Temporal lobe functional activity and connectivity in young adult APOE ɛ4 carriers
Nancy A. Dennis
Center for Cognitive Neuroscience, Duke University, Durham, NC, USA
Department of Psychology, Pennsylvania State University, University Park, PA, USA
Search for more papers by this authorCorresponding Author
Jeffrey N. Browndyke
Joseph and Kathleen Bryan Alzheimer's Disease Research Center, Duke University, Durham, NC, USA
Division of Medical Psychology, Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC, USA
Duke Institute for Brain Sciences, Duke University, Durham, NC, USA
Corresponding author. Tel.: 919-668-1586; Fax: 919-668-0828.
E-mail address: [email protected]
Search for more papers by this authorJared Stokes
Center for Cognitive Neuroscience, Duke University, Durham, NC, USA
Search for more papers by this authorAnna Need
Institute for Genome Sciences and Policy, Duke University, Durham, NC, USA
Search for more papers by this authorJames R. Burke
Joseph and Kathleen Bryan Alzheimer's Disease Research Center, Duke University, Durham, NC, USA
Division of Neurology, Department of Medicine, Duke University Medical Center, Durham, NC, USA
Search for more papers by this authorKathleen A. Welsh-Bohmer
Joseph and Kathleen Bryan Alzheimer's Disease Research Center, Duke University, Durham, NC, USA
Division of Medical Psychology, Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC, USA
Division of Neurology, Department of Medicine, Duke University Medical Center, Durham, NC, USA
Search for more papers by this authorRoberto Cabeza
Center for Cognitive Neuroscience, Duke University, Durham, NC, USA
Duke Institute for Brain Sciences, Duke University, Durham, NC, USA
Search for more papers by this authorNancy A. Dennis
Center for Cognitive Neuroscience, Duke University, Durham, NC, USA
Department of Psychology, Pennsylvania State University, University Park, PA, USA
Search for more papers by this authorCorresponding Author
Jeffrey N. Browndyke
Joseph and Kathleen Bryan Alzheimer's Disease Research Center, Duke University, Durham, NC, USA
Division of Medical Psychology, Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC, USA
Duke Institute for Brain Sciences, Duke University, Durham, NC, USA
Corresponding author. Tel.: 919-668-1586; Fax: 919-668-0828.
E-mail address: [email protected]
Search for more papers by this authorJared Stokes
Center for Cognitive Neuroscience, Duke University, Durham, NC, USA
Search for more papers by this authorAnna Need
Institute for Genome Sciences and Policy, Duke University, Durham, NC, USA
Search for more papers by this authorJames R. Burke
Joseph and Kathleen Bryan Alzheimer's Disease Research Center, Duke University, Durham, NC, USA
Division of Neurology, Department of Medicine, Duke University Medical Center, Durham, NC, USA
Search for more papers by this authorKathleen A. Welsh-Bohmer
Joseph and Kathleen Bryan Alzheimer's Disease Research Center, Duke University, Durham, NC, USA
Division of Medical Psychology, Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC, USA
Division of Neurology, Department of Medicine, Duke University Medical Center, Durham, NC, USA
Search for more papers by this authorRoberto Cabeza
Center for Cognitive Neuroscience, Duke University, Durham, NC, USA
Duke Institute for Brain Sciences, Duke University, Durham, NC, USA
Search for more papers by this authorAbstract
Background
We sought to determine if the APOE ε4 allele influences both the functional activation and connectivity of the medial temporal lobes (MTLs) during successful memory encoding in young adults.
Methods
Twenty-four healthy young adults, i.e., 12 carriers and 12 noncarriers of the APOE ε4 allele, were scanned in a subsequent-memory paradigm, using event-related functional magnetic resonance imaging. The neuroanatomic correlates of successful encoding were measured as greater neural activity for subsequently remembered versus forgotten task items, or in short, encoding success activity (ESA). Group differences in ESA within the MTLs, as well as whole-brain functional connectivity with the MTLs, were assessed.
Results
In the absence of demographic or performance differences, APOE ε4 allele carriers exhibited greater bilateral MTL activity relative to noncarriers while accomplishing the same encoding task. Moreover, whereas ε4 carriers demonstrated a greater functional connectivity of ESA-related MTL activity with the posterior cingulate and other peri-limbic regions, reductions in overall connectivity were found across the anterior and posterior cortices.
Conclusions
These results suggest that the APOE ɛ4 allele may influence not only functional activations within the MTL, but functional connectivity of the MTLs to other regions implicated in memory encoding. Enhanced functional connectivity of the MTLs with the posterior cingulate in young adult ε4 carriers suggests that APOE may be expressed early in brain regions known to be involved in Alzheimer's disease, long before late-onset dementia is a practical risk or consideration. These functional connectivity differences may also reflect pleiotropic effects of APOE during early development.
Supporting Information
Filename | Description |
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alzjjalz200907003-sup-0001.jpgapplication/jpg, 1.2 MB | Supplementary data: Supplementary Fig. 3 |
alzjjalz200907003-sup-0002.jpgapplication/jpg, 1.1 MB | Supplementary Fig. 4 |
alzjjalz200907003-sup-0003.docapplication/doc, 40 KB | Supplementary Table 4 |
Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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