Longitudinal structural MRI-based deep learning and radiomics features for predicting Alzheimer's disease progression.

IF 7.6 1区 医学 Q1 CLINICAL NEUROLOGY
Sepehr Aghajanian, Fateme Mohammadifard, Ida Mohammadi, Shahryar Rajai Firouzabadi, Ali Baradaran Bagheri, Elham Moases Ghaffary, Omid Mirmosayyeb
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引用次数: 0

Abstract

Background: Alzheimer's disease (AD) is the principal cause of dementia and requires the early diagnosis of people with mild cognitive impairment (MCI) who are at high risk of progressing. Early diagnosis is imperative for optimizing clinical management and selecting proper therapeutic interventions. Structural magnetic resonance imaging (MRI) markers have been widely investigated for predicting the conversion of MCI to AD, and recent advances in deep learning (DL) methods offer enhanced capabilities for identifying subtle neurodegenerative changes over time.

Methods: We selected 228 MCI participants from the Alzheimer's Disease Neuroimaging Initiative (ADNI) who had at least three T1-weighted MRI scans within 18 months of baseline. MRI volumes underwent bias correction, segmentation, and radiomics feature extraction. A 3D residual network (ResNet3D) was trained using a pairwise ranking loss to capture single-timepoint risk scores. Longitudinal analyses were performed by extracting deep convolutional neural network (CNN) embeddings and gray matter radiomics for each scan, which were put into a time-aware long short-term memory (LSTM) model with an attention mechanism.

Results: A single-timepoint ResNet3D model achieved modest performance (c-index ~ 0.70). Incorporating longitudinal MRI files or downstream survival models led to a pronounced prognostic improvement (c-index:0.80-0.90), but was not further improved by longitudinal radiomics data. Time-specific classification within two- and three-year and five-year windows after the last MRI acquisition showed high accuracy (AUC > 0.85). Several radiomics, including gray matter surface to volume and elongation, emerged as the most predictive features. Each SD change in the gray matter surface to volume change within the last visit was associated with an increased risk of developing AD (HR: 1.50; 95% CI: 1.25-1.79).

Conclusions: These findings emphasize the value of structural MRI within the advanced DL architectures for predicting MCI-to-AD conversion. The approach may enable earlier risk stratification and targeted interventions for individuals most likely to progress. limitations in sample size and computational resources warrant larger, more diverse studies to confirm these observations and explore additional improvements.

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基于纵向结构mri的深度学习和放射组学特征预测阿尔茨海默病的进展。
背景:阿尔茨海默病(AD)是痴呆症的主要原因,需要对进展风险较高的轻度认知障碍(MCI)患者进行早期诊断。早期诊断对于优化临床管理和选择适当的治疗干预措施至关重要。结构磁共振成像(MRI)标记物已被广泛研究用于预测MCI向AD的转化,深度学习(DL)方法的最新进展为识别随着时间推移的细微神经退行性变化提供了增强的能力。方法:我们从阿尔茨海默病神经影像学倡议(ADNI)中选择了228名MCI参与者,他们在基线后18个月内至少进行了三次t1加权MRI扫描。MRI体积进行了偏差校正、分割和放射组学特征提取。使用两两排序损失来训练3D残余网络(ResNet3D)以获取单时间点风险评分。通过提取每次扫描的深度卷积神经网络(CNN)嵌入和灰质放射组学进行纵向分析,并将其放入具有注意机制的时间感知长短期记忆(LSTM)模型中。结果:单时间点ResNet3D模型取得了一般的性能(c-index ~ 0.70)。结合纵向MRI文件或下游生存模型可显著改善预后(c-index:0.80-0.90),但纵向放射组学数据并未进一步改善预后。在最后一次MRI采集后的2年、3年和5年窗口内的时间特异性分类显示出较高的准确性(AUC > 0.85)。几种放射组学,包括灰质表面体积和伸长,成为最具预测性的特征。在最后一次访问中,灰质表面的每一次SD变化与体积变化都与患AD的风险增加相关(HR: 1.50;95% ci: 1.25-1.79)。结论:这些发现强调了结构MRI在高级DL架构中预测mci到ad转换的价值。该方法可能使早期风险分层和针对最有可能进展的个体的有针对性的干预成为可能。由于样本量和计算资源的限制,需要更大规模、更多样化的研究来证实这些观察结果,并探索进一步的改进。
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来源期刊
Alzheimer's Research & Therapy
Alzheimer's Research & Therapy 医学-神经病学
CiteScore
13.10
自引率
3.30%
发文量
172
审稿时长
>12 weeks
期刊介绍: Alzheimer's Research & Therapy is an international peer-reviewed journal that focuses on translational research into Alzheimer's disease and other neurodegenerative diseases. It publishes open-access basic research, clinical trials, drug discovery and development studies, and epidemiologic studies. The journal also includes reviews, viewpoints, commentaries, debates, and reports. All articles published in Alzheimer's Research & Therapy are included in several reputable databases such as CAS, Current contents, DOAJ, Embase, Journal Citation Reports/Science Edition, MEDLINE, PubMed, PubMed Central, Science Citation Index Expanded (Web of Science) and Scopus.
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