From the Department of Cardiology, Guy's and St Thomas' NHS Trust, London, England (V.O.P., A.I., R.H., L.F., G.C., E.N.); Institute of Experimental and Translational Cardiovascular Imaging, DZHK Centre for Cardiovascular Imaging, Goethe University Hospital Frankfurt, Theodor-Stern-Kai 7, Frankfurt am Main 60590, Germany (V.O.P., E.N.); Department of Cardiology, Goethe University Hospital Frankfurt, Frankfurt am Main, Germany (V.O.P.); Department of Cardiovascular Imaging, King's College London, St. Thomas' Hospital, London, England (V.O.P.); Ramón y Cajal University Hospital, University of Alcalá, Madrid, Spain (R.H.); and King's College Hospital NHS Trust, Denmark Hill, London, England (G.C.).
Radiology. 2017 Oct;285(1):63-72. doi: 10.1148/radiol.2017162732. Epub 2017 Apr 27.
Purpose To determine whether quantitative tissue characterization with T1 and T2 mapping supports recognition of myocardial involvement in patients with systemic sarcoidosis. Materials and Methods Fifty-three consecutive patients with a biopsy-proven extracardiac diagnosis of systemic sarcoidosis (21 men; median age, 45 years; interquartile range, 22 years) and 36 normotensive previously healthy control subjects (14 men; median age, 43 years; interquartile range, 18 years) underwent cardiovascular magnetic resonance imaging, which was performed to assess cardiac function and late gadolinium enhancement, and T1 and T2 mapping. A follow-up substudy was performed in 40 patients (mean follow-up interval, 144 days ± 35 [standard deviation]); of these 40 patients, 18 underwent anti-inflammatory treatment for systemic symptoms. Binary logistic regression and receiver operating characteristic curve analyses were used to assess discrimination between health and disease; Wilcoxon signed rank test was used to assess the effect of treatment. Results When compared with control subjects, patients had higher ventricular volume, higher myocardial native T1 and T2, and lower longitudinal strain and ejection fraction (P < .05 for all). Myocardial native T1 and T2 had higher discriminatory accuracy (area under the receiver operating characteristic curve [AUC]: 0.96 and 0.89, respectively) for separation between control subjects and patients when compared with the standard diagnostic criteria (AUC < 0.67). Native T1 was the independent discriminator between health and disease (specificity, 90%; sensitivity, 96%; accuracy, 94%). There was a significant reduction of native T1 and T2 in the patients who underwent treatment (z score: -3.72 and -2.88; P < .01) but not in the patients who did not (z score, -1.42 and -1.38; P > .15). Conclusion Quantitative myocardial tissue characterization with T1 and T2 mapping may enable noninvasive recognition of cardiac involvement and activity of myocardial inflammation in patients with systemic sarcoidosis. Future studies will be performed to confirm their role in risk stratification and guidance of clinical management. RSNA, 2017 Online supplemental material is available for this article.
目的 旨在确定 T1 和 T2 映射的定量组织特征是否支持识别系统性肉瘤病患者的心肌受累。
材料与方法 53 例经活检证实为系统性肉瘤病的患者(21 例男性;中位年龄 45 岁;四分位距 22 岁)和 36 例无高血压的健康对照者(14 例男性;中位年龄 43 岁;四分位距 18 岁)连续接受心血管磁共振成像检查,以评估心脏功能和晚期钆增强,并进行 T1 和 T2 映射。对 40 例患者进行了随访亚研究(平均随访间隔 144 天±35[标准差]);其中 40 例患者因系统性症状接受了抗炎治疗。采用二项逻辑回归和受试者工作特征曲线分析评估健康与疾病之间的区分;采用 Wilcoxon 符号秩检验评估治疗的效果。
结果 与对照组相比,患者的心室容积更大,心肌固有 T1 和 T2 值更高,纵向应变和射血分数更低(均 P<0.05)。与标准诊断标准(AUC<0.67)相比,心肌固有 T1 和 T2 对区分对照组和患者具有更高的准确性(AUC:分别为 0.96 和 0.89)。固有 T1 是区分健康与疾病的独立指标(特异性 90%;敏感性 96%;准确性 94%)。接受治疗的患者固有 T1 和 T2 值显著降低(z 值:-3.72 和-2.88;P<0.01),而未接受治疗的患者则无显著变化(z 值:-1.42 和-1.38;P>0.15)。
结论 T1 和 T2 映射的定量心肌组织特征可能能够无创识别系统性肉瘤病患者的心脏受累和心肌炎症活动。未来的研究将进一步证实它们在风险分层和临床管理指导中的作用。
放射学学会,2017 年
在线补充材料可在本文中获取。