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Age differences in brain signal variability are robust to multiple vascular controls

A host of studies support that younger, better performing adults express greater moment-to-moment blood oxygen level-dependent (BOLD) signal variability (SD(BOLD)) in various cortical regions, supporting an emerging view that the aging brain may undergo a generalized reduction in dynamic range. Howe...

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Detalles Bibliográficos
Autores principales: Garrett, Douglas D., Lindenberger, Ulman, Hoge, Richard D., Gauthier, Claudine J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5579254/
https://www.ncbi.nlm.nih.gov/pubmed/28860455
http://dx.doi.org/10.1038/s41598-017-09752-7
Descripción
Sumario:A host of studies support that younger, better performing adults express greater moment-to-moment blood oxygen level-dependent (BOLD) signal variability (SD(BOLD)) in various cortical regions, supporting an emerging view that the aging brain may undergo a generalized reduction in dynamic range. However, the exact physiological nature of age differences in SD(BOLD) remains understudied. In a sample of 29 younger and 45 older adults, we examined the contribution of vascular factors to age group differences in fixation-based SD(BOLD) using (1) a dual-echo BOLD/pseudo-continuous arterial spin labeling (pCASL) sequence, and (2) hypercapnia via a computer-controlled gas delivery system. We tested the hypothesis that, although SD(BOLD) may relate to individual differences in absolute cerebral blood flow (CBF), BOLD cerebrovascular reactivity (CVR), or maximum BOLD signal change (M), robust age differences in SD(BOLD) would remain after multiple statistical controls for these vascular factors. As expected, our results demonstrated that brain regions in which younger adults expressed higher SD(BOLD) persisted after comprehensive control of vascular effects. Our findings thus further establish BOLD signal variability as an important marker of the aging brain.