Biomedical Imaging Research Institute, Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, United States; Department of Bioengineering, University of California Los Angeles, CA, United States.
Biomedical Imaging Research Institute, Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, United States; Women's Heart Center, Cedars-Sinai Heart Institute, Los Angeles, CA, United States.
Int J Cardiol. 2018 Nov 1;270:48-53. doi: 10.1016/j.ijcard.2018.06.086. Epub 2018 Jun 22.
It has recently been shown that magnetic resonance (MR) "native T1" mapping is capable of characterizing abnormal microcirculation in patients with obstructive coronary artery disease (CAD). In studies involving women with signs and symptoms of ischemia and no obstructive CAD (INOCA), however, the potential role of native T1 as an imaging marker and its association with indices of diastolic function or vasodilator-induced myocardial ischemia have not been explored. We investigated whether native T1 in INOCA is associated with reduced myocardial perfusion reserve index (MPRI) or with diastolic dysfunction.
Twenty-two female patients with INOCA and twelve female reference controls with matching age and body-mass index were studied. The patients had evidence of vasodilator-induced ischemia without obstructive CAD or any prior infarction. All 34 subjects underwent stress/rest MR including native T1 mapping (MOLLI 5(3)3) at 1.5-Tesla.
Compared with controls, patients had similar morphology/function. As expected, MPRI was significantly reduced in patients compared to controls (1.78 ± 0.39 vs. 2.49 ± 0.41, p < 0.0001). Native T1 was significantly elevated in patients (1040.1 ± 29.3 ms vs. 1003.8 ± 18.5 ms, p < 0.001) and the increased T1 showed a significant inverse correlation with MPRI (r = -0.481, p = 0.004), but was not correlated with reduced diastolic strain rate.
Symptomatic women with INOCA have elevated native T1 compared to matched reference controls and there is a significant association between elevated native T1 and impaired MPRI, considered a surrogate measure of ischemia severity in this cohort. Future studies in a larger cohort are needed to elucidate the mechanism underlying this inverse relationship.
最近的研究表明,磁共振(MR)“原生 T1”mapping 能够对阻塞性冠状动脉疾病(CAD)患者的异常微循环进行特征描述。然而,在涉及有缺血症状和无阻塞性 CAD(INOCA)的女性的研究中,尚未探讨原生 T1 作为成像标志物的潜在作用及其与舒张功能或血管扩张剂诱导的心肌缺血的指标的关联。我们研究了 INOCA 中的原生 T1 是否与降低的心肌灌注储备指数(MPRI)或舒张功能障碍相关。
研究了 22 名 INOCA 女性患者和 12 名年龄和体重指数匹配的女性参考对照者。这些患者有血管扩张剂诱导的缺血但没有阻塞性 CAD 或任何先前的梗死。所有 34 名受试者均接受了包括原生 T1 mapping(MOLLI 5(3)3)在内的应激/休息 MR 检查,检查在 1.5-Tesla 磁共振扫描仪上进行。
与对照组相比,患者的形态/功能相似。正如预期的那样,与对照组相比,患者的 MPRI 显著降低(1.78±0.39 对 2.49±0.41,p<0.0001)。患者的原生 T1 显著升高(1040.1±29.3 ms 对 1003.8±18.5 ms,p<0.001),升高的 T1 与 MPRI 呈显著负相关(r=-0.481,p=0.004),但与舒张应变率降低无关。
与匹配的参考对照者相比,有 INOCA 症状的女性患者的原生 T1 升高,且升高的原生 T1 与 MPRI 受损之间存在显著关联,这在该队列中被认为是缺血严重程度的替代指标。需要在更大的队列中进行进一步的研究来阐明这种负相关关系的机制。