Psychiatric disorders and SLC6A4 gene variants: possible effects on alcohol dependence and alzheimer’s disease
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 ple...
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Published in | Molecular biology reports Vol. 47; no. 1; pp. 191 - 200 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Dordrecht
Springer Netherlands
01.01.2020
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
ISSN | 0301-4851 1573-4978 1573-4978 |
DOI | 10.1007/s11033-019-05119-5 |
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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 p
d
= 9.25 × 10
−03
, p
r
= 7.24 × 10
−03
; rs2066713 p
d
= 6.35 × 10
−08
; rs25531 p
d
= 2.95 × 10
−02
; rs4251417 p
d
= 2.46 × 10
−03
), and ALZ (rs6354 p
r
= 1.22 × 10
−02
; rs7224199 p
d
= 1.00 × 10
−08
, p
r
= 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. |
---|---|
AbstractList | 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. 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 p d = 9.25 × 10 −03 , p r = 7.24 × 10 −03 ; rs2066713 p d = 6.35 × 10 −08 ; rs25531 p d = 2.95 × 10 −02 ; rs4251417 p d = 2.46 × 10 −03 ), and ALZ (rs6354 p r = 1.22 × 10 −02 ; rs7224199 p d = 1.00 × 10 −08 , p r = 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. 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 p = 9.25 × 10 , p = 7.24 × 10 ; rs2066713 p = 6.35 × 10 ; rs25531 p = 2.95 × 10 ; rs4251417 p = 2.46 × 10 ), and ALZ (rs6354 p = 1.22 × 10 ; rs7224199 p = 1.00 × 10 , p = 2.65 × 10 ) 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. 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. 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.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. |
Author | Politis, Antonis Bellomo, Antonello Ducci, Giuseppe Landi, Stefano Di Nicola, Marco Calabrò, Marco Colombo, Roberto Vieta, Eduard Porcelli, Stefano Papadimitriou, George N. Serretti, Alessandro Frustaci, Alessandra Crisafulli, Concetta Martinotti, Giovanni Mandelli, Laura Albani, Diego Boccia, Stefania Bonassi, Stefano Janiri, Luigi |
Author_xml | – sequence: 1 givenname: Marco surname: Calabrò fullname: Calabrò, Marco organization: Department of Biomedical and Dental Sciences and Morphofunctional Imaging, University of Messina – sequence: 2 givenname: Laura surname: Mandelli fullname: Mandelli, Laura organization: Department of Biomedical and NeuroMotor Sciences, University of Bologna – sequence: 3 givenname: Concetta surname: Crisafulli fullname: Crisafulli, Concetta organization: Department of Biomedical and Dental Sciences and Morphofunctional Imaging, University of Messina – sequence: 4 givenname: Stefano surname: Porcelli fullname: Porcelli, Stefano organization: Department of Biomedical and NeuroMotor Sciences, University of Bologna – sequence: 5 givenname: Diego surname: Albani fullname: Albani, Diego organization: Laboratory of Biology of Neurodegenerative Disorders, Neuroscience Department, Istituto di Ricerche Farmacologiche Mario Negri IRCSS – sequence: 6 givenname: Antonis surname: Politis fullname: Politis, Antonis organization: Department of Psychiatry, University of Athens Medical School, Eginition Hospital – sequence: 7 givenname: George N. surname: Papadimitriou fullname: Papadimitriou, George N. organization: Department of Psychiatry, University of Athens Medical School, Eginition Hospital – sequence: 8 givenname: Marco surname: Di Nicola fullname: Di Nicola, Marco organization: Fondazione Policlinico Universitario “A. Gemelli” - IRCCS, Università Cattolica del Sacro Cuore – sequence: 9 givenname: Luigi surname: Janiri fullname: Janiri, Luigi organization: Fondazione Policlinico Universitario “A. Gemelli” - IRCCS, Università Cattolica del Sacro Cuore – sequence: 10 givenname: Roberto surname: Colombo fullname: Colombo, Roberto organization: Fondazione Policlinico Universitario “A. Gemelli” - IRCCS, Università Cattolica del Sacro Cuore – sequence: 11 givenname: Giovanni surname: Martinotti fullname: Martinotti, Giovanni organization: Department of Neuroscience, Imaging and Clinical Sciences, University “G. d’Annunzio” of Chieti – sequence: 12 givenname: Antonello surname: Bellomo fullname: Bellomo, Antonello organization: Psychiatry Unit, Department of Medical Sciences, University of Foggia – sequence: 13 givenname: Eduard surname: Vieta fullname: Vieta, Eduard organization: Bipolar Disorders Unit, Institute of Neuroscience, Hospital Clínic, University of Barcelona, IDIBAPS, CIBERSAM – sequence: 14 givenname: Stefano surname: Bonassi fullname: Bonassi, Stefano organization: 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 – sequence: 15 givenname: Alessandra surname: Frustaci fullname: Frustaci, Alessandra organization: Barnet, Enfield and Haringey Mental Health NHS Trust, St.Ann’s Hospital – sequence: 16 givenname: Giuseppe surname: Ducci fullname: Ducci, Giuseppe organization: Mental Health Department – sequence: 17 givenname: Stefano surname: Landi fullname: Landi, Stefano organization: Dipartimento di Biologia, Università di Pisa – sequence: 18 givenname: Stefania surname: Boccia fullname: Boccia, Stefania organization: Section of Hygiene, Institute of Public Health, Universita’ Cattolica del Sacro Cuore, Fondazione Policlinico “Agostino Gemelli” IRCCS – sequence: 19 givenname: Alessandro orcidid: 0000-0003-4363-3759 surname: Serretti fullname: Serretti, Alessandro email: alessandro.serretti@unibo.it organization: Department of Biomedical and NeuroMotor Sciences, University of Bologna |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31595439$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1080_10615806_2024_2388850 crossref_primary_10_1016_j_gene_2022_147061 crossref_primary_10_3390_biom11111635 crossref_primary_10_1016_j_neulet_2021_136086 crossref_primary_10_1097_YCO_0000000000000679 crossref_primary_10_1371_journal_pbio_3002642 crossref_primary_10_2139_ssrn_4109815 |
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Keywords | Schizophrenia Genetics Bipolar disorder Alzheimer’s disease Alcohol dependence disorder SLC6A4 |
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Title | Psychiatric disorders and SLC6A4 gene variants: possible effects on alcohol dependence and alzheimer’s disease |
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