Cargando…

Arterial spin labeling characterization of cerebral perfusion during normal maturation from late childhood into adulthood: normal ‘reference range' values and their use in clinical studies

The human brain changes structurally and functionally during adolescence, with associated alterations in cerebral perfusion. We performed dynamic arterial spin labeling (ASL) magnetic resonance imaging in healthy subjects between 8 and 32 years of age, to investigate changes in cerebral hemodynamics...

Descripción completa

Detalles Bibliográficos
Autores principales: Hales, Patrick W, Kawadler, Jamie M, Aylett, Sarah E, Kirkham, Fenella J, Clark, Christopher A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013758/
https://www.ncbi.nlm.nih.gov/pubmed/24496173
http://dx.doi.org/10.1038/jcbfm.2014.17
Descripción
Sumario:The human brain changes structurally and functionally during adolescence, with associated alterations in cerebral perfusion. We performed dynamic arterial spin labeling (ASL) magnetic resonance imaging in healthy subjects between 8 and 32 years of age, to investigate changes in cerebral hemodynamics during normal development. In addition, an inversion recovery sequence allowed quantification of changes in longitudinal relaxation time (T(1)) and equilibrium longitudinal magnetization (M(0)). We present mean and reference ranges for normal values of T(1), M(0), cerebral blood flow (CBF), bolus arrival time, and bolus duration in cortical gray matter, to provide a tool for identifying age-matched perfusion abnormalities in this age range in clinical studies. Cerebral blood flow and T(1) relaxation times were negatively correlated with age, without gender or hemisphere differences. The same was true for M(0) anteriorly, but posteriorly, males but not females showed a significant decline in M(0) with increasing age. Two examples of the clinical utility of these data in identifying age-matched perfusion abnormalities, in Sturge–Weber syndrome and sickle cell anemia, are illustrated.