MRI of healthy brain aging: A review. (6th June 2021)

• Record Type: Journal Article
• Authors: MacDonald, M. Ethan; Pike, G. Bruce
• Is Part Of: NMR in biomedicine. Volume 34:Number 9(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-06-06
• Subjects: Nuclear magnetic resonance -- Periodicals; Magnetic Resonance Spectroscopy -- Periodicals; 574
• DOI: 10.1002/nbm.4564
• Languages: English
• ISSNs: 0952-3480

Abstract

Abstract : We present a review of the characterization of healthy brain aging using MRI with an emphasis on morphology, lesions, and quantitative MR parameters. A scope review found 6612 articles encompassing the keywords "Brain Aging" and "Magnetic Resonance"; papers involving functional MRI or not involving imaging of healthy human brain aging were discarded, leaving 2246 articles. We first consider some of the biogerontological mechanisms of aging, and the consequences of aging in terms of cognition and onset of disease. Morphological changes with aging are reviewed for the whole brain, cerebral cortex, white matter, subcortical gray matter, and other individual structures. In general, volume and cortical thickness decline with age, beginning in mid‐life. Prevalent silent lesions such as white matter hyperintensities, microbleeds, and lacunar infarcts are also observed with increasing frequency. The literature regarding quantitative MR parameter changes includes T 1, T 2, T 2 *, magnetic susceptibility, spectroscopy, magnetization transfer, diffusion, and blood flow. We summarize the findings on how each of these parameters varies with aging. Finally, we examine how the aforementioned techniques have been used for age prediction. While relatively large in scope, we present a comprehensive review that should provide the reader with sound understanding of what MRI has been able to tell us about how the healthy brain ages. Abstract : This review covers normal healthy brain aging and findings of many MRI contrasts. Brain morphology, lesions and multiple quantitative parameters, including T, T 2, T 2 *, spectroscopy, magnetization transfer, diffusion, and blood flow, are reviewed with respect to their changes with age; we then review age modelling and some of the potential future directions.