TY - JOUR
T1 - Lower Cerebrospinal Fluid Concentration of Brain-Derived Neurotrophic Factor Predicts Progression from Mild Cognitive Impairment to Alzheimer’s Disease
AU - Forlenza, Orestes Vicente
AU - Diniz, Breno Satler
AU - Teixeira, Antonio Lucio
AU - Radanovic, Marcia
AU - Talib, Leda Leme
AU - Rocha, Natalia Pessoa
AU - Gattaz, Wagner Farid
N1 - Publisher Copyright:
© 2015, Springer Science+Business Media New York.
PY - 2015/9/14
Y1 - 2015/9/14
N2 - There is little information on the dynamics of BDNF in the CSF in the continuum between healthy aging, MCI and AD. We included 128 older adults (77 with amnestic MCI, 26 with AD and 25 healthy controls). CSF BDNF level was measured by ELISA assay, and AD biomarkers (Aβ42, T-Tau and P-Tau181) were measured using a Luminex xMAP assay. CSF BDNF levels were significantly reduced in AD subjects compared to MCI and healthy controls (p = 0.009). Logistic regression models showed that lower CSF BDNF levels (p = 0.008), lower CSF Aβ42 (p = 0.005) and lower MMSE scores (p = 0.007) are significantly associated with progression from MCI to AD. The present study adds strong evidence of the involvement of BDNF in the pathophysiology of neurodegenerative changes in AD. Interventions aiming to restore central neurotrophic support may represent future therapeutic targets to prevent or delay the progression from MCI to AD.
AB - There is little information on the dynamics of BDNF in the CSF in the continuum between healthy aging, MCI and AD. We included 128 older adults (77 with amnestic MCI, 26 with AD and 25 healthy controls). CSF BDNF level was measured by ELISA assay, and AD biomarkers (Aβ42, T-Tau and P-Tau181) were measured using a Luminex xMAP assay. CSF BDNF levels were significantly reduced in AD subjects compared to MCI and healthy controls (p = 0.009). Logistic regression models showed that lower CSF BDNF levels (p = 0.008), lower CSF Aβ42 (p = 0.005) and lower MMSE scores (p = 0.007) are significantly associated with progression from MCI to AD. The present study adds strong evidence of the involvement of BDNF in the pathophysiology of neurodegenerative changes in AD. Interventions aiming to restore central neurotrophic support may represent future therapeutic targets to prevent or delay the progression from MCI to AD.
KW - Alzheimer’s disease
KW - Biomarkers
KW - Brain-derived neurotrophic factor
KW - Cerebrospinal fluid
KW - Mild cognitive impairment
KW - Pathophysiology
UR - http://www.scopus.com/inward/record.url?scp=84938971568&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84938971568&partnerID=8YFLogxK
U2 - 10.1007/s12017-015-8361-y
DO - 10.1007/s12017-015-8361-y
M3 - Article
C2 - 26138246
AN - SCOPUS:84938971568
SN - 1535-1084
VL - 17
SP - 326
EP - 332
JO - NeuroMolecular Medicine
JF - NeuroMolecular Medicine
IS - 3
ER -