Evidence map›Paper›PMID 41907241›Full record

ArticleFrontiers in medicine2026

Diagnostic value of neutrophil-to-lymphocyte, platelet-to-lymphocyte, and lymphocyte-to-monocyte ratios for assessing organ and multiorgan involvement in sarcoidosis: a retrospective single-center study.

Estefanía Díaz-Martín, Andrea Fernández-Valmaña, Jesús López-Martínez, Alex Mayer-Fuentes, Joan María Mercadé-Torras, María García-González, Laia Mas-Maresma, Blanca Carrillo-Lampe, Joel Font-Majo, Begoña Marí-Alfonso and 1 more

Abstract read
In one paragraph

Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Estefanía Díaz-MartínDepartment of Systemic Autoimmune Diseases-Internal Medicine, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.
Andrea Fernández-ValmañaDepartment of Systemic Autoimmune Diseases-Internal Medicine, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.
Jesús López-MartínezDepartment of Systemic Autoimmune Diseases-Internal Medicine, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.
Alex Mayer-FuentesDepartment of Systemic Autoimmune Diseases-Internal Medicine, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.
Joan María Mercadé-TorrasDepartment of Systemic Autoimmune Diseases-Internal Medicine, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.
María García-GonzálezDepartment of Systemic Autoimmune Diseases-Internal Medicine, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.
Laia Mas-MaresmaDepartment of Systemic Autoimmune Diseases-Internal Medicine, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.
Blanca Carrillo-LampeDepartment of Systemic Autoimmune Diseases-Internal Medicine, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.
Joel Font-MajoDepartment of Systemic Autoimmune Diseases-Internal Medicine, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.
Begoña Marí-AlfonsoDepartment of Systemic Autoimmune Diseases-Internal Medicine, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.
Carlos Feijoo-MassóDepartment of Systemic Autoimmune Diseases-Internal Medicine, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sarcoidosis is a heterogeneous disease lacking reliable biomarkers for organ involvement. Indices derived from the complete blood count (CBC), including the neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and lymphocyte-to-monocyte ratio (LMR), have emerged as accessible markers of systemic inflammation. Objectives: To assess whether CBC parameters and NLR, PLR, and LMR vary across demographic and clinical features in sarcoidosis, and to evaluate their diagnostic performance for organ-specific and multiorgan involvement. Methods: A retrospective, single-center observational study included adults with sarcoidosis diagnosed between 2000 and 2025. Age- and sex-adjusted logistic regression evaluated associations between hematologic indices at diagnosis and organ involvement. Additional logistic regression using analytical parameters evaluated associations between blood count-derived ratios and multiorgan involvement. Firth's correction was applied when the events-per-variable ratio was < 10, and analyses were repeated using log-transformed hematologic ratios when skewness coefficient > 2. Diagnostic performance was assessed by receiver operating characteristic (ROC) curve analysis. Results: A total of 229 patients were included (mean age 51.34 years; 57.64% women). Median values for NLR, PLR, and LMR were 2.57, 158.97, and 3.17, respectively. Higher NLR and PLR were independently associated with extrathoracic lymph node involvement (NLR: OR = 13.42, 95% CI 1.91-94.32, Conclusion: NLR was independently associated with multiorgan disease, splenic and extrathoracic lymph node involvement. PLR was independently associated with extrathoracic lymph node involvement.

Indexed as

lymphocyte-to-monocyte ratiomultiorgan involvementneutrophil-to-lymphocyte ratioplatelet-to-lymphocyte ratiosarcoidosis

Identifiers

PMID41907241
PMCPMC13021668

What Socratic holds

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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 Socratic graph.