Nagy Muhammad, Azeem Muhammad U, Soliman Youssef, Nawab Sahil A, Jun-O'Connell Adalia H, Goddeau Richard P, Moonis Majaz, Silver Brian, Henninger Nils
Department of Neurology, University of Massachusetts Medical School, Worcester, Massachusetts.
Department of Neurology, University of Massachusetts Medical School, Worcester, Massachusetts; Department of Biochemistry, Worcester Polytechnic Institute, Worcester, Massachusetts.
J Stroke Cerebrovasc Dis. 2019 Apr;28(4):944-953. doi: 10.1016/j.jstrokecerebrovasdis.2018.12.022. Epub 2019 Jan 7.
There are no validated biomarkers that allow for reliable distinction between TIA and other transient neurological symptoms that mimic TIA. We sought to determine whether the degree of pre-existing white matter hyperintensity (WMH) lesion burden relates to the diagnostic certainty of TIA in a cohort of patients presenting with transient neurological symptoms.
We retrospectively analyzed 144 consecutive patients with available brain MRI to quantify and normalize the WMH volume for brain atrophy (adjusted white matter hyperintensity [aWMHV]). We first stratified subjects to probable (n = 62) versus possible (n = 82) TIA as per existing guidelines. Receiver-operating characteristic curves were used to determine a critical aWMHV-threshold (7.8 mL) that best differentiated probable from possible TIA. We then further stratified patients with possible TIA to likely (n = 52) versus unlikely (n = 30) TIA after independent chart review and adjudication. Finally, multivariable logistic and multinomial regression was used to determine whether the defined aWMHV independently related to probable and likely TIA after adjustment for pertinent confounders.
With the exception of age (P < .001) and use of antiplatelets (P = .017), baseline characteristics were similar between patients with probable, likely, and unlikely TIA. In the fully adjusted multinomial model, the aWMHV cut-off greater than 7.8 mL (odds ratio 3.8, 95% confidence interval 1.3-10.9, P = .012) was significantly more frequent in patients with a probable TIA as compared to those with an unlikely TIA diagnosis.
We provide proof-of-principle that WMH may serve as a neuroimaging marker of diagnostic certainty of TIA after neurological workup has been completed.
目前尚无经过验证的生物标志物能够可靠地区分短暂性脑缺血发作(TIA)与其他模仿TIA的短暂性神经症状。我们试图确定在一组出现短暂性神经症状的患者中,既往存在的白质高信号(WMH)病变负担程度是否与TIA的诊断确定性相关。
我们回顾性分析了144例有可用脑部MRI的连续患者,以量化WMH体积并针对脑萎缩进行标准化(调整后的白质高信号[aWMHV])。我们首先根据现有指南将受试者分为可能的TIA(n = 62)和疑似的TIA(n = 82)。采用受试者操作特征曲线来确定最佳区分可能的TIA与疑似的TIA的临界aWMHV阈值(7.8 mL)。然后,在独立的病历审查和判定后,我们将疑似TIA的患者进一步分为可能的TIA(n = 52)和不太可能的TIA(n = 30)。最后,使用多变量逻辑回归和多项回归来确定在调整相关混杂因素后,定义的aWMHV是否与可能的和很可能的TIA独立相关。
除年龄(P <.001)和使用抗血小板药物(P = 0.017)外,可能的、很可能的和不太可能的TIA患者的基线特征相似。在完全调整的多项模型中,与不太可能诊断为TIA的患者相比,aWMHV临界值大于7.8 mL(比值比3.8,95%置信区间1.3 - 10.9,P = 0.012)在可能诊断为TIA的患者中显著更常见。
我们提供了原理证明,即在完成神经学检查后,WMH可作为TIA诊断确定性的神经影像学标志物。