TITLE

Effects of androgen deprivation on brain function in prostate cancer patients - a prospective observational cohort analysis

AUTHOR(S)
Chao, Herta H.; Uchio, Edward; Zhang, Sheng; Hu, Sien; Bednarski, Sarah R.; Luo, Xi; Rose, Michal; Concato, John; Li, Chiang-shan R.
PUB. DATE
January 2012
SOURCE
BMC Cancer;2012, Vol. 12 Issue 1, p371
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
Background: Despite a lack of consensus regarding effectiveness, androgen deprivation therapy (ADT) is a common treatment for non-metastatic, low-risk prostate cancer. To examine a particular clinical concern regarding the possible impact of ADT on cognition, the current study combined neuropsychological testing with functional magnetic resonance imaging (fMRI) to assess both brain activation during cognitive performance as well as the integrity of brain connectivity. Methods: In a prospective observational cohort analysis of men with non-metastatic prostate cancer at a Veterans Affairs medical center, patients receiving ADT were compared with patients not receiving ADT at baseline and at 6 months. Assessments included fMRI, the N-back task (for working memory), the stop-signal task (for cognitive control), and a quality of life questionnaire. Results: Among 36 patients enrolled (18 in each group), 30 completed study evaluations (15 in each group); 5 withdrew participation and 1 died. Results for the N-back task, stop-signal task, and quality of life were similar at 6 months vs. baseline in each group. In contrast, statistically significant associations were found between ADT use (vs. non use) and decreased medial prefrontal cortical activation during cognitive control, as well as decreased connectivity between the medial prefrontal cortex and other regions involved with cognitive control. Conclusions: Although ADT for 6 months did not affect selected tests of cognitive function, brain activations during cognitive control and functional brain connectivity were impaired on fMRI. The long-term clinical implications of these changes are not known and warrant future study.
ACCESSION #
84511841

 

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