Evidence map›Paper›PMID 40266593›Full record

ArticleInvestigative ophthalmology & visual science2025

Macrophage-Hosted Porphyromonas gingivalis Is a Risk Factor for Cataract Development.

Dongzhe Zhang, Junwei Qu, Cuncun Ke, Xiumei Kong, Mengyun Liu, Iqbal Nawaz Khan, Shuxin Huang, Haijiao Tian, Tong Xie, Ke Qiu and 13 more

Abstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

23 authors.

Dongzhe ZhangDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Junwei QuDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Cuncun KeDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Xiumei KongDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Mengyun LiuDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Iqbal Nawaz KhanDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Shuxin HuangDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Haijiao TianDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Tong XieDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Ke QiuDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Jing LiDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Mingli WangDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Hui LiDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Fengling YuanDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Weikai GuoDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Mingya CaoDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Jing ZhangDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Keke ZhuKaifeng Key Lab for Cataract and Myopia, Institute of Eye Disease, Kaifeng Central Hospital, Kaifeng, China.
Jin LuoDepartment of Pathology, Sinopharm Dongfeng General Hospital, Hubei University of Medicine, Shiyan, China.
Fengyan ZhangDepartment of Ophthalmology, First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Xiukun CuiDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.
Hongmei MuKaifeng Key Lab for Cataract and Myopia, Institute of Eye Disease, Kaifeng Central Hospital, Kaifeng, China.
Yanzhong HuDivision of Vision Science, Joint National Laboratory for Antibody Drug Engineering, Henan University, Kaifeng, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: We studied the regulatory association of Porphyromonas gingivalis (PG) and cataracts. Methods: PCR and FISH assays were used for detecting PG 16s ribosomal RNA genome, Immunofluorescence was for expression of RpgA in anterior capsular epithelium and fibrosis markers in anterior subcapsular cataract (ASC) model. Flow cytometry was for reactive oxygen species and apoptosis. RNA deep sequencing is for differential gene expression analysis. Results: PG's 16s ribosomal RNA gene is positively in 43.3% (101/233 cases) of aqueous humor (AH) samples of patients with cataracts, which differs from 4.7% (6/127) of PG-positive AH in patients with glaucoma. Diabetic and high myopia cataracts increase PG-positive AH compared with age-related cataracts. No PG is observed in AH of congenital cataracts. PG is positive in 82% to 94% of the cataractous anterior capsule tissues from high myopia and age-related, congenital, and diabetic cataracts. The PG-positive cells in the cataractous anterior capsular epithelium are CD68+/CD14+ macrophages, but not anterior epithelial cells. In rat ASC models, PG injected via the tail vein or PG-carried bone marrow monocytes can migrate into the equatorial lens epithelium in form of PG-positive macrophages, which promote ASC progression with upregulation of collagen, fibronectin and α smooth muscle actin (α-SMA) expression, and increase 8-OHdG levels and α-SMA expression in the surrounding lens epithelial cells. Kyoto Encyclopedia of Genes and Genomes and Gene Ontology analysis of the RNA sequencing dataset of ASC tissues shows that signaling pathways related to epithelial-mesenchymal transition, oxidative stress, and cell death are up-regulated in PG + ASC compared with that in ASC alone. Co-culture of supernatants of Raw264.7/PG+ cells with rat primary lens epithelial cells increases the 8-OHdG levels, mitochondrial fission, apoptosis, and expression of α-SMA. Conclusions: Chronic infection with PG can access the lens epithelium via macrophages during stress conditions, which promotes cataract development by possibly elevating oxidative stress, apoptosis, and epithelial-mesenchymal transition in lens tissues. PG infection is a novel a risk factor for cataract development.

Indexed as

CataractEye Infections, BacterialMacrophagesPorphyromonas gingivalisAnimalsApoptosisAqueous HumorDisease Models, AnimalFemaleFlow CytometryHumansMaleMiddle AgedOxidative StressRatsRats, Sprague-DawleyReactive Oxygen SpeciesRNA, Ribosomal, 16S

Identifiers

PMID40266593
PMCPMC12025317

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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.