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Δευτέρα 24 Απριλίου 2017

Diffusion-Tensor Imaging Findings and Cognitive Function Following Hospitalised Mixed-Mechanism Mild Traumatic Brain Injury: A Systematic Review and Meta-Analysis.

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Diffusion-Tensor Imaging Findings and Cognitive Function Following Hospitalised Mixed-Mechanism Mild Traumatic Brain Injury: A Systematic Review and Meta-Analysis.

Arch Phys Med Rehabil. 2017 Apr 19;:

Authors: Oehr L, Anderson J

Abstract
OBJECTIVE: To undertake a systematic review and meta-analysis of the relationship between microstructural damage and cognitive function following hospitalised mixed-mechanism (HMM) mild traumatic brain injury (mTBI).
DATA SOURCES: PsycInfo, Embase, and Medline were used to find relevant empirical papers published between January 2002 to January 2016.
STUDY SELECTION: Studies that examined the specific relationship between diffusion tensor imaging (DTI) and cognitive test performance were included. The final sample comprised previously medically and psychiatrically healthy adults with HMM mTBI.
DATA EXTRACTION: Specific data was extracted including mTBI definitional criteria, descriptive statistics, outcome measures, and specific results of associations between DTI metrics and cognitive test performance.
DATA SYNTHESIS: Of the 248 original articles retrieved and reviewed, 8 studies met all inclusion criteria and were included in the meta-analysis. The meta-analysis revealed statistically significant associations between reduced white matter integrity and poor performance on measures of attention (FA: d=.413, p<.001; MD: d=-.407, p=.001), memory (FA: d=.347, p<.001; MD: d=-.568, p<.001), and executive function (FA: d=.246, p<.05), which persisted beyond one-month post-injury.
CONCLUSIONS: The findings from the meta-analysis provide clear support for an association between in vivo markers of underlying neuropathology and cognitive function following mTBI. Furthermore, these results demonstrate clearly for the first time that in vivo markers of structural neuropathology are associated with cognitive dysfunction within the domains of attention, memory and executive function. These findings provide an avenue for future research to examine the causal relationship between mTBI-related neuropathology and cognitive dysfunction. Furthermore, they have important implications for clinical management of mTBI patients as they provide a more comprehensive understanding of factors that are associated with cognitive dysfunction following mTBI.

PMID: 28433414 [PubMed - as supplied by publisher]



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