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Measuring inorganic phosphate and intracellular pH in the healthy and hypertrophic cardiomyopathy hearts by in vivo 7T 31P-cardiovascular magnetic resonance spectroscopy

机译:通过体内7T 31P-心血管磁共振波谱测量健康和肥厚型心肌病心脏中的无机磷酸盐和细胞内pH

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摘要

BackgroundCardiovascular phosphorus MR spectroscopy (31P-CMRS) is a powerful tool for probing energetics in the human heart, through quantification of phosphocreatine (PCr) to adenosine triphosphate (ATP) ratio. In principle, 31P-CMRS can also measure cardiac intracellular pH (pHi) and the free energy of ATP hydrolysis (ΔGATP). However, these require determination of the inorganic phosphate (Pi) signal frequency and amplitude that are currently not robustly accessible because blood signals often obscure the Pi resonance.Typical cardiac 31P-CMRS protocols use low (e.g. 30°) flip-angles and short repetition time (TR) to maximise signal-to-noise ratio (SNR) within hardware limits. Unfortunately, this causes saturation of Pi with negligible saturation of the flowing blood pool. We aimed to show that an adiabatic 90° excitation, long-TR, 7T 31P-CMRS protocol will reverse this balance, allowing robust cardiac pHi measurements in healthy subjects and patients with hypertrophic cardiomyopathy (HCM).
机译:背景心血管磷MR光谱法( 31 P-CMRS)是通过定量磷酸肌酸(PCr)与三磷酸腺苷(ATP)之比来探测人心中能量的有力工具。原则上, 31 P-CMRS还可以测量心脏的细胞内pH(pHi)和ATP水解的自由能(ΔGATP)。但是,这些方法需要确定当前无法可靠获取的无机磷酸盐(Pi)信号的频率和幅度,因为血液信号通常会掩盖Pi的共振。典型的心脏 31 P-CMRS协议使用的信号低(例如30 °)翻转角度和较短的重复时间(TR),可在硬件限制内最大化信噪比(SNR)。不幸的是,这导致Pi的饱和度和流动血池的饱和度可以忽略不计。我们旨在证明绝热的90°激发,长TR,7T 31 P-CMRS方案将逆转这种平衡,从而在健康受试者和肥厚型心肌病(HCM)患者中进行可靠的心脏pHi测量。

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