Department of Dermatology, Ministry of Health Diskapi Yildirim Beyazit Research and Education Hospital, Ankara, Turkey.
Int J Dermatol. 2010 Feb;49(2):167-71. doi: 10.1111/j.1365-4632.2009.04229.x.
Although the etiology of Behcet's disease is not clarified yet, the vascular endothelial damage and thrombosis are prominent features of the disease. The underlying mechanisms of increased risk of thrombosis in Behcet's disease are not completely understood. It is stated that the changes in blood rheology such as erythrocyte deformability take part in the thrombosis. There are limited numbers of studies with conflicting results about the erythrocyte deformability in Behcet's disease. The previous studies were not limited to the untreated patients with active disease.
Blood samples were filtered immediately by "Imugard- leukocyte removal filter". After plasma and erythrocytes were separated by centrifugation, 10% erythrocyte suspensions were prepared with isotonic Tris NaCl buffer solution. These erythrocyte suspensions were filtered under gravitational force by "Nucleopore" to determine the filtration time. The filtration times of the erythrocyte and buffer solutions were referred as t1 and t2 respectively. Finally, deformability indices were obtained by dividing the t1 by t2. A decrease in the deformability of the erythrocytes would result in an increase in the filtration time of the erythrocyte suspension and deformability indices.
The median deformability indices were 3.090 and 2.170 for patients and control subjects respectively and the difference was statistically significant (P = 0.000).
We suggest that the decrease in erythrocyte deformability in Behcet's disease may be related to oxidative damage of erythrocytes and subsequently takes part in the development of thrombosis in Behcet's disease.
尽管白塞病的病因尚未阐明,但血管内皮损伤和血栓形成是该病的突出特征。白塞病血栓形成风险增加的潜在机制尚未完全了解。有人指出,红细胞变形等血液流变学的变化参与了血栓形成。关于白塞病红细胞变形的研究数量有限,结果相互矛盾。以前的研究不仅限于未接受治疗的活动期患者。
血液样本立即通过“Imugard-白细胞去除过滤器”过滤。离心分离血浆和红细胞后,用等渗 Tris NaCl 缓冲液制备 10%红细胞悬液。这些红细胞悬浮液在重力下通过“Nucleopore”过滤以确定过滤时间。红细胞和缓冲液的过滤时间分别记为 t1 和 t2。最后,通过 t1 除以 t2 获得变形指数。红细胞变形能力下降会导致红细胞悬浮液的过滤时间和变形指数增加。
患者和对照组的中位变形指数分别为 3.090 和 2.170,差异具有统计学意义(P = 0.000)。
我们认为,白塞病中红细胞变形能力的降低可能与红细胞的氧化损伤有关,随后参与了白塞病血栓形成的发展。