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MRI in older patients-A focused review
Stephan Seiler1, Christian Enzinger1
1Department of Neurology, Medical University of Graz, Auenbruggerplatz 22, 8036 Graz, Austria; Division of Neuroradiology, Vascular and Interventional Radiology, Department of Radiology, Medical University of Graz, Auenbruggerplatz 9, 8036 Graz, Austria.
Abstract:
MRI has considerably increased our pathophysiological knowledge of age-related brain abnormalities. Brain abnormalities regularly seen on MRI of older adults are atrophy, and changes related to small vessel disease (SVD). SVD-related changes include white matter hyperintensities (WMH), lacunes, microbleeds, microinfarcts and perivascular spaces. While atrophy, WMH and lacunes are recognized as important contributors to cognitive decline and dementia, relationships are less clear for microbleeds, microinfarcts and perivascular spaces. Vascular risk factors are considered critical in the development of these changes and being potentially modifiable have become increasingly interesting to researchers and clinicians alike. Managing vascular risk early, particularly hypertension, is a key factor in slowing down the evolution of age-related brain abnormalities and decelerate their detrimental cognitive consequences. Cognition and visible brain abnormalities have a complex relationship, which reaches far beyond what we can understand using standard MRI. Remote effects of lesions and associated- as well as independent network changes likely explain much of the different cognitive trajectories observed with aging. Because of the versatility of MRI in the diagnostic of various diseases, including epilepsy, incident signs of brain aging will be encountered ever more frequently on standard MRI of older adults. To facilitate understanding and ultimately reporting these changes to patients, this review will give a brief overview of MRI findings encountered on MRI of older people. We will discuss their pathology, risk factors, and relationships with cognition. Special emphasis will be given to more recent developments, including remote effects of lesions, and effects on the structural brain network. Relationships between MRI findings in older people and epilepsy will be discussed as well.
Insights
Magnetic Resonance Imaging (MRI) reveals age-related brain changes like atrophy and small vessel disease (SVD). Managing vascular risks, especially hypertension, is crucial for slowing cognitive decline associated with these brain abnormalities.
Area of Science:
- Neurology
- Radiology
- Gerontology
Background:
- Magnetic Resonance Imaging (MRI) significantly enhances understanding of age-related brain abnormalities.
- Common MRI findings in older adults include atrophy and small vessel disease (SVD)-related changes such as white matter hyperintensities (WMH), lacunes, microbleeds, microinfarcts, and enlarged perivascular spaces.
Purpose of the Study:
- To provide an overview of common MRI findings in older adults.
- To discuss the pathology, risk factors, and cognitive relationships of these findings.
- To highlight recent advancements, including remote lesion effects and brain network alterations.
Main Methods:
- Literature review of MRI findings in aging brains.
- Discussion of pathophysiological mechanisms and vascular risk factors.
- Exploration of cognitive correlations and network effects.
Main Results:
- Atrophy, WMH, and lacunes are linked to cognitive decline; the role of microbleeds, microinfarcts, and perivascular spaces is less clear.
- Vascular risk factors, particularly hypertension, are critical in the development of these brain changes.
- Complex relationships exist between visible brain abnormalities, remote lesion effects, network changes, and cognitive trajectories.
Conclusions:
- Early management of vascular risks is vital for mitigating age-related brain abnormalities and cognitive consequences.
- Standard MRI increasingly detects signs of brain aging, necessitating clear patient communication.
- Further research into remote effects and network changes is needed to fully understand cognitive aging.
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