Craven Alexander R, Bell Tiffany K, Ersland Lars, Harris Ashley D, Hugdahl Kenneth, Oeltzschner Georg
Department of Biological and Medical Psychology, University of Bergen, Bergen, Norway.
Department of Clinical Engineering, Haukeland University Hospital, Bergen, Norway.
bioRxiv. 2024 Feb 28:2024.02.27.582249. doi: 10.1101/2024.02.27.582249.
J-difference-edited MRS is widely used to study GABA in the human brain. Editing for low-concentration target molecules (such as GABA) typically exhibits lower signal-to-noise ratio (SNR) than conventional non-edited MRS, varying with acquisition region, volume and duration. Moreover, spectral lineshape may be influenced by age-, pathology-, or brain-region-specific effects of metabolite T, or by task-related blood-oxygen level dependent (BOLD) changes in functional MRS contexts. Differences in both SNR and lineshape may have systematic effects on concentration estimates derived from spectral modelling. The present study characterises the impact of lineshape and SNR on GABA+ estimates from different modelling algorithms: FSL-MRS, Gannet, LCModel, Osprey, spant and Tarquin. Publicly available multi-site GABA-edited data (222 healthy subjects from 20 sites; conventional MEGA-PRESS editing; TE = 68 ms) were pre-processed with a standardised pipeline, then filtered to apply controlled levels of Lorentzian and Gaussian linebroadening and SNR reduction. Increased Lorentzian linewidth was associated with a 2-5% decrease in GABA+ estimates per Hz, observed consistently (albeit to varying degrees) across datasets and most algorithms. Weaker, often opposing effects were observed for Gaussian linebroadening. Variations are likely caused by differing baseline parametrization and lineshape constraints between models. Effects of linewidth on other metabolites (e.g., Glx and tCr) varied, suggesting that a linewidth confound may persist after scaling to an internal reference. These findings indicate a potentially significant confound for studies where linewidth may differ systematically between groups or experimental conditions, e.g. due to T differences between brain regions, age, or pathology, or varying T* due to BOLD-related changes. We conclude that linewidth effects need to be rigorously considered during experimental design and data processing, for example by incorporating linewidth into statistical analysis of modelling outcomes or development of appropriate lineshape matching algorithms.
J 差异编辑磁共振波谱(MRS)被广泛用于研究人类大脑中的γ-氨基丁酸(GABA)。针对低浓度目标分子(如GABA)进行编辑时,通常比传统的非编辑MRS表现出更低的信噪比(SNR),且会随采集区域、体积和持续时间而变化。此外,谱线形状可能会受到代谢物T的年龄、病理或脑区特异性影响,或在功能MRS环境中受到与任务相关的血氧水平依赖(BOLD)变化的影响。SNR和谱线形状的差异可能会对从光谱建模得出的浓度估计产生系统性影响。本研究描述了谱线形状和SNR对来自不同建模算法(FSL-MRS、Gannet、LCModel、Osprey、spant和Tarquin)的GABA+估计值的影响。公开可用的多站点GABA编辑数据(来自20个站点的222名健康受试者;传统的MEGA-PRESS编辑;回波时间(TE)=68毫秒)使用标准化流程进行预处理,然后进行滤波,以应用受控水平的洛伦兹和高斯线展宽以及SNR降低。洛伦兹线宽增加与每个赫兹的GABA+估计值降低2 - 5%相关,在各个数据集和大多数算法中均一致观察到(尽管程度不同)。对于高斯线展宽,观察到的影响较弱,且往往相反。这些变化可能是由模型之间不同的基线参数化和谱线形状约束导致的。线宽对其他代谢物(如谷氨酰胺-谷氨酸复合物(Glx)和磷酸肌酸(tCr))的影响各不相同,这表明在按内部参考进行缩放后,线宽混淆可能仍然存在。这些发现表明,对于线宽可能在组间或实验条件下存在系统性差异的研究,例如由于脑区之间的T差异、年龄或病理,或由于与BOLD相关的变化导致的T*变化,可能存在潜在的重大混淆因素。我们得出结论,在实验设计和数据处理过程中需要严格考虑线宽效应,例如通过将线宽纳入建模结果的统计分析或开发适当的谱线形状匹配算法。