PT - JOURNAL ARTICLE AU - Mathew R. Brier AU - Jewell B. Thomas AU - Abraham Z. Snyder AU - Tammie L. Benzinger AU - Dongyang Zhang AU - Marcus E. Raichle AU - David M. Holtzman AU - John C. Morris AU - Beau M. Ances TI - Loss of Intranetwork and Internetwork Resting State Functional Connections with Alzheimer's Disease Progression AID - 10.1523/JNEUROSCI.5698-11.2012 DP - 2012 Jun 27 TA - The Journal of Neuroscience PG - 8890--8899 VI - 32 IP - 26 4099 - http://www.jneurosci.org/content/32/26/8890.short 4100 - http://www.jneurosci.org/content/32/26/8890.full SO - J. Neurosci.2012 Jun 27; 32 AB - Alzheimer's disease (AD) is the most common cause of dementia. Much is known concerning AD pathophysiology but our understanding of the disease at the systems level remains incomplete. Previous AD research has used resting-state functional connectivity magnetic resonance imaging (rs-fcMRI) to assess the integrity of functional networks within the brain. Most studies have focused on the default-mode network (DMN), a primary locus of AD pathology. However, other brain regions are inevitably affected with disease progression. We studied rs-fcMRI in five functionally defined brain networks within a large cohort of human participants of either gender (n = 510) that ranged in AD severity from unaffected [clinical dementia rating (CDR) 0] to very mild (CDR 0.5) to mild (CDR 1). We observed loss of correlations within not only the DMN but other networks at CDR 0.5. Within the salience network (SAL), increases were seen between CDR 0 and CDR 0.5. However, at CDR 1, all networks, including SAL, exhibited reduced correlations. Specific networks were preferentially affected at certain CDR stages. In addition, cross-network relations were consistently lost with increasing AD severity. Our results demonstrate that AD is associated with widespread loss of both intranetwork and internetwork correlations. These results provide insight into AD pathophysiology and reinforce an integrative view of the brain's functional organization.