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Cerebrovascular reactivity in retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
Authors:Evelien S Hoogeveen  Nadine Pelzer  Eidrees Ghariq  Matthias JP van Osch  Albert Dahan  Gisela M Terwindt  Mark C Kruit
Institution:1.Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands;2.Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands;3.C.J. Gorter Center for High Field MRI, Leiden University Medical Center, Leiden, The Netherlands;4.Department of Anesthesiology, Leiden University Medical Center, Leiden, The Netherlands
Abstract:Retinal Vasculopathy with Cerebral Leukoencephalopathy and Systemic manifestations (RVCL-S) is a small vessel disease caused by TREX1 mutations. RVCL-S is characterized by retinal vasculopathy and brain white matter lesions with and without contrast enhancement. We aimed to investigate cerebrovascular reactivity (CVR) in RVCL-S. In this cross-sectional observational study, 21 RVCL-S patients, 23 mutation-negative family members, and 31 healthy unrelated controls were included. CVR to a hypercapnic challenge was measured using dual-echo arterial spin labeling magnetic resonance imaging. Stratified analyses based on age were performed. We found that CVR was decreased in gray and white matter of RVCL-S patients compared with family members and healthy controls (ANCOVA; P < 0.05 for all comparisons). This was most noticeable in RVCL-S patients aged ≥40 years (ANCOVA, P < 0.05 for all comparisons). In RVCL-S patients aged < 40 years, only CVR in white matter was lower when compared to healthy controls (P < 0.05). Gray matter CVR was associated with white matter lesion volume in RVCL-S patients (r = –0.527, P = 0.01). In conclusion, impaired cerebrovascular reactivity may play an important role in the pathophysiology of RVCL-S and may be an useful early biomarker of cerebrovascular disease severity.
Keywords:Cerebrovascular circulation  cerebrovascular disorders  leukoencephalopathies  magnetic resonance imaging  mutation
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