• Media type: E-Article
  • Title: Autism spectrum disorder and GABA levels in children with succinic semialdehyde dehydrogenase deficiency
  • Contributor: Tokatly Latzer, Itay; Hanson, Ellen; Bertoldi, Mariarita; García‐Cazorla, Àngeles; Tsuboyama, Melissa; MacMullin, Paul; Rotenberg, Alexander; Roullet, Jean‐Baptiste; Pearl, Phillip L.
  • Published: Wiley, 2023
  • Published in: Developmental Medicine & Child Neurology, 65 (2023) 12, Seite 1596-1606
  • Language: English
  • DOI: 10.1111/dmcn.15659
  • ISSN: 0012-1622; 1469-8749
  • Origination:
  • Footnote:
  • Description: AbstractAimTo elucidate the etiological aspects of autism spectrum disorder (ASD) in succinic semialdehyde dehydrogenase deficiency (SSADHD), related to dysregulation of γ‐aminobutyric acid (GABA) and the imbalance of excitatory and inhibitory neurotransmission.MethodIn this prospective, international study, individuals with SSADHD underwent neuropsychological assessments, as well as biochemical, neurophysiological, and neuroimaging evaluations.ResultsOf the 29 individuals (17 females) enrolled (median age [IQR] 10 years 5 months [5 years 11 months–18 years 1 month]), 16 were diagnosed with ASD. ASD severity significantly increased with age (r = 0.67, p < 0.001) but was inversely correlated with plasma GABA (r = −0.67, p < 0.001) and γ‐hydroxybutyrate levels (r = −0.538, p = 0.004), and resting motor threshold as measured by transcranial magnetic stimulation (r = −0.44, p = 0.03). A discriminative analysis indicated that an age older than 7 years 2 months (p = 0.004) and plasma GABA levels less than 2.47 μM (p = 0.01) are the threshold values beyond which the likelihood of ASD presenting in individuals with SSADHD is increased.InterpretationASD is prevalent but not universal in SSADHD, and it can be predicted by lower levels of plasma GABA and GABA‐related metabolites. ASD severity in SSADHD increases with age and the loss of cortical inhibition. These findings add insight into the pathophysiology of ASD and may facilitate its early diagnosis and intervention in individuals with SSADHD.