Evidence map›Paper›PMID 42816830›Full record

ArticleJournal of Alzheimer's disease : JAD2026

Exploring the interplay between frailty, Alzheimer's disease biomarkers, and cognitive functioning in patients with mild cognitive impairment: A cross-sectional study.

Manuela Pintus, Martina Valletta, Luca Sacchi, Tiziana Carandini, Laura Ghezzi, Anna Pietroboni, Chiara Fenoglio, Maria Serpente, Marina Arcaro, Giuseppe Bruno and 3 more

Abstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

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5 · Who and what money

Authors and funding

13 authors.

Manuela PintusFondazione IRCCS Cà Granda, Ospedale Maggiore Policlinico, Milan, Italy.ORCID 0009-0009-4292-060X
Martina VallettaAging Research Center, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet and Stockholm University, Stockholm, Sweden.
Luca SacchiFondazione IRCCS Cà Granda, Ospedale Maggiore Policlinico, Milan, Italy.
Tiziana CarandiniFondazione IRCCS Cà Granda, Ospedale Maggiore Policlinico, Milan, Italy.
Laura GhezziDepartment of Biomedical, Surgical and Dental Sciences, University of Milan, Milan, Italy.
Anna PietroboniFondazione IRCCS Cà Granda, Ospedale Maggiore Policlinico, Milan, Italy.
Chiara FenoglioFondazione IRCCS Cà Granda, Ospedale Maggiore Policlinico, Milan, Italy.
Maria SerpenteFondazione IRCCS Cà Granda, Ospedale Maggiore Policlinico, Milan, Italy.
Marina ArcaroFondazione IRCCS Cà Granda, Ospedale Maggiore Policlinico, Milan, Italy.ORCID 0000-0002-3821-0682
Giuseppe BrunoDepartment of Human Neuroscience, Sapienza University of Rome, Rome, Italy.
Daniela GalimbertiFondazione IRCCS Cà Granda, Ospedale Maggiore Policlinico, Milan, Italy.
Marco CanevelliAging Research Center, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet and Stockholm University, Stockholm, Sweden.
Andrea ArighiFondazione IRCCS Cà Granda, Ospedale Maggiore Policlinico, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BackgroundFrailty is characterized by declining homeostatic reserves and increased vulnerability to stressors, and has been associated with cognitive decline and dementia.ObjectiveTo examine the relationship between frailty, Alzheimer's disease (AD) biomarkers, and cognitive performance in individuals with mild cognitive impairment (MCI).MethodsWe enrolled 183 MCI patients from the Diagnostic Outpatient Service of the Neurodegenerative Diseases Unit at IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan. Cerebrospinal fluid (CSF) biomarkers amyloid-β42, total-tau, and phosphorylated-tau181were analyzed. Frailty was assessed using a 47-item frailty index (FI), and cognitive performance was measured with the Mini-Mental State Examination (MMSE).ResultsHigher FI scores were associated with lower MMSE scores, even after adjusting for amyloid and tau biomarkers (β = -0.72, 95% CI -1.20, -0.24). Compared to robust (FI ≤ 0.11) amyloid-negative subjects, individuals with higher FI (>0.11) and CSF amyloid positivity had significantly lower MMSE scores. Patients with lower FI had twice the odds ratio (OR 2.00, 95% CI 1.02-3.90) of presenting an amyloid-positive (A+) CSF profile compared to those with higher FI; similar trends were found for the amyloid and tau-positive (A + T+) profile (OR 2.29, 95% CI 1.14-4.61).ConclusionsFrailty modulates the phenotypic variability of AD, influencing its clinical expression in MCI. Specifically, it is associated with lower cognitive performance in MCI independently of AD biomarker status and contributes synergistically with amyloid pathology to cognitive decline. Moreover, lower frailty levels are associated with a higher likelihood of an AD-compatible CSF profile, suggesting that frailty assessment may aid in identifying patients at greater risk.

Indexed as

Alzheimer's diseasecerebrospinal fluid biomarkerscognitive declinefrailtymild cognitive impairment

Identifiers

PMID42816830
PMCPMC13675565

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