TY - JOUR
T1 - Machine learning reveals distinct neuroanatomical signatures of cardiovascular and metabolic diseases in cognitively unimpaired individuals
AU - Govindarajan, Sindhuja Tirumalai
AU - Mamourian, Elizabeth
AU - Erus, Guray
AU - Abdulkadir, Ahmed
AU - Melhem, Randa
AU - Doshi, Jimit
AU - Pomponio, Raymond
AU - Tosun, Duygu
AU - Bilgel, Murat
AU - An, Yang
AU - Sotiras, Aristeidis
AU - Marcus, Daniel S.
AU - LaMontagne, Pamela
AU - Benzinger, Tammie L.S.
AU - Espeland, Mark A.
AU - Masters, Colin L.
AU - Maruff, Paul
AU - Launer, Lenore J.
AU - Fripp, Jurgen
AU - Johnson, Sterling C.
AU - Morris, John C.
AU - Albert, Marilyn S.
AU - Bryan, R. Nick
AU - Resnick, Susan M.
AU - Habes, Mohamad
AU - Shou, Haochang
AU - Wolk, David A.
AU - Nasrallah, Ilya M.
AU - Davatzikos, Christos
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12
Y1 - 2025/12
N2 - Comorbid cardiovascular and metabolic risk factors (CVM) differentially impact brain structure and increase dementia risk, but their specific magnetic resonance imaging signatures (MRI) remain poorly characterized. To address this, we developed and validated machine learning models to quantify the distinct spatial patterns of atrophy and white matter hyperintensities related to hypertension, hyperlipidemia, smoking, obesity, and type-2 diabetes mellitus at the patient level. Using harmonized MRI data from 37,096 participants (45–85 years) in a large multinational dataset of 10 cohort studies, we generated five in silico severity markers that: i) outperformed conventional structural MRI markers with a ten-fold increase in effect sizes, ii) captured subtle patterns at sub-clinical CVM stages, iii) were most sensitive in mid-life (45–64 years), iv) were associated with brain beta-amyloid status, and v) showed stronger associations with cognitive performance than diagnostic CVM status. Integrating personalized measurements of CVM-specific brain signatures into phenotypic frameworks could guide early risk detection and stratification in clinical studies.
AB - Comorbid cardiovascular and metabolic risk factors (CVM) differentially impact brain structure and increase dementia risk, but their specific magnetic resonance imaging signatures (MRI) remain poorly characterized. To address this, we developed and validated machine learning models to quantify the distinct spatial patterns of atrophy and white matter hyperintensities related to hypertension, hyperlipidemia, smoking, obesity, and type-2 diabetes mellitus at the patient level. Using harmonized MRI data from 37,096 participants (45–85 years) in a large multinational dataset of 10 cohort studies, we generated five in silico severity markers that: i) outperformed conventional structural MRI markers with a ten-fold increase in effect sizes, ii) captured subtle patterns at sub-clinical CVM stages, iii) were most sensitive in mid-life (45–64 years), iv) were associated with brain beta-amyloid status, and v) showed stronger associations with cognitive performance than diagnostic CVM status. Integrating personalized measurements of CVM-specific brain signatures into phenotypic frameworks could guide early risk detection and stratification in clinical studies.
UR - http://www.scopus.com/inward/record.url?scp=105000392237&partnerID=8YFLogxK
U2 - 10.1038/s41467-025-57867-7
DO - 10.1038/s41467-025-57867-7
M3 - Article
C2 - 40108173
AN - SCOPUS:105000392237
SN - 2041-1723
VL - 16
JO - Nature communications
JF - Nature communications
IS - 1
M1 - 2724
ER -