{"title":"Developing and validating an elderly brain template: A comprehensive comparison with MNI152 for age-specific neuroimaging analyses","authors":"Kazumichi Ota, Yoshihiko Nakazato, Genko Oyama","doi":"10.1016/j.neuroimage.2025.121473","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>The Montreal Neurological Institute 152 (MNI152) brain template, constructed from young adult brains, may not accurately represent older age–specific morphological changes. Accordingly, we developed and validated the new Elderly template.</div></div><div><h3>Methods</h3><div>MRI scans from 90 OASIS-1 participants, matching Japanese census demographics, were used to construct the Elderly template. Spatial normalization accuracy was compared with that of the MNI152 in the IXI dataset. Following UK Biobank–based intracranial volume quality control (±2 SD; 1232–1850 mL), 282 of 313 scans from individuals aged 20–80+ years were included. Whole-brain similarity was assessed with cross-correlation (CC), mean-squared error (MSE), and 3D structural similarity index measure (3D-SSIM). Dice coefficients were computed for white matter (WM), gray matter (GM), cerebrospinal fluid (CSF), and seven subcortical regions. Generalized linear models were used to test the Age × Template interactions (β₃).</div></div><div><h3>Results</h3><div>Significant Age × Template interactions were observed for CC and MSE (<em>p</em> < 0.001); 3D-SSIM showed a positive but non-significant trend. Dice analyses mirrored this pattern: WM and GM showed minor differences between templates, and the Dice coefficient was parallel. CSF showed a sharp difference at the age ≥60 years. The largest interaction effects (≈1–4 % gain) occurred in the caudate, thalamus, hippocampus, and amygdala, whereas the brainstem, pallidum, and putamen showed minimal differences between templates.</div></div><div><h3>Conclusions</h3><div>The Elderly template more accurately reflects older age–specific morphological changes and enhances spatial normalization accuracy, compared with the MNI152 template. This improvement suggests advancements in age-specific analyses and neurodegenerative disease research, enabling clinical applications.</div></div>","PeriodicalId":19299,"journal":{"name":"NeuroImage","volume":"320 ","pages":"Article 121473"},"PeriodicalIF":4.5000,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"NeuroImage","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1053811925004768","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NEUROIMAGING","Score":null,"Total":0}
引用次数: 0
Abstract
Background
The Montreal Neurological Institute 152 (MNI152) brain template, constructed from young adult brains, may not accurately represent older age–specific morphological changes. Accordingly, we developed and validated the new Elderly template.
Methods
MRI scans from 90 OASIS-1 participants, matching Japanese census demographics, were used to construct the Elderly template. Spatial normalization accuracy was compared with that of the MNI152 in the IXI dataset. Following UK Biobank–based intracranial volume quality control (±2 SD; 1232–1850 mL), 282 of 313 scans from individuals aged 20–80+ years were included. Whole-brain similarity was assessed with cross-correlation (CC), mean-squared error (MSE), and 3D structural similarity index measure (3D-SSIM). Dice coefficients were computed for white matter (WM), gray matter (GM), cerebrospinal fluid (CSF), and seven subcortical regions. Generalized linear models were used to test the Age × Template interactions (β₃).
Results
Significant Age × Template interactions were observed for CC and MSE (p < 0.001); 3D-SSIM showed a positive but non-significant trend. Dice analyses mirrored this pattern: WM and GM showed minor differences between templates, and the Dice coefficient was parallel. CSF showed a sharp difference at the age ≥60 years. The largest interaction effects (≈1–4 % gain) occurred in the caudate, thalamus, hippocampus, and amygdala, whereas the brainstem, pallidum, and putamen showed minimal differences between templates.
Conclusions
The Elderly template more accurately reflects older age–specific morphological changes and enhances spatial normalization accuracy, compared with the MNI152 template. This improvement suggests advancements in age-specific analyses and neurodegenerative disease research, enabling clinical applications.
期刊介绍:
NeuroImage, a Journal of Brain Function provides a vehicle for communicating important advances in acquiring, analyzing, and modelling neuroimaging data and in applying these techniques to the study of structure-function and brain-behavior relationships. Though the emphasis is on the macroscopic level of human brain organization, meso-and microscopic neuroimaging across all species will be considered if informative for understanding the aforementioned relationships.