AI Article Synopsis

  • Traumatic brain injury (TBI) can impair consciousness, and recent studies suggest that diffusion tensor imaging metrics like fractional anisotropy (FA) and apparent diffusion coefficient (ADC) are linked to consciousness levels.
  • A meta-analysis of 16 studies with 701 participants found that FA showed moderate to strong positive correlations with consciousness levels in certain brain regions, particularly the corpus callosum.
  • In contrast, ADC showed negative correlations that weren't significant, indicating FA is a more reliable measure for assessing consciousness affected by TBI, especially in the body's and splenium of the corpus callosum.

Article Abstract

Traumatic brain injury (TBI) often leads to impaired consciousness. Recent diffusion tensor imaging studies associated consciousness with imaging metrics including fractional anisotropy (FA) and apparent diffusion coefficient (ADC). We evaluated their correlations and determined the best index in candidate regions. Six databases were searched, including PubMed and Embase, and 16 studies with 701 participants were included. Data from region-of-interest and whole-brain analysis methods were meta-analysed separately. The FA-consciousness correlation was marginal in the whole-brain white matter (r = 0.63, 95% CI [0.47, 0.79], p = 0.000) and the corpus callosum (CC) (r = 0.60, 95% CI [0.48, 0.71], p = 0.000), and moderate in the internal capsule (r = 0.48, 95% CI [0.24, 0.72], p = 0.000). Correlations with ADC trended negative and lacked significance. Further subgroup analysis revealed that consciousness levels correlated strongly with FA in the CC body (r = 0.66, 95% CI [0.43, 0.89]), moderately in the splenium (r = 0.58, 95% CI [0.38, 0.78]), but insignificantly in the genu. In conclusion, FA correlates better with consciousness levels than ADC in TBI. The degree of correlation varies among brain regions. The CC (especially its splenium and body) is a reliable candidate region to quantitatively reflect consciousness levels.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5459858PMC
http://dx.doi.org/10.1038/s41598-017-02950-3DOI Listing

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