Greiner K, Peetz D, Winkgen A, Prellwitz W, Pfeiffer N, Hafner G
Department of Ophthalmology, Johannes-Gutenberg-University, Mainz, Germany.
Int Ophthalmol. 1999;23(3):155-60. doi: 10.1023/a:1010639332737.
This study was carried out to determine the prevalence of genetic thrombophilia in patients with retinal vascular occlusion.
We investigated 116 consecutive patients with central retinal vein occlusion (CRVO, n = 48), branch retinal vein occlusion (BRVO, n = 33), central retinal artery occlusion (CRAO, n = 21), branch retinal artery occlusion (BRAO, n = 14). All patients underwent comprehensive tests for coagulation disorders including determinations of protein C, protein S, lupus anticoagulants, prothrombin gene mutation (G20210A), resistance to activated protein C (APCR), and were screened for vascular disease risk factors. APC resistance was confirmed by a PCR method to detect the factor V R506Q mutation. A PCR method was also used to detect the G20210A mutation. For comparative purposes, we screened 209 consecutive patients with deep vein thrombosis (DVT) and 581 patients with coronary heart disease (control group) for APC resistance.
13 (27%) of 48 patients with CRVO had the factor V R506Q mutation. The factor V R506Q mutation was detected in six (18%) of 33 patients with BRVO, but in only one patient with CRAO and in two patients with BRAO. Other thrombophilic defects were not detected. The APCR prevalence within the CRVO group was significantly increased when compared to the control group (8%). There was no significant difference in the factor V R506Q mutation prevalence between the CRVO group and the DVT group (19%).
The factor V R506Q mutation is the most common cause of genetic thrombophilia in patients with CRVO and has a similar prevalence as in DVT patients.
本研究旨在确定视网膜血管阻塞患者中遗传性血栓形成倾向的患病率。
我们调查了116例连续性视网膜中央静脉阻塞(CRVO,n = 48)、视网膜分支静脉阻塞(BRVO,n = 33)、视网膜中央动脉阻塞(CRAO,n = 21)、视网膜分支动脉阻塞(BRAO,n = 14)患者。所有患者均接受了凝血障碍的全面检测,包括蛋白C、蛋白S、狼疮抗凝物、凝血酶原基因突变(G20210A)的测定以及活化蛋白C抵抗(APCR)检测,并对血管疾病危险因素进行了筛查。通过PCR方法检测因子V R506Q突变以确认APCR抵抗。还使用PCR方法检测G20210A突变。为作比较,我们对209例连续性深静脉血栓形成(DVT)患者和581例冠心病患者(对照组)进行了APCR抵抗筛查。
48例CRVO患者中有13例(27%)存在因子V R506Q突变。33例BRVO患者中有6例(18%)检测到因子V R506Q突变,但CRAO患者中仅1例、BRAO患者中仅2例检测到该突变。未检测到其他血栓形成倾向缺陷。与对照组(8%)相比,CRVO组中APCR患病率显著升高。CRVO组与DVT组之间因子V R506Q突变患病率无显著差异(19%)。
因子V R506Q突变是CRVO患者遗传性血栓形成倾向的最常见原因,其患病率与DVT患者相似。