Effects of beta-amyloid accumulation on neural function during encoding across the adult lifespan.
Effects of beta-amyloid accumulation on neural function during encoding across the adult lifespan.
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DOI:
10.1016/j.neuroimage.2012.03.077
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发表时间:
2012-08-01
期刊:
影响因子:
5.7
通讯作者:
Park, Denise C.
中科院分区:
文献类型:
--
作者:
Kennedy, Kristen M.;Rodrigue, Karen M.;Devous, Michael D., Sr.;Hebrank, Andrew C.;Bischof, Gerard N.;Park, Denise C.
Limited functional imaging evidence suggests increased beta-amyloid deposition is associated with alterations in brain function, even in healthy older adults. However, the majority of these findings report on resting-state activity or functional connectivity in adults over age 60. Much less is known about the impact of beta-amyloid on neural activations during cognitive task performance, or the impact of amyloid in young and middle-aged adults. The current study measured beta-amyloid burden from PET imaging using18Florbetapir, in a large continuous age sample of highly-screened, healthy adults (N = 137; aged 30–89 years). The same participants also underwent fMRI scanning, performing a memory encoding task. Using both beta-amyloid burden and age as continuous predictors of encoding activity, we report a dose-response relationship of beta-amyloid load to neural function, beyond the effects of age. Specifically, individuals with greater amyloid burden evidence less neural activation in bilateral dorsolateral prefrontal cortex, a region important for memory encoding, as well as reduced neural modulation in areas associated with default network activity: bilateral superior/medial frontal and lateral temporal cortex. Importantly, this reduction of both activation and suppression as a function of amyloid load was found across the lifespan, even in young- and middle-aged individuals. Moreover, this frontal and temporal amyloid-reduced activation/suppression was associated with poorer processing speed, verbal fluency, and fluid reasoning in a subgroup of individuals with elevated amyloid, suggesting that it is detrimental, rather than compensatory in nature.
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DOI:
10.1093/geronb/gbq035
发表时间:
2010-07-01
影响因子:
6.2
作者:
Reuter-Lorenz, Patricia A.;Park, Denise C.
通讯作者:
Park, Denise C.
影响因子:
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Park DC;Reuter-Lorenz P
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Reuter-Lorenz P
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14.5
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通讯作者:
Johnson, Keith A.
影响因子:
10.6
作者:
Sheline YI;Raichle ME;Snyder AZ;Morris JC;Head D;Wang S;Mintun MA
通讯作者:
Mintun MA