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Amyloid-related imaging abnormalities (ARIA), thought to reflect immune responses to vascular amyloid, have been detected in several amyloid-modifying therapy trials for Alzheimer's disease (AD). We report a case of ARIA developing spontaneously during the course of Presenilin 1 (PSEN1)-associated familial AD (FAD), in an APOE4 homozygous patient. Severe cerebral amyloid angiopathy with associated inflammation was subsequently found at autopsy. Recognition that ARIA may arise spontaneously during FAD and of the potential risk factors for its development are important observations given the recent launch of amyloid-modifying therapy trials for FAD.

作者:Natalie S, Ryan;Tammaryn, Lashley;Tamas, Revesz;Kiran, Dantu;Nick C, Fox;Huw R, Morris

来源:Journal of Alzheimer's disease : JAD 2015 年 44卷 4期

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作者:
Natalie S, Ryan;Tammaryn, Lashley;Tamas, Revesz;Kiran, Dantu;Nick C, Fox;Huw R, Morris
来源:
Journal of Alzheimer's disease : JAD 2015 年 44卷 4期
标签:
APOE Presenilin 1 cerebral amyloid angiopathy-related inflammation familial Alzheimer's disease magnetic resonance imaging
Amyloid-related imaging abnormalities (ARIA), thought to reflect immune responses to vascular amyloid, have been detected in several amyloid-modifying therapy trials for Alzheimer's disease (AD). We report a case of ARIA developing spontaneously during the course of Presenilin 1 (PSEN1)-associated familial AD (FAD), in an APOE4 homozygous patient. Severe cerebral amyloid angiopathy with associated inflammation was subsequently found at autopsy. Recognition that ARIA may arise spontaneously during FAD and of the potential risk factors for its development are important observations given the recent launch of amyloid-modifying therapy trials for FAD.