Working memory recall precision is a more sensitive index than span

被引:54
|
作者
Zokaei, Nahid [1 ,2 ]
Burnett Heyes, Stephanie [1 ]
Gorgoraptis, Nikos [3 ]
Budhdeo, Sanjay [4 ]
Husain, Masud [1 ,2 ]
机构
[1] Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX1 3UD, England
[2] Univ Oxford, Dept Expt Psychol, Oxford OX1 3UD, England
[3] Univ London Imperial Coll Sci Technol & Med, Dept Med, Div Brain Sci, London SW7 2AZ, England
[4] Univ Cambridge, Dept Clin Neurosci, Cambridge CB2 1TN, England
基金
英国惠康基金;
关键词
Working memory; Span; Parkinson's Disease; SHORT-TERM-MEMORY; PARKINSONS-DISEASE; DEFICITS; BINDING; PERFORMANCE; DYSFUNCTION; IMPAIRMENT; RESOURCES; BACKWARD;
D O I
10.1111/jnp.12052
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Delayed adjustment tasks have recently been developed to examine working memory (WM) precision, that is, the resolution with which items maintained in memory are recalled. However, despite their emerging use in experimental studies of healthy people, evaluation of patient populations is sparse. We first investigated the validity of adjustment tasks, comparing precision with classical span measures of memory across the lifespan in 114 people. Second, we asked whether precision measures can potentially provide a more sensitive measure of WM than traditional span measures. Specifically, we tested this hypothesis examining WM in a group with early, untreated Parkinson's disease (PD) and its modulation by subsequent treatment on dopaminergic medication. Span measures correlated with precision across the lifespan: in children, young, and elderly participants. However, they failed to detect changes in WM in PD patients, either pre- or post-treatment initiation. By contrast, recall precision was sensitive enough to pick up such changes. PD patients pre-medication were significantly impaired compared to controls, but improved significantly after 3months of being established on dopaminergic medication. These findings suggest that precision methods might provide a sensitive means to investigate WM and its modulation by interventions in clinical populations.
引用
收藏
页码:319 / 329
页数:11
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