PMID- 25784293 OWN - NLM STAT- MEDLINE DCOM- 20160509 LR - 20181113 IS - 1531-135X (Electronic) IS - 1530-7026 (Print) IS - 1530-7026 (Linking) VI - 15 IP - 3 DP - 2015 Sep TI - Lack of an association of BDNF Val66Met polymorphism and plasma BDNF with hippocampal volume and memory. PG - 625-43 LID - 10.3758/s13415-015-0343-x [doi] AB - Brain-derived neurotrophic factor (BDNF) has been shown to be important for neuronal survival and synaptic plasticity in the hippocampus in nonhuman animals. The Val66Met polymorphism in the BDNF gene, involving a valine (Val) to methionine (Met) substitution at codon 66, has been associated with lower BDNF secretion in vitro. However, there have been mixed results regarding associations between either circulating BDNF or the BDNF Val66Met polymorphism with hippocampal volume and memory in humans. The current study examined the association of BDNF genotype and plasma BDNF with hippocampal volume and memory in two large independent cohorts of middle-aged and older adults (both cognitively normal and early-stage dementia). Sample sizes ranged from 123 to 649. Measures of the BDNF genotype, plasma BDNF, MRI-based hippocampal volume, and memory performance were obtained from the Knight Alzheimer Disease Research Center (ADRC) and the Alzheimer's Disease Neuroimaging Initiative (ADNI). There were no significant differences between BDNF Met+ and Met- groups on either hippocampal volume or memory in either cohort. In addition, plasma BDNF was not significantly associated with either hippocampal volume or memory in either cohort. Neither age, cognitive status, nor gender moderated any of the relationships. Overall, current findings suggest that BDNF genotype and plasma BDNF may not be robust predictors for variance in hippocampal volume and memory in middle age and older adult cohorts. FAU - Kim, Ana AU - Kim A AD - Program in Neuroscience, Division of Biology and Biomedical Sciences, Washington University, St. Louis, MO, USA. FAU - Fagan, Anne M AU - Fagan AM FAU - Goate, Alison M AU - Goate AM FAU - Benzinger, Tammie L S AU - Benzinger TL FAU - Morris, John C AU - Morris JC FAU - Head, Denise AU - Head D CN - Alzheimer's Disease Neuroimaging Initiative LA - eng GR - P50 AG05861/AG/NIA NIH HHS/United States GR - U01 AG024904/AG/NIA NIH HHS/United States GR - P01 AG003991/AG/NIA NIH HHS/United States GR - P50 AG005681/AG/NIA NIH HHS/United States GR - P01 AG026276/AG/NIA NIH HHS/United States GR - P01 AG03991/AG/NIA NIH HHS/United States GR - P30 NS098577/NS/NINDS NIH HHS/United States GR - P30 NS048056/NS/NINDS NIH HHS/United States GR - UL1 TR000448/TR/NCATS NIH HHS/United States GR - T32 AG000030/AG/NIA NIH HHS/United States GR - F32 AG005861/AG/NIA NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't PL - United States TA - Cogn Affect Behav Neurosci JT - Cognitive, affective & behavioral neuroscience JID - 101083946 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 7171WSG8A2 (BDNF protein, human) SB - IM MH - Aged MH - Aging/blood/genetics/pathology/psychology MH - Association Learning/physiology MH - Brain-Derived Neurotrophic Factor/*blood/*genetics MH - Cohort Studies MH - Dementia/genetics/pathology/psychology MH - Female MH - Genotyping Techniques MH - Hippocampus/*anatomy & histology/pathology MH - Humans MH - Magnetic Resonance Imaging MH - Male MH - Memory/*physiology MH - Organ Size MH - *Polymorphism, Single Nucleotide MH - Psychological Tests MH - Sex Characteristics PMC - PMC4529376 MID - NIHMS673156 COIS- The authors have no conflicts of interest related to this work. EDAT- 2015/03/19 06:00 MHDA- 2016/05/10 06:00 PMCR- 2016/09/01 CRDT- 2015/03/19 06:00 PHST- 2015/03/19 06:00 [entrez] PHST- 2015/03/19 06:00 [pubmed] PHST- 2016/05/10 06:00 [medline] PHST- 2016/09/01 00:00 [pmc-release] AID - 10.3758/s13415-015-0343-x [doi] PST - ppublish SO - Cogn Affect Behav Neurosci. 2015 Sep;15(3):625-43. doi: 10.3758/s13415-015-0343-x.