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White matter is altered with parental family history of Alzheimer's disease
Author(s) -
Bendlin Barbara B.,
Ries Michele L.,
Canu Elisa,
Sodhi Aparna,
Lazar Mariana,
Alexander Andrew L.,
Carlsson Cynthia M.,
Sager Mark A.,
Asthana Sanjay,
Johnson Sterling C.
Publication year - 2010
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1016/j.jalz.2009.11.003
Subject(s) - family history , cingulum (brain) , white matter , fractional anisotropy , apolipoprotein e , psychology , diffusion mri , uncinate fasciculus , corpus callosum , alzheimer's disease , brain structure and function , boston naming test , medicine , dementia , disease , neuroscience , neuroimaging , magnetic resonance imaging , radiology
Background Brain alterations in structure and function have been identified in people with risk factors for sporadic type Alzheimer's disease (AD), suggesting that alterations can be detected decades before AD diagnosis. Although the effect of apolipoprotein E ( APOE ) ɛ4 on the brain is well‐studied, less is known about the effect of family history of AD. We examined the main effects of family history and APOE ɛ4 on brain integrity, in addition to assessing possible additive effects of these two risk factors. Methods Diffusion tensor imaging was performed in 136 middle‐aged asymptomatic participants stratified on family history and APOE ɛ4. Mean diffusivity and fractional anisotropy (FA) were entered in factorial analyses to test the effect of AD risk on microstructural brain integrity. We performed a post hoc analysis of the three principal diffusivities (λ1, λ2, λ3) to provide potential additional insight on underlying tissue differences. Results Parental family history of AD was associated with lower FA in regions of the brain known to be affected by AD, including cingulum, corpus callosum, tapetum, uncinate fasciculus, hippocampus, and adjacent white matter. Contrary to previous reports, there was no main effect of APOE ɛ4; however, there was an additive effect of family history and APOE ɛ4 in which family history–positive participants who were also APOE ɛ4 carriers had the lowest FA compared with the other groups. Conclusions The data indicate that unknown risk factors contained in family history are associated with changes in microstructural brain integrity in areas of the brain known to be affected by AD. Importantly, the results provide further evidence that AD pathology might be detected before cognitive changes, perhaps decades before disease onset.