Evidence map›Paper›PMID 25180891›Full record

ArticlePloS one2014

Oral microbiome link to neurodegeneration in glaucoma.

Konstantin Astafurov, Eman Elhawy, Lizhen Ren, Cecilia Q Dong, Christina Igboin, Leslie Hyman, Ann Griffen, Thomas Mittag, John Danias

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed, 3 pooled it
5.7field-weighted citation impact, top 4% 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

86 citing papers in PubMed, 3 syntheses or guidelines pooled it, 139 citations in OpenAlex.

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26 more citing papers are in PubMed but not listed here.

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 at 5 institutions in 1 country.

Konstantin AstafurovDepartment of Cell Biology, State University of New York (SUNY) Downstate Medical Center, Brooklyn, New York, United States of America.
Eman ElhawyDepartment of Ophthalmology, State University of New York (SUNY) Downstate Medical Center, Brooklyn, New York, United States of America.
Lizhen RenDepartment of Cell Biology, State University of New York (SUNY) Downstate Medical Center, Brooklyn, New York, United States of America.
Cecilia Q DongDepartment of Ophthalmology, State University of New York (SUNY) Downstate Medical Center, Brooklyn, New York, United States of America.
Christina IgboinDivision of Pediatric Dentistry, Ohio State University, Columbus, Ohio, United States of America.
Leslie HymanDepartment of Preventive Medicine, Stony Brook University Medical Center, Stony Brook, New York, United States of America; State University of New York (SUNY) Eye Institute, Brooklyn, New York, United States of America.
Ann GriffenDivision of Pediatric Dentistry, Ohio State University, Columbus, Ohio, United States of America.
Thomas MittagDepartment of Ophthalmology, Mount Sinai School of Medicine, New York, New York, United States of America.
John DaniasDepartment of Cell Biology, State University of New York (SUNY) Downstate Medical Center, Brooklyn, New York, United States of America; Department of Ophthalmology, State University of New York (SUNY) Downstate Medical Center, Brooklyn, New York, United States of America; State University of New York (SUNY) Eye Institute, Brooklyn, New York, United States of America.
State University of New York · USSUNY Downstate Health Sciences University · USThe Ohio State University · USIcahn School of Medicine at Mount Sinai · USStony Brook University Hospital · US

Funding

Retinal gene expression changes in glaucomaR01EY015224 · NEI · SUNY DOWNSTATE MEDICAL CENTER · PI DANIAS, JOHN · 2004 to 2012
$3.9M
NEI NIH HHS R01 EY015224
6 · The paper itself

Abstract

backgroundGlaucoma is a progressive optic nerve degenerative disease that often leads to blindness. Local inflammatory responses are implicated in the pathology of glaucoma. Although inflammatory episodes outside the CNS, such as those due to acute systemic infections, have been linked to central neurodegeneration, they do not appear to be relevant to glaucoma. Based on clinical observations, we hypothesized that chronic subclinical peripheral inflammation contributes to neurodegeneration in glaucoma.

methodsMouthwash specimens from patients with glaucoma and control subjects were analyzed for the amount of bacteria. To determine a possible pathogenic mechanism, low-dose subcutaneous lipopolysaccharide (LPS) was administered in two separate animal models of glaucoma. Glaucomatous neurodegeneration was assessed in the retina and optic nerve two months later. Changes in gene expression of toll-like receptor 4 (TLR4) signaling pathway and complement as well as changes in microglial numbers and morphology were analyzed in the retina and optic nerve. The effect of pharmacologic blockade of TLR4 with naloxone was determined.

findingsPatients with glaucoma had higher bacterial oral counts compared to control subjects (p<0.017). Low-dose LPS administration in glaucoma animal models resulted in enhancement of axonal degeneration and neuronal loss. Microglial activation in the optic nerve and retina as well as upregulation of TLR4 signaling and complement system were observed. Pharmacologic blockade of TLR4 partially ameliorated the enhanced damage.

conclusionsThe above findings suggest that the oral microbiome contributes to glaucoma pathophysiology. A plausible mechanism by which increased bacterial loads can lead to neurodegeneration is provided by experiments in animal models of the disease and involves activation of microglia in the retina and optic nerve, mediated through TLR4 signaling and complement upregulation. The finding that commensal bacteria may play a role in the development and/or progression of glaucomatous pathology may also be relevant to other chronic neurodegenerative disorders.

Indexed as

MicrobiotaAnimalsBlack or African AmericanBrainComplement System ProteinsFemaleGlaucomaHumansIntraocular PressureLipopolysaccharidesMaleMice, Inbred C57BLMice, Inbred DBAMicrogliaMouthNerve DegenerationComplement System ProteinsLipopolysaccharidesToll-Like Receptor 4

Identifiers

PMID25180891
PMCPMC4152129
OpenAlexW2076838517

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.