Anatomical Variations of the Willis Circle: A Risk Factor for Brain Lesions in Sickle Cell Patients

Nwatsock Joseph-Francis, Gharingam Marie Laure, Moulion-Tapouh Jean-Roger, Simoni Paolo, Moifo Boniface
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Abstract

: Background and objective : The brain lesions observed in sickle cell patients are often known to be due to vessels occlusions. But other factors could be associated with the genesis of these lesions. The objective of this study was to assess the association between the presence of anatomical variations in the Willis circle and that of brain lesions found on MRI in sickle cell patients. Methods : We conducted a bicentric cross-sectional study with retrolective analysis of images at the medical imaging departments of the HUDERF in Brussels (Belgium) and the Yaoundé General Hospital (Cameroon), over a period of 12 months from November 2020 to October 2021. We included 187 homozygous sickle cell patients with documented electrophoresis and brain MRI results. The MRI were carried out in T1, T2, T2*, FLAIR, Diffusion and 3D TOF sequences on Siemens ® 1.5 Tesla devices. The collected data were analyzed using SPSS ® software version 20.0 for Windows ® with a significant p<0.05. Results : The mean age of patients was 8.76 years with no significant difference between the sexes. Variations in the Willis circle were present in 20 cases (10.70%) with a predominance in the posterior hemicircle (6.96% versus 3.74% for the anterior hemicircle; p=0.04). The most common variation was type G corresponding to hypoplasia or absence of the anterior communicating artery in the anterior hemicircle, and hypoplasia or unilateral absence of a posterior communicating artery in the posterior hemicircle. At the parenchymal level, brain lesions were found in 11 cases (5.88%) including ischemic lesions (3.21%) and leukopathies (1.07%). In general, the existence of these lesions was significantly associated with the presence of the Willis circle variations (p=0.01). Conclusion and recommendation : The presence of anatomical variations of the Willis arterial circle in sickle cell patients is associated with the existence of brain lesions. We therefore conclude that anatomical variations of the Willis circle could be an unknown factor increasing the risk of brain damages and therefore morbidity in these patients. We recommend that a larger sample study be conducted to verify our findings.
威利斯圈的解剖变异:镰状细胞患者脑损伤的危险因素
背景与目的:镰状细胞病患者的脑部病变通常是由血管闭塞引起的。但其他因素可能与这些病变的发生有关。本研究的目的是评估镰状细胞患者威利斯环解剖变异与MRI发现的脑病变之间的关系。方法:在2020年11月至2021年10月的12个月期间,我们对比利时布鲁塞尔HUDERF和喀麦隆雅温德格总医院医学影像部门的图像进行了一项双中心横断面研究,并进行了回顾性分析。我们纳入了187例有记录的电泳和脑MRI结果的纯合子镰状细胞患者。MRI在Siemens®1.5 Tesla设备上按T1、T2、T2*、FLAIR、Diffusion和3D TOF序列进行。采用SPSS®软件20.0 for Windows®进行统计分析,差异有统计学意义p<0.05。结果:患者平均年龄为8.76岁,性别差异无统计学意义。20例(10.70%)患者出现Willis环变异,以后半圆为主(6.96% vs 3.74%);p = 0.04)。最常见的变异是G型,对应于前半圆的前交通动脉发育不全或缺失,以及后半圆的后交通动脉发育不全或单侧缺失。脑实质病变11例(5.88%),包括缺血性病变(3.21%)和白质病变(1.07%)。一般来说,这些病变的存在与Willis环变异的存在显著相关(p=0.01)。结论和建议:镰状细胞患者威利斯动脉圈解剖变异的存在与脑病变的存在有关。因此,我们得出结论,威利斯环的解剖变异可能是增加脑损伤风险的未知因素,因此在这些患者中发病率增加。我们建议进行更大样本的研究来验证我们的发现。
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