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首页> 外文期刊>Brain imaging and behavior >Validated Alzheimer's Disease Risk Index (ANU-ADRI) is associated with smaller volumes in the default mode network in the early 60s
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Validated Alzheimer's Disease Risk Index (ANU-ADRI) is associated with smaller volumes in the default mode network in the early 60s

机译:验证的阿尔茨海默病风险指数(ANU-ADRI)在60年代初期与默认模式网络中的较小卷相关联

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摘要

Strong evidence is available suggesting that effective reduction of exposure to demonstrated modifiable risk factors in mid-life or before could significantly decrease the incidence of Alzheimer's disease (AD) and delay its onset. A key ingredient to achieving this goal is the reliable identification of individuals at risk well before they develop clinical symptoms. The aim of this study was to provide further neuroimaging evidence of the effectiveness of a validated tool, the ANU Alzheimer's Disease Risk Index, for the assessment of future risk of cognitive decline. Participants were 461 (60-64 years, 48% female) community-living individuals free of dementia at baseline. Associations between risk estimates obtained with the ANU-ADRI, total and regional brain volumes including in the default mode network (DMN) measured at the same assessment and diagnosis of MCI/dementia over a 12-year follow-up were tested in a large sample of community-living individuals free of dementia at baseline. Higher risk estimates on the ANU-ADRI were associated with lower cortical gray matter and particularly in the DMN. Importantly, difference in participants with high and low risk scores explained 7-9% of the observed difference in gray matter volume. In this sample, every one additional risk point on the ANU-ADRI was associated with an 8% increased risk of developing MCI/dementia over a 12-year follow-up and this association was partly mediated by a sub-region of the DMN. Risk of cognitive decline assessed with a validated instrument is associated with gray matter volume, particularly in the DMN, a region known to be implicated in the pathological process of the disease.
机译:有强有力的证据表明,有效减少暴露于中生中的可修改的风险因素,或之前可以显着降低阿尔茨海默病(AD)的发病率并延迟发病。实现这一目标的关键因素是在发展临床症状之前,良好危险的个人识别。本研究的目的是提供进一步的神经影像学证据证明验证工具的有效性,Anu Alzheimer的疾病风险指数,用于评估未来认知衰退的风险。参与者是461(60-64岁,48%的女性)社区生活在基线上没有痴呆症。用ANU-ADRI,总和区域脑体积获得的风险估算之间的关联在一个大型样本中测试了在同一评估和诊断的默认模式网络(DMN)中测量的默认模式网络(DMN)中进行了在一个大型样本中进行了测试在基线上没有痴呆的社区生活中的人。 ANU-ADRI的较高风险估计与较低的皮质灰质相关,特别是DMN相关。重要的是,高风险评分的参与者的差异解释了灰质体积中观察到的7-9%。在该样品中,ANU-ADRI上的每一个额外风险点与在12年的随访中发育MCI /痴呆的风险增加8%,这种关联部分由DMN的子区域介导。用验证仪器评估的认知性下降的风险与灰质体积相关,特别是在DMN中,已知在疾病的病理过程中涉及的区域。

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