Impaired dynamic cerebral autoregulation is associated with the severity of neuroimaging features of cerebral small vessel disease

Z Liu, H Ma, ZN Guo, L Wang, Y Qu… - CNS neuroscience & …, 2022 - Wiley Online Library
Z Liu, H Ma, ZN Guo, L Wang, Y Qu, L Fan, X Liu, J Liu, Y Zhu, Y Yang
CNS neuroscience & therapeutics, 2022Wiley Online Library
Aims Cerebral small vessel disease (CSVD) is characterized by functional and structural
changes in small vessels. We aimed to elucidate the relationship between dynamic cerebral
autoregulation (dCA) and neuroimaging characteristics of CSVD. Methods A case‐control
study was performed. Cerebral blood flow velocity (CBFV) of bilateral middle cerebral
arteries and spontaneous arterial blood pressure were simultaneously recorded. Transfer
function analysis was used to calculate dCA parameters (phase, gain, and the rate of …
Aims
Cerebral small vessel disease (CSVD) is characterized by functional and structural changes in small vessels. We aimed to elucidate the relationship between dynamic cerebral autoregulation (dCA) and neuroimaging characteristics of CSVD.
Methods
A case‐control study was performed. Cerebral blood flow velocity (CBFV) of bilateral middle cerebral arteries and spontaneous arterial blood pressure were simultaneously recorded. Transfer function analysis was used to calculate dCA parameters (phase, gain, and the rate of recovery of CBFV [RoRc]). Neuroimaging characteristics of CSVD patients were evaluated, including lacunes, white matter hyperintensities (WMH), cerebral microbleeds (CMBs), perivascular spaces (PVS), and the total CSVD burden.
Results
Overall, 113 patients and 83 controls were enrolled. Compared with the control group, the phase at low frequency and the RoRc in CSVD patients were lower, and the gain at very low and low frequencies were higher, indicating bilaterally impaired dCA. Total CSVD burden, WMH (total, periventricular and deep), severe PVS, and lobar CMBs were independently correlated with the phase at low frequency.
Conclusions
Our findings suggested that dCA was compromised in CSVD patients, and some specific neuroimaging characteristics (the total CSVD burden, WMH, severe PVS and lobar CMBs) might indicate more severe dCA impairment in CSVD patients.
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