Evidence map›Paper›PMID 41615542›Full record

ArticleGeroScience2026

Functional connectivity correlates of sequence memory decline in healthy older adults.

Catalina Trujillo-Llano, Nina M Ehrhardt, Anna Elisabeth Fromm, Friederike Thams, Dayana Hayek, Shu-Chen Li, Agnes Flöel, Daria Antonenko

Abstract read
In one paragraph

Article in GeroScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Catalina Trujillo-LlanoDepartment of Neurology, Universitätsmedizin Greifswald, Greifswald, Germany.
Nina M EhrhardtDepartment of Neurology, Universitätsmedizin Greifswald, Greifswald, Germany.
Anna Elisabeth FrommDepartment of Neurology, Universitätsmedizin Greifswald, Greifswald, Germany.
Friederike ThamsDepartment of Neurology, Universitätsmedizin Greifswald, Greifswald, Germany.
Dayana HayekDepartment of Neurology, Universitätsmedizin Greifswald, Greifswald, Germany.
Shu-Chen LiChair of Lifespan Developmental Neuroscience, Technische Universität Dresden, Dresden, Germany.
Agnes FlöelDepartment of Neurology, Universitätsmedizin Greifswald, Greifswald, Germany.
Daria AntonenkoDepartment of Neurology, Universitätsmedizin Greifswald, Greifswald, Germany. daria.antonenko@med.uni-greifswald.de.ORCID http://orcid.org/0000-0002-2839-4609

Funding

Deutsche Forschungsgemeinschaft FL 379/35-1)Deutsche Forschungsgemeinschaft Grant 426477764 (AN 1103/3-1)Deutsche Forschungsgemeinschaft Grant 426477764 (FL 379/24-1)Deutsche Forschungsgemeinschaft Project number 539593253 (AN 1103/6-1)Deutsche Forschungsgemeinschaft Research Unit 5429/1 (467143400) (AN 1103/5-1)Deutsche Forschungsgemeinschaft Research Unit 5429/1 (467143400) (FL 379/34-1Deutsche Forschungsgemeinschaft SFB1315/B03 (327654276)German Academic Exchange Service scholarship: 91828451
6 · The paper itself

Abstract

Episodic sequence memory is crucial for daily functioning and typically declines during aging. However, the neural mechanisms underlying this decline remain poorly understood. We examined the resting-state functional connectivity (FC) correlates of sequence memory in healthy older adults (OA), with a young adult (YA) group included for comparison. Thirty-eight OA (mean ± SD age: 69.9 ± 3.9 years; 24 women) and 20 YA (mean ± SD age: 24.2 ± 3.4 years; 14 women) completed a sequence memory task and resting-state functional magnetic resonance imaging (rsfMRI). Participants encoded sequences of greyscale pictures presented in colored frames and retrieved their sequential order. We compared the sequence memory performance (% correct) between age groups and examined associations between performance and seed-based FC patterns within each group, focusing on hippocampal and default mode network (DMN) regions. OA exhibited poorer sequence memory performance than YA. In OA, lower performance was associated with reduced FC between the left posterior hippocampus and DMN hubs, and the DMN and right posterior parietal cortex, suggesting that reduced intrinsic coupling within memory networks and between memory and attention networks contributes to sequence memory decline in aging. In YA, superior sequence memory performance correlated with higher FC between the left posterior hippocampus and right medial occipital cortex, indicating that hippocampal-perceptual integration benefits memory function. The FC in these networks did not differ between age groups, indicating a potential shift in memory-relevant connectivity in older adults rather than reduced network function per se. Our findings provide novel evidence of large-scale network correlates underlying sequence memory decline in old age and suggest qualitatively distinct connectivity patterns supporting sequence memory in young and older adults.

Indexed as

AgingMemory DisordersMemory, EpisodicAdultAgedBrain MappingFemaleHippocampusHumansMagnetic Resonance ImagingMaleNeuropsychological TestsYoung AdultAgingDefault mode networkEpisodic memoryHippocampusResting-state functional connectivitySerial order memory

Identifiers

PMID41615542
PMCPMC13638877

What OpenQuestion holds

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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.