Decreased cerebral blood flow velocity in apolipoprotein E epsilon4 allele carriers with mild cognitive impairment

Z-W Sun1, Y-X Zhu, H-Y Liu

  • 1Department of Neurology, Anhui Geriatric Institute, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.

Insights

Mild cognitive impairment (MCI) is linked to reduced cerebral blood flow velocity (CBFV). Apolipoprotein E (apoE) epsilon4 carriers with MCI exhibit even lower CBFV, suggesting potential for early Alzheimer's disease detection.

Area of Science:

  • Neurology
  • Neuroscience
  • Medical Imaging

Background:

  • Mild cognitive impairment (MCI) represents a transitional stage between normal aging and dementia.
  • Cerebral blood flow velocity (CBFV) is a crucial indicator of brain perfusion and vascular health.
  • The apolipoprotein E (apoE) epsilon4 allele is a known genetic risk factor for Alzheimer's disease.

Purpose of the Study:

  • To investigate alterations in CBFV in individuals with MCI.
  • To examine the association between the apoE epsilon4 allele and CBFV in MCI patients.
  • To explore the potential of CBFV as a biomarker for early detection of cognitive decline.

Main Methods:

  • Transcranial Doppler ultrasonography was used to measure CBFV in the anterior (ACA), middle (MCA), and basilar (BA) cerebral arteries.
  • Participants included 30 individuals with MCI and 30 healthy controls.
  • Cognitive function was assessed using the Mini-Mental State Examination (MMSE) and Cambridge Cognitive Examination-Chinese version (CAMCOG-C).

Main Results:

  • MCI patients demonstrated significantly reduced mean (V(m)), systolic (V(s)), and diastolic (V(d)) CBFV in the bilateral MCA and ACA compared to controls.
  • No significant differences in CBFV were observed in the BA between groups.
  • Within the MCI group, apoE epsilon4 allele carriers showed significantly lower CBFV in the bilateral MCA compared to non-carriers.

Conclusions:

  • Reduced CBFV in the cerebral arteries is associated with MCI.
  • The presence of the apoE epsilon4 allele exacerbates CBFV reduction in individuals with MCI.
  • Longitudinal studies tracking CBFV and cognitive changes are warranted for potential early diagnosis of Alzheimer's disease.

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