ArticleLearning & memory (Cold Spring Harbor, N.Y.)2015
Memory for sequences of events impaired in typical aging.
Article in Learning & memory (Cold Spring Harbor, N.Y.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
10 citing papers in PubMed, 22 citations in OpenAlex.
- Functional connectivity correlates of sequence memory decline in healthy older adults.GeroScience · 2026Article
- Aging and memory for temporal order in naturalistic events.Psychology and aging · 2026Article
- Order, please! Explicit sequence learning in hybrid search in younger and older age.Memory & cognition · 2021Article
- Medial prefrontal cortex and hippocampal activity differentially contribute to ordinal and temporal context retrieval during sequence memory.Learning & memory (Cold Spring Harbor, N.Y.) · 2021Article
- A Hierarchical Bayesian Model for Differential Connectivity in Multi-trial Brain Signals.Econometrics and statistics · 2020Article
- Article
- Nonspatial sequence coding varies along the CA1 transverse axis.Behavioural brain research · 2018Article
- Multiple Types of Memory and Everyday Functional Assessment in Older Adults.Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists · 2017Article
- Nonspatial Sequence Coding in CA1 Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016Article
- Longitudinal Development of Memory for Temporal Order in Early to Middle Childhood.The Journal of genetic psychologyArticle
Corrections and comments
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Authors and funding
5 authors at 2 institutions in 1 country.
Funding
Abstract
Typical aging is associated with diminished episodic memory performance. To improve our understanding of the fundamental mechanisms underlying this age-related memory deficit, we previously developed an integrated, cross-species approach to link converging evidence from human and animal research. This novel approach focuses on the ability to remember sequences of events, an important feature of episodic memory. Unlike existing paradigms, this task is nonspatial, nonverbal, and can be used to isolate different cognitive processes that may be differentially affected in aging. Here, we used this task to make a comprehensive comparison of sequence memory performance between younger (18-22 yr) and older adults (62-86 yr). Specifically, participants viewed repeated sequences of six colored, fractal images and indicated whether each item was presented "in sequence" or "out of sequence." Several out of sequence probe trials were used to provide a detailed assessment of sequence memory, including: (i) repeating an item from earlier in the sequence ("Repeats"; e.g., AB A: DEF), (ii) skipping ahead in the sequence ("Skips"; e.g., AB D: DEF), and (iii) inserting an item from a different sequence into the same ordinal position ("Ordinal Transfers"; e.g., AB 3: DEF). We found that older adults performed as well as younger controls when tested on well-known and predictable sequences, but were severely impaired when tested using novel sequences. Importantly, overall sequence memory performance in older adults steadily declined with age, a decline not detected with other measures (RAVLT or BPS-O). We further characterized this deficit by showing that performance of older adults was severely impaired on specific probe trials that required detailed knowledge of the sequence (Skips and Ordinal Transfers), and was associated with a shift in their underlying mnemonic representation of the sequences. Collectively, these findings provide unambiguous evidence that the capacity to remember sequences of events is fundamentally affected by typical aging.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.