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Published on: May 25, 2020
The correlation between C-reactive protein and normal tension glaucoma disease: A meta-analysis
Yen Thi Thao Le1,2, Shu-Han Chuang3, Duy Nguyen Anh Tran1,4
1International Master Program in Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Elevated C-reactive protein (CRP) levels are linked to normal tension glaucoma (NTG), suggesting inflammation plays a role. This finding may help identify individuals at higher risk for NTG.
Area of Science:
- Ophthalmology
- Immunology
- Cardiovascular Disease
Background:
- Normal tension glaucoma (NTG) is a prevalent form of glaucoma characterized by optic nerve damage and vision loss without elevated intraocular pressure.
- Systemic inflammation and vascular dysfunction are increasingly implicated in NTG pathogenesis.
- C-reactive protein (CRP) is a well-established marker of systemic inflammation and atherosclerosis, but its association with NTG is not well-defined.
Purpose of the Study:
- To investigate the association between C-reactive protein (CRP) levels and normal tension glaucoma (NTG).
- To compare CRP levels in individuals with NTG versus controls.
- To evaluate CRP as a potential indicator in NTG.
Main Methods:
- A systematic meta-analysis of observational studies (case-control) was conducted.
- Studies were identified through comprehensive searches of PubMed, Embase, and Scopus up to October 31, 2023.
- Data from ten studies involving 766 participants were analyzed using standardized mean differences (SMDs) and 95% confidence intervals (CIs).
Main Results:
- Meta-analysis revealed significantly higher CRP levels in individuals with NTG compared to controls (SMD: 0.731, P=0.014).
- No significant difference in CRP levels was found between primary open-angle glaucoma (POAG) patients and controls (SMD=0.093, P=0.472).
Conclusions:
- Elevated circulating CRP levels are significantly associated with NTG.
- This suggests a potential role for systemic inflammation in the pathogenesis of NTG.
- CRP may serve as an adjunctive marker for identifying high-risk individuals, warranting further prospective research.
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