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Decoding neurovascular signatures: advanced imaging insights in DADA2-Related Cerebral Microangiopathy
Yaping Zhou1, Min Shen2, Nan Jiang1
1Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Dongcheng District, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, No.1 Shuaifuyuan, DongdanBeijing, 100730, China.
Background And Purpose:
Neuroimaging phenotypes remain poorly characterized in patients with deficiency of adenosine deaminase 2 (DADA2). We aimed to characterize cerebral microangiopathy patterns and establish diagnostic imaging biomarkers for DADA2.
Methods:
We retrospectively analyzed consecutively enrolled DADA2 patients with neurological involvement from two ongoing prospective cohorts. The demographic, clinical, and neuroimaging data were evaluated, focusing on neuroimaging lesion patterns and cerebral small vessel disease (CSVD) imaging markers.
Results:
Thirteen patients were included, with 69.2% males. The median age at neurological onset was 17 (7-26) years. A striking disparity emerged between acute ischemic burden and chronic small vessel injury markers. During a follow-up of 51 (0.5-193) months,138 ischemic lesions were observed in all patients, primarily involving the pons (38 lesions), thalamus (21 lesions), internal capsule (20 lesions), and basal ganglia (18 lesions). Conversely, only one cerebral microbleed (CMB) was detected in all patients. Mild white matter hyperintensities (WMH) were observed in 9 patients. Infratentorial atrophy was prevailing and present in 69.2% (n = 9) patients. Additionally, hemorrhagic stroke was less frequent (n = 6, 46.2%) than infarction.
Conclusion:
DADA2 exhibited a profoundly high risk of stroke recurrence, with substantial lesions being clinically asymptomatic, underscoring the importance of routine neuroimaging evaluation for DADA2 patients. This disease presents a unique CSVD phenotype characterized by brainstem-deep gray nucleus ischemic predominance and infratentorial atrophy yet paradoxically low burdens of CMBs and WMH compared to other CSVD. This distinctive imaging triad not only facilitates early recognition and timely intervention, but also suggests a pathophysiological divergence from other CSVD.
