Evidence map›Paper›PMID 41930609›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2026

Neutrophil inflammation metrics are associated with the risk of future dementia in large data from NYU Langone Hospitals and the Veterans Health Administration.

Tianshe He, Rebecca A Betensky, Ricardo S Osorio, Kaitlin Swinnerton, Chunlei Zheng, Tovia Jacobs, Alok Vedvyas, Karyn Marsh, Joshua Chodosh, Ula Y Hwang and 7 more

Abstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 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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0cells of the map it votes in
0citing 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

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

17 authors.

Tianshe HeVA Boston Cooperative Studies Program, MAVERIC, VA Boston Healthcare System, Boston, Massachusetts, USA.ORCID 0000-0001-9752-1256
Rebecca A BetenskyDepartment of Biostatistics, NYU School of Global Public Health, New York, New York, USA.
Ricardo S OsorioDepartment of Psychiatry, New York University Grossman School of Medicine, New York, New York, USA.
Kaitlin SwinnertonVA Boston Cooperative Studies Program, MAVERIC, VA Boston Healthcare System, Boston, Massachusetts, USA.
Chunlei ZhengVA Boston Cooperative Studies Program, MAVERIC, VA Boston Healthcare System, Boston, Massachusetts, USA.
Tovia JacobsDepartment of Psychiatry, New York University Grossman School of Medicine, New York, New York, USA.
Alok VedvyasCenter for Cognitive Neurology, Department of Neurology, New York University Grossman School of Medicine, New York, New York, USA.
Karyn MarshCenter for Cognitive Neurology, Department of Neurology, New York University Grossman School of Medicine, New York, New York, USA.
Joshua ChodoshDivision of Geriatrics and Palliative Care, Department of Medicine, New York University Grossman School of Medicine, New York, New York, USA.
Ula Y HwangDepartment of Population Health, New York University Grossman School of Medicine, New York, New York, USA.
Natalia SifnugelDepartment of Population Health, New York University Grossman School of Medicine, New York, New York, USA.
Omonigho M BubuDepartment of Psychiatry, New York University Grossman School of Medicine, New York, New York, USA.
Thomas WisniewskiDepartment of Psychiatry, New York University Grossman School of Medicine, New York, New York, USA.
Mary BrophyVA Boston Cooperative Studies Program, MAVERIC, VA Boston Healthcare System, Boston, Massachusetts, USA.
Nhan V DoVA Boston Cooperative Studies Program, MAVERIC, VA Boston Healthcare System, Boston, Massachusetts, USA.
Nathanael R FillmoreVA Boston Cooperative Studies Program, MAVERIC, VA Boston Healthcare System, Boston, Massachusetts, USA.
Jaime Ramos-CejudoVA Boston Cooperative Studies Program, MAVERIC, VA Boston Healthcare System, Boston, Massachusetts, USA.ORCID 0000-0002-0993-9909

Funding

PSYCHOSOCIAL COREP30AG008051 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI RUSINEK, HENRY · 1990 to 2019
$36.1M
Research Education ComponentP30AG066512 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Mary Sherman Mittelman · 2020 to 2026
$28.4M
Using a Health Disparity Research Framework to examine mechanisms linking Obstructive Sleep Apnea with higher Alzheimer’s disease risk in older Blacks/African-AmericansR01AG082278 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI OMONIGHO A MICHAEL Bubu · 2023 to 2026
$6.9M
Treatment of OSA on sleep-dependent memory and blood biomarkers in blacksRF1AG083975 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI OMONIGHO A MICHAEL Bubu, Korey Kam · 2023 to 2026
$4.2M
The mediating role of Slow Wave Sleep and Vascular Risk Factors on Alzheimer Disease related disparity between African-Americans and non-Hispanic WhitesK23AG068534 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BUBU, OMONIGHO A MICHAEL · 2021 to 2025
$958k
Alzheimer's Association grant AARG-21-848397and BrightFocus Foundation A2022033SFoundation for the National Institutes of Health K23AG068534Foundation for the National Institutes of Health R01AG082278Foundation for the National Institutes of Health RF1AG083975National Alzheimer's Coordinating Center AY2022/23 New Investigator Award to J.R.C., and the Cooperative Studies Program, VA Boston Healthcare System. O.M.B. is supported by the NIH through the following grants K23AG068534National Alzheimer's Coordinating Center AY2022/23 New Investigator Award to J.R.C., and the Cooperative Studies Program, VA Boston Healthcare System. O.M.B. is supported by the NIH through the following grants R01AG082278National Alzheimer's Coordinating Center AY2022/23 New Investigator Award to J.R.C., and the Cooperative Studies Program, VA Boston Healthcare System. O.M.B. is supported by the NIH through the following grants RF1AG083975NIA NIH HHS P30 AG008051NIA NIH HHS P30 AG066512the National Institutes of Health P30AG066512the National Institutes of Health R01AG070821the National Institutes of Health R01AG079282U.S. Department of Veterans Affairs Cooperative Studies Program
6 · The paper itself

Abstract

introductionNeutrophil-to-lymphocyte ratio (NLR), a marker of systemic inflammation, has been linked to dementia risk, but prior studies were limited by small sample sizes.

methodsWe assessed the association between baseline NLR and incident Alzheimer's disease (AD) and Alzeimer's disease and related dementias (AD/ADRD) using electronic health records from New York University (NYU) (n = 284,530) and the Veterans Health Administration [VA] (n = 85,836) Hospitals from 2011 to 2023. AD/ADRD diagnoses were identified via International Classification of Diseases (ICD) codes ≥6 months post-baseline. Cox models and cumulative incidence functions (CIFs) adjusted for demographic and clinical variables, with death as a competing risk.

resultsHigher NLR was associated significantly with increased AD/ADRD risk in both cohorts (NYU hazard ratio [HR] = 1.07, 95% confidence interval [CI] 1.02-1.15; VA HR = 1.21, 95% CI 1.10-1.34). Spline analysis further confirmed a continuous dose-response relationship, and subgroup analyses showed higher risk among female and Hispanic patients. DISCUSSION: Elevated NLR is independently associated with higher AD/ADRD risk across diverse populations, highlighting the role of systemic inflammation and neutrophil-mediated pathways in neurodegeneration.

Indexed as

Alzheimer DiseaseDementiaInflammationLymphocytesNeutrophilsAgedAged, 80 and overFemaleHumansIncidenceMaleRisk FactorsUnited StatesUnited States Department of Veterans AffairsADADRDAlzheimer's diseaseCBCdementianeutrophilsneutrophil‐to‐lymphocyte ratioNLR

Identifiers

PMID41930609
PMCPMC13052120

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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.