Evidence map›Paper›PMID 40594347›Full record

ArticleScientific reports2025

Age-related decline in retinal function in marmosets.

Takahiko Noro, Xiaoli Guo, Rika Kikuchi, Kenya Sato, Kazuhiko Namekata, Youichi Shinozaki, Chikako Harada, Terumi Yurimoto, Nanako Hashimoto, Keiko Moriya-Ito and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Takahiko NoroVisual Research Project, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-ku, Tokyo, 156-8506, Japan.
Xiaoli GuoVisual Research Project, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-ku, Tokyo, 156-8506, Japan.
Rika KikuchiCentral Institute for Experimental Medicine and Life Science, Kawasaki, Japan.
Kenya SatoCentral Institute for Experimental Medicine and Life Science, Kawasaki, Japan.
Kazuhiko NamekataVisual Research Project, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-ku, Tokyo, 156-8506, Japan.
Youichi ShinozakiVisual Research Project, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-ku, Tokyo, 156-8506, Japan.
Chikako HaradaVisual Research Project, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-ku, Tokyo, 156-8506, Japan.
Terumi YurimotoCentral Institute for Experimental Medicine and Life Science, Kawasaki, Japan.
Nanako HashimotoCenter for Basic Technology Research, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
Keiko Moriya-ItoDevelopmental Neuroscience Project, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
Tadashi NakanoDepartment of Ophthalmology, The Jikei University School of Medicine, Tokyo, Japan.
Erika SasakiCentral Institute for Experimental Medicine and Life Science, Kawasaki, Japan.
Takayuki HaradaVisual Research Project, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-ku, Tokyo, 156-8506, Japan. harada-tk@igakuken.or.jp.

Funding

Japan Agency for Medical Research and Development 24zf0127007h0003Japan Agency for Medical Research and Development JP20dm0207065Japan Society for the Promotion of Science JP19KK0229Japan Society for the Promotion of Science JP20KK0366Japan Society for the Promotion of Science JP21H04756Japan Society for the Promotion of Science JP22K07368Japan Society for the Promotion of Science JP22K09804Japan Society for the Promotion of Science JP23K06818Japan Society for the Promotion of Science JP23K09019Japan Society for the Promotion of Science JP24K12795
6 · The paper itself

Abstract

Vision deterioration caused by natural aging have a detrimental impact on an individual's quality of life, which has become a serious problem as the world's population is aging rapidly. Rodents are the commonly used animal species to investigate the physiological aging process or to identify possible therapeutic targets. However, due to anatomical differences and their genetic distance to humans, translation of findings is sometimes complicated. In the present study, as a step toward aging study in vision using non-human primate marmosets, we examined the eyes of aged marmosets non-invasively. We found that the retinal response deteriorated along with the retinal structure in aged marmosets and the retinal peripheral region was more susceptible to aging. Moreover, the expression of the oxidative stress biomarker 4-HNE was increased in the serum of aged marmosets although no significant correlation was found between 4-HNE levels and the retinal thickness. Our study demonstrated that marmosets offer a promising translational model for the research of age-related vision declination.

Indexed as

AgingRetinaAldehydesAnimalsBiomarkersCallithrixFemaleMaleOxidative Stress4-hydroxy-2-nonenalAldehydesBiomarkersAge-related retinal degenerationMarmosetsOxidative stress

Identifiers

PMID40594347
PMCPMC12217975

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.