Effects of androgen deprivation on cerebral morphometry in prostate cancer patients--an exploratory study

PLoS One. 2013 Aug 19;8(8):e72032. doi: 10.1371/journal.pone.0072032. eCollection 2013.

Abstract

Background: Androgen deprivation therapy (ADT) is a common treatment for non-metastatic, low-risk prostate cancer, but a potential side effect of ADT is impaired brain functioning. Previous work with functional magnetic resonance imaging (MRI) demonstrated altered prefrontal cortical activations in cognitive control, with undetectable changes in behavioral performance. Given the utility of brain imaging in identifying the potentially deleterious effects of ADT on brain functions, the current study examined the effects of ADT on cerebral structures using high resolution MRI and voxel-based morphometry (VBM).

Methods: High resolution T1 weighted image of the whole brain were acquired at baseline and six months after ADT for 12 prostate cancer patients and 12 demographically matched non-exposed control participants imaged at the same time points. Brain images were segmented into gray matter, white matter and cerebral ventricles using the VBM toolbox as implemented in Statistical Parametric Mapping 8.

Results: Compared to baseline scan, prostate cancer patients undergoing ADT showed decreased gray matter volume in frontopolar cortex, dorsolateral prefrontal cortex and primary motor cortex, whereas the non-exposed control participants did not show such changes. In addition, the decrease in gray matter volume of the primary motor cortex showed a significant correlation with longer reaction time to target detection in a working memory task.

Conclusions: ADT can affect cerebral gray matter volumes in prostate cancer patients. If replicated, these results may facilitate future studies of cognitive function and quality of life in men receiving ADT, and can also help clinicians weigh the benefits and risks of hormonal therapy in the treatment of prostate cancer.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Androgen Antagonists / adverse effects*
  • Androgen Antagonists / therapeutic use
  • Animals
  • Antineoplastic Agents, Hormonal / adverse effects*
  • Antineoplastic Agents, Hormonal / therapeutic use
  • Case-Control Studies
  • Cognitive Dysfunction / chemically induced
  • Cognitive Dysfunction / physiopathology
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Memory / drug effects
  • Middle Aged
  • Motor Cortex / drug effects
  • Motor Cortex / pathology
  • Neuroimaging
  • Organ Size / drug effects
  • Prefrontal Cortex / drug effects
  • Prefrontal Cortex / pathology*
  • Prefrontal Cortex / physiopathology
  • Prostatic Neoplasms / drug therapy*
  • Quality of Life

Substances

  • Androgen Antagonists
  • Antineoplastic Agents, Hormonal