MR spectroscopy

MR spectrosopy  spectroscopy (MRS) allows tissue to be interrogated for the presence and concentration of various metabolites. Grossman and Yousem said "If you need this to help you, go back to page 1; everything except Canavan has low NAA, high Choline"¹. This is perhaps a little harsh, however it is fair to say that MRS often does not add a great deal to an overall MR study but does increase specificity, and may help in improving our ability to predict histological grade.

Physics

The basic principle that enables MR spectroscopy (MRS) is the fact that the electron cloud around an atom that shields the nucleus from the magnetic field to a greater or lesser degree. This naturally therefore results in slightly resonant frequencies, which in turn return a slightly different signal.

When we see spectra in general radiology practice, this is usually of protons, although phosphorus can also be targeted to examine ATP.

If raw signal was processed then the spectra would be dominated by water, which would make all other spectra invisible. Water suppression is therefore part of any MRS sequence, either via Inversion Recoveryinversion recovery or Chemicalchemical shift selective (CHESS). If water suppression is not successful then a general slope to the base line can be demonstrated, changing the relative heights of peaks.

Magnetic resonance spectroscopy (MRS) is performed with a variety of pulse sequences. The simplest sequence consists of a 90 degree RF pulse without any gradients with reception of the signal by the RF coil immediately after the single RF pulse.

Many sequences used for imaging can be used for spectroscopy also (such as the spin echo sequence). The important difference between an imaging sequence and a spectroscopy sequence is that for spectroscopy, a read out gradient is not used during the time the RF coil is receiving the signal from the person or object being examined. Instead of using the frequency information (provided by the read out or frequency gradient) to provide spatial or positional information, the frequency information is used to identify different chemical compounds. This is possible because the electron cloud surrounding different chemical compounds shields the resonant atoms of spectroscopic interest to varying degrees depending on the specific compound and the specific position in the compound. This electron shielding causes the observed resonance frequency of the atoms to slightly different and therefore identifiable with MRS.

History

Magnetic resonance spectroscopy (MRS)MRS of intact biological tissues was first reported by two groups: Moon and Richards using P-31 MRS to examine intact red blood cells in 1973, and Hoult et al. using P-31 MRS to examine excised leg muscle from the rat in 1974.  

Peaks

• lactate peak: resonates at 1.3 ppm
• lipid peak: resonates at 1.3 ppm
• alanine peak: resonates at 1.48 ppm
• N-acetylaspartate (NAA) peak: resonates at 2.0
• glutamine / glutamate peak: resonate sat 2.2-2.4 ppm 
• GABA peak: resonates at 2.2-2.4 ppm
• citrate peak: resonates 2.6 ppm 
• creatine peak: resonates at 3.0 ppm
• choline peak: resonates at 3.2 ppm
• myo-inositol peak: resonates at 3.5 ppm

Spectra in specific conditions

Glioma

MRS can help increase our ability to predict grade. As the grade increases NAA and creatine decrease and choline, lipids and lactate increase.

Non-glial tumours 

May be difficult but in general non-glial tumours will not have little, if any, NAA. In the setting of gliomas, choline will be elevated beyond the margins contrast enhancement in keeping with cellular infiltration.

Radiation effects 

Distinguishing radiation change and tumour recurrence can be problematic. In recurrent tumour choline will be elevated, whereas in radiation change, NAA, choline and creatine will all be low.

Ischaemia and infarction 

Lactate will increase as the brain switches to anaerobic metabolism. When infarction takes place then lipids are released and peaks appear.

Infection 

As in all processes which destroy normal brain tissue, NAA is absent. Within bacterial abscess cavities, lactate, alanine, cytosolic acid and acetate are elevated / present/present.

Of note choline is low or absent in toxoplasmosis, whereas it is elevated in lymphoma, helping to distinguish the two.

White matter diseases

• progressive multifocal leukoencephalopathy (PML) may demonstrate elevated myo-inositol.
• Canavan disease characteristically demonstrates elevated NAA.

Hepatic encephalopathy 

Markedly reduced myo-inositol, and to a lesser degree choline. Glutamine is increased.

Mitochondrial disorders

• Leigh syndrome: elevated choline, reduced NAA and occasionally elevated lactate.

Mnemonic

My ChoCrNaaLa (think of a new chocolate energy bar or something)

• My: Myoinisitol 3.3
• Cho: Choline 3.2
• Cr: Creatine 3.0
• Naa: Naa 2.0
• L: Lactate 1.3