Vascular risk factors and the relationships between cognitive impairment and hypoperfusion in late-onset Alzheimer's disease

Acta Neuropsychiatr. 2018 Dec;30(6):350-358. doi: 10.1017/neu.2018.17. Epub 2018 Aug 22.

Abstract

Objective: Our recent single-photon emission computed tomography (SPECT) study of patients with late-onset Alzheimer's disease (AD) revealed that regional cerebral blood flow (rCBF) was reduced in the frontal, temporal, and limbic lobes, and to a lesser degree in the parietal and occipital lobes. Moreover, these patients' scores on the Alzheimer's Disease Assessment Scale-cognitive subscale (ADAS-cog) were significantly correlated with rCBF in some gyri of the frontal, parietal, and limbic lobes. Our present study aimed to understand how vascular factors and metabolic disease influenced the relationship between rCBF and ADAS-cog scores.

Methods: We divided late-onset AD patients into two groups according to their Hachinski Ischemic Score (HIS), low vascular risk patients had values of ≤4 (n=25) and high vascular risk patients had scores ≥5 (n=15). We examined rCBF using brain perfusion SPECT data.

Results: The degrees and patterns of reduced rCBF were largely similar between late-onset AD patients in both groups, regardless of HIS values. Cognitive function was significantly associated with rCBF among late-onset AD patients with low vascular risk (HIS≤4), but not among those with high vascular risk (HIS≥5). Furthermore, metabolic diseases, such as hypertension and diabetes mellitus, disrupted the relationships between hypoperfusion and cognitive impairments in late-onset AD patients.

Conclusion: Factors other than hypoperfusion, such as hypertension and diabetes mellitus, could be involved in the cognitive dysfunction of late-onset AD patients with high vascular risk.

Keywords: SPECT; cognitive function; dementia; metabolic disease.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / complications
  • Alzheimer Disease / diagnostic imaging
  • Alzheimer Disease / physiopathology*
  • Alzheimer Disease / psychology*
  • Brain / blood supply*
  • Brain / diagnostic imaging
  • Brain / physiopathology*
  • Cognitive Dysfunction / etiology
  • Female
  • Humans
  • Male
  • Neuropsychological Tests
  • Risk Factors
  • Tomography, Emission-Computed, Single-Photon