Evidence map›Paper›PMID 40836983›Full record

ArticleFrontiers in drug delivery2024

Investigation of novel combination therapy for age-related macular degeneration on ARPE-19 cells.

Madhuri Dandamudi, Peter McLoughlin, Gautam Behl, Lee Coffey, Anuj Chauhan, David Kent, Sweta Rani, Laurence Fitzhenry

Abstract read
In one paragraph

Article in Frontiers in drug delivery, 2024. 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

8 authors.

Madhuri DandamudiOcular Therapeutics Research Group, Pharmaceutical and Molecular Biotechnology Research Centre, Department of Science, South East Technological University, Waterford, Ireland.
Peter McLoughlinOcular Therapeutics Research Group, Pharmaceutical and Molecular Biotechnology Research Centre, Department of Science, South East Technological University, Waterford, Ireland.
Gautam BehlEirgen Pharma Ltd, Waterford, Ireland.
Lee CoffeyOcular Therapeutics Research Group, Pharmaceutical and Molecular Biotechnology Research Centre, Department of Science, South East Technological University, Waterford, Ireland.
Anuj ChauhanDepartment of Chemical and Biological Engineering, Colorado School of Mines, Colorado, CO, United States.
David KentThe Vision Clinic, Kilkenny, Ireland.
Sweta RaniOcular Therapeutics Research Group, Pharmaceutical and Molecular Biotechnology Research Centre, Department of Science, South East Technological University, Waterford, Ireland.
Laurence Fitzhenry *Ocular Therapeutics Research Group, Pharmaceutical and Molecular Biotechnology Research Centre, Department of Science, South East Technological University, Waterford, Ireland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Age-related macular degeneration (AMD) is a multifactorial degenerative disease characterised by the gradual loss of central vision in individuals aged more than 50 years. There is currently no cure for this disease, but treatment can delay its progression. Consequently, there is an urgent need for the development of both new and cost-effective therapeutics. In this study, a novel combination of a corticosteroid and flavonoid was investigated on human retinal pigment epithelial cell lines to explore its potential pharmacological effect on AMD. Combination therapies, such as anti-VEGF (vascular endothelial growth factor) agents combined with photodynamic therapy and anti-VEGF agents in conjunction with corticosteroids, have been utilized previously and are known to be effective. However anti-VEGF injections are associated with serious side effects and are costly. Various disease conditions associated with AMD were stimulated on human retinal cells, which were then exposed to different concentrations of triamcinolone acetonide (TA) and quercetin (QCN) individually and in combination. This investigation aimed to assess their potential for the treatment of AMD. The combination of TA and QCN demonstrated a superior anti-inflammatory effect, as TA and QCN primarily act on different inflammatory signaling pathways. Furthermore, in terms of anti-VEGF activity, both drugs exert their effects through different mechanisms: QCN inhibits kinase pathways leading to the deactivation of VEGF receptors, whereas TA destabilises VEGF mRNA, resulting in increased suppression of VEGF-C with combination treatments. The anti-oxidant assay yielded similar outcomes, demonstrating a synergetic effect when treated with combination drugs. These findings collectively suggest TA and QCN as a promising combination therapy for targeting AMD with multiple pathological conditions.

Indexed as

AMDARPE-19combination therapycorticosteroidflavonoidmacular degenerationquercetintriamcinolone acetonide

Identifiers

PMID40836983
PMCPMC12363285

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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.