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The neutrophil to lymphocyte ratio associates with markers of Alzheimer's disease pathology in cognitively unimpaired elderly people
Jacobs, Tovia (New York University)
Jacobson, Sean R. (Veterans Affairs Boston Healthcare System)
Fortea, Juan (Institut de Recerca Sant Pau)
Berger, Jeffrey S. (New York University)
Vedvyas, Alok (New York University)
Marsh, Karyn (New York University)
He, Tianshe (New York University)
Gutierrez-Jimenez, Eugenio (Aarhus University)
Fillmore, Nathanael R. (Harvard Medical School)
Gonzalez, Moses (New York University)
Figueredo, Luisa (New York University)
Gaggi, Naomi L. (New York University)
Plaska, Chelsea Reichert (Nathan Kline Institute)
Pomara, Nunzio (New York University)
Blessing, Esther (New York University)
Betensky, Rebecca (New York University)
Rusinek, Henry (New York University)
Zetterberg, Henrik (University of Wisconsin-Madison)
Blennow, Kaj (University of Science and Technology of China and First Affiliated Hospital of USTC)
Glodzik, Lidia (Weill Cornell Medicine)
Wisniweski, Thomas M. (New York University)
de Leon, Mony J. (New York University)
Osorio, Ricardo S. (Nathan Kline Institute)
Ramos-Cejudo, Jaime (Veterans Affairs Boston Healthcare System)
Universitat Autònoma de Barcelona

Fecha: 2024
Resumen: An elevated neutrophil-lymphocyte ratio (NLR) in blood has been associated with Alzheimer's disease (AD). However, an elevated NLR has also been implicated in many other conditions that are risk factors for AD, prompting investigation into whether the NLR is directly linked with AD pathology or a result of underlying comorbidities. Herein, we explored the relationship between the NLR and AD biomarkers in the cerebrospinal fluid (CSF) of cognitively unimpaired (CU) subjects. Adjusting for sociodemographics, APOE4, and common comorbidities, we investigated these associations in two cohorts: the Alzheimer's Disease Neuroimaging Initiative (ADNI) and the M. J. de Leon CSF repository at NYU. Specifically, we examined associations between the NLR and cross-sectional measures of amyloid-β42 (Aβ42), total tau (t-tau), and phosphorylated tau (p-tau), as well as the trajectories of these CSF measures obtained longitudinally. A total of 111 ADNI and 190 NYU participants classified as CU with available NLR, CSF, and covariate data were included. Compared to NYU, ADNI participants were older (73. 79 vs. 61. 53, p < 0. 001), had a higher proportion of males (49. 5% vs. 36. 8%, p = 0. 042), higher BMIs (27. 94 vs. 25. 79, p < 0. 001), higher prevalence of hypertensive history (47. 7% vs. 16. 3%, p < 0. 001), and a greater percentage of Aβ-positivity (34. 2% vs. 20. 0%, p = 0. 009). In the ADNI cohort, we found cross-sectional associations between the NLR and CSF Aβ42 (β = -12. 193, p = 0. 021), but not t-tau or p-tau. In the NYU cohort, we found cross-sectional associations between the NLR and CSF t-tau (β = 26. 812, p = 0. 019) and p-tau (β = 3. 441, p = 0. 015), but not Aβ42. In the NYU cohort alone, subjects classified as Aβ + (n = 38) displayed a stronger association between the NLR and t-tau (β = 100. 476, p = 0. 037) compared to Aβ- subjects or the non-stratified cohort. In both cohorts, the same associations observed in the cross-sectional analyses were observed after incorporating longitudinal CSF data. We report associations between the NLR and Aβ42 in the older ADNI cohort, and between the NLR and t-tau and p-tau in the younger NYU cohort. Associations persisted after adjusting for comorbidities, suggesting a direct link between the NLR and AD. However, changes in associations between the NLR and specific AD biomarkers may occur as part of immunosenescence.
Derechos: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. Creative Commons
Lengua: Anglès
Documento: Article ; recerca ; Versió publicada
Materia: Alzheimer's disease ; Amyloid-β ; CSF ; NLR ; Neutrophil to lymphocyte ratio ; P-tau ; T-tau
Publicado en: Immunity and Ageing, Vol. 21 Núm. 1 (december 2024) , p. 32, ISSN 1742-4933

DOI: 10.1186/s12979-024-00435-2
DOI: 10.21203/rs.3.rs-4076789/v1
PMID: 38760856
PMID: 38559231


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Documentos de investigación > Documentos de los grupos de investigación de la UAB > Centros y grupos de investigación (producción científica) > Ciencias de la salud y biociencias > Institut de Recerca Sant Pau
Artículos > Artículos de investigación
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 Registro creado el 2025-01-17, última modificación el 2025-04-24



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