Impaired cerebral autoregulation in Fabry disease: A case‐control study

Abstract

AbstractBackground and PurposeCerebral small vessel disease is a common manifestation among patients with Fabry disease (FD). As a biomarker of cerebral small vessel disease, the prevalence of impaired cerebral autoregulation as assessed by transcranial Doppler (TCD) ultrasonography was evaluated in FD patients and healthy controls.MethodsTCD was performed to assess pulsatility index (PI) and vasomotor reactivity expressed by breath‐holding index (BHI) for the middle cerebral arteries of included FD patients and healthy controls. Prevalence of increased PI (>1.2) and decreased BHI (<0.69) and ultrasound indices of cerebral autoregulation were compared in FD patients and controls. The potential association of ultrasound indices of impaired cerebral autoregulation with white matter lesions and leukoencephalopathy on brain MRI in FD patients was also evaluated.ResultsDemographics and vascular risk factors were similar in 23 FD patients (43% women, mean age: 51 ± 13 years) and 46 healthy controls (43% women, mean age: 51 ± 13 years). The prevalence of increased PI (39%; 95% confidence interval [CI]: 20%‐61%), decreased BHI (39%; 95% CI: 20%‐61%), and the combination of increased PI and/or decreased BHI (61%; 95% CI: 39%‐80%) was significantly (p < .001) higher in FD patients compared to healthy controls (2% [95% CI: 0.1%‐12%], 2% [95% CI: 0.1%‐12%], and 4% [95% CI: 0.1%‐15%], respectively). However, indices of abnormal cerebral autoregulation were not associated independently with white matter hyperintensities and presented a low‐to‐moderate predictive ability for the discrimination of FD patients with and without white matter hyperintensities.ConclusionsImpaired cerebral autoregulation as assessed by TCD appears to be highly more prevalent among FD patients compared to healthy controls.