Literature DB >> 19281802

Influence of the 5-HTTLPR polymorphism and environmental risk factors in a Brazilian sample of patients with autism spectrum disorders.

Dânae Longo1, Lavínia Schüler-Faccini, Ana Paula Carneiro Brandalize, Rudimar dos Santos Riesgo, Claiton Henrique Dotto Bau.   

Abstract

The 5-HTTLPR polymorphism of serotonin transporter gene is widely investigated in association studies in autism spectrum disorders (ASD). The results of such studies, however, remain controversial possibly due to the great genetic heterogeneity related to ASD and the lack of evaluation of the triallelic functional structure of 5-HTTLPR. This study tested for association between the 5-HTTLPR and ASD in a Brazilian sample by case-control and family-based association test (FBAT) methods, considering the biallelic and triallelic structures of this polymorphism. In addition, we performed an exploratory analysis of associations between specific clinical outcomes of ASD patients and 5-HTTLPR as well as several prenatal environmental factors. Genotyping was achieved in 151 ASD patients, 179 unrelated controls and 105 complete trios. There was no evidence of association between the 5-HTTLPR with ASD in both case-control and FBAT tests, but the LaLa 5-HTTLPR genotype was associated with mood instability in patients (P=0.006). The prenatal exposure to potential neuroteratogenic drugs was associated with epilepsy (P<0.001). Our findings suggest that the 5-HTTLPR is not associated with ASD in the Brazilian population, even considering the triallelic structure. Additionally, this study suggested a role of the 5-HTTLPR and environmental factors in the clinical expression of ASD.

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Year:  2009        PMID: 19281802     DOI: 10.1016/j.brainres.2009.02.072

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  5 in total

1.  Altered Global mRNA Expressions of Pain and Aggression Related Genes in the Blood of Children with Autism Spectrum Disorders.

Authors:  Elif Funda Sener; Serpil Taheri; Mustafa Caglar Sahin; Keziban Korkmaz Bayramov; Mert Kahraman Marasli; Gokmen Zararsiz; Ecmel Mehmetbeyoglu; Didem Behice Oztop; Mehmet Canpolat; Halit Canatan; Yusuf Ozkul
Journal:  J Mol Neurosci       Date:  2018-12-05       Impact factor: 3.444

2.  Evidence for Association Between OXTR Gene and ASD Clinical Phenotypes.

Authors:  Lucas de Oliveira Pereira Ribeiro; Pedro Vargas-Pinilla; Djenifer B Kappel; Danae Longo; Josiane Ranzan; Michele Michelin Becker; Rudimar Dos Santos Riesgo; Lavinia Schuler-Faccini; Tatiana Roman; Jaqueline Bohrer Schuch
Journal:  J Mol Neurosci       Date:  2018-06-01       Impact factor: 3.444

3.  ADGRL3 rs6551665 as a Common Vulnerability Factor Underlying Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder.

Authors:  Djenifer B Kappel; Jaqueline B Schuch; Diego L Rovaris; Bruna S da Silva; Diana Müller; Vitor Breda; Stefania P Teche; Rudimar S Riesgo; Lavínia Schüler-Faccini; Luís A Rohde; Eugenio H Grevet; Claiton H D Bau
Journal:  Neuromolecular Med       Date:  2019-01-16       Impact factor: 3.843

4.  Parent-of-origin effects of the serotonin transporter gene associated with autism.

Authors:  Emily Kistner-Griffin; Camille W Brune; Lea K Davis; James S Sutcliffe; Nancy J Cox; Edwin H Cook
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2010-12-08       Impact factor: 3.568

5.  The role of 5-HTTLPR in autism spectrum disorder: New evidence and a meta-analysis of this polymorphism in Latin American population with psychiatric disorders.

Authors:  D L Nuñez-Rios; R Chaskel; A Lopez; L Galeano; M C Lattig
Journal:  PLoS One       Date:  2020-07-02       Impact factor: 3.240

  5 in total

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