Transient peripheral blood transcriptomic response to ketamine treatment in children with ADNP syndrome.
Ariela S Buxbaum GriceLaura SloofmanTess LevyHannah WalkerGauri GaneshMiguel Rodriguez de Los SantosPardis AminiJoseph D BuxbaumAlexander KolevzonAna KosticMichael S BreenPublished in: Translational psychiatry (2024)
Activity-dependent neuroprotective protein (ADNP) syndrome is a rare neurodevelopmental disorder resulting in intellectual disability, developmental delay and autism spectrum disorder (ASD) and is due to mutations in the ADNP gene. Ketamine treatment has emerged as a promising therapeutic option for ADNP syndrome, showing safety and apparent behavioral improvements in a first open label study. However, the molecular perturbations induced by ketamine remain poorly understood. Here, we investigated the longitudinal effect of ketamine on the blood transcriptome of 10 individuals with ADNP syndrome. Transcriptomic profiling was performed before and at multiple time points after a single low-dose intravenous ketamine infusion (0.5 mg/kg). We show that ketamine triggers immediate and profound gene expression alterations, with specific enrichment of monocyte-related expression patterns. These acute alterations encompass diverse signaling pathways and co-expression networks, implicating upregulation of immune and inflammatory-related processes and down-regulation of RNA processing mechanisms and metabolism. Notably, these changes exhibit a transient nature, returning to baseline levels 24 hours to 1 week after treatment. These findings enhance our understanding of ketamine's molecular effects and lay the groundwork for further research elucidating its specific cellular and molecular targets. Moreover, they contribute to the development of therapeutic strategies for ADNP syndrome and potentially, ASD more broadly.
Keyphrases
- autism spectrum disorder
- intellectual disability
- gene expression
- pain management
- low dose
- peripheral blood
- poor prognosis
- single cell
- case report
- open label
- attention deficit hyperactivity disorder
- rna seq
- magnetic resonance imaging
- signaling pathway
- clinical trial
- binding protein
- dna methylation
- computed tomography
- oxidative stress
- squamous cell carcinoma
- cerebral ischemia
- genome wide
- randomized controlled trial
- magnetic resonance
- study protocol
- small molecule
- brain injury
- extracorporeal membrane oxygenation
- single molecule
- amino acid
- liver failure
- smoking cessation
- locally advanced
- congenital heart disease
- phase iii
- mass spectrometry
- diffusion weighted imaging
- immune response
- double blind