Association of tumour necrosis factor alpha-308 gene polymorphism with primary open-angle glaucoma in Chinese

被引:60
作者
Lin, HJ
Tsai, FJ
Chen, WC
Shi, YR
Hsu, Y
Tsai, SW
机构
[1] China Med Coll Hosp, Dept Med Genet & Pediat, Taichung 404, Taiwan
[2] China Med Coll Hosp, Dept Ophthalmol, Taichung 404, Taiwan
[3] China Med Coll Hosp, Dept Occupat Safety & Hlth, Taichung 404, Taiwan
[4] China Med Coll Hosp, Inst Environm Med, Taichung 404, Taiwan
关键词
tumour necrosis factor; genetic polymorphism; glaucoma;
D O I
10.1038/sj.eye.6700227
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose Genetic factors are known to play a role in the aetiology of glaucoma, and in particular the role of the immune system is highly suspected. In this study, we evaluated the association between tumour necrosis factor alpha -308 (TNF alpha -308) and primary open-angle glaucoma (POAG). Methods A total of sixty POAG patients and 103 healthy volunteers as control group were enrolled in this case-controlled study. Furthermore, we used polymerase chain reaction based analysis to resolve the TNF alpha -308 polymorphism. Statistical analysis for the relative risk of TNF alpha -308 polymorphism was compared by the chi(2) test. Results There were significant differences in the distribution of the polymorphism between the POAG patients and the control subjects (P = 0.00016; P < 0.05) and it was found that the A(-308) allele occurred more frequently in POAG patients (odds ratio: 2.72; 95% confidence interval: 1.66-4.45). Conclusion The results of our study concluded that the distribution of TNF alpha -308 was significantly higher in the POAG patients than in the control group. Therefore, the A(-308) allele appears to be associated with POAG and, therefore, could be used as a genetic marker for disease mapping. POAG is a complex disease, and a single gene could not be responsible. Understanding the role of genetic polymorphisms, like TNF alpha, could be a prediction of the disease and useful for developing new treatments for POAG.
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页码:31 / 34
页数:4
相关论文
共 21 条
[1]   Impact of the-308 TNF promoter polymorphism on the transcriptional regulation of the TNF gene: relevance to disease [J].
Abraham, LJ ;
Kroeger, KM .
JOURNAL OF LEUKOCYTE BIOLOGY, 1999, 66 (04) :562-566
[2]   Comparison study for identifying promoter allelic polymorphism in interleukin 10 and tumor necrosis factor α genes [J].
Agarwal, P ;
Oldenburg, MC ;
Czarneski, JE ;
Morse, RM ;
Hameed, MR ;
Cohen, S ;
Fernandes, H .
DIAGNOSTIC MOLECULAR PATHOLOGY, 2000, 9 (03) :158-164
[3]   Polymorphism of the human TNF-α promoter -: random variation or functional diversity? [J].
Allen, RD .
MOLECULAR IMMUNOLOGY, 1999, 36 (15-16) :1017-1027
[5]   HETEROZYGOSITY EFFECTS IN STUDIES OF GENETIC-MARKERS AND DISEASE [J].
BECKMAN, L ;
FROHLANDER, N .
HUMAN HEREDITY, 1990, 40 (06) :322-329
[6]  
Courtney RH, 1931, J AMER MED ASSOC, V97, P1602
[7]   GENETICS AND PRIMARY OPEN-ANGLE GLAUCOMA [J].
FRANCOIS, J .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1966, 61 (04) :652-&
[8]  
GALBRAITH GMP, 1995, HUM GENET, V96, P433
[9]  
HOSKIN H, 1989, BECKER SHAFFERS DIAG, P277
[10]   GENETIC CLUES TO GLAUCOMAS SECRETS - THE L-EDWARD-JACKSON-MEMORIAL-LECTURE .2. [J].
LICHTER, PR .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1994, 117 (06) :706-727