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fMRI activation in late‐life anxious depression: a potential biomarker
Author(s) -
Andreescu Carmen,
Butters Meryl,
Lenze Eric J.,
Venkatraman Vijay K.,
Nable Megan,
Reynolds Charles F.,
Aizenstein Howard J.
Publication year - 2009
Publication title -
international journal of geriatric psychiatry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 129
eISSN - 1099-1166
pISSN - 0885-6230
DOI - 10.1002/gps.2327
Subject(s) - depression (economics) , biomarker , psychology , late life depression , anxiety , psychiatry , clinical psychology , neuroscience , medicine , cognition , biology , biochemistry , macroeconomics , economics
Objective and Methods The neurobiology of late‐life anxious depression (LLAD) is poorly characterized despite evidence that this is a common and severe subtype of late‐life depression. To identify the neuroanatomical substrate of LLAD, we examined event‐related fMRI data collected in eight subjects with late‐life depression, half of whom had high levels of comorbid anxiety. Subjects were trained on the Preparing to Overcome Prepotency (POP) task, which is an executive control task that reliably activates the lateral prefrontal cortex–anterior cingulate cortex (ACC) cognitive control circuit. Results Time series analysis showed that, when compared with elderly depressed subjects, elderly subjects with anxious depression performing the POP task produced a significantly greater and more sustained signal in three regions: BA24 (dorsal anterior cingulate), BA31 (posterior cingulate), and BA6 (prefrontal cortex). While elderly subjects with pure depression presented a bimodal activation curve in the dorsal anterior cingulate and the posterior cingulate, elderly subjects with anxious depression presented a sustained unimodal activation pattern. Conclusions Our preliminary results suggest specific activation patterns unique to anxious depression that may suggest greater and more sustained efforts of the ACC to carry out cognitive control tasks. Further research is needed to clarify the neuroanatomical basis of LLAD. Copyright © 2009 John Wiley & Sons, Ltd.