Modeling brain compartmental lactate response to metabolic challenge: a feasibility study

被引:10
作者
Friedman, SD
Dager, SR
Richards, TL
Petropoulos, H
Posse, S
机构
[1] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98105 USA
[2] Univ Washington, Dept Bioengn, Seattle, WA 98105 USA
[3] Univ Washington, Dept Radiol, Seattle, WA 98105 USA
[4] Univ Washington, Sch Med, Diagnost Imaging Sci Ctr, Seattle, WA 98105 USA
[5] Univ New Mexico, Clin & Magnet Resonance Res Ctr, Albuquerque, NM USA
[6] Inst Med, Ctr MR Res, Julich, Germany
关键词
magnetic resonance spectroscopy; brain metabolism; water; quantification; modeling;
D O I
10.1016/S0925-4927(99)00053-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Magnetic resonance spectroscopy has been used to characterize abnormal brain lactate response in panic disorder (PD) subjects following lactate infusion. The present study integrated water quantification and tissue segmentation to evaluate compartmental lactate response within brain and cerebrospinal fluid (CSF). As there is evidence of brain parenchymal pH changes during lactate infusion, water scans were collected at baseline and post-infusion to address brain water stability. Water levels remained essentially stable across the protocol suggesting internal water provides an improved reference signal for measuring dynamic changes in response to metabolic challenge paradigms such as lactate infusion. To model brain lactate changes by compartments, we took the null hypothesis that lactate rises occur only in tissue. The approach referenced lactate amplitude (potentially from both compartments) to 'voxel' water (water scan corrected for differential T-2 between CSF brain at long-echo times - synonymous to a short-echo water scan). If the magnitude of lactate rise in CSF was equal to or greater than brain, voxels with substantial CSF fractions should demonstrate an equivalent or elevated response to voxels comprised only of tissue. The magnitude of lactate increases paralleled voxel tissue fraction suggesting the abnormal lactate rise observed in PD is tissue-based. The feasibility of lactate quantification and compartmental modeling are discussed. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:55 / 66
页数:12
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