Yang Zhijian, Wen Junhao, Erus Guray, Govindarajan Sindhuja T, Melhem Randa, Mamourian Elizabeth, Cui Yuhan, Srinivasan Dhivya, Abdulkadir Ahmed, Parmpi Paraskevi, Wittfeld Katharina, Grabe Hans J, Bülow Robin, Frenzel Stefan, Tosun Duygu, Bilgel Murat, An Yang, Yi Dahyun, Marcus Daniel S, LaMontagne Pamela, Benzinger Tammie L S, Heckbert Susan R, Austin Thomas R, Waldstein Shari R, Evans Michele K, Zonderman Alan B, Launer Lenore J, Sotiras Aristeidis, Espeland Mark A, Masters Colin L, Maruff Paul, Fripp Jurgen, Toga Arthur, O'Bryant Sid, Chakravarty Mallar M, Villeneuve Sylvia, Johnson Sterling C, Morris John C, Albert Marilyn S, Yaffe Kristine, Völzke Henry, Ferrucci Luigi, Bryan Nick R, Shinohara Russell T, Fan Yong, Habes Mohamad, Lalousis Paris Alexandros, Koutsouleris Nikolaos, Wolk David A, Resnick Susan M, Shou Haochang, Nasrallah Ilya M, Davatzikos Christos
Artificial Intelligence in Biomedical Imaging Laboratory (AIBIL), Center for and Data Science for Integrated Diagnostics (AID), Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Graduate Group in Applied Mathematics and Computational Science, University of Pennsylvania, Philadelphia, PA, USA.
medRxiv. 2023 Dec 30:2023.12.29.23300642. doi: 10.1101/2023.12.29.23300642.
Brain aging is a complex process influenced by various lifestyle, environmental, and genetic factors, as well as by age-related and often co-existing pathologies. MRI and, more recently, AI methods have been instrumental in understanding the neuroanatomical changes that occur during aging in large and diverse populations. However, the multiplicity and mutual overlap of both pathologic processes and affected brain regions make it difficult to precisely characterize the underlying neurodegenerative profile of an individual from an MRI scan. Herein, we leverage a state-of-the art deep representation learning method, Surreal-GAN, and present both methodological advances and extensive experimental results that allow us to elucidate the heterogeneity of brain aging in a large and diverse cohort of 49,482 individuals from 11 studies. Five dominant patterns of neurodegeneration were identified and quantified for each individual by their respective (herein referred to as) R-indices. Significant associations between R-indices and distinct biomedical, lifestyle, and genetic factors provide insights into the etiology of observed variances. Furthermore, baseline R-indices showed predictive value for disease progression and mortality. These five R-indices contribute to MRI-based precision diagnostics, prognostication, and may inform stratification into clinical trials.
大脑衰老过程复杂,受多种生活方式、环境和遗传因素以及与年龄相关且常并存的病理状况影响。磁共振成像(MRI)以及最近的人工智能方法,对于理解不同人群衰老过程中发生的神经解剖学变化起到了重要作用。然而,病理过程和受影响脑区的多样性及相互重叠,使得难以从MRI扫描中精确表征个体潜在的神经退行性特征。在此,我们利用一种先进的深度表征学习方法——超现实生成对抗网络(Surreal-GAN),展示了方法学的进展和广泛的实验结果,这些使我们能够在来自11项研究的49482名个体组成的多样化大群体中阐明大脑衰老的异质性。通过各自的(在此称为)R指数为每个个体识别并量化了五种主要的神经退行性模式。R指数与不同的生物医学、生活方式和遗传因素之间的显著关联,为观察到的差异的病因提供了见解。此外,基线R指数对疾病进展和死亡率具有预测价值。这五个R指数有助于基于MRI的精准诊断、预后评估,并可为临床试验的分层提供参考。