4.6 Article

Prediction of Depression in Individuals at High Familial Risk of Mood Disorders Using Functional Magnetic Resonance Imaging

期刊

PLOS ONE
卷 8, 期 3, 页码 -

出版社

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0057357

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资金

  1. Royal Society [DH080018]
  2. Medical Research Council
  3. Scottish Senior Clinical Fellowship
  4. Wellcome Trust
  5. Health Foundation through Clinician Scientist Fellowship [2268/4295]
  6. Brain and Behaviour Research Foundation through NARSAD Independent Investigator Award
  7. Scottish Funding Council Senior Clinical Fellowship
  8. National Health Service (NHS) Research Scotland, through the Scottish Mental Health Research Network
  9. Dr Mortimer and Theresa Sackler Foundation
  10. Pfizer
  11. SINAPSE (Scottish Imaging Network, a Platform for Scientific Excellence)
  12. MRC [G0600429] Funding Source: UKRI
  13. Royal Society [DH080018] Funding Source: Royal Society
  14. Academy of Medical Sciences (AMS) [AMS-CSF2-McIntosh] Funding Source: researchfish
  15. Medical Research Council [G0600429, G0801418B] Funding Source: researchfish

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Objective: Bipolar disorder is a highly heritable condition. First-degree relatives of affected individuals have a more than a ten-fold increased risk of developing bipolar disorder (BD), and a three-fold risk of developing major depressive disorder (MDD) than the general population. It is unclear however whether differences in brain activation reported in BD and MDD are present before the onset of illness. Methods: We studied 98 young unaffected individuals at high familial risk of BD and 58 healthy controls using functional Magnetic Resonance Imaging (fMRI) scans and a task involving executive and language processing. Twenty of the high-risk subjects subsequently developed MDD after the baseline fMRI scan. Results: At baseline the high-risk subjects who later developed MDD demonstrated relatively increased activation in the insula cortex, compared to controls and high risk subjects who remained well. In the healthy controls and high-risk group who remained well, this region demonstrated reduced engagement with increasing task difficulty. The high risk subjects who subsequently developed MDD did not demonstrate this normal disengagement. Activation in this region correlated positively with measures of cyclothymia and neuroticism at baseline, but not with measures of depression. Conclusions: These results suggest that increased activation of the insula can differentiate individuals at high-risk of bipolar disorder who later develop MDD from healthy controls and those at familial risk who remain well. These findings offer the potential of future risk stratification in individuals at risk of mood disorder for familial reasons.

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