Metabolic connectivity as index of verbal working memory.
Zou NDepartment of Industrial Engineering, Arizona State University, Tempe, Arizona, USA.
Chetelat GInserm-EPHE-Université de Caen, Caen, France.
Baydogan MGDepartment of Industrial Engineering, Bogazici University, Istanbul, Turkey.
Li JDepartment of Industrial Engineering, Arizona State University, Tempe, Arizona, USA.
Fischer FUDepartment of Psychiatry and Psychotherapy, University Medical Center Mainz, Mainz, Germany.
Titov DDepartment of Nuclear Medicine, Technische Universität München, Munich, Germany.
Dukart J1] Service of Neurology, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland [2] Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.
Fellgiebel ADepartment of Psychiatry and Psychotherapy, University Medical Center Mainz, Mainz, Germany.
Schreckenberger MDepartment of Nuclear Medicine, University Medical Center Mainz, Mainz, Germany.
Yakushev I1] Department of Psychiatry and Psychotherapy, University Medical Center Mainz, Mainz, Germany [2] Department of Nuclear Medicine, Technische Universität München, Munich, Germany [3] Neuroimaging Center (TUM-NIC), Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
English
Positron emission tomography (PET) data are commonly analyzed in terms of regional intensity, while covariant information is not taken into account. Here, we searched for network correlates of healthy cognitive function in resting state PET data. PET with [(18)F]-fluorodeoxyglucose and a test of verbal working memory (WM) were administered to 35 young healthy adults. Metabolic connectivity was modeled at a group level using sparse inverse covariance estimation. Among 13 WM-relevant Brodmann areas (BAs), 6 appeared to be robustly connected. Connectivity within this network was significantly stronger in subjects with above-median WM performance. In respect to regional intensity, i.e., metabolism, no difference between groups was found. The results encourage examination of covariant patterns in FDG-PET data from non-neurodegenerative populations.