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Sex differences in predictors and regional patterns of brain age gap estimates

The brain‐age‐gap estimate (brainAGE) quantifies the difference between chronological age and age predicted by applying machine‐learning models to neuroimaging data and is considered a biomarker of brain health. Understanding sex differences in brainAGE is a significant step toward precision medicin...

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Detalles Bibliográficos
Autores principales: Sanford, Nicole, Ge, Ruiyang, Antoniades, Mathilde, Modabbernia, Amirhossein, Haas, Shalaila S., Whalley, Heather C., Galea, Liisa, Popescu, Sebastian G., Cole, James H., Frangou, Sophia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491279/
https://www.ncbi.nlm.nih.gov/pubmed/35790053
http://dx.doi.org/10.1002/hbm.25983
Descripción
Sumario:The brain‐age‐gap estimate (brainAGE) quantifies the difference between chronological age and age predicted by applying machine‐learning models to neuroimaging data and is considered a biomarker of brain health. Understanding sex differences in brainAGE is a significant step toward precision medicine. Global and local brainAGE (G‐brainAGE and L‐brainAGE, respectively) were computed by applying machine learning algorithms to brain structural magnetic resonance imaging data from 1113 healthy young adults (54.45% females; age range: 22–37 years) participating in the Human Connectome Project. Sex differences were determined in G‐brainAGE and L‐brainAGE. Random forest regression was used to determine sex‐specific associations between G‐brainAGE and non‐imaging measures pertaining to sociodemographic characteristics and mental, physical, and cognitive functions. L‐brainAGE showed sex‐specific differences; in females, compared to males, L‐brainAGE was higher in the cerebellum and brainstem and lower in the prefrontal cortex and insula. Although sex differences in G‐brainAGE were minimal, associations between G‐brainAGE and non‐imaging measures differed between sexes with the exception of poor sleep quality, which was common to both. While univariate relationships were small, the most important predictor of higher G‐brainAGE was self‐identification as non‐white in males and systolic blood pressure in females. The results demonstrate the value of applying sex‐specific analyses and machine learning methods to advance our understanding of sex‐related differences in factors that influence the rate of brain aging and provide a foundation for targeted interventions.