Evidence map›Paper›PMID 32155173›Full record

ArticlePloS one2020

Aqueous humour proteins and treatment outcomes of anti-VEGF therapy in neovascular age-related macular degeneration.

Yusuke Arai, Hidenori Takahashi, Satoru Inoda, Xue Tan, Shinichi Sakamoto, Yuji Inoue, Yujiro Fujino, Hidetoshi Kawashima, Yasuo Yanagi

Abstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
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

9 authors.

Yusuke AraiDepartment of Ophthalmology, Jichi Medical University, Shimotsuke-shi, Tochigi, Japan.ORCID 0000-0003-1677-3713
Hidenori TakahashiDepartment of Ophthalmology, Jichi Medical University, Shimotsuke-shi, Tochigi, Japan.ORCID 0000-0001-5331-4730
Satoru InodaDepartment of Ophthalmology, Jichi Medical University, Shimotsuke-shi, Tochigi, Japan.
Xue TanDepartment of Ophthalmology, Graduate School of Medicine, the University of Tokyo, Bunkyo-ku, Tokyo, Japan.
Shinichi SakamotoDepartment of Ophthalmology, Jichi Medical University, Shimotsuke-shi, Tochigi, Japan.
Yuji InoueDepartment of Ophthalmology, Jichi Medical University, Shimotsuke-shi, Tochigi, Japan.
Yujiro FujinoJapan Community Health Care Organization Tokyo Shinjuku Medical Center, Shinjuku-ku, Tokyo, Japan.
Hidetoshi KawashimaDepartment of Ophthalmology, Jichi Medical University, Shimotsuke-shi, Tochigi, Japan.
Yasuo YanagiDepartment of Ophthalmology, Asahikawa Medical University, Asahikawa-shi, Hokkaido, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to construct a better model for predicting treatment outcomes of anti-vascular endothelial growth factor therapy for neovascular age-related macular degeneration (nAMD) using the concentrations of aqueous humour proteins at baseline and during treatment. From the data of 48 treatment-naïve nAMD eyes that received intravitreal ranibizumab pro re nata for up to 12 months, we used the aqueous humour concentrations of C-X-C motif chemokine ligand 1 (CXCL1), CXCL12, CXCL13, interferon-γ-induced protein 10, monocyte chemoattractant protein 1 (MCP-1), C-C motif chemokine ligand 11, interleukin 6 (IL-6), IL-10, and matrix metalloproteinase 9 (MMP-9). After stepwise regression, multivariate analysis was performed to identify which predictors were significantly associated with best-corrected visual acuity (BCVA) changes and the number of injections. The results demonstrated that besides male sex (β coefficient = -0.088, P = 0.040) and central retinal thickness (β coefficient = 0.00051 per μm, P = 0.027), MCP-1 (β coefficient = 0.44, P < 0.001) and IL-10 (β coefficient = -0.16, P = 0.033) were significantly correlated with baseline BCVA. Additionally, high MCP-1 at baseline (β coefficient = -0.20, P = 0.015) and low CXCL13 at baseline (β coefficient = 0.10, P = 0.0054) were independently associated with better BCVA change at 12 months. High MMP-9 at the first injection (β coefficient = 0.56, P = 0.01), CXCL12 at the third injection (β coefficient = 0.10, P = 0.0002), and IL-10 at the third injection (β coefficient = 1.3, P = 0.001) were predictor variables associated with the increased number of injections. In conclusion, aqueous humour protein concentrations may have predictive abilities of BCVA change over 12 months and the number of injections in pro re nata treatment of exudative nAMD.

Indexed as

AgedAngiogenesis InhibitorsAqueous HumorEye ProteinsFemaleGene Expression RegulationHumansMacular DegenerationMaleNeovascularization, PathologicProspective StudiesRanibizumabTreatment OutcomeVascular Endothelial Growth Factor AAngiogenesis InhibitorsEye ProteinsRanibizumabVascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID32155173
PMCPMC7064238

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.