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J Neurol Neurosurg Psychiatry doi:10.1136/jnnp.2007.124149

Hippocampal activation in adults with mild cognitive impairment predicts subsequent cognitive decline

  1. Saul L Miller
  1. Massachusetts General Hospital, United States
    1. Elizabeth Fenstermacher
    1. Massachusetts General Hospital, United States
      1. Julie Bates
      1. Massachusetts General Hospital, United States
        1. Deborah Blacker
        1. Massachusetts General Hospital, United States
          1. Reisa A Sperling
          1. Massachusetts General Hospital, United States
            1. Bradford C Dickerson (bradd{at}nmr.mgh.harvard.edu)
            1. Massachusetts General Hospital, United States
              • Published Online First 10 September 2007

              Abstract

              Objective: To use fMRI to investigate whether hippocampal activation during a memory task can predict cognitive decline in individuals with mild cognitive impairment (MCI).

              Methods: Twenty-five older individuals with MCI performed a visual scene-encoding task during fMRI scanning, and were followed clinically for at least 4 years after scanning. A hypothesis-driven analysis of fMRI data was performed. First, fMRI data were analyzed at the group level to identify the regions of the hippocampal formation that were engaged by this memory task. Parameter estimates of each subject’s memory-related hippocampal activation (% signal change) were extracted, and were analyzed with a linear regression model to determine whether hippocampal activation predicted the degree or rate of cognitive decline, defined as change in CDR Sum-of-Boxes (CDR-SB).

              Results:Over 5.9 (± 1.2) years of follow-up after scanning, subjects varied widely in degree and rate of cognitive decline (change in CDR-SB ranged from 0 to 6, and rate ranged from 0 to 1 CDR-SB unit/year). Greater hippocampal activation predicted greater degree and rate of subsequent cognitive decline (p<0.05). This finding was present even after controlling for baseline degree of impairment (CDR-SB), age, education, and hippocampal volume, as well as gender and apolipoprotein E status. In addition, an exploratory whole-brain analysis produced convergent results, demonstrating that the hippocampal formation was the only brain region where activation predicted cognitive decline.

              Conclusions In individuals with MCI, greater memory task-related hippocampal activation is predictive of a greater degree and rate of cognitive decline subsequent to scanning. fMRI may provide a physiologic imaging biomarker useful for identifying the subgroup of MCI individuals at highest risk of cognitive decline for potential inclusion in disease-modifying clinical trials.

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