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SNAP-25 Polymorphisms in Autism Spectrum Disorder: A Pilot Study towards a Possible Endophenotype.
Mensi, Martina Maria; Guerini, Franca Rosa; Marchesi, Michele; Chiappedi, Matteo; Bolognesi, Elisabetta; Borgatti, Renato.
Afiliação
  • Mensi MM; Child Neuropsychiatry Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.
  • Guerini FR; IRCCS Don Carlo Gnocchi Foundation-ONLUS, 20148 Milan, Italy.
  • Marchesi M; Child Neurology and Psychiatry Unit, ASST Pavia, 27029 Vigevano, Italy.
  • Chiappedi M; Department of Brain and Behavioural Sciences, University of Pavia, 27100 Pavia, Italy.
  • Bolognesi E; IRCCS Don Carlo Gnocchi Foundation-ONLUS, 20148 Milan, Italy.
  • Borgatti R; Child Neuropsychiatry Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.
Pediatr Rep ; 15(4): 766-773, 2023 Dec 18.
Article em En | MEDLINE | ID: mdl-38133436
ABSTRACT
While there is substantial agreement on the diagnostic criteria for autism spectrum disorder, it is also acknowledged that it has a broad range of clinical presentations. This can complicate the diagnostic process and aggravate the choice of the most suitable rehabilitative strategy for each child. Attentional difficulties are among the most frequently reported comorbidities in autism spectrum disorder. We investigated the role of SNAP-25 polymorphisms. Synaptosome-associated protein 25 (SNAP25) is a presynaptic membrane-binding protein; it plays a crucial role in neurotransmission and has already been studied in numerous psychiatric disorders. It was also seen to be associated with hyperactivity in children with autism spectrum disorder. We collected clinical, behavioral and neuropsychological data on 41 children with a diagnosis of autism spectrum disorder, and then genotyped them for five single-nucleotide polymorphisms of SNAP-25. Participants were divided into two groups according to the Autism Diagnostic Observation Schedule (ADOS-2) Severity Score. In the group with the highest severity score, we found significant associations of clinical data with polymorphism rs363050 (A/G) children with the GG genotype had lower total IQ, more severe autistic functioning and more attentional difficulties. Our research could be the starting point for outlining a possible endophenotype among patients with autism spectrum disorder who are clinically characterized by severe autistic functioning and significant attentional difficulties.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Pediatr Rep Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Pediatr Rep Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália