Effect of BDNF Val66Met polymorphism on hippocampal subfields in multiple sclerosis patients

Author(s):  
Ermelinda De Meo ◽  
Emilio Portaccio ◽  
Elio Prestipino ◽  
Benedetta Nacmias ◽  
Silvia Bagnoli ◽  
...  
PLoS ONE ◽  
2013 ◽  
Vol 8 (4) ◽  
pp. e61063 ◽  
Author(s):  
Francesco Fera ◽  
Luca Passamonti ◽  
Antonio Cerasa ◽  
Maria Cecilia Gioia ◽  
Maria Liguori ◽  
...  

2010 ◽  
Vol 32 (1) ◽  
pp. 117-123 ◽  
Author(s):  
D. Dinacci ◽  
A. Tessitore ◽  
A. Russo ◽  
M. L. De Bonis ◽  
L. Lavorgna ◽  
...  

2010 ◽  
Vol 207 (2) ◽  
pp. 377-386 ◽  
Author(s):  
Antonio Cerasa ◽  
Enrico Tongiorgi ◽  
Francesco Fera ◽  
Maria C. Gioia ◽  
Paola Valentino ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Emilio Portaccio ◽  
Angelo Bellinvia ◽  
Elio Prestipino ◽  
Benedetta Nacmias ◽  
Silvia Bagnoli ◽  
...  

Introduction: Brain-derived neurotrophic factor (BDNF) is a member of the neurotrophin family, involved in neuronal survival and synaptic plasticity. The BDNF Val66Met polymorphism is known to reduce BDNF expression and secretion; its role in multiple sclerosis (MS) is poorly investigated.Objectives and Methods: In this multicenter, retrospective study, we assessed the role of BDNF Val66Met polymorphism on cognitive and motor disability in MS patients consecutively referred to the University of Florence and the Hospital of Barletta. All patients underwent a genetic analysis for the presence of Val66Met polymorphism and a comprehensive neuropsychological examination on the Rao's Brief Repeatable Battery and the Stroop Color Word Test. Possible predictors of the Expanded Disability Status Scale (EDSS) score and number of failed neuropsychological tests were assessed through linear multivariable regression models.Results: Ninety-eight patients were recruited. Patients with the BDNF Val66Met polymorphism (35.7%) were more frequently males (p = 0.020), more disabled (p = 0.026) and, marginally, older (p = 0.064). In the multivariable analysis, BDNF Val66Met polymorphism was associated with a better cognitive performance (B = −1.1 ± 0.5, p = 0.027). Higher EDSS score was associated with a progressive disease course (B = 3.4, p < 0.001) and, marginally, with the presence of the BDNF Val66Met polymorphism (B = 0.56, p = 0.066).Discussion: Our results preliminarily suggest a protective role of BDNF Val66Met polymorphism against cognitive impairment in MS patients, possibly related to a detrimental effect of increased BDNF concentration in a neuroinflammatory environment.


2019 ◽  
Vol 15 ◽  
pp. P286-P288
Author(s):  
Natalia Vilor-Tejedor ◽  
Grégory Operto ◽  
Carles Falcon ◽  
Marta Crous-Bou ◽  
Diego Garrido-Martín ◽  
...  

2005 ◽  
Vol 167 (1-2) ◽  
pp. 183-185 ◽  
Author(s):  
S. Lindquist ◽  
B.H. Schott ◽  
M. Ban ◽  
D.A.S. Compston ◽  
S. Sawcer ◽  
...  

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