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Updated: Feb 2, 2026

A Simple Bioassay for the Evaluation of Vascular Endothelial Growth Factors
Published on: March 15, 2016
[The genetic factors of non-response to anti-vascular endothelial growth factor therapy]
1Eye Center of the Second Hospital, Jilin University, Changchun 130022, China.
Abstract:
The response to anti-vascular endothelial growth factor (VEGF) treatment is variable. It is generally measured in terms of changes in correlated functional and/or anatomical outcomes, and patients are then classified as optimal response, poor response and non-response. The precise cause of non-response remains undetermined. A variety of factors could account for poor or non-response to anti-VEGF therapy, such as age, baseline vision, disease course, lesion characteristics and genomic polymorphism. At the present time, many studies on the genetic factors of non-response or poor response to anti-VEGF treatment mainly focus on VEGF genes (VEGF-A, VEGFR-2), complement factor H (CFH), age-related maculopathy susceptibility 2 (LOC387715/ARMS2), high temperature factor A-1 (HTRA1), interleukin-related gene (IL-8 rs4073) and so forth. It is still worthy of further investigations that how to assess genetic reasons for non-response or poor response, so that we can provide individualized treatment sequences and predict the response to anti-VEGF therapy. (Chin J Ophthalmol, 2018, 54:873-878).
Insights
Patient response to anti-vascular endothelial growth factor (VEGF) therapy varies. Genetic factors influencing poor or non-response require further investigation for personalized treatment strategies.
Area of Science:
- Ophthalmology
- Genetics
- Molecular Biology
Background:
- Anti-vascular endothelial growth factor (VEGF) treatments are crucial for various eye conditions.
- Treatment efficacy is variable, with patients classified as optimal responders, poor responders, or non-responders.
- The exact reasons for poor or non-response to anti-VEGF therapy are not fully understood.
Purpose of the Study:
- To explore the genetic factors contributing to variable responses to anti-VEGF treatment.
- To identify potential genetic markers for predicting treatment outcomes.
- To facilitate personalized treatment strategies and improve therapeutic efficacy.
Main Methods:
- Review of existing literature on genetic polymorphisms associated with anti-VEGF treatment response.
- Analysis of studies focusing on genes such as VEGF-A, VEGFR-2, CFH, ARMS2, HTRA1, and IL-8.
- Discussion of the implications of genomic variations on treatment outcomes.
Main Results:
- Non-response to anti-VEGF therapy can be influenced by multiple factors including age, baseline vision, disease progression, lesion characteristics, and genetic variations.
- Current research primarily focuses on specific genes (e.g., VEGF, CFH, ARMS2) but a comprehensive understanding is lacking.
- Genomic polymorphism is a significant area for further investigation.
Conclusions:
- Understanding the genetic basis of non-response is critical for optimizing anti-VEGF therapy.
- Further research into genetic factors can lead to individualized treatment plans.
- Predicting patient response based on genetic profiles holds promise for improving ophthalmic care.
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