Radiomics-Derived Brain Age Predicts Functional Outcome After Acute Ischemic Stroke.
Bretzner, M
Bonkhoff, AK
Schirmer, MD
Hong, S
Dalca, A
Donahue, K
Giese, A-K
Etherton, MR
Rist, PM
Nardin, M
Regenhardt, RW
Leclerc, X
Lopes, R
Gautherot, M
Wang, C
Benavente, OR
Cole, JW
Donatti, A
Griessenauer, C
Heitsch, L
Holmegaard, L
Jood, K
Jimenez-Conde, J
Kittner, SJ
Lemmens, R
Levi, CR
McArdle, PF
McDonough, CW
Meschia, JF
Phuah, C-L
Rolfs, A
Ropele, S
Rosand, J
Roquer, J
Rundek, T
Sacco, RL
Schmidt, R
Sharma, P
Slowik, A
Sousa, A
Stanne, TM
Strbian, D
Tatlisumak, T
Thijs, V
Vagal, A
Wasselius, J
Woo, D
Wu, O
Zand, R
Worrall, BB
Maguire, J
Lindgren, AG
Jern, C
Golland, P
Kuchcinski, G
Rost, NS
- Publisher:
- LIPPINCOTT WILLIAMS & WILKINS
- Publication Type:
- Journal Article
- Citation:
- Neurology, 2023, 100, (8), pp. e822-e833
- Issue Date:
- 2023
Closed Access
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Radiomics-Derived Brain Age Predicts Functional Outcome After Acute Ischemic Stroke.pdf | Published version | 441.42 kB | Adobe PDF |
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Bretzner, M | |
dc.contributor.author | Bonkhoff, AK | |
dc.contributor.author | Schirmer, MD | |
dc.contributor.author | Hong, S | |
dc.contributor.author | Dalca, A | |
dc.contributor.author | Donahue, K | |
dc.contributor.author | Giese, A-K | |
dc.contributor.author | Etherton, MR | |
dc.contributor.author | Rist, PM | |
dc.contributor.author | Nardin, M | |
dc.contributor.author | Regenhardt, RW | |
dc.contributor.author | Leclerc, X | |
dc.contributor.author | Lopes, R | |
dc.contributor.author | Gautherot, M | |
dc.contributor.author | Wang, C | |
dc.contributor.author | Benavente, OR | |
dc.contributor.author | Cole, JW | |
dc.contributor.author | Donatti, A | |
dc.contributor.author | Griessenauer, C | |
dc.contributor.author | Heitsch, L | |
dc.contributor.author | Holmegaard, L | |
dc.contributor.author | Jood, K | |
dc.contributor.author | Jimenez-Conde, J | |
dc.contributor.author | Kittner, SJ | |
dc.contributor.author | Lemmens, R | |
dc.contributor.author | Levi, CR | |
dc.contributor.author | McArdle, PF | |
dc.contributor.author | McDonough, CW | |
dc.contributor.author | Meschia, JF | |
dc.contributor.author | Phuah, C-L | |
dc.contributor.author | Rolfs, A | |
dc.contributor.author | Ropele, S | |
dc.contributor.author | Rosand, J | |
dc.contributor.author | Roquer, J | |
dc.contributor.author | Rundek, T | |
dc.contributor.author | Sacco, RL | |
dc.contributor.author | Schmidt, R | |
dc.contributor.author | Sharma, P | |
dc.contributor.author | Slowik, A | |
dc.contributor.author | Sousa, A | |
dc.contributor.author | Stanne, TM | |
dc.contributor.author | Strbian, D | |
dc.contributor.author | Tatlisumak, T | |
dc.contributor.author | Thijs, V | |
dc.contributor.author | Vagal, A | |
dc.contributor.author | Wasselius, J | |
dc.contributor.author | Woo, D | |
dc.contributor.author | Wu, O | |
dc.contributor.author | Zand, R | |
dc.contributor.author | Worrall, BB | |
dc.contributor.author |
Maguire, J https://orcid.org/0000-0001-5722-8311 |
|
dc.contributor.author | Lindgren, AG | |
dc.contributor.author | Jern, C | |
dc.contributor.author | Golland, P | |
dc.contributor.author | Kuchcinski, G | |
dc.contributor.author | Rost, NS | |
dc.date.accessioned | 2024-01-25T05:32:06Z | |
dc.date.available | 2022-10-06 | |
dc.date.available | 2024-01-25T05:32:06Z | |
dc.date.issued | 2023 | |
dc.identifier.citation | Neurology, 2023, 100, (8), pp. e822-e833 | |
dc.identifier.issn | 0028-3878 | |
dc.identifier.issn | 1526-632X | |
dc.identifier.uri | http://hdl.handle.net/10453/174947 | |
dc.description.abstract | BACKGROUND AND OBJECTIVES: While chronological age is one of the most influential determinants of post-stroke outcomes, little is known of the impact of neuroimaging-derived biological "brain age". We hypothesized that radiomics analyses of T2-FLAIR images texture would provide brain age estimates and that advanced brain age of stroke patients will be associated with cardiovascular risk factors and worse functional outcomes. METHODS: We extracted radiomics from T2-FLAIR images acquired during acute stroke clinical evaluation. Brain age was determined from brain parenchyma radiomics using an ElasticNet linear regression model. Subsequently, relative brain age (RBA), which expresses brain age in comparison to chronological age-matched peers, was estimated. Finally, we built a linear regression model of RBA using clinical cardiovascular characteristics as inputs, and a logistic regression model of favorable functional outcomes taking RBA as input. RESULTS: We reviewed 4,163 patients from a large multisite ischemic stroke cohort (mean age=62.8 years, 42.0% females). T2-FLAIR radiomics predicted chronological ages (mean absolute error=6.9 years, r=0.81). After adjustment for covariates, RBA was higher and therefore described older-appearing brains in patients with hypertension, diabetes mellitus, a history of smoking, and a history of a prior stroke. In multivariate analyses, age, RBA, NIHSS, and a history of prior stroke were all significantly associated with functional outcome (respective adjusted Odds-Ratios: 0.58, 0.76, 0.48, 0.55; all p-values<0.001). Moreover, the negative effect of RBA on outcome was especially pronounced in minor strokes. DISCUSSION: T2-FLAIR radiomics can be used to predict brain age and derive RBA. Older appearing brains, characterized by a higher RBA, reflect cardiovascular risk factor accumulation and are linked to worse outcomes after stroke. | |
