Evidence map›Paper›PMID 24098476›Full record

ArticlePloS one2013

CEP biomarkers as potential tools for monitoring therapeutics.

Kutralanathan Renganathan, Jiayin Gu, Mary E Rayborn, John S Crabb, Robert G Salomon, Robert J Collier, Michael A Kapin, Carmelo Romano, Joe G Hollyfield, John W Crabb

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Glycative stress as a cause of macular degeneration.Progress in retinal and eye research · 2024
    Review
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  7. Involvement of a gut-retina axis in protection against dietary glycemia-induced age-related macular degeneration.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
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  14. Adrenergic and serotonin receptors affect retinal superoxide generation in diabetic mice: relationship to capillary degeneration and permeability.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
    Article
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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

10 authors at 2 institutions in 1 country.

Kutralanathan RenganathanCole Eye Institute, Cleveland Clinic Foundation, Cleveland, Ohio, United States of America ; Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio, United States of America ; Department of Chemistry, Case Western Reserve University, Cleveland, Ohio, United States of America.
Jiayin Gu
Mary E Rayborn
John S Crabb
Robert G Salomon
Robert J Collier
Michael A Kapin
Carmelo Romano
Joe G Hollyfield
John W Crabb
Cleveland Clinic · USCase Western Reserve University · US

Funding

TISSUE CULTURE AND HYBRIDOMA MODULEP30EY011373 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI Irina A Pikuleva · 1997 to 2026
$17.7M
Preprostaglandin Endoperoxides (supplement)R01GM021249 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI SALOMON, ROBERT GERD · 1985 to 2014
$5.2M
Initiating Events in AMD: An Animal Model for the Human DiseaseR01EY014240 · NEI · CLEVELAND CLINIC LERNER COM-CWRU · PI HOLLYFIELD, JOE GILBERT · 2002 to 2015
$4.9M
REACTIVE INTERMEDIATES OF OXIDATIVE LIPID FRAGMENTATIONR01EY016813 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI SALOMON, ROBERT GERD · 2006 to 2018
$3.9M
Proteomic Studies of Age Related Macular DegenerationR01EY014239 · NEI · CLEVELAND CLINIC LERNER COL/MED-CWRU · PI CRABB, JOHN W · 2002 to 2005
$1.5M
Vision Research Infrastructure Development GrantR24EY015638 · NEI · CLEVELAND CLINIC LERNER COM-CWRU · PI HOLLYFIELD, JOE GILBERT · 2004 to 2008
$1.1M
Proteomic Biomarkers for AMDR21EY022134 · NEI · CLEVELAND CLINIC LERNER COM-CWRU · PI CRABB, JOHN W · 2013 to 2014
$428k
Initiating Events in AMD: An Animal Model for the Human DiseaseR56EY014240 · NEI · CLEVELAND CLINIC LERNER COM-CWRU · PI HOLLYFIELD, JOE GILBERT · 2007 to 2007
$386k
NEI NIH HHS EY14239NEI NIH HHS EY14240NEI NIH HHS EY15638NEI NIH HHS R01 EY014239NEI NIH HHS R01 EY014240NEI NIH HHS R01 EY016813NEI NIH HHS R21 EY022134NEI NIH HHS R24 EY015638NEI NIH HHS R56 EY014240NIGMS NIH HHS GM21249NIGMS NIH HHS R01 GM021249
6 · The paper itself

Abstract

backgroundCarboxyethylpyrrole (CEP) adducts are oxidative modifications derived from docosahexaenoate-containing lipids that are elevated in ocular tissues and plasma in age-related macular degeneration (AMD) and in rodents exposed to intense light. The goal of this study was to determine whether light-induced CEP adducts and autoantibodies are modulated by pretreatment with AL-8309A under conditions that prevent photo-oxidative damage of rat retina. AL-8309A is a serotonin 5-HT1A receptor agonist.

methodsAlbino rats were dark adapted prior to blue light exposure. Control rats were maintained in normal cyclic light. Rats were injected subcutaneously 3x with 10 mg/kg AL-8309A (2 days, 1 day and 0 hours) before light exposure for 6 h (3.1 mW/cm(2), λ=450 nm). Animals were sacrificed immediately following light exposure and eyes, retinas and plasma were collected. CEP adducts and autoantibodies were quantified by Western analysis or ELISA.

resultsANOVA supported significant differences in mean amounts of CEP adducts and autoantibodies among the light + vehicle, light + drug and dark control groups from both retina and plasma. Light-induced CEP adducts in retina were reduced ~20% following pretreatment with AL-8309A (n = 62 rats, p = 0.006) and retinal CEP immunoreactivity was less intense by immunohistochemistry. Plasma levels of light-induced CEP adducts were reduced at least 30% (n = 15 rats, p = 0.004) by drug pretreatment. Following drug treatment, average CEP autoantibody titer in light exposed rats (n = 22) was unchanged from dark control levels, and ~20% (p = 0.046) lower than in vehicle-treated rats.

conclusionsLight-induced CEP adducts in rat retina and plasma were significantly decreased by pretreatment with AL-8309A. These results are consistent with and extend previous studies showing AL-8309A reduces light-induced retinal lesions in rats and support CEP biomarkers as possible tools for monitoring the efficacy of select therapeutics.

Indexed as

AnimalsAutoantibodiesBiomarkersDisease Models, AnimalDocosahexaenoic AcidsLightMacular DegenerationMaleOxidation-ReductionPyrrolesRatsRetinaAutoantibodiesBiomarkersDocosahexaenoic AcidsPyrroles

Identifiers

PMID24098476
PMCPMC3788138
OpenAlexW2054846680

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Registered trials

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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.