Evidence map›Paper›PMID 38779354›Full record

ArticleBrain communications2024

Investigating the brain's neurochemical profile at midlife in relation to dementia risk factors.

Maria-Eleni Dounavi, Elizabeth McKiernan, Michael Langsen, Sarah Gregory, Graciela Muniz-Terrera, Maria Angeles Prats-Sedano, Marius Ovidiu Mada, Guy B Williams, Brian Lawlor, Lorina Naci and 8 more

Abstract read
In one paragraph

Article in Brain communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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

18 authors.

Maria-Eleni DounaviDepartment of Psychiatry, School of Clinical Medicine, University of Cambridge, Cambridge, CB2 0SP, UK.ORCID https://orcid.org/0000-0001-8287-346X
Elizabeth McKiernanDepartment of Psychiatry, School of Clinical Medicine, University of Cambridge, Cambridge, CB2 0SP, UK.
Michael LangsenCenter for Clinical Brain Sciences, University of Edinburgh, Edinburgh, EH16 4SB, UK.
Sarah GregoryCentre for Dementia Prevention, University of Edinburgh, Edinburgh, EH16 4UX, UK.ORCID https://orcid.org/0000-0001-9864-8240
Graciela Muniz-TerreraCentre for Dementia Prevention, University of Edinburgh, Edinburgh, EH16 4UX, UK.
Maria Angeles Prats-SedanoDepartment of Psychiatry, School of Clinical Medicine, University of Cambridge, Cambridge, CB2 0SP, UK.
Marius Ovidiu MadaMedical Research Council Cognition and Brain Sciences Unit, University of Cambridge, Cambridge, CB2 7EF, UK.
Guy B WilliamsDepartment of Clinical Neurosciences and Wolfson Brain Imaging Centre, University of Cambridge, Cambridge, CB2 0QQ, UK.
Brian LawlorInstitute of Neuroscience, Trinity College Dublin, University of Dublin, Dublin, D02 PX31, Ireland.
Lorina NaciInstitute of Neuroscience, Trinity College Dublin, University of Dublin, Dublin, D02 PX31, Ireland.
Clare MackayDepartment of Psychiatry, Oxford University, Oxford, OX3 7JX, UK.ORCID https://orcid.org/0000-0001-6111-8318
Ivan KoychevDepartment of Psychiatry, Oxford University, Oxford, OX3 7JX, UK.ORCID https://orcid.org/0000-0001-6813-8493
Paresh MalhotraDepartment of Brain Sciences, Imperial College Healthcare NHS Trust, London, W12 0NN, UK.ORCID https://orcid.org/0000-0002-1897-0780
Karen RitchieINM, Univ Montpellier, INSERM, Montpellier, 34090, France.
Craig W RitchieCentre for Dementia Prevention, University of Edinburgh, Edinburgh, EH16 4UX, UK.
Li SuDepartment of Psychiatry, School of Clinical Medicine, University of Cambridge, Cambridge, CB2 0SP, UK.
Adam D WaldmanCenter for Clinical Brain Sciences, University of Edinburgh, Edinburgh, EH16 4SB, UK.
John T O' BrienDepartment of Psychiatry, School of Clinical Medicine, University of Cambridge, Cambridge, CB2 0SP, UK.ORCID https://orcid.org/0000-0002-0837-5080

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Changes in the brain's physiology in Alzheimer's disease are thought to occur early in the disease's trajectory. In this study our aim was to investigate the brain's neurochemical profile in a midlife cohort in relation to risk factors for future dementia using single voxel proton magnetic resonance spectroscopy. Participants in the multi-site PREVENT-Dementia study (age range 40-59 year old) underwent 3T magnetic resonance spectroscopy with the spectroscopy voxel placed in the posterior cingulate/precuneus region. Using LCModel, we quantified the absolute concentrations of myo-inositol, total N-acetylaspartate, total creatine, choline, glutathione and glutamate-glutamine for 406 participants (mean age 51.1; 65.3% female). Underlying partial volume effects were accounted for by applying a correction for the presence of cerebrospinal fluid in the magnetic resonance spectroscopy voxel. We investigated how metabolite concentrations related to apolipoprotein ɛ4 genotype, dementia family history, a risk score (Cardiovascular Risk Factors, Aging and Incidence of Dementia -CAIDE) for future dementia including non-modifiable and potentially-modifiable factors and dietary patterns (adherence to Mediterranean diet). Dementia family history was associated with decreased total N-acetylaspartate and no differences were found between apolipoprotein ɛ4 carriers and non-carriers. A higher Cardiovascular Risk Factors, Aging, and Incidence of Dementia score related to higher myo-inositol, choline, total creatine and glutamate-glutamine, an effect which was mainly driven by older age and a higher body mass index. Greater adherence to the Mediterranean diet was associated with lower choline, myo-inositol and total creatine; these effects did not survive correction for multiple comparisons. The observed associations suggest that at midlife the brain demonstrates subtle neurochemical changes in relation to both inherited and potentially modifiable risk factors for future dementia.

Indexed as

Alzheimer’s diseaseAPOE4brain metabolismMRSpreclinical dementia

Identifiers

PMID38779354
PMCPMC11109818

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Registered trials

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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.