Abstract | OBJECTIVE: METHODS: Odds ratios (OR) of MYOC Gln368STOP genotype distributions in POAG patients verse the controls were analyzed. All the relevant reported studies were identified. Poor-qualified studies were eliminated, and the risk of publication bias was excluded. Meta-analysis software, RevMan 4.2, was applied for investigating heterogeneity among individual studies and summarizing the effects across studies. RESULTS: A total of 3077 POAG cases and 2063 controls from 11 studies were included. No heterogeneity among these studies was noticed (P = 0.79). The pooled OR (with 95% CI) of MYOC Gln368STOP in POAG cases versus that in the controls was 6.01 (2.57 - 14.04, P < 0.01). CONCLUSION: MYOC Gln368STOP mutation might be associated with the increased risk of POAG and is one of its risk factors.
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Authors | Ting Liu, Xiang-Ge He |
Journal | [Zhonghua yan ke za zhi] Chinese journal of ophthalmology
(Zhonghua Yan Ke Za Zhi)
Vol. 43
Issue 4
Pg. 361-6
(Apr 2007)
ISSN: 0412-4081 [Print] China |
PMID | 17605937
(Publication Type: English Abstract, Journal Article, Meta-Analysis)
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Chemical References |
- Cytoskeletal Proteins
- Eye Proteins
- Glycoproteins
- trabecular meshwork-induced glucocorticoid response protein
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Topics |
- Cytoskeletal Proteins
(genetics)
- Eye Proteins
(genetics)
- Genotype
- Glaucoma, Open-Angle
(genetics)
- Glycoproteins
(genetics)
- Humans
- Mutation
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