dc.format | Print-Electronic | |
dc.language | eng | |
dc.publisher | LIPPINCOTT WILLIAMS & WILKINS | |
dc.relation.ispartof | Neurology | |
dc.relation.isbasedon | 10.1212/WNL.0000000000201596 | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | 1103 Clinical Sciences, 1109 Neurosciences, 1702 Cognitive Sciences | |
dc.subject.classification | Neurology & Neurosurgery | |
dc.subject.classification | 3202 Clinical sciences | |
dc.subject.classification | 3209 Neurosciences | |
dc.subject.mesh | Child | |
dc.subject.mesh | Female | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Male | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Brain | |
dc.subject.mesh | Brain Ischemia | |
dc.subject.mesh | Ischemic Stroke | |
dc.subject.mesh | Magnetic Resonance Imaging | |
dc.subject.mesh | Stroke | |
dc.subject.mesh | Brain | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Brain Ischemia | |
dc.subject.mesh | Magnetic Resonance Imaging | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Child | |
dc.subject.mesh | Female | |
dc.subject.mesh | Male | |
dc.subject.mesh | Stroke | |
dc.subject.mesh | Ischemic Stroke | |
dc.subject.mesh | Child | |
dc.subject.mesh | Female | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Male | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Brain | |
dc.subject.mesh | Brain Ischemia | |
dc.subject.mesh | Ischemic Stroke | |
dc.subject.mesh | Magnetic Resonance Imaging | |
dc.subject.mesh | Stroke | |
dc.title | Radiomics-Derived Brain Age Predicts Functional Outcome After Acute Ischemic Stroke. | |
dc.type | Journal Article | |
utslib.citation.volume | 100 | |
utslib.location.activity | United States | |
utslib.for | 1103 Clinical Sciences | |
utslib.for | 1109 Neurosciences | |
utslib.for | 1702 Cognitive Sciences | |
pubs.organisational-group | University of Technology Sydney | |
pubs.organisational-group | University of Technology Sydney/Faculty of Health | |
utslib.copyright.status | closed_access | * |
pubs.consider-herdc | false | |
dc.date.updated | 2024-01-25T05:32:03Z | |
pubs.issue | 8 | |
pubs.publication-status | Published online | |
pubs.volume | 100 | |
utslib.citation.issue | 8 |
Abstract:
BACKGROUND AND OBJECTIVES: While chronological age is one of the most influential determinants of post-stroke outcomes, little is known of the impact of neuroimaging-derived biological "brain age". We hypothesized that radiomics analyses of T2-FLAIR images texture would provide brain age estimates and that advanced brain age of stroke patients will be associated with cardiovascular risk factors and worse functional outcomes. METHODS: We extracted radiomics from T2-FLAIR images acquired during acute stroke clinical evaluation. Brain age was determined from brain parenchyma radiomics using an ElasticNet linear regression model. Subsequently, relative brain age (RBA), which expresses brain age in comparison to chronological age-matched peers, was estimated. Finally, we built a linear regression model of RBA using clinical cardiovascular characteristics as inputs, and a logistic regression model of favorable functional outcomes taking RBA as input. RESULTS: We reviewed 4,163 patients from a large multisite ischemic stroke cohort (mean age=62.8 years, 42.0% females). T2-FLAIR radiomics predicted chronological ages (mean absolute error=6.9 years, r=0.81). After adjustment for covariates, RBA was higher and therefore described older-appearing brains in patients with hypertension, diabetes mellitus, a history of smoking, and a history of a prior stroke. In multivariate analyses, age, RBA, NIHSS, and a history of prior stroke were all significantly associated with functional outcome (respective adjusted Odds-Ratios: 0.58, 0.76, 0.48, 0.55; all p-values<0.001). Moreover, the negative effect of RBA on outcome was especially pronounced in minor strokes. DISCUSSION: T2-FLAIR radiomics can be used to predict brain age and derive RBA. Older appearing brains, characterized by a higher RBA, reflect cardiovascular risk factor accumulation and are linked to worse outcomes after stroke.
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