El-Shazly Sherien F, El-Bradey Mohamed H, Tameesh Mohamed K
Department of Clinical Pathology, Faculty of Medicine, Tanta University, Tanta, Egypt.
Clin Exp Ophthalmol. 2014 May-Jun;42(4):369-78. doi: 10.1111/ceo.12182. Epub 2013 Sep 24.
To study the possible association between vascular endothelial growth factor gene polymorphism and diabetic macular oedema, and its correlation to the outcomes of anti-vascular endothelial growth factor treatment.
Prospective study.
392 diabetic patients were included; 180 patients of them had no retinopathy, 212 patients had diabetic retinopathy. Diabetic retinopathy patients were classified into four groups as defined by the absence or presence of macular oedema or proliferative retinopathy.
In all subjects, polymerase chain reaction-restriction fragment length polymorphism was conducted to detect the vascular endothelial growth factor gene C-634G polymorphism. Serum levels of vascular endothelial growth factor were estimated. Changes of visual acuity and central macular thickness after bevacizumab treatment in diabetic macular oedema patients of different genotypes were monitored for 9-12 months.
Vascular endothelial growth factor C-634G genotypes distribution in different groups; correlation between genotypes, and changes in visual acuity and central macular thickness after intravitreal bevacizumab treatment.
CC genotype was significantly prevalent among diabetic macular oedema patients (P = 0.019). Significant higher serum levels of vascular endothelial growth factor were detected in diabetic retinopathy and diabetic macular oedema patients with CC genotype (P = 0.02, 0.016). After bevacizumab treatment, individuals with genotypes CG and GG have a decreased chance of positive treatment outcomes compared t with CC genotype (P < 0.001).
Vascular endothelial growth factor C-634G polymorphism (CC genotype) is a genetic risk factor for diabetic macular oedema, and its presence provides significantly better visual outcome following bevacizumab treatment.
研究血管内皮生长因子基因多态性与糖尿病性黄斑水肿之间的可能关联,以及其与抗血管内皮生长因子治疗效果的相关性。
前瞻性研究。
纳入392例糖尿病患者;其中180例无视网膜病变,212例有糖尿病视网膜病变。糖尿病视网膜病变患者根据是否存在黄斑水肿或增殖性视网膜病变分为四组。
对所有受试者进行聚合酶链反应-限制性片段长度多态性检测,以检测血管内皮生长因子基因C-634G多态性。测定血清血管内皮生长因子水平。对不同基因型的糖尿病性黄斑水肿患者进行贝伐单抗治疗后,监测其视力和黄斑中心厚度变化9至12个月。
不同组中血管内皮生长因子C-634G基因型分布;基因型与玻璃体内注射贝伐单抗治疗后视力及黄斑中心厚度变化的相关性。
CC基因型在糖尿病性黄斑水肿患者中显著多见(P = 0.019)。CC基因型的糖尿病视网膜病变和糖尿病性黄斑水肿患者血清血管内皮生长因子水平显著更高(P = 0.02,0.016)。贝伐单抗治疗后,与CC基因型相比,CG和GG基因型个体治疗效果为阳性的几率降低(P < 0.001)。
血管内皮生长因子C-634G多态性(CC基因型)是糖尿病性黄斑水肿的遗传危险因素,其存在使贝伐单抗治疗后的视力改善明显更好。