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首页> 外文期刊>Brain: A journal of neurology >A 10-year follow-up of hippocampal volume on magnetic resonance imaging in early dementia and cognitive decline.
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A 10-year follow-up of hippocampal volume on magnetic resonance imaging in early dementia and cognitive decline.

机译:对早期痴呆和认知功能下降的磁共振成像海马体积进行10年随访。

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Hippocampal atrophy is frequently observed on magnetic resonance images from patients with Alzheimer's disease and persons with mild cognitive impairment. Even in asymptomatic elderly, a small hippocampal volume on magnetic resonance imaging is a risk factor for developing Alzheimer's disease. However, not everyone with a small hippocampus develops dementia. With the increased interest in the use of sequential magnetic resonance images as potential surrogate biomarkers of the disease process, it has also been shown that the rate of hippocampal atrophy is higher in persons with Alzheimer's disease compared to those with mild cognitive impairment and the healthy elderly. Whether a higher rate of hippocampal atrophy also predicts Alzheimer's disease or subtle cognitive decline in non-demented elderly is unknown. We examine these associations in a group of 518 elderly (age 60-90 years, 50% female), taken from the population-based Rotterdam Scan Study. A magnetic resonance imaging examination was performed at baseline in 1995-96 that was repeated in 1999-2000 (in 244 persons) and in 2006 (in 185 persons). Using automated segmentation procedures, we assessed hippocampal volumes on all magnetic resonance imaging scans. All persons were free of dementia at baseline and followed over time for cognitive decline and incident dementia. Persons had four repeated neuropsychological tests at the research centre over a 10-year period. We also continuously monitored the medical records of all 518 participants for incident dementia. During a total follow-up of 4360 person-years, (mean 8.4, range 0.1-11.3), 50 people developed incident dementia (36 had Alzheimer's disease). We found an increased risk to develop incident dementia per standard deviation faster rate of decline in hippocampal volume [left hippocampus 1.6 (95% confidence interval 1.2-2.3, right hippocampus 1.6 (95% confidence interval 1.2-2.1)]. Furthermore, decline in hippocampal volume predicted onset of clinical dementia when corrected for baseline hippocampal volume. In people who remained free of dementia during the whole follow-up period, we found that decline in hippocampal volume paralleled, and preceded, specific decline in delayed word recall. No associations were found in this sample between rate of hippocampal atrophy, Mini Mental State Examination and tests of executive function. Our results suggest that rate of hippocampal atrophy is an early marker of incipient memory decline and dementia, and could be of additional value when compared with a single hippocampal volume measurement as a surrogate biomarker of dementia.
机译:在阿尔茨海默氏病患者和轻度认知障碍患者的磁共振图像上经常观察到海马萎缩。即使在无症状的老年人中,磁共振成像中较小的海马体积也是发展为阿尔茨海默氏病的危险因素。但是,并不是每个人都有一个小的海马体会发展为痴呆症。随着人们越来越关注使用顺序磁共振图像作为疾病过程的潜在替代生物标志物,研究还表明,与轻度认知障碍和健康老人相比,阿尔茨海默氏病患者海马萎缩的发生率更高。尚不清楚海马萎缩率升高是否也预示着老年痴呆症患者的阿尔茨海默氏病或​​微妙的认知功能下降。我们从基于人口的鹿特丹扫描研究中抽取了518名老年人(60-90岁,女性50%)作为研究对象。 1995-96年在基线进行了磁共振成像检查,1999-2000年(244人)和2006年(185人)重复进行了磁共振检查。使用自动分割程序,我们在所有磁共振成像扫描中评估了海马体积。所有患者在基线时都没有痴呆症,并随着时间的推移进行认知下降和突发性痴呆症的随访。在过去的10年中,人们在研究中心进行了四次重复的神经心理学测试。我们还持续监控了所有518名参与者的医疗记录,以记录他们的痴呆事件。在总共4360人年的随访中(平均8.4,范围0.1-11.3),有50人发展为痴呆(36人患有老年痴呆症)。我们发现,每标准偏差,发生痴呆的风险增加,海马体积下降的速度更快[左海马1.6(95%置信区间1.2-2.3,右海马1.6(95%置信区间1.2-2.1)]。在校正基线海马体积后,海马体积可预测临床痴呆症的发作;在整个随访期间仍无痴呆的人群中,我们发现,海马体积的下降与延迟词回想的特定下降相平行,并且在此之前是特定的。在该样本中发现了海马萎缩率,迷你精神状态检查与执行功能测试之间的关系,我们的研究结果表明,海马萎缩率是早期记忆衰退和痴呆的早期标志,当与海马萎缩率相比时可能具有附加价值。单个海马体积测量作为痴呆的替代生物标志物。

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