Open AccessPlasma BDNF levels associate with Pittsburgh Compound B binding in the brain
Author(s) -
Hwang Kristy S.,
Lazaris Andreas S.,
Eastman Jennifer A.,
Teng Edmond,
Thompson Paul M.,
Gylys Karen H.,
Cole Gregory M.,
Apostolova Liana G.
Publication year - 2015
Publication title -
alzheimer's and dementia: diagnosis, assessment and disease monitoring
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.497
H-Index - 37
ISSN - 2352-8729
DOI - 10.1016/j.dadm.2015.01.005
Subject(s) - pittsburgh compound b , brain derived neurotrophic factor , medicine , alzheimer's disease neuroimaging initiative , alzheimer's disease , psychology , neuroimaging , posterior cingulate , amyloid (mycology) , neuroscience , neurotrophic factors , endocrinology , pathology , cognition , disease , receptor
Background Brain‐derived neurotrophic factor (BDNF) plays an important role in Alzheimer's disease (AD) and other neurodegenerative disorders. BDNF function is adversely affected by amyloid beta in AD. BDNF levels in brain and peripheral tissues are lower in patients with AD and mild cognitive impairment (MCI) than in controls. Here we examined the association between plasma levels of BDNF and amyloid deposition in the brain measured with Pittsburgh Compound B (PiB). Method Our data set consisted of 18 AD, 56 MCI, and 3 normal control Alzheimer's Disease Neuroimaging Initiative‐1 (ADNI1) subjects with available [ 11 C] PiB and peripheral blood protein data. Magnetic resonance imaging (MRI)‐coregistered positron emission tomography data were smoothed with a 15 mm kernel and mapped onto three‐dimensional (3D) hemispheric models using the warping deformations computed in cortical pattern matching of the associated MRI scans. We applied linear regression to examine in 3D the associations between BDNF and PiB standard uptake value ratio, while adjusting for age and sex. We used permutation statistics thresholded at P < .01 for multiple comparisons correction. Results Plasma BDNF levels showed significant negative associations with left greater than right amyloid burden in the lateral temporal, inferior parietal, inferior frontal, anterior and posterior cingulate, and orbitofrontal regions (left P corrected = .03). Conclusions As hypothesized, lower plasma levels of BDNF were significantly associated with widespread brain amyloidosis.