Department of Human Development, Cornell University.
J Exp Psychol Learn Mem Cogn. 2014 Jan;40(1):41-65. doi: 10.1037/a0034057. Epub 2013 Aug 26.
Advances in dual-retrieval models of recall make it possible to use clinical data to test theoretical hypotheses about mild cognitive impairment (MCI) and Alzheimer's dementia (AD), the most common forms of neurocognitive impairment. Hypotheses about the nature of the episodic memory declines in these diseases, about decline versus sparing of specific processes, and about which individuals will become impaired over time can all be rigorously tested. Basic theoretical principles, such as whether recollection and reconstruction are distinct retrieval processes, can also be evaluated. In 3 studies, measurements of recollective retrieval, reconstructive retrieval, and familiarity judgment were extracted from standard clinical instruments, for healthy subjects and for subjects with MCI and AD diagnoses. Differences in reconstructive retrieval consistently distinguished MCI and AD, in nationally representative subject samples as well as in highly educated samples, and recollective retrieval also distinguished them in highly educated samples. Dual-retrieval processes were accurate predictors of future conversion to MCI and AD over periods of 1.5-6 years and were better predictors than the best genetic marker of these conditions (the ε4 allele of the APOE genotype). The standard recollection-deficit account of memory declines in MCI and AD was not supported, but the data were consistent with an alternative account that stresses the increasing importance of reconstruction deficits as older adults convert to these diseases.
双重提取模型的进展使得利用临床数据检验关于轻度认知障碍 (MCI) 和阿尔茨海默病 (AD) 的理论假设成为可能,这两种疾病是最常见的神经认知障碍形式。关于这些疾病中情景记忆下降的本质、特定过程的下降与保留、以及哪些个体随时间推移会受损的假设,都可以进行严格的检验。关于诸如回忆和重构是否是不同的提取过程等基本理论原则也可以进行评估。在 3 项研究中,从标准临床仪器中提取了对健康受试者、MCI 和 AD 受试者的回忆提取、重构提取和熟悉度判断的测量值。在全国代表性受试者样本和高教育程度样本中,重构提取的差异始终可以区分 MCI 和 AD,而在高教育程度样本中,回忆提取也可以区分它们。在 1.5 至 6 年的时间内,双重提取过程是未来转化为 MCI 和 AD 的准确预测指标,并且比这些疾病的最佳遗传标志物(APOE 基因型的 ε4 等位基因)更能准确预测。MCI 和 AD 中记忆下降的标准回忆缺陷理论没有得到支持,但数据与强调随着老年人向这些疾病转化,重构缺陷变得越来越重要的替代理论一致。