmática de Transporte de Serotonina / Doença de Alzheimer / Transtornos Mentais Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Humans / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Alcoolismo / Proteínas da Membrana Plasmática de Transporte de Serotonina / Doença de Alzheimer / Transtornos Mentais Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Humans / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2020 Tipo de documento: Article