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Association Between Cerebral Hypoperfusion and Cognitive Impairment in Patients With Chronic Vertebra-Basilar
Yiming Deng1,2,3, Luyao Wang4, Xuan Sun1,2,3
1Department of Interventional Neuroradiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Insights
Chronic vertebra-basilar (VB) stenosis leads to cognitive impairment due to reduced cerebral blood flow. Reduced perfusion in the posterior circulation significantly impacts memory and executive functions.
Area of Science:
- Neurology
- Neuroimaging
- Cognitive Neuroscience
Background:
- Chronic vertebra-basilar (VB) stenosis is a significant risk factor for cerebrovascular events.
- Cognitive impairment is a common complication in patients with VB stenosis.
- Cerebral haemodynamic changes play a crucial role in cognitive function.
Purpose of the Study:
- To investigate the association between cognitive impairment and cerebral haemodynamic changes in patients with severe VB stenosis.
- To identify specific cognitive deficits related to different levels of cerebral perfusion.
- To determine independent risk factors for cognitive impairment in this patient population.
Main Methods:
- A cohort of 96 patients with severe posterior circulation VB stenosis was divided into three groups based on computed tomography perfusion (CTP) status: normal, compensated, and decompensated.
- Cognitive function was assessed using the Mini-Mental State Examination (MMSE), Frontal Assessment Battery (FAB), and Repeatable Battery for the Assessment of Neuropsychological Status (RBANS).
- Multiple regression analyses were performed to identify independent risk factors for cognitive impairment.
Main Results:
- Patients in the CTP decompensated group showed significantly lower MMSE and FAB scores compared to the CTP normal and compensated groups.
- RBANS scores, including immediate memory, visual acuity, and delayed memory, were significantly lower in both CTP compensated and decompensated groups compared to the CTP normal group.
- CTP compensation, CTP decompensation, severe VB tandem stenosis, and multiple infarctions were identified as independent risk factors for cognitive impairment.
Conclusions:
- Low cerebral perfusion resulting from severe VB stenosis is associated with extensive cognitive impairments.
- Specific cognitive domains affected include immediate memory, visual span, and delayed memory.
- Cerebral haemodynamic status is a critical determinant of cognitive function in patients with VB stenosis.
Abstract:
Objective: This study aimed to investigate the association between cognitive impairment and cerebral haemodynamic changes in patients with chronic vertebra-basilar (VB) stenosis. Methods: Patients with severe posterior circulation VB stenosis and infarction or a history of infarction for more than 2 weeks from January 2014 to January 2015 were enrolled (n = 96). They were divided into three groups, namely, the computed tomography perfusion (CTP) normal group, the CTP compensated group, and the CTP decompensated group. Cognitive function was assessed using a validated Chinese version of the Mini-Mental State Examination (MMSE), the Frontal Assessment Battery (FAB), and the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS). Regression models were used to identify independent risk factors for cognitive impairment. Results: The MMSE and FAB scores of patients in the CTP decompensated group were significantly lower than those of patients in the CTP normal and CTP compensated groups (all p < 0.05). The RBANS total and its domain scores, including immediate memory, visual acuity, and delayed memory, in the CTP compensated and CTP decompensated groups were significantly lower than those in the CTP normal group (all p < 0.05). Multiple regression analyses showed that CTP compensation, CTP decompensation, severe VB tandem stenosis, and multiple infarctions were independent risk factors for cognitive impairment. Conclusions: Low perfusion caused by severe VB stenosis can lead to extensive cognitive impairments in areas such as immediate memory, visual span, and delayed memory.
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