Evidence map›Paper›PMID 41667691›Full record

Observational studyNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2026

Characterization of neuropsychiatric symptoms in patients with early-stage Alzheimer's disease in a specialized outpatient clinic.

Manuel Alanís-Bernal, Laura Melgarejo, Laia Boada-Oller, Santiago Rios, Olga Maisterra, Alejandro Ballvé, Mariateresa Buongiorno, Darly Giraldo, Pilar Delgado, Belén Gutiérrez and 2 more

Abstract readObservational Study
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In one paragraph

Observational study in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

12 authors.

Manuel Alanís-Bernal *Neurology Department, University Hospital Vall d'Hebron, Barcelona, Spain.ORCID http://orcid.org/0009-0009-0956-6506
Laura Melgarejo *Neurology Department, University Hospital Vall d'Hebron, Barcelona, Spain.ORCID http://orcid.org/0000-0002-0477-0286
Laia Boada-Oller *Neurology Department, University Hospital Vall d'Hebron, Barcelona, Spain.ORCID http://orcid.org/0009-0002-5418-4418
Santiago RiosDepartment of Genetics, Microbiology, and Statistics, Faculty of Biology, University of Barcelona, Barcelona, Spain.ORCID http://orcid.org/0000-0003-2492-9247
Olga MaisterraNeurology Department, University Hospital Vall d'Hebron, Barcelona, Spain.
Alejandro BallvéNeurology Department, University Hospital Vall d'Hebron, Barcelona, Spain.ORCID http://orcid.org/0000-0001-7587-2768
Mariateresa BuongiornoNeurology Department, University Hospital Vall d'Hebron, Barcelona, Spain.ORCID http://orcid.org/0000-0002-1745-5744
Darly GiraldoNeurology Department, University Hospital Vall d'Hebron, Barcelona, Spain.ORCID http://orcid.org/0009-0005-8821-7662
Pilar DelgadoNeurology Department, University Hospital Vall d'Hebron, Barcelona, Spain.ORCID http://orcid.org/0000-0002-1628-4488
Belén GutiérrezNeurology Department, University Hospital Vall d'Hebron, Barcelona, Spain.
Diana LiébanaNeurology Department, University Hospital Vall d'Hebron, Barcelona, Spain.
Antonio PalasíNeurology Department, University Hospital Vall d'Hebron, Barcelona, Spain. antonio.palasi@vallhebron.cat.ORCID http://orcid.org/0000-0001-8772-8245

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo describe the frequency and temporal onset of neuropsychiatric symptoms (NPS) around the diagnosis of Alzheimer's disease (AD) and to explore their associations with clinical and paraclinical variables.

methodsWe conducted a retrospective observational study of patients diagnosed with AD between 2020 and 2024, including NPS emerging from six years before to four years after diagnosis. Symptoms were classified by temporal onset as preNPS or postNPS and categorized into affective, psychotic, and behavioral domains. Clinical and demographic data, cerebrospinal fluid (CSF) biomarkers, and FDG-PET imaging findings were collected.

resultsAmong 184 patients (mean age 76.7 ± 9.0 years; 68% female), preNPS occurred in 78.2% and postNPS in 53.8%. Psychotic preNPS were associated with older age (81.4 ± 8.6 vs. 76.3 ± 8.9 years; p = 0.049), lower Mini-Mental State Examination scores (19.9 ± 3.7 vs. 22.1 ± 4.1; p = 0.033), and use of benzodiazepines (38.5% vs. 14.0%; p = 0.036) and antipsychotics (61.5% vs. 7.0%; p < 0.001). Affective preNPS were more common in women (71.9% vs. 55.4%; p = 0.029) and were associated with antidepressant use (p < 0.001) and lower alcohol intake (p = 0.018). Behavioral preNPS predominated in men (57.1% vs. 30.1%; p = 0.013) and were associated with a greater preservation of temporal lobe metabolism in FDG-PET imaging (28.0% vs. 76.2%; p = 0.04). PostNPS correlated with disease duration (r = 0.19; p = 0.01) and higher CSF total tau levels (386.9 ± 112.8 vs. 347.1 ± 148.9; p = 0.04).

conclusionNPS are frequent in early-stage AD, with psychotic preNPS linked to older age and greater cognitive decline, and postNPS correlating with disease duration and CSF tau, indicating an association with neurodegeneration.

Indexed as

Alzheimer DiseasePsychotic DisordersAgedAged, 80 and overAmbulatory Care FacilitiesBiomarkersFemaleHumansMalePositron-Emission TomographyRetrospective Studiestau ProteinsBiomarkerstau ProteinsAlzheimer’s diseaseCerebrospinal fluid biomarkersFDG-PETNeuropsychiatric symptoms

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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.