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Table of Contents
CASE REPORT
Year : 2014  |  Volume : 17  |  Issue : 1  |  Page : 123-124
 

Glutamate-based magnetic resonance spectroscopy in neuroleptic malignant syndrome


Department of Medicine, Nil Ratan Sircar Medical College, Kolkata, West Bengal, India

Date of Submission18-Feb-2013
Date of Decision10-Mar-2013
Date of Acceptance27-Mar-2013
Date of Web Publication12-Mar-2014

Correspondence Address:
Atri Chatterjee
Rajdeep Apartments, 18/1E, D. P. P. Road, Kolkata - 700 047, West Bengal
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0972-2327.128579

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   Abstract 

Glutamate neurotoxicity is implicated in a number of neurological diseases, including Neuroleptic Malignant syndrome. Therefore, functional magnetic resonance imaging can help in diagnosis and monitoring such conditions. However, reports of this application are scarce in the literature. In this manuscript, glutamate based imaging of the basal ganglia showed increased levels of the neurotransmitter bilaterally. In addition, a radon transform of the functional image was performed to look for any asymmetry in cerebral activation. Although no asymmetry was detected in this case, this novel analysis can be applied in physiological and pathological scenarios to visualize contribution of different brain structures.


Keywords: Glutamate, magnetic resonance spectroscopy, neuroleptic malignant syndrome


How to cite this article:
Chatterjee A. Glutamate-based magnetic resonance spectroscopy in neuroleptic malignant syndrome. Ann Indian Acad Neurol 2014;17:123-4

How to cite this URL:
Chatterjee A. Glutamate-based magnetic resonance spectroscopy in neuroleptic malignant syndrome. Ann Indian Acad Neurol [serial online] 2014 [cited 2019 Oct 14];17:123-4. Available from: http://www.annalsofian.org/text.asp?2014/17/1/123/128579



   Introduction Top


Glutamate is one of the most ubiquitous neurotransmitters in the brain and it has been clearly implicated in Neuroleptic Malignant syndrome (NMS). [1] A rapid rise in intracerebral levels of glutamate in NMS results in features of hyperthermia, severe hypertonia, and tremors. Although, intracerebral concentration of glutamate is being investigated with proton-based magnetic resonance spectroscopy (HMRS) in cognitive decline, [2] Alzheimer's disease, [3] and autistic spectrum disorders, [4] to the best of our knowledge, there are no reports of similar efforts in NMS.

It can be rationally hypothesized that HMRS would reveal an increased concentration of glutamate in the basal ganglia in a patient of NMS. Here, we report the case of a patient of NMS, in whom HMRS proved this hypothesis. This report is a proof-of-concept investigation of pathogenesis of NMS using glutamate-based functional magnetic resonance imaging.


   Case Report Top


A 55-year-old man was admitted with a history of acute-onset high-grade fever, severe generalized tremors and an altered level of consciousness for the last 2 days. On admission, the patient had a pulse rate of 116 beats/min, blood pressure 140/80 mm Hg, temperature 103.4°F respiratory rate of 32/min, and oxygen saturation of 95% although inhaling room air. The patient was being treated for bipolar disorder for the last year. He was on risperidone (30 mg/day), clonazepam (0.5 mg/day) and olanzapine (7.5 mg/day). Neurological examination revealed Glasgow coma score 12/15, disorientation, lead-pipe rigidity, brisk jerks, and coarse tremors. Examination of the other systems was normal.

The patient's treatment was initiated with cooling blankets, intravenous infusion of acetaminophen, and lorazepam. Routine investigations of blood revealed elevated erythrocyte sedimentation rate (100 mm 1 st h), raised serum creatinine (1.5 mg/dl), and a very high creatine phosphokinase level (3522 Units/dl). His electrocardiogram and chest X-ray were normal. Bacterial and fungal cultures of blood were negative.

Magnetic resonance imaging of the brain was obtained with a 1.5T scanner (General Electric, USA). T2 sequences showed mild hyperintensities in basal ganglia bilaterally [Figure 1]a. Simultaneously, magnetic resonance spectroscopy was carried out with single [inner green box in [Figure 1]b] and multi-voxel regions [outer white box in [Figure 1]b] of interest. The regions of interest (ROI) were specified manually. [Figure 1]c shows a similar image at a different level. [Figure 1]d shows the presence of increased levels of glutamate in the single-voxel ROI (625 mm 2 ) (arrowhead) with relaxation time (TR) 4200 and excitation time TE 103.8. A heat map of the glutamate concentration was generated [Figure 1]b and c, which showed increased levels of glutamate in both the basal ganglia.
Figure 1: HMRS study of brain. (a) T2 sequence showed hyperintensities in both basal ganglia. (b, c) Showed concentrations of glutamate by multivoxel imaging (TR 4200 TE 103.8). The inner green square identified a single voxel. (d) Magnetic resonance spectroscopy curve showed elevated glutamate levels (arrowhead)

