Evidence map›Paper›PMID 40507969›Full record

ReviewInternational journal of molecular sciences2025

Neutrophil-to-Lymphocyte Ratio in the Alzheimer's Disease Continuum.

Davide Aprile, Fabiola De Marchi, Federico Menegon, Cristoforo Comi, Giacomo Tondo

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–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

7 citing papers in PubMed.

  1. Observational
  2. Article
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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

5 authors.

Davide AprileNeurology Unit, Department of Translational Medicine, Università del Piemonte Orientale (UPO), 28100 Novara, Italy.
Fabiola De MarchiNeurology Unit, Department of Translational Medicine, Università del Piemonte Orientale (UPO), 28100 Novara, Italy.ORCID 0000-0003-0197-1880
Federico MenegonNeurology Unit, Department of Translational Medicine, Università del Piemonte Orientale (UPO), 28100 Novara, Italy.ORCID 0009-0005-2432-2762
Cristoforo ComiNeurology Unit, Department of Translational Medicine, Università del Piemonte Orientale (UPO), 28100 Novara, Italy.ORCID 0000-0002-6862-9468
Giacomo TondoNeurology Unit, Department of Translational Medicine, Università del Piemonte Orientale (UPO), 28100 Novara, Italy.ORCID 0000-0002-0057-3103

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) is a neurodegenerative disorder defined clinically by progressive cognitive decline and memory impairment and pathologically by the accumulation of amyloid-beta plaques, tau neurofibrillary tangles, neuroinflammation, and immune system dysregulation. Peripheral biomarkers are gaining attention as valuable tools for elucidating neuroinflammatory mechanisms in the AD continuum, with potential implications for diagnosis and prognosis. Among these, the neutrophil-to-lymphocyte ratio (NLR) has emerged as a promising systemic inflammatory marker. NLR, a readily available and cost-effective parameter derived from routine blood tests, reflects the balance between innate and adaptive immune responses. Elevated NLR has been associated with AD and mild cognitive impairment (MCI), showing correlations with disease severity, amyloid burden, and neuroinflammation. Increased neutrophil counts may contribute to neurodegeneration through oxidative stress and pro-inflammatory cytokine release, while decreased lymphocyte levels suggest impaired adaptive immunity. However, despite growing evidence, the clinical utility of NLR in AD remains debated due to heterogeneity in study populations and confounding factors, such as comorbidities and medication effects. This review provides a comprehensive analysis of the association between NLR and AD throughout the disease continuum. Future research should prioritize longitudinal studies and integrative approaches that combine NLR with other inflammatory and neurodegenerative markers to enhance early diagnosis and personalized therapeutic strategies.

Indexed as

Alzheimer DiseaseLymphocytesNeutrophilsBiomarkersCognitive DysfunctionHumansBiomarkersbiomarkerscognitive declinemild cognitive impairmentneuroinflammation

Identifiers

PMID40507969
PMCPMC12154037

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.