用结构MRI评估从轻度认知障碍到阿尔茨海默病的转化:一项机器学习研究。

IF 4.5 Q1 CLINICAL NEUROLOGY Brain communications Pub Date : 2025-01-21 eCollection Date: 2025-01-01 DOI:10.1093/braincomms/fcaf027
Daniela Vecchio, Federica Piras, Federica Natalizi, Nerisa Banaj, Clelia Pellicano, Fabrizio Piras
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摘要

阿尔茨海默病是一种致残的神经退行性疾病,目前尚无有效的治疗方法。预测阿尔茨海默病的诊断可能对患者的预后至关重要,但目前的阿尔茨海默病生物标志物具有侵入性、耗时或昂贵。因此,开发基于核磁共振成像的阿尔茨海默病早期诊断计算方法对于缩小预测认知能力下降的表型测量范围至关重要。遗忘性轻度认知障碍(aMCI)与阿尔茨海默病的高风险相关,在这里,我们旨在确定基于mri的定量规则来预测aMCI可能转化为阿尔茨海默病,依次应用不同的机器学习算法。在基线时,收集104例aMCI患者的t1加权脑图像,并对其进行处理,获得146个脑灰质区域[感兴趣区域(roi)]的体积测量值。一年后,根据认知表现将患者分为转换者(aMCI-c = 32)和非转换者,即临床和神经心理稳定(aMCI-s = 72)。采用随机森林(random forest, RF)进行特征选择,并利用识别出的7个roi体积数据实现支持向量机(SVM)和决策树(DT)分类算法。SVM和DT识别aMCI-c和aMCI-s的平均准确率均达到86%。DT发现右内嗅皮层临界阈值体积(EC-r)是区分aMCI-c/aMCI-s的第一个特征。几乎所有的aMCI-c都有EC-r容量3,而超过一半的aMCI-s患者的容量高于该结构的确定阈值。aMCI-c/aMCI-s分类的其他关键区域是左枕侧(loc - 1)、颞中回和颞极皮质。我们的研究强化了先前的证据,表明EC-r和loc - 1的形态测定可以最好地预测aMCI向阿尔茨海默病的转化。在认为我们的发现是一个广泛适用的预测框架之前,需要进一步的调查。然而,在这里,容积阈值的第一个指征很容易获得,可能有助于在临床实践中早期识别阿尔茨海默病,从而有助于将MRI作为痴呆症发病的有用的非侵入性预后工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Evaluating conversion from mild cognitive impairment to Alzheimer's disease with structural MRI: a machine learning study.

Alzheimer's disease is a disabling neurodegenerative disorder for which no effective treatment currently exists. To predict the diagnosis of Alzheimer's disease could be crucial for patients' outcome, but current Alzheimer's disease biomarkers are invasive, time consuming or expensive. Thus, developing MRI-based computational methods for Alzheimer's disease early diagnosis would be essential to narrow down the phenotypic measures predictive of cognitive decline. Amnestic mild cognitive impairment (aMCI) is associated with higher risk for Alzheimer's disease, and here, we aimed to identify MRI-based quantitative rules to predict aMCI to possible Alzheimer's disease conversion, applying different machine learning algorithms sequentially. At baseline, T1-weighted brain images were collected for 104 aMCI patients and processed to obtain 146 volumetric measures of cerebral grey matter regions [regions of interest (ROIs)]. One year later, patients were classified as converters (aMCI-c = 32) or non-converters, i.e. clinically and neuropsychologically stable (aMCI-s = 72) based on cognitive performance. Feature selection was performed by random forest (RF), and the identified seven ROIs volumetric data were used to implement support vector machine (SVM) and decision tree (DT) classification algorithms. Both SVM and DT reached an average accuracy of 86% in identifying aMCI-c and aMCI-s. DT found a critical threshold volume of the right entorhinal cortex (EC-r) as the first feature for differentiating aMCI-c/aMCI-s. Almost all aMCI-c had an EC-r volume <1286 mm3, while more than half of the aMCI-s patients had a volume above the identified threshold for this structure. Other key regions for the classification between aMCI-c/aMCI-s were the left lateral occipital (LOC-l), the middle temporal gyrus and the temporal pole cortices. Our study reinforces previous evidence suggesting that the morphometry of the EC-r and LOC-l best predicts aMCI to Alzheimer's disease conversion. Further investigations are needed prior to deeming our findings as a broadly applicable predictive framework. However, here, a first indication was derived for volumetric thresholds that, being easy to obtain, may assist in early identification of Alzheimer's disease in clinical practice, thus contributing to establishing MRI as a useful non-invasive prognostic instrument for dementia onset.

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