Evidence map›Paper›PMID 31467395›Full record

ArticleScientific reports2019

Fundamental differences in patterns of retinal ageing between primates and mice.

Jaimie Hoh Kam, Tobias W Weinrich, Harpreet Shinhmar, Michael B Powner, Nicholas W Roberts, Asmaa Aboelnour, Glen Jeffery

Open access · goldAbstract readComparative Study
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Diabetic retinopathy and Alzheimer's disease: Convergence of the unfolded protein response in neurodegeneration.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
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  8. Modeling Retinitis Pigmentosa with Patient-Derived iPSCs.Advances in experimental medicine and biology · 2023
    Review
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  11. Review
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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

7 authors at 5 institutions in 3 countries.

Jaimie Hoh KamUniversity College London, Institute of Ophthalmology, EC1V9EL, London, UK.
Tobias W WeinrichUniversity College London, Institute of Ophthalmology, EC1V9EL, London, UK.
Harpreet ShinhmarUniversity College London, Institute of Ophthalmology, EC1V9EL, London, UK.
Michael B PownerCity, University of London, Centre of Applied Vision Research, EC1V0HB, London, UK.ORCID http://orcid.org/0000-0003-4913-1004
Nicholas W RobertsSchool of Biological Sciences, University of Bristol, BS8 1TQ, Bristol, UK.ORCID http://orcid.org/0000-0002-4540-6683
Asmaa AboelnourHistology and Cytology Department, Faculty of Veterinary Medicine, Damanhour University, Damanhour, Egypt.
Glen JefferyUniversity College London, Institute of Ophthalmology, EC1V9EL, London, UK. g.jeffery@ucl.ac.uk.ORCID http://orcid.org/0000-0002-8777-4521
University College London · GBCity, University of London · GBDamanhour University · EGInstitute of Ophthalmology · MXUniversity of Bristol · GB

Funding

RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BB/N000250/1
6 · The paper itself

Abstract

Photoreceptors have high metabolic demands and age rapidly, undermining visual function. We base our understanding mainly on ageing mice where elevated inflammation, extracellular deposition, including that of amyloid beta, and rod and cone photoreceptor loss occur, but cones are not lost in ageing primate although their function declines, revealing that primate and mouse age differently. We examine ageing primate retinae and show elevated stress but low inflammation. However, aged primates have a >70% reduction in adenosine triphosphate (ATP) and a decrease in cytochrome c oxidase. There is a shift in cone mitochondrial positioning and glycolytic activity increases. Bruch's membrane thickens but unlike in mice, amyloid beta is absent. Hence, reduced ATP may explain cone functional decline in ageing but their retained presence offers the possibility of functional restoration if they can be fuelled appropriately to restore cellular function. This is important because as humans we largely depend on cone function to see and are rarely fully dark adapted. Presence of limited aged inflammation and amyloid beta deposition question some of the therapeutic approaches taken to resolve problems of retinal ageing in humans and the possible lack of success in clinical trials in macular degeneration that have targeted inflammatory agents.

Indexed as

Adenosine TriphosphateAgingAnimalsBruch MembraneExtracellular SpaceMiceMitochondriaPrimatesRetinaSpecies SpecificityStress, PhysiologicalAdenosine Triphosphate

Identifiers

PMID31467395
PMCPMC6715671
OpenAlexW2971092797

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.