AI Article Synopsis

  • Delirium can lead to long-term brain problems, and the study looked at specific brain markers related to both delirium and dementia.
  • Researchers studied 35 people with ongoing delirium and compared them to 20 people with dementia to see how their brain markers were different.
  • The findings showed that certain brain markers were higher in people with persistent delirium, suggesting that this condition affects the brain in specific ways even if someone has dementia too.

Article Abstract

Delirium is associated with the risk of future long-term cognitive impairment, but the degree to which markers of neuronal injury may be distinct or shared with dementia has yet to be comprehensively described. We investigated CSF biomarkers of dementia, astrocytosis and neuronal damage in a clinical cohort with persistent delirium, comparing them with an outpatient memory clinic sample. Our aim was to determine if different patterns of biomarker changes could implicate specific mechanisms for delirium-related neuronal injury over and above that attributable to comorbid dementia. We recruited 35 participants from the Prince of Wales Hospital, Sydney, Australia. We included inpatients with delirium persisting for at least 5 days ( = 15, 10 with underlying dementia) and participants from outpatient memory clinics ( = 20, 17 with dementia). CSF assays were as follows: amyloid-β, amyloid-β, phosphorylated tau181, neurofilament light chain and glial fibrillary acidic protein. We used propensity score matching to estimate effect sizes for each standardized CSF biomarker separately for persistent delirium (irrespective of underlying dementia) and dementia (irrespective of superimposed delirium). Compared with individuals without delirium, persistent delirium was associated with elevated glial fibrillary acidic protein (normalized coefficient per transformed standard deviation, = 0.85; 95% confidence interval: 0.03-1.68) and neurofilament light chain ( = 1.1; 95% confidence interval: 0.5-1.6), but not phosphorylated tau181. Compared with individuals without dementia, glial fibrillary acidic protein, neurofilament light chain and phosphorylated tau181 were all increased to expected levels in dementia cases, with the former two biomarkers at levels comparable to those seen in persistent delirium [glial fibrillary acidic protein ( = 1.54; 95% confidence interval: 1.05-2.0) and neurofilament light chain ( = 0.65; 95% confidence interval: 0.24-1.1)]. Persistent delirium was linked with changes in CSF biomarkers not necessarily attributable to dementia. These findings support the potential that delirium is associated with direct neuronal injury independent of dementia pathophysiology. Whether this neuronal injury involves astrocyte dysfunction or direct axonal damage are both possibilities. Future work examining acute brain injury in delirium is needed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11443447PMC
http://dx.doi.org/10.1093/braincomms/fcae319DOI Listing

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