The prevalence of 4G/5G polymorphism of plasminogen activator inhibitor-1 (PAI-1) gene in central serous chorioretinopathy and its association with plasma PAI-1 levels

被引:14
|
作者
Sari, Esin Sogutlu [1 ]
Yazici, Alper [1 ]
Eser, Betul [2 ]
Erol, Muhammet Kazim [3 ]
Kilic, Adil [1 ]
Ermis, Sitki Samet [1 ]
Koytak, Arif [4 ]
Aksit, Hasan [5 ]
Yakut, Tahsin [6 ]
机构
[1] Balikesir Univ, Dept Ophthalmol, Fac Med, Balikesir, Turkey
[2] Balikesir Univ, Dept Genet, Fac Med, Balikesir, Turkey
[3] Bezmialem Vakif Univ, Fac Med, Dept Ophthalmol, Balikesir, Turkey
[4] Antalya Educ & Res Hosp, Dept Ophthalmol, Antalya, Turkey
[5] Balikesir Univ, Dept Biochem, Fac Vet, Balikesir, Turkey
[6] Uludag Univ, Fac Med, Dept Genet, Bursa, Turkey
关键词
4G/5G polymorphism of PAI-1 gene; central serous chorioretinopathy; serum PAI-1 level; PROMOTER; ABNORMALITIES; RISK;
D O I
10.3109/15569527.2013.854372
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Context: Central serous chorioretinopathy (CSCR) is a poorly understood disease and the choroidal circulation abnormality induced by the plasminogen activator inhibitor type 1 (PAI-1) seems to be associated with the pathogenesis. There are many reports indicating that 4G/5G polymorphism of the PAI-1 gene is a risk factor for several diseases related to the elevated serum levels of PAI-1. Objective: To evaluate the 4G/5G polymorphism of the PAI-1 gene and its association with serum levels of PAI-1 in acute CSCR patients. Materials and methods: Sixty CSCR patients and 50 healthy control patients were included. The PAI-1 4G/5G was genotyped using the polymerase chain reaction-restriction technique. Serum PAI-1 level was measured using enzyme-linked immunosorbent assay. Demographic data consisting of age, sex, body mass index (BMI) as well as genotype disturbances and serum PAI-1 levels were compared between the groups. Statistical significance for differences in the serum PAI-1 levels of each group with different genotypes was also analyzed. Results: The CSCR group consisted of 40 male (66.7%) and 20 female (33.3%) patients with a mean age of 46.7 +/- 8.39 years. The control group consisted of 32 male (64%) and 18 female (36%) healthy subjects with a mean age of 45.8 +/- 8.39 years. There was no statistically significant difference between the groups in terms of age, sex and BMI. In the CSCR group the genotype frequencies were 4G/4G: 30% (n = 18), 4G/5G: 50% (n = 30), 5G/5G: 20% (n = 12) and in the control group genotype frequencies were 34% (n = 17), 42% (n = 21) and 24% (n = 12), respectively. There was no statistically significant difference in the distribution of genotypes among the groups (chi-squared, p = 0.70). The CSCR group had a significantly higher serum PAI-1 concentration than the control group (p = 0.001). In both groups the mean plasma PAI-1 concentration did not vary significantly among the different genotypes (p > 0.05). Discussion and conclusion: Although our results demonstrated that the patients with acute CSCR have higher serum PAI-1 concentrations than the controls, no significant difference was found in the genotype disturbances of the PAI-1 gene between the groups. The current study indicates that 4G/5G polymorphism in the promoter of the PAI-1 gene cannot be considered a risk factor for the elevated serum PAI-1 levels and consequent development of CSCR.
引用
收藏
页码:270 / 274
页数:5
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