TY - JOUR
T1 - Radiomics-Derived Brain Age Predicts Functional Outcome after Acute Ischemic Stroke
AU - Bretzner, Martin
AU - Bonkhoff, Anna K.
AU - Schirmer, Markus D.
AU - Hong, Sungmin
AU - Dalca, Adrian
AU - Donahue, Kathleen
AU - Giese, Anne Katrin
AU - Etherton, Mark R.
AU - Rist, Pamela M.
AU - Nardin, Marco
AU - Regenhardt, Robert W.
AU - Leclerc, Xavier
AU - Lopes, Renaud
AU - Gautherot, Morgan
AU - Wang, Clinton
AU - Benavente, Oscar R.
AU - Cole, John W.
AU - Donatti, Amanda
AU - Griessenauer, Christoph
AU - Heitsch, Laura
AU - Holmegaard, Lukas
AU - Jood, Katarina
AU - Jimenez-Conde, Jordi
AU - Kittner, Steven J.
AU - Lemmens, Robin
AU - Levi, Christopher R.
AU - McArdle, Patrick F.
AU - McDonough, Caitrin W.
AU - Meschia, James F.
AU - Phuah, Chia Ling
AU - Rolfs, Arndt
AU - Ropele, Stefan
AU - Rosand, Jonathan
AU - Roquer, Jaume
AU - Rundek, Tatjana
AU - Sacco, Ralph L.
AU - Schmidt, Reinhold
AU - Sharma, Pankaj
AU - Slowik, Agnieszka
AU - Sousa, Alessandro
AU - Stanne, Tara M.
AU - Strbian, Daniel
AU - Tatlisumak, Turgut
AU - Thijs, Vincent
AU - Vagal, Achala
AU - Wasselius, Johan
AU - Woo, Daniel
AU - Wu, Ona
AU - Zand, Ramin
AU - Worrall, Bradford B.
AU - Maguire, Jane
AU - Lindgren, Arne G.
AU - Jern, Christina
AU - Golland, Polina
AU - Kuchcinski, Grégory
AU - Rost, Natalia S.
N1 - Funding Information:
The MRI-GENIE study was funded by NIH NINDS (R01NS086905, NSR PI). M.B was supported by the ISITE-ULNE Fundation, the Société Française de Neuroradiologie, the Société Française de Radiologie, and the Thérèse and René Planiol Fundation. A.K.B. is supported by a MGH ECOR Fund for Medical Discovery (FMD) Clinical Research Fellowship Award. MRE is supported by the American Academy of Neurology and MGH Executive Council on Research. PMR is supported by NIH K01 HL128791. TT was supported by the Helsinki University Central Hospital, Sigrid Juselius Foundation, Sahlgrenska University Hospital, and University of Gothenburg. A.G.L was supported by the Swedish Heart and Lung Foundation, Region Skåne, Lund University, Skåne University Hospital, Sparbanksstiftelsen Färs och Frosta, Fremasons Lodge of Instruction Eos in Lund, CaNVAS project was funded by NIH (US), the Swedish Government (under the Avtal om Läkarutbildning och Medicinsk Forskning, ALF); C.J. was supported by the Swedish Heart and Lung Foundation (20190203); and the Swedish state under the agreement between the Swedish government and the county councils, the ALF agreement (ALFGBG-720081) PL is supported by NIH NIBIB NAC P41EB015902; The funders had no role in design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
Funding Information:
M. Etherton has received personal fees for consulting from Astra Zeneca and WorldCare Clinical Group. C. Griessenauer has received consulting honoraria from Microvention and Stryker and research funding from Medtronic and Penumbra. A. Vagal has received research funding from Cerenovus. A.G. Lindgren has received personal fees from Bayer, Astra Zeneca, BMS Pfizer, and Portola. N.S. Rost has received compensation as scientific advisory consultant from Omniox, Sanofi Genzyme, and AbbVie Inc. The other authors report no relevant disclosures. Go to Neurology.org/N for full disclosures.
Publisher Copyright:
© American Academy of Neurology.
PY - 2023/2/21
Y1 - 2023/2/21
N2 - Background and ObjectivesWhile chronological age is one of the most influential determinants of poststroke 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 patients with stroke will be associated with cardiovascular risk factors and worse functional outcomes.MethodsWe 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 with 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.ResultsWe reviewed 4,163 patients from a large multisite ischemic stroke cohort (mean age = 62.8 years, 42.0% female patients). 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.DiscussionT2-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.
AB - Background and ObjectivesWhile chronological age is one of the most influential determinants of poststroke 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 patients with stroke will be associated with cardiovascular risk factors and worse functional outcomes.MethodsWe 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 with 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.ResultsWe reviewed 4,163 patients from a large multisite ischemic stroke cohort (mean age = 62.8 years, 42.0% female patients). 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.DiscussionT2-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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U2 - 10.1212/WNL.0000000000201596
DO - 10.1212/WNL.0000000000201596
M3 - Article
C2 - 36443016
AN - SCOPUS:85149484351
SN - 0028-3878
VL - 100
SP - E822-E833
JO - Neurology
JF - Neurology
IS - 8
ER -