Evidence map›Paper›PMID 25589767›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

Cholinergic basal forebrain structure influences the reconfiguration of white matter connections to support residual memory in mild cognitive impairment.

Nicola J Ray, Claudia Metzler-Baddeley, Mizanur R Khondoker, Michel J Grothe, Stefan Teipel, Paul Wright, Helmut Heinsen, Derek K Jones, John P Aggleton, Michael J O'Sullivan

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.3field-weighted citation impact, top 6% of its field
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

26 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. TACR3 variant confers resilience to aging and Alzheimer's disease.medRxiv : the preprint server for health sciences · 2026
    Article
  3. The cholinergic basal forebrain and its role in neurodegeneration.Journal of neuropathology and experimental neurology · 2025
    Review
  4. Review
  5. Review
  6. The fornix supports episodic memory during childhood.Cerebral cortex (New York, N.Y. : 1991) · 2022
    Article
  7. Article
  8. Article
  9. Review
  10. Cholinergic Basal Forebrain Volumes Predict Gait Decline in Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2021
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Neural regeneration research · 2019
    Article
  17. Article
  18. Article
  19. Article
  20. The cingulum bundle: Anatomy, function, and dysfunction.Neuroscience and biobehavioral reviews · 2018
    Review
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

10 authors at 5 institutions in 2 countries.

Nicola J RayDepartment of Basic and Clinical Neuroscience and.
Claudia Metzler-BaddeleyCardiff University Brain Research Imaging Centre, School of Psychology, and Neuroscience and Mental Health Research Institute, Cardiff, CF10 3AT, United Kingdom.ORCID http://orcid.org/0000-0002-8646-1144
Mizanur R KhondokerBiostatistics, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 8AF, United Kingdom.
Michel J GrotheDepartment of Psychosomatic Medicine, University Medicine Rostock, D-18147 Rostock, Germany, and.ORCID http://orcid.org/0000-0003-2600-9022
Stefan TeipelGerman Center for Neurodegenerative Diseases Rostock/Greifswald, D-18471 Rostock, Germany.
Paul WrightDepartment of Basic and Clinical Neuroscience and.ORCID http://orcid.org/0000-0001-5297-6257
Helmut HeinsenLaboratory of Morphological Brain Research, Department of Psychiatry, Psychosomatic Medicine and Psychotherapy, University of Würzburg, D-97080 Würzburg, Germany.ORCID http://orcid.org/0000-0002-4688-4441
Derek K JonesCardiff University Brain Research Imaging Centre, School of Psychology, and Neuroscience and Mental Health Research Institute, Cardiff, CF10 3AT, United Kingdom.
John P AggletonCardiff University Brain Research Imaging Centre, School of Psychology, and Neuroscience and Mental Health Research Institute, Cardiff, CF10 3AT, United Kingdom.
Michael J O'SullivanDepartment of Basic and Clinical Neuroscience and Cardiff University Brain Research Imaging Centre, School of Psychology, and Neuroscience and Mental Health Research Institute, Cardiff, CF10 3AT, United Kingdom, mike.osullivan@kcl.ac.uk.
Cardiff University · GBGerman Center for Neurodegenerative Diseases · DEKing's College London · GBUniversity of Rostock · DEUniversity of Würzburg · DE

Funding

Medical Research Council G0701912Medical Research Council MR/K022113/1Wellcome Trust 096646
6 · The paper itself

Abstract

The fornix and hippocampus are critical to recollection in the healthy human brain. Fornix degeneration is a feature of aging and Alzheimer's disease. In the presence of fornix damage in mild cognitive impairment (MCI), a recognized prodrome of Alzheimer's disease, recall shows greater dependence on other tracts, notably the parahippocampal cingulum (PHC). The current aims were to determine whether this shift is adaptive and to probe its relationship to cholinergic signaling, which is also compromised in Alzheimer's disease. Twenty-five human participants with MCI and 20 matched healthy volunteers underwent diffusion MRI, behavioral assessment, and volumetric measurement of the basal forebrain. In a regression model for recall, there was a significant group × fornix interaction, indicating that the association between recall and fornix structure was weaker in patients. The opposite trend was present for the left PHC. To further investigate this pattern, two regression models were generated to account for recall performance: one based on fornix microstructure and the other on both fornix and left PHC. The realignment to PHC was positively correlated with free recall but not non-memory measures, implying a reconfiguration that is beneficial to residual memory. There was a positive relationship between realignment to PHC and basal forebrain gray matter volume despite this region demonstrating atrophy at a group level, i.e., the cognitive realignment to left PHC was most apparent when cholinergic areas were relatively spared. Therefore, cholinergic systems appear to enable adaptation to injury even as they degenerate, which has implications for functional restoration.

Indexed as

Memory, EpisodicMental RecallAgedAged, 80 and overCognitive DysfunctionFemaleFornix, BrainHumansMaleMiddle AgedModels, NeurologicalProsencephalonWhite Mattercholinergic systemdiffusionepisodic memoryfornixmild cognitive impairmentwhite matter

Identifiers

PMID25589767
PMCPMC4293419
OpenAlexW2170978105

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.