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Brain-predicted age difference estimated using DeepBrainNet is significantly associated with pain and function—a multi-institutional and multiscanner study

慢性疼痛 医学 大脑结构与功能 脑形态计量学 神经病理学 脑功能 磁共振成像 神经影像学 物理医学与康复 心理学 物理疗法 内科学 神经科学 精神科 疾病 放射科
作者
Pedro A. Valdés-Hernández,Chavier Laffitte Nodarse,Alisa J. Johnson,Soamy Montesino-Goicolea,Vishnu Bashyam,Christos Davatzikos,Julio A. Peraza,James H. Cole,Zhiguang Huo,Roger B. Fillingim,Yenisel Cruz‐Almeida
出处
期刊:Pain [Ovid Technologies (Wolters Kluwer)]
卷期号:164 (12): 2822-2838 被引量:4
标识
DOI:10.1097/j.pain.0000000000002984
摘要

Abstract Brain age predicted differences (brain-PAD: predicted brain age minus chronological age) have been reported to be significantly larger for individuals with chronic pain compared with those without. However, a debate remains after one article showed no significant differences. Using Gaussian Process Regression, an article provides evidence that these negative results might owe to the use of mixed samples by reporting a differential effect of chronic pain on brain-PAD across pain types. However, some remaining methodological issues regarding training sample size and sex-specific effects should be tackled before settling this controversy. Here, we explored differences in brain-PAD between musculoskeletal pain types and controls using a novel convolutional neural network for predicting brain-PADs, ie, DeepBrainNet. Based on a very large, multi-institutional, and heterogeneous training sample and requiring less magnetic resonance imaging preprocessing than other methods for brain age prediction, DeepBrainNet offers robust and reproducible brain-PADs, possibly highly sensitive to neuropathology. Controlling for scanner-related variability, we used a large sample (n = 660) with different scanners, ages (19-83 years), and musculoskeletal pain types (chronic low back [CBP] and osteoarthritis [OA] pain). Irrespective of sex, brain-PAD of OA pain participants was ∼3 to 4.7 years higher than that of CBP and controls, whereas brain-PAD did not significantly differ among controls and CBP. Moreover, brain-PAD was significantly related to multiple variables underlying the multidimensional pain experience. This comprehensive work adds evidence of pain type–specific effects of chronic pain on brain age. This could help in the clarification of the debate around possible relationships between brain aging mechanisms and pain.

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