Chen Alan M, Karani Kunal B, Taylor J Michael, Zhang Bin, Furthmiller Andrew, De Vela Gabriel, Leach James L, Vadivelu Sudhakar, Abruzzo Todd A
1Radiology Associates of Tallahassee, Tallahassee, Florida.
2Department of Radiology and.
J Neurosurg Pediatr. 2019 Jul 26;24(4):389-396. doi: 10.3171/2019.5.PEDS1982. Print 2019 Oct 1.
Although intracranial arterial aneurysms (IAAs) of childhood are usually idiopathic, it is possible that underlying arteriopathy escapes detection when using conventional diagnostic tools. Quantitative arterial tortuosity (QAT) has been studied as a biomarker of arteriopathy. The authors analyzed cervicocerebral QAT in children with idiopathic IAAs to assess the possibility of arteriopathy.
Cases were identified by text-string searches of imaging reports spanning the period January 1993 through June 2017. QAT of cervicocerebral arterial segments was measured from cross-sectional studies using image-processing software. Other imaging and clinical data were confirmed by retrospective electronic record review. Children with idiopathic IAAs and positive case controls, with congenital arteriopathy differentiated according to aneurysm status (with and without an aneurysm), were compared to each other and to healthy controls without vascular risk factors.
Cervicocerebral QAT was measured in 314 children: 24 with idiopathic IAAs, 163 with congenital arteriopathy (including 14 arteriopathic IAAs), and 127 healthy controls. QAT of all vertebrobasilar segments was larger in children with IAAs (idiopathic and arteriopathic forms) (p < 0.05). In children with congenital arteriopathy without an aneurysm, QAT was decreased for the distal cervical vertebral arteries and increased for the supraspinal vertebral artery relative to healthy children. QAT of specific cervicocerebral segments correlated with IAA size and rupture status.
Cervicocerebral QAT is a biomarker of arteriopathy in children with IAA, even in the absence of other disease markers. Additional findings suggest a correlation of cervicocerebral QAT with IAA size and rupture status and with the presence of IAA in children with congenital arteriopathy.
尽管儿童颅内动脉瘤(IAA)通常为特发性,但使用传统诊断工具时,潜在的动脉病变可能无法被检测到。定量动脉迂曲度(QAT)已被作为动脉病变的生物标志物进行研究。作者分析了特发性IAA患儿的颈脑QAT,以评估动脉病变的可能性。
通过对1993年1月至2017年6月期间的影像学报告进行文本串搜索来确定病例。使用图像处理软件从横断面研究中测量颈脑动脉段的QAT。通过回顾性电子病历审查确认其他影像学和临床数据。将特发性IAA患儿和阳性病例对照(根据动脉瘤状态分为有和无动脉瘤的先天性动脉病变)相互比较,并与无血管危险因素的健康对照进行比较。
对314名儿童进行了颈脑QAT测量:24名特发性IAA患儿、163名先天性动脉病变患儿(包括14名动脉病变性IAA患儿)和127名健康对照。IAA患儿(特发性和动脉病变性)所有椎基底动脉段的QAT均较大(p<0.05)。在无动脉瘤的先天性动脉病变患儿中,相对于健康儿童,颈段椎动脉远端的QAT降低,而椎动脉上段的QAT升高。特定颈脑段的QAT与IAA大小和破裂状态相关。
颈脑QAT是IAA患儿动脉病变的生物标志物,即使在没有其他疾病标志物的情况下也是如此。其他研究结果表明,颈脑QAT与IAA大小和破裂状态以及先天性动脉病变患儿中IAA的存在相关。