Brandsen Rajani P, Diederen Roselie M H, Klaassen Ingeborg, Veldthuis Martijn, Korsten Herbert, van Zwieten Rob, Schlingemann Reinier O, Nur Erfan, Biemond Bart J
Department of Ophthalmology, Amsterdam UMC, Amsterdam, The Netherlands.
Department of Haematology, Amsterdam UMC, Amsterdam, The Netherlands.
Br J Haematol. 2025 Jun;206(6):1796-1805. doi: 10.1111/bjh.20124. Epub 2025 Apr 29.
Sickle cell disease (SCD), encompassing genotypes such as HbSS and HbSC, causes chronic haemolysis and microvascular occlusion, leading to organ damage. The retina is particularly vulnerable, often resulting in sickle cell retinopathy (SCR) or sickle cell maculopathy (SCM). The precise underlying mechanisms are unclear, though various factors are suggested to contribute. This study explored the role of whole blood viscosity and red blood cell (RBC) deformability in SCR and SCM. Adult HbSS (n = 34) and HbSC patients (n = 34) were offered an ophthalmic examination to determine SCR stage. A venous ethylenediaminetetraacetic acid (EDTA) sample was collected from each participant. Whole blood viscosity was measured using a Brookfield viscometer and RBC deformability was assessed using the Oxygenscan feature of the Laser Optical Rotational Red Cell Analyser as a function of the (varying) partial oxygen pressure. HbSC patients with proliferative sickle cell retinopathy (PSCR) had a lower delta elongation index (p = 0.012) and point of sickling (p = 0.002) than those without PSCR, suggesting that RBC sickling might not play a central role in the pathogenesis of PSCR in HbSC patients. Despite hyperviscosity being a commonly proposed mechanism, no associations were found between blood viscosity, SCR and SCM. These results point to alternative mechanisms contributing to SCR and SCM, highlighting the complexity and need for further research to fully understand the underlying factors.
镰状细胞病(SCD)包括HbSS和HbSC等基因型,会导致慢性溶血和微血管阻塞,进而造成器官损伤。视网膜尤其脆弱,常常引发镰状细胞视网膜病变(SCR)或镰状细胞黄斑病变(SCM)。尽管有多种因素被认为与之相关,但其确切的潜在机制尚不清楚。本研究探讨了全血粘度和红细胞(RBC)变形性在SCR和SCM中的作用。为成年HbSS患者(n = 34)和HbSC患者(n = 34)进行眼科检查以确定SCR分期。从每位参与者采集静脉乙二胺四乙酸(EDTA)样本。使用布鲁克菲尔德粘度计测量全血粘度,并使用激光光学旋转红细胞分析仪的氧扫描功能评估RBC变形性,该功能是部分氧分压(变化)的函数。患有增殖性镰状细胞视网膜病变(PSCR)的HbSC患者的伸长指数变化值(p = 0.012)和镰变点(p = 0.002)低于无PSCR的患者,这表明RBC镰变可能在HbSC患者PSCR的发病机制中不发挥核心作用。尽管高粘度是一种常见的推测机制,但未发现血液粘度、SCR和SCM之间存在关联。这些结果表明存在导致SCR和SCM的其他机制,凸显了其复杂性以及进一步研究以充分了解潜在因素的必要性。