Evidence map›Paper›PMID 24854852›Full record

ArticleInvestigative ophthalmology & visual science2014

Angiographic features of transgenic mice with increased expression of human serine protease HTRA1 in retinal pigment epithelium.

Sandeep Kumar, Zachary Berriochoa, Balamurali K Ambati, Yingbin Fu

Open access · bronzeAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.4field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Modeling complex age-related eye disease.Progress in retinal and eye research · 2024
    Review
  6. Article
  7. International journal of molecular sciences · 2022
    Article
  8. Review
  9. Evolving treatment paradigms for PCV.Eye (London, England) · 2022
    Review
  10. Classification of Transgenic Mice by Retinal Imaging Using SVMS.Computational intelligence and neuroscience · 2022
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. A functional approach to examine the role of HTRA1 versus ARMS2 in AMD.Investigative ophthalmology & visual science · 2014
    Article
  19. Article
  20. Role ofTaiwan journal of ophthalmology
    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

4 authors at 1 institution in 1 country.

Sandeep KumarDepartment of Ophthalmology and Visual Sciences, University of Utah Health Sciences Center, Salt Lake City, Utah, United States.
Zachary BerriochoaDepartment of Ophthalmology and Visual Sciences, University of Utah Health Sciences Center, Salt Lake City, Utah, United States.
Balamurali K AmbatiDepartment of Ophthalmology and Visual Sciences, University of Utah Health Sciences Center, Salt Lake City, Utah, United States Department of Neurobiology and Anatomy, University of Utah Health Sciences Center, Salt Lake City, Utah, United States.
Yingbin FuDepartment of Ophthalmology and Visual Sciences, University of Utah Health Sciences Center, Salt Lake City, Utah, United States Department of Neurobiology and Anatomy, University of Utah Health Sciences Center, Salt Lake City, Utah, United States.
University of Utah · US

Funding

University of Utah, Core Vision Research GrantP30EY014800 · NEI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Behrad Noudoost · 2005 to 2026
$14.6M
Mechanisms and treatment strategies for polypoidal choroidal vasculopathR01EY022901 · NEI · UNIVERSITY OF UTAH · PI FU, YINGBIN · 2014 to 2016
$1.3M
NEI NIH HHS 1R01EY022901NEI NIH HHS 5P30EY014800NEI NIH HHS P30 EY014800NEI NIH HHS R01 EY022901
6 · The paper itself

Abstract

purposePolypoidal choroidal vasculopathy (PCV) is characterized by a branching vascular network (BVN) of choroid that terminates in polypoidal dilations. We have previously reported the generation of the first PCV model by transgenically expressing human HTRA1 (hHTRA1(+)), a multifunctional serine protease, in mouse RPE. The purpose of this study was to perform a comprehensive examination of the PCV phenotypes (e.g., lesion type and distribution) of hHTRA1(+) mice by a variety of in vivo imaging techniques.

methodsWe generated improved hHTRA1(+) mice with a more consistent phenotype. Transgenic mice were examined by indocyanine green angiography (ICGA), fluorescein angiography, funduscopy, and spectral-domain optical coherence tomography. In particular, we performed ICGA by tail vein injection of ICG to obtain high-quality ICGA comparable to human studies in terms of the three phases (early, middle, and late) of angiography.

resultsThe polyps can be detected in the early "fill-in" phase of ICGA, and most lesions become visible in the middle phase and are more distinct in the late phase with the fading of surrounding vessels. In addition to the two key features of PCV (polypoidal dilations and BVNs), hHTRA1(+) mice exhibit other features of PCV (i.e., late geographic hyperfluorescence, pigment epithelial detachment, and hyperfluorescent plaque). Polypoidal lesions appear as reddish orange nodules on funduscopy.

conclusionsTransgenic hHTRA1(+) mice exhibit a rich spectrum of "clinical" features that closely mimic human PCV. This animal model will serve as an invaluable tool for future mechanistic and translational studies of PCV and other forms of choroidal vasculopathies.

Indexed as

Disease Models, AnimalFluorescein AngiographyAgedAnimalsBlotting, WesternChoroidal NeovascularizationColoring AgentsFemaleGene Expression RegulationHigh-Temperature Requirement A Serine Peptidase 1HumansImmunohistochemistryIndocyanine GreenMaleMiceMice, Inbred C57BLColoring AgentsHigh-Temperature Requirement A Serine Peptidase 1HTRA1 protein, humanIndocyanine GreenSerine EndopeptidasesHTRA1indocyanine green angiographylate geographic hyperfluorescencepigment epithelial detachmentpolypoidal choroidal vasculopathy

Identifiers

PMID24854852
PMCPMC4581615
OpenAlexW2006517100

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.