BrainAgeNeXt:推进多发性硬化症患者的脑年龄建模

Francesco La Rosa, Jonadab Dos, Santos Silva, Emma Dereskewicz, A. Invernizzi, Noa Cahan, Julia Galasso, Nadia Garcia, Robin Graney, Sarah Levy, Gaurav Verma, P. Balchandani, Daniel S Reich, Megan Horton, H. Greenspan, James Sumowski, M. B. Cuadra, Erin S Beck
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摘要

衰老与大脑结构变化、认知能力下降和神经退行性疾病有关。脑年龄是一种对健康老化偏差敏感的成像生物标志物,它提供了对结构性老化变化的洞察力,是神经退行性疾病的潜在预后生物标志物。本研究介绍了受 MedNeXt 框架启发的新型卷积神经网络 BrainAgeNeXt,该网络旨在通过 T1 加权磁共振成像(MRI)扫描预测脑年龄。BrainAgeNeXt 在 33 个私人和公开数据集的 11,574 次核磁共振成像扫描上进行了训练和验证,这些数据集包含 5 至 95 岁的健康志愿者,并使用 3T 和 7T 核磁共振成像成像。将其性能与三种最先进的脑年龄预测方法进行了比较。BrainAgeNeXt 的平均绝对误差 (MAE) 为 2.78 岁,低于比较过的方法(MAE = 3.55、3.59 和 4.16 岁)。我们还在不同的图像质量水平上对所有方法进行了测试,BrainAgeNeXt 即使在运动伪影和不常见的 7T MRI 数据上也表现出色。在三个多发性硬化症(MS)纵向队列(273 人)中,脑年龄平均比实际年龄大 4.21 岁。纵向分析表明,多发性硬化症患者的脑龄每增加 1.15 岁(95% CI = [1.05, 1.26])。此外,在早期多发性硬化症患者中,与临床评估稳定的患者相比,残疾恶化的患者脑龄的年增长率更高(1.24 vs. 0.75,p < 0.01)。这些研究结果表明,脑年龄是一种很有希望的多发性硬化症进展预后生物标志物,并有可能成为临床试验的一个有价值的终点。
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BrainAgeNeXt: Advancing Brain Age Modeling for Individuals with Multiple Sclerosis
Aging is associated with structural brain changes, cognitive decline, and neurodegenerative diseases. Brain age, an imaging biomarker sensitive to deviations from healthy aging, offers insights into structural aging variations and is a potential prognostic biomarker in neurodegenerative conditions. This study introduces BrainAgeNeXt, a novel convolutional neural network inspired by the MedNeXt framework, designed to predict brain age from T1-weighted magnetic resonance imaging (MRI) scans. BrainAgeNeXt was trained and validated on 11,574 MRI scans from 33 private and publicly available datasets of healthy volunteers, aged 5 to 95 years, imaged with 3T and 7T MRI. Performance was compared against three state-of-the-art brain age prediction methods. BrainAgeNeXt achieved a mean absolute error (MAE) of 2.78 years, lower than the compared methods (MAE = 3.55, 3.59, and 4.16 years, respectively). We tested all methods also across different levels of image quality, and BrainAgeNeXt performed well even with motion artifacts and less common 7T MRI data. In three longitudinal multiple sclerosis (MS) cohorts (273 individuals), brain age was, on average, 4.21 years greater than chronological age. Longitudinal analysis indicated that brain age increased by 1.15 years per chronological year in individuals with MS (95% CI = [1.05, 1.26]). Moreover, in early MS, individuals with worsening disability had a higher annual increase in brain age compared to those with stable clinical assessments (1.24 vs. 0.75, p < 0.01). These findings suggest that brain age is a promising prognostic biomarker for MS progression and potentially a valuable endpoint for clinical trials.
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