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The contribution of each hemisphere to the clinical scenario was analysed by parallel-beam radon transformation analysis of the heat map generated by magnetic resonance. This was carried out using the image analysis toolbox of MATLAB (MATLAB 2008a, MA, USA). The result showed marked symmetry [Figure 2], confirming equal participation of both hemispheres.
Figure 2: Radon transformation of the glutamate concentrations in the multi - voxel regions of interest in Figure 1. This revealed a bilaterally symmetric involvement of basal ganglia

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   Discussion Top


The potential of HMRS to assess concentration of neurotransmitters in specific ROIs have opened up avenues of patient monitoring in dementia and other psychiatric diseases. NMS can be considered as a scenario where well-known pathways of glutamate excitotoxicity are greatly exaggerated. However, there is little objective evidence of this knowledge in the literature. Although the incidence of NMS is lower than conditions like Alzheimer's disease, this was the rationale for selection of the patient.

Multi-voxel imaging has been shown to correlate with clinical severity of autism. [5] Therefore, a single voxel HMRS was carried out initially to prove the excess of glutamate, followed by a multi-voxel imaging to map the concentrations of glutamate. In our patient, the severity of the clinical features and laboratory values correlated with the heat map. However, larger studies that include suitable controls are necessary to comment on its usefulness as a clinical application.

Language function in humans are linked with inter-hemispheric asymmetry and is possibly a result of functional specialization. [6] In schizophrenia, there is decreased activation of cortico-cerebellar-thalamic circuit in the right hemisphere. [7] Although bilateral affection is biologically plausible in NMS, no evidence has emerged until date. I performed radon transformation of the image obtained by HMRS to clearly visualize the level of symmetry of glutamate levels in the basal ganglia. Radon transformation has been utilized to detect red blood cells in microscopic images. [8] Our report suggests that, it can have applications in detection of cerebral in homogeneities.

 
   References Top

1.Kornhuber J, Weller M, Riederer P. Glutamate receptor antagonists for neuroleptic malignant syndrome and akinetic hyperthermic parkinsonian crisis. J Neural Transm Park Dis Dement Sect 1993;6:63-72.  Back to cited text no. 1
    
2.Zahr NM, Mayer D, Pfefferbaum A, Sullivan EV. Low striatal glutamate levels underlie cognitive decline in the elderly: Evidence from in vivo molecular spectroscopy. Cereb Corte×2008;18:2241-50.  Back to cited text no. 2
    
3.Fayed N, Modrego PJ, Rojas-Salinas G, Aguilar K. Brain glutamate levels are decreased in Alzheimer′s disease: A magnetic resonance spectroscopy study. Am J Alzheimers Dis Other Demen 2011;26:450-6.  Back to cited text no. 3
    
4.Joshi G, Biederman J, Wozniak J, Goldin RL, Crowley D, Furtak S, et al. Magnetic resonance spectroscopy study of the glutamatergic system in adolescent males with high-functioning autistic disorder: A pilot study at 4T. Eur Arch Psychiatry Clin Neurosci 2013;263:379-84.  Back to cited text no. 4
    
5.Coutanche MN, Thompson-Schill SL, Schultz RT. Multi-voxel pattern analysis of fMRI data predicts clinical symptom severity. Neuroimage 2011;57:113-23.  Back to cited text no. 5
    
6.Chance SA, Sawyer EK, Clover LM, Wicinski B, Hof PR, Crow TJ. Hemispheric asymmetry in the fusiform gyrus distinguishes Homo sapiens from chimpanzees. Brain Struct Funct2013;218:1391-405.  Back to cited text no. 6
    
7.Ortuño F, Guillén-Grima F, López-García P, Gómez J, Pla J. Functional neural networks of time perception: Challenge and opportunity for schizophrenia research. Schizophr Res 2011;125:129-35.  Back to cited text no. 7
    
8.Ljosa V, Carpenter AE. Introduction to the quantitative analysis of two-dimensional fluorescence microscopy images for cell-based screening. PLoS Comput Biol 2009;5:e1000603.  Back to cited text no. 8
    


    Figures

  [Figure 1], [Figure 2]


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[Pubmed] | [DOI]



 

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