Abstract

Lactate is a product of glucose metabolism. In tumour tissues, which exhibit enhanced glycolytic metabolism, lactate signals may be elevated, making lactate a potential useful tumour biomarker. Methods of lactate quantitation are complicated because of overlap between the lactate methyl doublet CH3 resonance and a lipid resonance at 1.3 ppm. This study presents the use of a selective homonuclear multiple quantum coherence transfer sequence (SelMQC-CSI), at 1.5 T, to better quantify lactate in the presence of lipids. Work performed on phantoms showed good lactate detection (49%) and lipid suppression (98%) efficiencies. To evaluate the method in the brain, the sequence was tested on a group of 23 patients with treated brain tumours, either glioma (N = 20) or secondary metastases in the brain (N = 3). Here it was proved to be of use in determining lactate concentrations in vivo. Lactate was clearly seen in SelMQC spectra of glioma, even in the presence of lipids, with high grade glioma (7.3 ± 1.9 mM, mean ± standard deviation) having higher concentrations than low grade glioma (1.9 ± 1.5 mM, p = 0.048). Lactate was not seen in secondary metastases in the brain. SelMQC-CSI is shown to be a useful technique for measuring lactate in tumours whose signals are otherwise contaminated by lipid. © 2015 The Authors NMR in Biomedicine Published by John Wiley & Sons Ltd.

Highlights

  • While there is a small bias, since single voxel spectroscopy (SVS) measurements take significantly less time, in comparison with chemical shift imaging (CSI), this justified the use of SVS to measure the water reference signal in further experiments

  • This study has successfully shown that selective multiple quantum coherence (SelMQC)-CSI provides better quantification of lactate in regions of elevated lipid signal

  • A previous report stated that lactate is present in higher concentrations in newly diagnosed high grade glioma compared with low grade [5], in keeping with what we present here in a group of treated gliomas

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Summary

Introduction

Lactate has been shown to be elevated in rodent glioma models [7]. Measuring the concentration of lactate in animal models has been used to monitor response to both chemotherapy and radiotherapy [9]. 18 F-fluorodeoxyglucose (18FDG) positron emission tomography is used to detect tumours and monitor their response to treatment by imaging their increased glucose uptake compared with normal tissue. In this situation, quantifying lactate potentially offers complementary information on (steadystate) lactate concentrations, in organs such as the brain where the high glucose consumption and 18FDG uptake of normal tissue obscures their differentiation

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