Preserved self-awareness following extensive bilateral brain damage to the insula, anterior cingulate, and medial prefrontal cortices.

TitlePreserved self-awareness following extensive bilateral brain damage to the insula, anterior cingulate, and medial prefrontal cortices.
Publication TypeJournal Article
Year of Publication2012
AuthorsPhilippi CL, Feinstein JS, Khalsa SS, Damasio A, Tranel D, Landini G, Williford K, Rudrauf D
JournalPLoS One
Volume7
Issue8
Paginatione38413
Date Published2012
ISSN1932-6203
KeywordsAwareness, Behavior, Brain Injuries, Consciousness, Face, Functional Neuroimaging, Gyrus Cinguli, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Prefrontal Cortex, Recognition (Psychology), Smell
Abstract

It has been proposed that self-awareness (SA), a multifaceted phenomenon central to human consciousness, depends critically on specific brain regions, namely the insular cortex, the anterior cingulate cortex (ACC), and the medial prefrontal cortex (mPFC). Such a proposal predicts that damage to these regions should disrupt or even abolish SA. We tested this prediction in a rare neurological patient with extensive bilateral brain damage encompassing the insula, ACC, mPFC, and the medial temporal lobes. In spite of severe amnesia, which partially affected his "autobiographical self", the patient's SA remained fundamentally intact. His Core SA, including basic self-recognition and sense of self-agency, was preserved. His Extended SA and Introspective SA were also largely intact, as he has a stable self-concept and intact higher-order metacognitive abilities. The results suggest that the insular cortex, ACC and mPFC are not required for most aspects of SA. Our findings are compatible with the hypothesis that SA is likely to emerge from more distributed interactions among brain networks including those in the brainstem, thalamus, and posteromedial cortices.

DOI10.1371/journal.pone.0038413
Alternate JournalPLoS ONE
PubMed ID22927899
PubMed Central IDPMC3425501
Grant ListP01 NS19632 / NS / NINDS NIH HHS / United States
R01 DA022549 / DA / NIDA NIH HHS / United States