AI Article Synopsis

  • Cerebral infarcts in older adults can lead to cognitive impairment, and this study evaluates the use of quantitative electroencephalography (qEEG) as a predictive tool for this risk.
  • The research involved EEG recordings and cognitive assessments over time, focusing on various brain wave patterns, particularly background rhythm frequency (BRF) and θ band power.
  • Results indicated that low BRF significantly increases the likelihood of cognitive impairment, alongside elevated θ band power, suggesting these qEEG measures could serve as early indicators for cognitive decline in patients with cerebral infarcts.

Article Abstract

In clinical settings, cerebral infarct is a common disease of older adults, which usually increases the risk of cognitive impairment. This study aims to assess the quantitative electroencephalography (qEEG) as a predictive biomarker for the development of cognitive impairment, post-cerebral infarcts, in subjects from the Department of Neurology. They underwent biennial EEG recording. Cerebral infarct subjects, with follow-up cognitive evaluation, were analyzed for qEEG measures of background rhythm frequency (BRF) and relative δ, θ, α, and β band power. The relationship between cognitive impairment and qEEG, and other possible predictors, was assessed by Cox regression. The results showed that the risk hazard of developing cognitive impairment was 14 times higher for those with low BRF than for those with high BRF (P < .001). Hazard ratio (HR) was also significant for more than median θ band power (HR = 5, P = .002) compared with less than median θ band power. The HRs for δ, α, and β bands were equal to the baseline demographic, and clinical characteristics were not significantly different. In conclusion, qEEG measures of BRF, and relative power in θ band, are potential predictive biomarkers for cognitive impairment in patients with cerebral infarcts. These biomarkers might be valuable in early prediction of cognitive impairment in patients with cerebral infarcts.

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Source
http://dx.doi.org/10.1177/1550059413517492DOI Listing

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