PMID- 24586380 OWN - NLM STAT- MEDLINE DCOM- 20150109 LR - 20231110 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 9 IP - 2 DP - 2014 TI - Preservation of general intelligence following traumatic brain injury: contributions of the Met66 brain-derived neurotrophic factor. PG - e88733 LID - 10.1371/journal.pone.0088733 [doi] LID - e88733 AB - Brain-derived neurotrophic factor (BDNF) promotes survival and synaptic plasticity in the human brain. The Val66Met polymorphism of the BDNF gene interferes with intracellular trafficking, packaging, and regulated secretion of this neurotrophin. The human prefrontal cortex (PFC) shows lifelong neuroplastic adaption implicating the Val66Met BDNF polymorphism in the recovery of higher-order executive functions after traumatic brain injury (TBI). In this study, we examined the effect of this BDNF polymorphism on the preservation of general intelligence following TBI. We genotyped a sample of male Vietnam combat veterans (n = 156) consisting of a frontal lobe lesion group with focal penetrating head injuries for the Val66Met BDNF polymorphism. Val/Met did not differ from Val/Val genotypes in general cognitive ability before TBI. However, we found substantial average differences between these groups in general intelligence ( approximately half a standard deviation or 8 IQ points), verbal comprehension (6 IQ points), perceptual organization (6 IQ points), working memory (8 IQ points), and processing speed (8 IQ points) after TBI. These results support the conclusion that Val/Met genotypes preserve general cognitive functioning, whereas Val/Val genotypes are largely susceptible to TBI. FAU - Barbey, Aron K AU - Barbey AK AD - Decision Neuroscience Laboratory, University of Illinois, Urbana, Illinois, United States of America ; Beckman Institute for Advanced Science and Technology, University of Illinois, Urbana, Illinois, United States of America ; Department of Internal Medicine, University of Illinois, Champaign, Illinois, United States of America ; Department of Psychology, University of Illinois, Champaign, Illinois, United States of America ; Department of Speech and Hearing Science, University of Illinois, Champaign, Illinois, United States of America ; Neuroscience Program, University of Illinois, Champaign, Illinois, United States of America. FAU - Colom, Roberto AU - Colom R AD - Universidad Autonoma de Madrid, Fundacion CIEN/Fundacion Reina Sofia, Madrid, Spain. FAU - Paul, Erick AU - Paul E AD - Decision Neuroscience Laboratory, University of Illinois, Urbana, Illinois, United States of America ; Beckman Institute for Advanced Science and Technology, University of Illinois, Urbana, Illinois, United States of America. FAU - Forbes, Chad AU - Forbes C AD - Department of Psychology, University of Delaware, Delaware, Maryland, United States of America. FAU - Krueger, Frank AU - Krueger F AD - Department of Molecular Neuroscience, George Mason University, Virginia, United States of America. FAU - Goldman, David AU - Goldman D AD - Laboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland, United States of America. FAU - Grafman, Jordan AU - Grafman J AD - Traumatic Brain Injury Research Laboratory, Rehabilitation Institute of Chicago, Chicago, Illinois, United States of America. LA - eng GR - Intramural NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Intramural PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, Non-P.H.S. DEP - 20140226 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - 0 (Brain-Derived Neurotrophic Factor) RN - AE28F7PNPL (Methionine) SB - IM MH - Aged MH - Brain Injuries/physiopathology/*psychology MH - Brain-Derived Neurotrophic Factor/chemistry/genetics/*physiology MH - Humans MH - *Intelligence MH - Male MH - Methionine/*chemistry MH - Middle Aged MH - Neuropsychological Tests MH - Polymorphism, Single Nucleotide PMC - PMC3935849 COIS- Competing Interests: The authors have declared that no competing interests exist. EDAT- 2014/03/04 06:00 MHDA- 2015/01/13 06:00 PMCR- 2014/02/26 CRDT- 2014/03/04 06:00 PHST- 2013/10/30 00:00 [received] PHST- 2014/01/10 00:00 [accepted] PHST- 2014/03/04 06:00 [entrez] PHST- 2014/03/04 06:00 [pubmed] PHST- 2015/01/13 06:00 [medline] PHST- 2014/02/26 00:00 [pmc-release] AID - PONE-D-13-44492 [pii] AID - 10.1371/journal.pone.0088733 [doi] PST - epublish SO - PLoS One. 2014 Feb 26;9(2):e88733. doi: 10.1371/journal.pone.0088733. eCollection 2014.