PMID- 25444596 OWN - NLM STAT- MEDLINE DCOM- 20151124 LR - 20220316 IS - 1558-1497 (Electronic) IS - 0197-4580 (Linking) VI - 36 IP - 3 DP - 2015 Mar TI - BDNF polymorphism associates with decline in set shifting in Parkinson's disease. PG - 1605.e1-6 LID - S0197-4580(14)00536-3 [pii] LID - 10.1016/j.neurobiolaging.2014.08.023 [doi] AB - Parkinson's disease (PD) is a neurodegenerative disorder caused by nigrostriatal dopaminergic degeneration. Brain-derived neurotrophic factor (BDNF) is a key protein in brain plasticity and is particularly important for survival of dopaminergic neurons. The Val66Met polymorphism of BDNF (rs6265) has been associated with functional differences (mainly cognitive) between healthy adults and also with differences in the clinical expression of several other neuropsychiatric illnesses including PD. However, these studies used different outcome measures, have not been replicated, and were cross sectional, making it difficult to establish the role of BDNF in the clinical variability of PD. Here, a large cohort of 384 PD patients were followed up for 2 years, and associations between BDNF genotype and various clinical characteristics were examined. The BDNF Met-allele carriers showed a significantly smaller decline in set shifting during follow-up compared with the homozygous BDNF Val-allele carriers. Contrary to previous assumptions, these results indicate that mental flexibility is one of the cognitive processes that may benefit from the BDNF Met allele in PD patients. CI - Copyright (c) 2015 Elsevier Inc. All rights reserved. FAU - van der Kolk, Nicolien M AU - van der Kolk NM AD - Department of Neurology, Donders Institute for Brain, Cognition, and Behavior, Radboud University Medical Center, Nijmegen, the Netherlands. FAU - Speelman, Arlene D AU - Speelman AD AD - Department of Neurology, Donders Institute for Brain, Cognition, and Behavior, Radboud University Medical Center, Nijmegen, the Netherlands. FAU - van Nimwegen, Marlies AU - van Nimwegen M AD - Department of Neurology, Donders Institute for Brain, Cognition, and Behavior, Radboud University Medical Center, Nijmegen, the Netherlands. FAU - Kessels, Roy P C AU - Kessels RP AD - Department of Medical Psychology, Radboud University Medical Center, Nijmegen, the Netherlands. FAU - IntHout, Joanna AU - IntHout J AD - Department for Health Evidence, Radboud University Medical Center, Nijmegen, the Netherlands. FAU - Hakobjan, Marina AU - Hakobjan M AD - Department of Human Genetics, Research Lab for Multifactorial Diseases, Radboud University Medical Center, Nijmegen, the Netherlands. FAU - Munneke, Marten AU - Munneke M AD - Department of Neurology, Donders Institute for Brain, Cognition, and Behavior, Radboud University Medical Center, Nijmegen, the Netherlands. FAU - Bloem, Bastiaan R AU - Bloem BR AD - Department of Neurology, Donders Institute for Brain, Cognition, and Behavior, Radboud University Medical Center, Nijmegen, the Netherlands. FAU - van de Warrenburg, Bart P AU - van de Warrenburg BP AD - Department of Neurology, Donders Institute for Brain, Cognition, and Behavior, Radboud University Medical Center, Nijmegen, the Netherlands. Electronic address: Bart.vandewarrenburg@radboudumc.nl. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20140827 PL - United States TA - Neurobiol Aging JT - Neurobiology of aging JID - 8100437 RN - 0 (Brain-Derived Neurotrophic Factor) RN - AE28F7PNPL (Methionine) SB - IM MH - Aged MH - Alleles MH - Brain-Derived Neurotrophic Factor/chemistry/*genetics MH - Cohort Studies MH - Dopaminergic Neurons/pathology MH - Executive Function MH - Female MH - *Genetic Association Studies MH - Genetic Predisposition to Disease/*genetics MH - Genotype MH - Humans MH - Male MH - Methionine/genetics MH - Middle Aged MH - Neuronal Plasticity/genetics MH - Parkinson Disease/*genetics/pathology/psychology MH - Polymorphism, Genetic/*genetics OTO - NOTNLM OT - BDNF OT - Executive function OT - Parkinson's disease EDAT- 2014/12/03 06:00 MHDA- 2015/12/15 06:00 CRDT- 2014/12/03 06:00 PHST- 2014/03/10 00:00 [received] PHST- 2014/08/14 00:00 [revised] PHST- 2014/08/22 00:00 [accepted] PHST- 2014/12/03 06:00 [entrez] PHST- 2014/12/03 06:00 [pubmed] PHST- 2015/12/15 06:00 [medline] AID - S0197-4580(14)00536-3 [pii] AID - 10.1016/j.neurobiolaging.2014.08.023 [doi] PST - ppublish SO - Neurobiol Aging. 2015 Mar;36(3):1605.e1-6. doi: 10.1016/j.neurobiolaging.2014.08.023. Epub 2014 Aug 27.