Evidence map›Paper›PMID 29021717›Full record

ArticleTransactions of the American Ophthalmological Society2017

Enhanced Detection of Sub-Retinal Pigment Epithelial Cell Layer Deposits in Human and Murine Tissue: Imaging Zinc as a Biomarker for Age-Related Macular Degeneration (An American Ophthalmological Society Thesis).

Frederik J G M van Kuijk, Scott W McPherson, Heidi Roehrich

Open access · greenAbstract read
In one paragraph

Article in Transactions of the American Ophthalmological Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 35% of its field
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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. Zinc and Autophagy in Age-Related Macular Degeneration.International journal of molecular sciences · 2020
    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

3 authors.

Frederik J G M van KuijkDepartments of Ophthalmology and Pediatrics, Department of Ophthalmology and Visual Neurosciences, University of Minnesota Medical School (Dr. van Kuijk), Department of Ophthalmology and Visual Neurosciences, University of Minnesota Medical School (Dr. McPherson) and Histology Core for Vision Research Department of Ophthalmology and Visual Neurosciences (Roehrich).
Scott W McPhersonDepartments of Ophthalmology and Pediatrics, Department of Ophthalmology and Visual Neurosciences, University of Minnesota Medical School (Dr. van Kuijk), Department of Ophthalmology and Visual Neurosciences, University of Minnesota Medical School (Dr. McPherson) and Histology Core for Vision Research Department of Ophthalmology and Visual Neurosciences (Roehrich).
Heidi RoehrichDepartments of Ophthalmology and Pediatrics, Department of Ophthalmology and Visual Neurosciences, University of Minnesota Medical School (Dr. van Kuijk), Department of Ophthalmology and Visual Neurosciences, University of Minnesota Medical School (Dr. McPherson) and Histology Core for Vision Research Department of Ophthalmology and Visual Neurosciences (Roehrich).

Funding

Visual TestingP30EY011374 · NEI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI NEWMAN, ERIC A · 1996 to 2019
$8.8M
NEI NIH HHS P30 EY011374
6 · The paper itself

Abstract

purposeUnderstanding the apparent paradoxical role of zinc in the pathogenesis and prevention of age-related macular degeneration (AMD) has been limited by the lack of animal models for its detection in sub-retinal epithelial deposits (drusen), a definitive early hallmark of AMD. In-vitro studies using Zinpyr-1 showed drusen contained high levels of zinc, but the probe was not suitable for in-vivo studies. This study compares Zinpyr-1 to ZPP1, a new fluorescein-based probe for zinc, to assess the potential of ZPP1 for in-vivo detection of zinc in drusen.

methodsFlat mounts of human sub-RPE tissue using the probes were analyzed by fluorescence and confocal microscopy. Flat mounts of sub-RPE tissue from mice deficient in superoxide dismutase isoform-1 (CuZn-SOD-KO) or isoform-2 (Mn-SOD-RPE-KO) were analyzed with sub-RPE deposits confirmed by histology.

resultsDrusen are detected in greater numbers and intensity with ZPP1 compared to Zinpyr-1. Using ZPP1, drusen was detected in a sample from a 46-year old human donor without ocular history, suggesting that ZPP1 might be sensitive enough to detect drusen at an early stage. With CuZn-SOD KO mice, ZPP1 detected sub-RPE deposits at 10 months of age, whereas Zinpyr-1 required 14 months.

conclusionDetection of sub-RPE deposits by ZPP1 was greatly enhanced compared to Zinpyr-1. This enhanced sensitivity will allow for more insightful analysis of zinc in AMD using human specimens and mouse models. This could result in the development of a sensitive in-vivo probe to enhance research on the role zinc in drusen formation and the early clinical diagnosis of AMD.

Indexed as

AnimalsBiomarkersDisease Models, AnimalHumansMiceMice, KnockoutMicroscopy, ConfocalOphthalmologyRetinal Pigment EpitheliumSocieties, MedicalUnited StatesWet Macular DegenerationZincBiomarkersZinc

Identifiers

PMID29021717
PMCPMC5598790
OpenAlexW2784328141

What OpenQuestion holds

Textmetadata
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.