Center for Cognitive Neuroscience, Duke University, Durham, NC, USA.
Alzheimers Dement. 2010 Jul;6(4):303-11. doi: 10.1016/j.jalz.2009.07.003. Epub 2009 Sep 9.
We sought to determine if the APOE epsilon4 allele influences both the functional activation and connectivity of the medial temporal lobes (MTLs) during successful memory encoding in young adults.
Twenty-four healthy young adults, i.e., 12 carriers and 12 noncarriers of the APOE epsilon4 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.
In the absence of demographic or performance differences, APOE epsilon4 allele carriers exhibited greater bilateral MTL activity relative to noncarriers while accomplishing the same encoding task. Moreover, whereas epsilon4 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.
These results suggest that the APOE varepsilon4 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 epsilon4 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.
我们试图确定 APOE epsilon4 等位基因是否会影响年轻成年人成功记忆编码期间内侧颞叶(MTL)的功能激活和连接。
24 名健康的年轻成年人,即 12 名 APOE epsilon4 等位基因携带者和 12 名非携带者,在随后的记忆范式中使用事件相关功能磁共振成像进行扫描。成功编码的神经解剖学相关性是通过随后记住的任务项与忘记的任务项相比,或简而言之,编码成功活动(ESA)的神经活动来测量的。评估了 MTL 内 ESA 的组间差异,以及与 MTL 的全脑功能连接。
在没有人口统计学或表现差异的情况下,APOE epsilon4 等位基因携带者在完成相同的编码任务时相对于非携带者表现出双侧 MTL 活动增加。此外,虽然 epsilon4 携带者表现出 ESA 相关 MTL 活动与后扣带回和其他边缘区域的功能连接增加,但在前皮质和后皮质的整体连接减少。
这些结果表明,APOE varepsilon4 等位基因不仅可能影响 MTL 内的功能激活,而且可能影响 MTL 与其他参与记忆编码的区域的功能连接。年轻的 APOE epsilon4 携带者的 MTL 与后扣带回的功能连接增强表明,APOE 可能在阿尔茨海默病相关的大脑区域中很早就表达出来,远在迟发性痴呆成为实际风险或考虑因素之前。这些功能连接差异也可能反映了 APOE 在早期发育过程中的多效性影响。