Key result
Better dynamic cerebral autoregulation is linked to less brain atrophy and better functional recovery after stroke.
Observational (n=142)
p-value: p=0.029, 0.018, 0.002
Dynamic cerebral autoregulation (dCA) is impaired following stroke. However, the relationship between dCA, brain atrophy, and functional outcomes following stroke remains unclear. In this study, we aimed to determine whether impairment of dCA is associated with atrophy in specific regions or globally, thereby affecting daily functions in stroke patients.We performed a retrospective analysis of 33 subjects with chronic infarctions in the middle cerebral artery territory, and 109 age-matched non-stroke subjects. dCA was assessed via the phase relationship between arterial blood pressure and cerebral blood flow velocity. Brain tissue volumes were quantified from MRI. Functional status was assessed by gait speed, instrumental activities of daily living (IADL), modified Rankin Scale, and NIH Stroke Score.Compared to the non-stroke group, stroke subjects showed degraded dCA bilaterally, and showed gray matter atrophy in the frontal, parietal and temporal lobes ipsilateral to infarct. In stroke subjects, better dCA was associated with less temporal lobe gray matter atrophy on the infracted side ([Formula: see text] = 0.029), faster gait speed ([Formula: see text] = 0.018) and lower IADL score ([Formula: see text]0.002). Our results indicate that better dynamic cerebral perfusion regulation is associated with less atrophy and better long-term functional status in older adults with chronic ischemic infarctions.
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Aoi et al. (2012) conducted an observational in Chronic Ischemic Stroke (n=142). Impaired dynamic cerebral autoregulation (dCA) vs. Non-stroke subjects / Better dCA was evaluated on Brain tissue volumes and functional status (gait speed, instrumental activities of daily living, modified Rankin Scale, NIH Stroke Score) (p=0.029, 0.018, 0.002). In chronic ischemic stroke patients, better dynamic cerebral autoregulation is associated with less temporal lobe atrophy (P=0.029), faster gait speed (P=0.018), and lower IADL scores (P=0.002).
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