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Age and sex effects on advanced white matter microstructure measures in 15,628 older adults: A UK biobank study

A comprehensive characterization of the brain’s white matter is critical for improving our understanding of healthy and diseased aging. Here we used diffusion-weighted magnetic resonance imaging (dMRI) to estimate age and sex effects on white matter microstructure in a cross-sectional sample of 15,6...

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Detalles Bibliográficos
Autores principales: Lawrence, Katherine E., Nabulsi, Leila, Santhalingam, Vigneshwaran, Abaryan, Zvart, Villalon-Reina, Julio E., Nir, Talia M., Ba Gari, Iyad, Zhu, Alyssa H., Haddad, Elizabeth, Muir, Alexandra M., Laltoo, Emily, Jahanshad, Neda, Thompson, Paul M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8761720/
https://www.ncbi.nlm.nih.gov/pubmed/34537917
http://dx.doi.org/10.1007/s11682-021-00548-y
Descripción
Sumario:A comprehensive characterization of the brain’s white matter is critical for improving our understanding of healthy and diseased aging. Here we used diffusion-weighted magnetic resonance imaging (dMRI) to estimate age and sex effects on white matter microstructure in a cross-sectional sample of 15,628 adults aged 45–80 years old (47.6% male, 52.4% female). Microstructure was assessed using the following four models: a conventional single-shell model, diffusion tensor imaging (DTI); a more advanced single-shell model, the tensor distribution function (TDF); an advanced multi-shell model, neurite orientation dispersion and density imaging (NODDI); and another advanced multi-shell model, mean apparent propagator MRI (MAPMRI). Age was modeled using a data-driven statistical approach, and normative centile curves were created to provide sex-stratified white matter reference charts. Participant age and sex substantially impacted many aspects of white matter microstructure across the brain, with the advanced dMRI models TDF and NODDI detecting such effects the most sensitively. These findings and the normative reference curves provide an important foundation for the study of healthy and diseased brain aging. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11682-021-00548-y.