Evidence map›Paper›PMID 40782213›Full record

ArticleInternational ophthalmology2025

Aqueous humor cytokine profile in insufficient responder to aflibercept for neovascular age-related macular degeneration.

Ryo Terao, Ryo Obata, Atsushi Okubo, Shuichiro Aoki, Keiko Azuma, Satoru Inoda, Yuto Hashimoto, Hana Yoshida, Manami Misawa, Hironori Takahashi and 1 more

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in International ophthalmology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

11 authors.

Ryo TeraoDepartment of Ophthalmology, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo, Tokyo, 113-8655, Japan.ORCID http://orcid.org/0000-0001-6182-4343
Ryo ObataDepartment of Ophthalmology, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo, Tokyo, 113-8655, Japan. robata-tky@umin.ac.jp.ORCID http://orcid.org/0000-0002-1762-0797
Atsushi OkuboDepartment of Ophthalmology, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo, Tokyo, 113-8655, Japan.
Shuichiro AokiDepartment of Ophthalmology, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo, Tokyo, 113-8655, Japan.
Keiko AzumaDepartment of Ophthalmology, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo, Tokyo, 113-8655, Japan.
Satoru InodaDepartment of Ophthalmology, Jichi Medical University, Tochigi, Japan.ORCID http://orcid.org/0000-0003-4577-8169
Yuto HashimotoDepartment of Ophthalmology, Jichi Medical University, Tochigi, Japan.
Hana YoshidaDepartment of Ophthalmology, Jichi Medical University, Tochigi, Japan.
Manami MisawaDepartment of Ophthalmology, Jichi Medical University, Tochigi, Japan.
Hironori TakahashiDepartment of Ophthalmology, Jichi Medical University, Tochigi, Japan.
Hidenori TakahashiDepartment of Ophthalmology, Jichi Medical University, Tochigi, Japan.ORCID http://orcid.org/0000-0001-5331-4730

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo identify cytokines associated with insufficient response to aflibercept against neovascular age-related macular degeneration.

methodsThis prospective, comparative control study enrolled 40 eyes of 40 patients with nAMD. Aqueous humor (AH) samples were collected at the baseline before the intravitreal administration of aflibercept. The patients were further classified into responder and non-responder groups based on the clinical course. Patients were classified as "responders" if they required three or fewer additional injections after the three initial monthly loading doses within one year, and as non-responders, if they required four or more injections after the initial three-monthly loading doses or were switched to alternative anti-VEGF agents or treatments such as photodynamic therapy. The concentration of Angiopoietin 1, angiopoietin like 4 (ANGPTL4), interferon gamma-induced protein 10, hepatocyte growth factor, interleukin 10, platelet derived growth factor BB, plasminogen activator inhibitor 1 (PAI1), vascular endothelial growth factor A, angiopoietin 2, monocyte chemotactic protein 1, IL8, IL12, platelet-derived growth factor (PlGF), and vascular cell adhesion molecule 1 in AH samples were analyzed using a multiplex immunoassay, in order to compare between responders and non-responders.

results21 eyes were defined as responders, and 19 eyes were defined as non-responders. There were no significant differences in baseline characteristics. Multiple variate analysis using logistic regression analysis found that PAI1 (p = 0.023, coefficient = 0.025), PlGF (p = 0.016, coefficient = - 1.4), and ANGPTL4 (p = 0.032, coefficient = - 0.00070) at the baseline were significantly associated with the resistance to aflibercept.

conclusionBaseline higher PAI1 and lower PlGF and ANGPTL4 were associated with insufficient response to aflibercept in 1 year. These cytokines can potentially predict the treatment effect against nAMD.

Indexed as

Aqueous HumorCytokinesReceptors, Vascular Endothelial Growth FactorRecombinant Fusion ProteinsWet Macular DegenerationAgedAged, 80 and overAngiogenesis InhibitorsBiomarkersFemaleFollow-Up StudiesHumansIntravitreal InjectionsMaleMiddle AgedProspective StudiesafliberceptAngiogenesis InhibitorsBiomarkersCytokinesReceptors, Vascular Endothelial Growth FactorRecombinant Fusion ProteinsAge-related macular degenerationCytokinesInterferon gamma-induced protein 10Placenta growth factorPlasminogen activator inhibitor 1Vascular endothelial growth factor

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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.