栓塞
医学
动静脉畸形
免疫组织化学
病理
放射科
作者
Yingkun He,Yanyan He,Weixing Bai,Dehua Guo,Taoyuan Lu,Lin Duan,Zhen Li,Lingfei Kong,Juha Hernesniemi,Tianxiao Li,Juha A. Hernesniemi,Tianxiao Li
摘要
Abstract Introduction Brain arteriovenous malformation (bAVM) might have a higher risk of rupture after partial embolization, and previous studies have shown that some metrics of vascular stability are related to bAVM rupture risk. Objective To analyze vascular stability of bAVM in patients after partial embolization. Methods Twenty‐four patients who underwent partial embolization were classified into the short‐term, medium‐term, and long‐term groups, according to the time interval between partial embolization and surgery. The control group consisted of 9 bAVM patients who underwent surgery alone. Hemodynamic changes after partial embolization were measured by angiogram. The inflammatory infiltrates and cell–cell junctions were evaluated by MMP‐9 and VE‐cadherin. At the protein level, the proliferative and apoptotic events of bAVMs were analyzed by immunohistochemical staining of VEGFA, eNOS, and caspase‐3. Finally, neovascularity and apoptotic cells were assessed by CD31 staining and TUNEL staining. Results Immediately after partial embolization, the blood flow velocity of most bAVMs increased. The quantity of MMP‐9 in the medium‐term group was the highest, and VE‐cadherin in the medium‐term group was the lowest. The expression levels of VEGFA, eNOS, and neovascularity were highest in the medium‐term group. Similarly, the expression level of caspase‐3 and the number of apoptotic cells were highest in the medium‐term group. Conclusion The biomarkers for bAVM vascular stability were most abnormal between 1 and 28 days after partial embolization.
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