4.5 Article

Longitudinal Study of Impaired Intra- and Inter-Network Brain Connectivity in Subjects at High Risk for Alzheimer's Disease

期刊

JOURNAL OF ALZHEIMERS DISEASE
卷 52, 期 3, 页码 913-927

出版社

IOS PRESS
DOI: 10.3233/JAD-160008

关键词

Default mode network; early mild cognitive impairment; late mild cognitive impairment; resting-state network; salience network

资金

  1. Natural Science Foundation of China [81571062, 81270020, 81471120, 81371544, 61305143]
  2. Natural Science Foundation of Beijing [7152096]
  3. Youth Innovation Promotion Association CAS [2014119]
  4. Beijing Nova Program [Z1511000003150112]
  5. Open Project Program of the National Laboratory of Pattern Recognition [201407344]
  6. Alzheimer's Disease Neuroimaging Initiative (ADNI) (National Institutes of Health Grant) [U01AG024904]
  7. DOD ADNI (Department of Defense) [W81XWH-12-2-0012]
  8. National Institute on Aging
  9. National Institute of Biomedical Imaging and Bioengineering
  10. AbbVie
  11. Alzheimer's Association
  12. Alzheimer's Drug Discovery Foundation
  13. Araclon Biotech
  14. BioClinica, Inc.
  15. Biogen
  16. Bristol-Myers Squibb Company
  17. CereSpir, Inc.
  18. Eisai Inc.
  19. Elan Pharmaceuticals, Inc.
  20. Eli Lilly and Company
  21. EuroImmun
  22. F.Hoffmann-La Roche Ltd and its affiliated company Genentech, Inc.
  23. Fujirebio
  24. GE Healthcare
  25. IXICO Ltd.
  26. Janssen Alzheimer Immunotherapy Research & Development, LLC.
  27. Johnson & Johnson Pharmaceutical Research & Development LLC.
  28. Lumosity
  29. Lundbeck
  30. Merck Co., Inc.
  31. Meso Scale Diagnostics, LLC.
  32. NeuroRx Research
  33. Neurotrack Technologies
  34. Novartis Pharmaceuticals Corporation
  35. Pfizer Inc.
  36. Piramal Imaging
  37. Servier
  38. Takeda Pharmaceutical Company
  39. Transition Therapeutics
  40. Canadian Institutes of Health Research
  41. NATIONAL INSTITUTE ON AGING [U01AG024904] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Alzheimer's disease (AD) is associated with abnormal resting-state network (RSN) architecture of the default mode network (DMN), the dorsal attention network (DAN), the executive control network (CON), the salience network (SAL), and the sensory-motor network (SMN). However, little is known about the disrupted intra- and inter-network architecture in mild cognitive impairment (MCI). Here, we employed a priori defined regions of interest to investigate the intra- and inter-network functional connectivity profiles of these RSNs in longitudinal participants, including normal controls (n = 23), participants with early MCI (n = 26), and participants with late MCI (n = 19). We found longitudinal alterations of functional connectivity within the DMN, where they were correlated with variation in cognitive ability. The SAL as well as the interaction between the DMN and the SAL were disrupted in MCI. Furthermore, our results demonstrate that longitudinal alterations of functional connectivity are more profound in earlier stages as opposed to later stages of the disease. The increased severity of cognitive impairment is associated with increasingly altered RSN connectivity patterns, suggesting that disruptions in functional connectivity may contribute to cognitive dysfunction and may represent a potential biomarker of impaired cognitive ability in MCI. Earlier prevention and treatment may help to delay disease progression to AD.

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