Cancer 'survivor-care': II. Disruption of prefrontal brain activation top-down control of working memory capacity as possible mechanism for chemo-fog/brain (chemotherapy-associated cognitive impairment)

J Clin Pharm Ther. 2013 Aug;38(4):265-8. doi: 10.1111/jcpt.12071. Epub 2013 May 8.

Abstract

What is known and objective: Cancer chemotherapy-associated cognitive impairments (termed 'chemo-fog' or 'chemo-brain'), particularly in memory, have been self-reported or identified in cancer survivors previously treated with chemotherapy. Although a variety of deficits have been detected, a consistent theme is a detriment in visuospatial working memory. The parietal cortex, a major site of storage of such memory, is implicated in chemotherapy-induced damage. However, if the findings of two recent publications are combined, the (pre)frontal cortex might be an equally viable target. Two recent studies, one postulating a mechanism for 'top-down control' of working memory capacity and another visualizing chemotherapy-induced alterations in brain activation during working memory processing, are reviewed and integrated.

Comment: A computational model and the proposal that the prefrontal cortex plays a role in working memory via top-down control of parietal working memory capacity is consistent with a recent demonstration of decreased frontal hyperactivation following chemotherapy.

What is new and conclusion: Chemotherapy-associated impairment of visuospatial working memory might include the (pre)frontal cortex in addition to the parietal cortex. This provides new opportunity for basic science and clinical investigation.

Keywords: chemo-brain; chemo-fog; control model; frontal cortex; working memory.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Antineoplastic Agents / adverse effects*
  • Cognition Disorders / chemically induced*
  • Cognition Disorders / physiopathology*
  • Humans
  • Memory, Short-Term / drug effects*
  • Memory, Short-Term / physiology*
  • Models, Neurological*
  • Prefrontal Cortex / drug effects*
  • Prefrontal Cortex / physiology*
  • Survivors

Substances

  • Antineoplastic Agents