Fiehler J, Geisler B, Siemonsen S, Saager C, Speck O, Thomalla G, Grzyska U, Kucinski T
Neuroradiology, University Hospital Hamburg-Eppendorf, Hamburg.
Rofo. 2007 Jan;179(1):17-20. doi: 10.1055/s-2006-927183.
Delineation of brain tissue that is at risk but not yet infarcted (penumbra) continues to be a major challenge for stroke imaging. Metabolic characterization of the penumbra might be able to be achieved using blood-oxygen-level-dependent (BOLD) imaging.
We analyzed MRI data from 20 patients within the first 6 hours after stroke onset and after 5-8 days. Among other sequences, the MRI protocol consisted of diffusion-weighted (DWI/ADC = apparent diffusion coefficient) and quantitative T2 and T2* imaging (qT2, qT2*). BOLD images (T2') were calculated using 1/T2' = 1/qT2* - 1/qT2. BOLD lesions were rated by two blinded observers.
Based on the primary blinded reading of the BOLD images, the lesion side was rated correctly by observers 1 and 2 in 80/50 % of the cases, incorrectly in 5/40 % of the cases, and rated as not visible in 15/10 % of the cases. After unblinding the observers, the visibility was rated in 45/45 % of the cases as good, in 35/40 % of the cases as reasonable, and in 20/15 % of the cases as insufficient for diagnostic purposes. The sensitivity for subsequent infarct growth was 0.88 (95 % confidence interval, CI 0.47 to 0.99), the specificity was 0.33 (95 % CI 0.07 to 0.70), the positive predictive value (PPV) was 0.54 (95 % CI 0.25 to 0.81), and the negative predictive value (NPV) was 0.75 (95 % CI 0.19 to 0.99). The odds ratio for subsequent infarct growth was 3.5 (95 % CI 0.20 to 115.53).
Hypo-intense lesions in BOLD imaging were visible and exceeded the lesion in diffusion-weighted imaging in most of the stroke patients. The encouraging results justify further testing of the hypothesis that BOLD lesions, when larger than DWI lesions, are associated with infarct growth from initial DWI to final infarct.
描绘有风险但尚未梗死的脑组织(半暗带)仍然是中风成像的一项重大挑战。利用血氧水平依赖(BOLD)成像或许能够实现对半暗带的代谢特征描述。
我们分析了20例患者在中风发作后最初6小时内以及5 - 8天后的MRI数据。在其他序列中,MRI方案包括扩散加权成像(DWI/ADC = 表观扩散系数)以及定量T2和T2成像(qT2,qT2)。利用1/T2' = 1/qT2* - 1/qT2计算BOLD图像(T2')。由两名不知情的观察者对BOLD病变进行评级。
基于对BOLD图像的初次不知情解读,观察者1和观察者2在80/50%的病例中正确判断出病变侧,在5/40%的病例中判断错误,在15/10%的病例中判断病变不可见。在观察者解除不知情状态后,45/45%的病例中病变可见性被评为良好,35/40%的病例中评为尚可,20/15%的病例中评为对诊断目的而言不足。对后续梗死灶扩大的敏感性为0.88(95%置信区间,CI 0.47至0.99),特异性为0.33(95% CI 0.07至0.70),阳性预测值(PPV)为0.54(95% CI 0.25至0.81),阴性预测值(NPV)为0.75(95% CI 0.19至0.99)。后续梗死灶扩大的优势比为3.5(95% CI 0.20至115.53)。
在大多数中风患者中,BOLD成像中的低信号病变可见,且大于扩散加权成像中的病变。这些令人鼓舞的结果证明有必要进一步验证这一假设,即当BOLD病变大于DWI病变时,与从初始DWI到最终梗死灶的梗死灶扩大相关。