Mazzeo S, Padiglioni S, Bagnoli S, Carraro M, Piaceri I, Bracco L, Nacmias B, Sorbi S, Bessi V
Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Azienda Ospedaliera-Universitaria Careggi, Florence, Italy.
IRCCS Fondazione Don Carlo Gnocchi, Florence, Italy.
Eur J Neurol. 2020 May;27(5):894-899. doi: 10.1111/ene.14167. Epub 2020 Mar 8.
Subjective cognitive decline (SCD) is a self-experienced decline in cognitive capacity with normal performance on standardized cognitive tests and has been shown to increase the risk of Alzheimer's disease (AD). SCD could also be related to other conditions such as normal aging, psychiatric, neurological or medical disorders. The SCD Initiative proposed a set of features (SCD-plus) that increase the likelihood of preclinical AD in individuals with SCD. Our aim was to assess the effect of these features on the risk of conversion from SCD to AD.
In total 150 SCD subjects who underwent extensive neuropsychological investigation, assessment of cognitive complaints and apolipoprotein E (ApoE) genotyping at baseline and clinical-neuropsychological follow-up for a mean time of 11 years were included.
During the follow-up, 20 subjects developed AD. Considering SCD-plus features, age at onset ≥60 years and ApoE ε4 significantly increased the risk of conversion from SCD to AD. When our sample was stratified into three groups (no risk factor, one risk factor, two risk factors), the proportion of conversion was statistically significantly different between the three groups.
Our model allows the risk of AD to be stratified in patients experiencing SCD according to age at onset and ApoE genotype.
主观认知下降(SCD)是一种自我感知的认知能力下降,在标准化认知测试中表现正常,且已被证明会增加患阿尔茨海默病(AD)的风险。SCD也可能与其他情况有关,如正常衰老、精神、神经或医学疾病。SCD倡议提出了一组特征(SCD加),这些特征增加了SCD个体发生临床前AD的可能性。我们的目的是评估这些特征对SCD转化为AD风险的影响。
总共纳入了150名SCD受试者,他们在基线时接受了广泛的神经心理学调查、认知主诉评估和载脂蛋白E(ApoE)基因分型,并进行了平均11年的临床神经心理学随访。
在随访期间,20名受试者患上了AD。考虑SCD加特征,发病年龄≥60岁和ApoE ε4显著增加了从SCD转化为AD的风险。当我们的样本分为三组(无危险因素、一个危险因素、两个危险因素)时,三组之间的转化比例在统计学上有显著差异。
我们的模型允许根据发病年龄和ApoE基因型对SCD患者的AD风险进行分层。