Evidence map›Paper›PMID 38877658›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2024

Mild behavioral impairment domains are longitudinally associated with pTAU and metabolic biomarkers in dementia-free older adults.

Emmanuel Gonzalez-Bautista, Marie Momméja, Adelaïde de Mauléon, Zahinoor Ismail, Bruno Vellas, Julien Delrieu, Maria E Soto Martin

Abstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

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

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  10. Mild Behavioral Impairment: A Population-Based Study.The Journal of neuropsychiatry and clinical neurosciences · 2026
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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

7 authors.

Emmanuel Gonzalez-BautistaResearch and Clinical Alzheimer's Disease Center, CMRR, CHU Toulouse, IHU HealthAge, Toulouse, France.ORCID 0000-0001-9844-3034
Marie MomméjaResearch and Clinical Alzheimer's Disease Center, CMRR, CHU Toulouse, IHU HealthAge, Toulouse, France.
Adelaïde de MauléonResearch and Clinical Alzheimer's Disease Center, CMRR, CHU Toulouse, IHU HealthAge, Toulouse, France.
Zahinoor IsmailDepartments of Psychiatry, Clinical Neurosciences, Community Health Sciences, and Pathology, Hotchkiss Brain Institute and O'Brien Institute for Public Health, University of Calgary, Calgary, Alberta, Canada.
Bruno VellasResearch and Clinical Alzheimer's Disease Center, CMRR, CHU Toulouse, IHU HealthAge, Toulouse, France.
Julien DelrieuResearch and Clinical Alzheimer's Disease Center, CMRR, CHU Toulouse, IHU HealthAge, Toulouse, France.
Maria E Soto MartinResearch and Clinical Alzheimer's Disease Center, CMRR, CHU Toulouse, IHU HealthAge, Toulouse, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe mechanisms linking mild behavioral impairment (MBI) and Alzheimer's disease (AD) have been insufficiently explored, with conflicting results regarding tau protein and few data on other metabolic markers. We aimed to evaluate the longitudinal association of the MBI domains and a spectrum of plasma biomarkers.

methodsOur study is a secondary analysis of data from NOLAN. The longitudinal association of the MBI domains with plasma biomarkers, including pTau181, was tested using adjusted linear mixed-effects models.

resultsThe sample comprised 359 participants (60% female, mean age: 78.3, standard deviation: 0.3 years). After 1 year, the MBI domain of abnormal perception was associated with steeper increases in plasma pTau181. Abnormal perception, decreased motivation, and impulse dyscontrol were associated with homocysteine or insulin dysregulation. DISCUSSION: Apart from the association with plasma pTau181, our results suggest that MBI might also represent metabolic dysregulation, probably contributing to dementia transition among older adults with subjective cognitive decline or mild cognitive impairment. HIGHLIGHTS: Mild behavioral impairment (MBI) psychosis was associated with steeper increases in plasma p. pTau could be a pharmacological target to treat agitation and psychosis symptoms. MBI domains were linked to metabolic dysregulation involving insulin and homocysteine.

Indexed as

BiomarkersCognitive Dysfunctiontau ProteinsAgedAged, 80 and overAlzheimer DiseaseFemaleHomocysteineHumansLongitudinal StudiesMalePsychotic DisordersBiomarkersHomocysteinetau Proteinshomocysteinemild behavioral impairmentneuropsychiatric symptomstau protein

Identifiers

PMID38877658
PMCPMC11247706

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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.