Background: Studies implicate single nucleotide polymorphism (SNP) rs17070145, a common T→C polymorphism on the KIBRA gene, in mediating differences in episodic memory. In healthy adults, T-allele carriers perform better than non-carriers on episodic memory measures. However, this association is reversed in adults with subjective memory complaints and populations vulnerable to memory deficits, a problem common in traumatic brain injury (TBI). Methods: This study assessed associations between variation in the KIBRA gene and cognitive function in 129 adults with severe TBI. In addition to other executive functioning and functional/global outcomes, the Buschke Selective Reminding Test (SRT), Rey-Osterrieth Complex Figure Test and California Verbal Learning Test-II (CVLT-II) were administered 6 and 12 months post-injury. Results: T-allele non-carriers performed better than carriers on multiple episodic memory measures. At 6 months, T-allele non-carriers performed better for delayed recall measures on the SRT. At 12 months, T-allele non-carriers performed better on multiple SRT measures and on List-B learning with CVLT-II. No associations occurred with executive function or global outcome measures. Conclusion: These results suggest that rs17070145 T-allele effects are specific to episodic memory and support the hypothesis that associations between rs17070145 variation and memory are disparate between healthy and impaired populations. © 2012 Informa UK Ltd.
CITATION STYLE
Wagner, A. K., Hatz, L. E., Scanlon, J. M., Niyonkuru, C., Miller, M. A., Ricker, J. H., … Ferrell, R. E. (2012). Association of KIBRA rs17070145 polymorphism and episodic memory in individuals with severe TBI. Brain Injury, 26(13–14), 1658–1669. https://doi.org/10.3109/02699052.2012.700089
Mendeley helps you to discover research relevant for your work.