AI Article Synopsis

  • Chromosome 22q11.2 deletion syndrome (22q11.2DS) is linked to high rates of anxiety and psychosis, influenced by the COMT gene, which regulates important neurotransmitters.
  • A study examined the relationship between COMT gene variations and anxiety as well as stress hormone responses in 30 affected children and adolescents.
  • The findings revealed that those with the active COMTval allele experienced higher anxiety levels, while there was no significant difference in cortisol levels, indicating that COMT variations affect sympathetic stress responses more than hypothalamic ones.

Article Abstract

Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a developmental disorder with high rates of anxiety and psychosis. Catechol-O-methyltransferase (COMT) regulates epinephrine (E), norepinephrine (NE), and dopamine (DA) and is implicated in both anxiety and psychotic disorders. The aim of this study was to determine how COMT variation relates to psychological anxiety and associated stress physiology responsiveness to better understand symptom heterogeneity in people with 22q11.2DS. We examined COMT allelic variation in relation to anxiety and hypothalamic-pituitary-adrenocortical (HPA) and sympathetic-adrenomedullary (SAM) hormonal stress indicators in 30 children and adolescents with 22q11.2DS. Contrary to expectation, individuals with the higher activity COMTval allele had higher anxiety levels versus those with the low activity (COMTmet) allele (p = 0.021; Glass' Δ = 0.69). Anxiety was not correlated with salivary cortisol (CORT) or alpha-amylase (sAA) in either group. Groups did not differ in CORT levels (p = 0.58), but the COMTmet group had higher sAA (p = 0.026; Glass' Δ = 0.67, uncorrected) suggesting greater SAM reactivity but not HPA activity. This suggests that COMT allelic variation may contribute to differences in acute SAM but not slower HPA stress reactivity in those with 22q11.2DS.

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Source
http://dx.doi.org/10.1007/s13353-024-00898-5DOI Listing

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