4.7 Article

Loss of Intranetwork and Internetwork Resting State Functional Connections with Alzheimer's Disease Progression

期刊

JOURNAL OF NEUROSCIENCE
卷 32, 期 26, 页码 8890-8899

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.5698-11.2012

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资金

  1. Medical Scientist Training Program [5T32GM007200-37]
  2. Knight Alzheimer's Disease Research Center (ADRC) Pilot Grant [3255 ADRC 26]
  3. NIMH Grant [K23MH081786, P30NS048056]
  4. National Institute of Nursing Research [R01NR012907, R01NR012657]
  5. Dana Foundation Grant [DF10052]
  6. Alene and Meyer Kopolov Fund for Geriatric Psychiatry and Neurology
  7. National Institute of Aging [P01AG026276, P01AG03991, P50 AG05681]
  8. National Institute of Neurological Disorders and Stroke Grant [NS06833]
  9. Washington University Center for Translational Neuroscience Grant [P30NS057105]
  10. American Roentgen Ray Society Foundation
  11. Avid Radiopharmaceuticals
  12. Janssen Alzheimer Immunotherapy
  13. Eli Lilly
  14. Pfizer

向作者/读者索取更多资源

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.

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