4.4 Review

Neuroprogression in bipolar disorder

期刊

BIPOLAR DISORDERS
卷 14, 期 4, 页码 356-374

出版社

WILEY-BLACKWELL
DOI: 10.1111/j.1399-5618.2012.01024.x

关键词

bipolar disorder; degeneration; development; magnetic resonance imaging (MRI) neuroimaging; progression

资金

  1. National Institute of Health (NIH) [R01MH078043, R01MH078043S1, P50MH077138, R01MH080973, R34MH083924, R01MH07193]
  2. AstraZeneca
  3. Bristol-Myers Squibb
  4. Eli Lilly Co.
  5. Forrest
  6. Amylin
  7. GlaxoSmithKline
  8. Pfizer
  9. Janssen
  10. Merck
  11. Novartis
  12. Johnson Johnson
  13. Martek Biosciences Inc.
  14. Inflammation Research Foundation
  15. Ortho-McNeil Janssen
  16. NARSAD
  17. NIMH
  18. NIA
  19. Sumatomo
  20. NIDA
  21. NIAAA
  22. Otzuka
  23. Sunovion

向作者/读者索取更多资源

Schneider MR, DelBello MP, McNamara RK, Strakowski SM, Adler CM. Neuroprogression in bipolar disorder. ?Bipolar Disord 2012: 14: 356374. (c) 2012 The Authors. Journal compilation (c) 2012 John Wiley & Sons A/S. Objective: Recent theories regarding the neuropathology of bipolar disorder suggest that both neurodevelopmental and neurodegenerative processes may play a role. While magnetic resonance imaging has provided significant insight into the structural, functional, and connectivity abnormalities associated with bipolar disorder, research assessing longitudinal changes has been more limited. However, such research is essential to elucidate the pathophysiology of the disorder. The aim of our review is to examine the extant literature for developmental and progressive structural and functional changes in individuals with and at risk for bipolar disorder. Methods: We conducted a literature review using MEDLINE and the following search terms: bipolar disorder, risk, child, adolescent, bipolar offspring, MRI, fMRI, DTI, PET, SPECT, cross-sectional, longitudinal, progressive, and developmental. Further relevant articles were identified by cross-referencing with identified manuscripts. Conclusions: There is some evidence for developmental and progressive neurophysiological alterations in bipolar disorder, but the interpretation of correlations between neuroimaging findings and measures of illness exposure or age in cross-sectional studies must be performed with care. Prospective longitudinal studies placed in the context of normative developmental and atrophic changes in neural structures and pathways thought to be involved in bipolar disorder are needed to improve our understanding of the neurodevelopmental underpinnings and progressive changes associated with bipolar disorder.

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