Bartha Robert
Centre for Functional and Metabolic Mapping, Robarts Research Institute, 100 Perth Drive, London, Ontario, Canada.
NMR Biomed. 2007 Aug;20(5):512-21. doi: 10.1002/nbm.1122.
The accuracy and precision of measurements of metabolite concentrations from short echo-time spectra has previously been characterized at l.5 T as a function of signal-to-noise ratio (SNR) and peak linewidth. The purpose of this study was to characterize the systematic error in quantification of metabolite concentrations associated with linewidth and SNR for the major metabolites of interest in the short echo-time 1H-MR spectrum at 4 T. Simulated 4 T LASER localized spectra (TE = 46 ms) were generated with full width at half maximum (FWHM) over the range 4-14 Hz, and SNR over the range 5-500 by adding 100 Gaussian-distributed noise realizations at each combination of SNR and linewidth. Linewidth and SNR were treated as independent parameters, and therefore an increase in linewidth at a constant SNR resulted in increased metabolite areas. All spectra were fitted in the time domain using identical prior-knowledge and relative parameter starting values. Six metabolites (N-acetylaspartate, glutamate, creatine, myo-inositol, glycerophosphocholine, phosphocholine) were quantified with >90% accuracy and <10% standard deviation at SNR = 10 for linewidths ranging from 8 to 14 Hz FWHM. These simulations did not consider additional sources of variation, including eddy current artifacts, incomplete macromolecule baseline removal, and incomplete water suppression. Regardless, the results show that metabolite quantification from 4 T short echo-time 1H-MRS is sensitive to SNR and linewidth.
短回波时间谱代谢物浓度测量的准确性和精密度此前已在1.5 T条件下,作为信噪比(SNR)和峰线宽的函数进行了表征。本研究的目的是表征在4 T条件下短回波时间1H-MR谱中,与感兴趣的主要代谢物的线宽和SNR相关的代谢物浓度定量中的系统误差。通过在SNR和线宽的每种组合下添加100个高斯分布的噪声实现,生成了模拟的4 T激光定位谱(TE = 46 ms),半高宽(FWHM)范围为4 - 14 Hz,SNR范围为5 - 500。线宽和SNR被视为独立参数,因此在恒定SNR下线宽增加会导致代谢物面积增加。所有谱在时域中使用相同的先验知识和相对参数起始值进行拟合。对于线宽范围为8至14 Hz FWHM且SNR = 10的情况,六种代谢物(N - 乙酰天门冬氨酸、谷氨酸、肌酸、肌醇、甘油磷酸胆碱、磷酸胆碱)的定量准确率>90%,标准差<10%。这些模拟未考虑其他变化来源,包括涡流伪影、大分子基线去除不完全以及水抑制不完全。尽管如此,结果表明从4 T短回波时间1H-MRS进行代谢物定量对SNR和线宽敏感。