Evidence map›Paper›PMID 41971217›Full record

ArticleRomanian journal of ophthalmology

Progressive Inflammatory Coupling Drives Glaucoma Progression - a Longitudinal Analysis of Cytokine-RNFL Dynamics.

Raluca Neacșa, Daniela Manasia, Cristiana Tănase, Mădălina-Elena Tobă, Adina-Diana Moldovan

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In one paragraph

Article in Romanian journal of ophthalmology. 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

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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

5 authors.

Raluca NeacșaDepartment of Medico-Surgical Disciplines, Faculty of Medicine, "Titu Maiorescu" University of Bucharest, Bucharest, Romania.
Daniela ManasiaDepartment of Medico-Surgical Disciplines, Faculty of Medicine, "Titu Maiorescu" University of Bucharest, Bucharest, Romania.
Cristiana TănaseDepartment of Preclinical Disciplines, Faculty of Medicine, "Titu Maiorescu" University of Bucharest, Bucharest, Romania.
Mădălina-Elena TobăDepartment of Medico-Surgical Disciplines, Faculty of Medicine, "Titu Maiorescu" University of Bucharest, Bucharest, Romania.
Adina-Diana MoldovanDepartment of Preclinical Disciplines, Faculty of Medicine, "Titu Maiorescu" University of Bucharest, Bucharest, Romania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Inflammatory biomarkers in glaucoma have shown promise but lack the longitudinal analysis necessary for clinical translation. We developed a comprehensive mixed-effects modeling approach to characterize temporal cytokine-RNFL dynamics and reveal patterns in the cytokine-RNFL progression. Methods: We analyzed a 24-month longitudinal cohort of 57 patients (19 each: controls, untreated POAG, treated POAG) using: (1) mixed-effects models with individual heterogeneity modeling; (2) censoring-informed cytokine analysis; and (3) temporal correlation network analysis.fi. Results: Mixed-effects models revealed significant group differences in RNFL progression: controls (-0.20 ± 0.10 μm/year), untreated POAG (-1.94 ± 0.54 μm/year), and treated POAG (-1.06 ± 0.49 μm/year). Cytokine censoring patterns provided biological validation-pro-inflammatory cytokines showed 1.37-fold higher detection in untreated POAG versus controls (TNF-alpha: 85.3% vs. 62.1%), independently confirming elevated disease inflammation. Temporal correlation analysis showed progressive inflammatory coupling, with the TNF-alpha of ~ IL6 correlation increasing from r = 0.23 to r = 0.49 over 24 months. Discussion: Our findings suggest that POAG pathogenesis can be linked to a progressive inflammatory dysregulation, in which other cytokines follow increases in an initial inflammatory cytokine. The doubling of the correlation between TNF alpha and IL6 over time could suggest that the disease progression could be self-amplifying. Conclusions: This study establishes that glaucoma involves progressive inflammatory coupling, in which initially independent cytokine signals evolve into self-reinforcing mechanisms. The differential censoring patterns provide compelling biological validation. These findings enable precision medicine approaches based on inflammatory phenotypes and support early intervention strategies targeting network establishment.

Indexed as

CytokinesGlaucoma, Open-AngleInflammationIntraocular PressureOptic DiskRetinal Ganglion CellsAgedBiomarkersDisease ProgressionFemaleFollow-Up StudiesHumansLongitudinal StudiesMaleMiddle AgedTomography, Optical CoherenceBiomarkersCytokinesANOVA = Analysis of VariancecytokineIFN-γ = Interferon gammaIL-10 = Interleukin-10IL-1β = Interleukin-1 betaIL-4 = Interleukin-4IL-6 = Interleukin-6inflammationIOP = Intraocular PressureOCT = Optical Coherence TomographyPGAs = Prostaglandin AnalogsPOAG = Primary Open-Angle GlaucomaRGCs = Retinal Ganglion CellsRNFLRNFL = Retinal Nerve Fiber LayerSD = Standard DeviationTNF-α = Tumor Necrosis Factor alphatreated POAGuntreated POAG

Identifiers

PMID41971217
PMCPMC13065147

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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.