Zapaishchykova Anna, Tak Divyanshu, Ye Zezhong, Liu Kevin X, Likitlersuang Jirapat, Vajapeyam Sridhar, Chopra Rishi B, Seidlitz Jakob, Bethlehem Richard A I, Mak Raymond H, Mueller Sabine, Haas-Kogan Daphne A, Poussaint Tina Y, Aerts Hugo J W L, Kann Benjamin H
Artificial Intelligence in Medicine (AIM) Program, Mass General Brigham, Harvard Medical School, Boston, MA, United States.
Department of Radiation Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
Imaging Neurosci (Camb). 2024 Mar 25;2. doi: 10.1162/imag_a_00114. eCollection 2024.
Deep learning (DL)-based prediction of biological age in the developing human from a brain magnetic resonance imaging (MRI) ("") may have important diagnostic and therapeutic applications as a non-invasive biomarker of brain health, aging, and neurocognition. While previous deep learning tools for predicting brain age have shown promising capabilities using single-institution, cross-sectional datasets, our work aims to advance the field by leveraging multi-site, longitudinal data with externally validated and independently implementable code to facilitate clinical translation and utility. This builds on prior foundational efforts in brain age modeling to enable broader generalization and individual's longitudinal brain development. Here, we leveraged 32,851 T1-weighted MRI scans from healthy children and adolescents aged 3 to 30 from 16 multisite datasets to develop and evaluate several DL brain age frameworks, including a novel regression diffusion DL network (AgeDiffuse). In a multisite external validation (5 datasets), we found that AgeDiffuse outperformed conventional DL frameworks, with a mean absolute error (MAE) of 2.78 years (interquartile range [IQR]: [1.2-3.9]). In a second, separate external validation (3 datasets), AgeDiffuse yielded an MAE of 1.97 years (IQR: [0.8-2.8]). We found that AgeDiffuse brain age predictions reflected age-related brain structure volume changes better than biological age (R= 0.48 vs. R= 0.37). Finally, we found that longitudinal predicted brain age tracked closely with chronological age at the individual level. To enable independent validation and application, we made AgeDiffuse publicly available and usable for the research community.
基于深度学习(DL)从脑磁共振成像(MRI)预测发育中人类的生物学年龄,作为脑健康、衰老和神经认知的非侵入性生物标志物,可能具有重要的诊断和治疗应用。虽然先前用于预测脑年龄的深度学习工具在使用单机构横断面数据集时已显示出有前景的能力,但我们的工作旨在通过利用多站点纵向数据以及经过外部验证且可独立实施的代码来推动该领域发展,以促进临床转化和应用。这建立在脑年龄建模先前的基础工作之上,以实现更广泛的泛化和个体的纵向脑发育。在此,我们利用来自16个多站点数据集的32851例3至30岁健康儿童和青少年的T1加权MRI扫描,来开发和评估多个DL脑年龄框架,包括一种新型回归扩散DL网络(AgeDiffuse)。在多站点外部验证(5个数据集)中,我们发现AgeDiffuse优于传统DL框架,平均绝对误差(MAE)为2.78岁(四分位间距[IQR]:[1.2 - 3.9])。在第二次单独的外部验证(3个数据集)中,AgeDiffuse的MAE为1.97岁(IQR:[0.8 - 2.8])。我们发现AgeDiffuse脑年龄预测比生物学年龄更能反映与年龄相关的脑结构体积变化(R = 0.48对R =