The Molecular Pathogenesis Study of Cataract

January 3, 2023 updated by: Jin Yang, Eye & ENT Hospital of Fudan University
To study the molecular pathogenesis of cataract and explore possible treatments,anterior lens capsules were collected from cataract patients

Study Overview

Status

Recruiting

Conditions

Detailed Description

Anterior lens capsules were collected from the patients with DC and ARC, and transparent crystals of cadaveric eyes. M6A epitranscriptomic microarray was performed to investigate the altered m6A modifications and determine the differentially expressed mRNAs. The potential role of dysregulated m6A modification levels was predicted through Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analyses. Real-time polymerase chain reaction was performed to identify the dysregulated expression of RNA methyltransferases, demethylases, and readers.

Study Type

Observational

Enrollment (Anticipated)

150

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Shanghai
      • Shanghai, Shanghai, China, 200031
        • Recruiting
        • Eye & ENT Hospital of Fudan University
        • Contact:
        • Principal Investigator:
          • Lei Cai, MD
        • Principal Investigator:
          • Dongmei Ma, MD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 90 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Anterior lens capsule tissues from cataract patients with diabetes mellitus more than 10 years, patients with age related cataract, and transparent crystals of cadaveric eyes.

Description

Inclusion Criteria:

  • diabetic cataract
  • underwent cataract surgery

Exclusion Criteria:

  • Combined with other eye diseases
  • underwent other eye surgery

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Control
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
DC group
Anterior lens capsule tissues from DC patients
ARC group
Anterior lens capsule tissues from ARC patients
NC group
anterior lens capsules collected from three age-matched transparent crystals of cadaveric eyes

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
m6A modification of mRNAs
Time Frame: 1 month
Epitranscriptomic microarray analysis reveals the differential m6A modification of mRNAs in DC samples
1 month
expression level of mRNAs
Time Frame: 1 month
the m6A microarray analyses provide data for mRNA expression levels
1 month
levels of methylated mRNA
Time Frame: 1 month
in vitro validation of the diverse expression levels of methylated mRNA
1 month
levels of RNA methyltransferase
Time Frame: 1 month
in vitro validation of the diverse expression levels of RNA methyltransferase
1 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jin Yang, PhD, Eye & ENT Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2022

Primary Completion (Anticipated)

December 1, 2023

Study Completion (Anticipated)

December 30, 2025

Study Registration Dates

First Submitted

December 6, 2022

First Submitted That Met QC Criteria

January 3, 2023

First Posted (Actual)

January 12, 2023

Study Record Updates

Last Update Posted (Actual)

January 12, 2023

Last Update Submitted That Met QC Criteria

January 3, 2023

Last Verified

January 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CMP

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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