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Distinct cerebral small vessel disease impairment in early‐ and late‐onset Alzheimer's disease

医学 认知 疾病 内科学 认知功能衰退 阿尔茨海默病 心脏病学 认知障碍 早发性阿尔茨海默病 痴呆 精神科
作者
Xiao Luo,Hong Hui,Kaicheng Li,Qingze Zeng,Shuyue Wang,Zheyu Li,Yanv Fu,Xiaocao Liu,Luwei Hong,Jixuan Li,Xinyi Zhang,Siyan Zhong,Yeerfan Jiaerken,Zhirong Liu,Yan-Xing Chen,Pei-Yu Huang,Minming Zhang,for the Alzheimer's Disease Neuroimaging Initiative (ADNI)
出处
期刊:Annals of clinical and translational neurology [Wiley]
卷期号:10 (8): 1326-1337 被引量:12
标识
DOI:10.1002/acn3.51824
摘要

Abstract Objective This study investigated cerebral small vessel disease (CSVD) damage patterns in early‐onset and late‐onset Alzheimer's disease (EOAD and LOAD) and their effects on cognitive function. Methods This study included 93 participants, 45 AD patients (14 EOAD and 31 LOAD), and 48 normal controls (13 YNC and 35 ONC) from the ADNI database. All participants had diffusion tensor imaging data; some had amyloid PET and plasma p‐tau 181 data. The study used peak width of skeletonized mean diffusivity (PSMD) to measure CSVD severity and compared PSMD between patients and age‐matched controls. The effect of age on the relationship between PSMD and cognition was also examined. The study also repeated the analysis in amyloid‐positive AD patients and amyloid‐negative controls in another independent database (31 EOAD and 38 LOAD), and the merged database. Results EOAD and LOAD showed similar cognitive function and disease severity. PSMD was validated as a reliable correlate of cognitive function. In the ADNI database, PSMD was significantly higher for LOAD and showed a tendency to increase for EOAD; in the independent and merged databases, PSMD was significantly higher for both LOAD and EOAD. The impact of PSMD on cognitive function was notably greater in the younger group (YNC and EOAD) than in the older group (ONC and LOAD), as supported by the ADNI and merged databases. Interpretation EOAD has less CSVD burden than LOAD, but has a greater impact on cognition. Proactive cerebrovascular prevention strategies may have potential clinical value for younger older adults with cognitive decline.
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