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October 04, 2011; 77 (14) Articles

Presymptomatic spinal cord neurometabolic findings in SOD1-positive people at risk for familial ALS

J.D. Carew, G. Nair, P.M. Andersen, J. Wuu, S. Gronka, X. Hu, M. Benatar
First published September 21, 2011, DOI: https://doi.org/10.1212/WNL.0b013e318231526a
J.D. Carew
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Citation
Presymptomatic spinal cord neurometabolic findings in SOD1-positive people at risk for familial ALS
J.D. Carew, G. Nair, P.M. Andersen, J. Wuu, S. Gronka, X. Hu, M. Benatar
Neurology Oct 2011, 77 (14) 1370-1375; DOI: 10.1212/WNL.0b013e318231526a

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Abstract

Objective: It has been speculated that amyotrophic lateral sclerosis (ALS) is characterized by a premanifest period during which neurodegeneration precedes the appearance of clinical manifestations. Magnetic resonance spectroscopy (MRS) was used to measure ratios of neurometabolites in the cervical spine of asymptomatic individuals with a mutation in the SOD1 gene (SOD1+) and compare their neurometabolic ratios to patients with ALS and healthy controls.

Methods: A cross-sectional study of 1H-MRS of the cervical spine was performed on 24 presymptomatic SOD1+ volunteers, 29 healthy controls, and 23 patients with ALS. All presymptomatic subjects had no symptoms of disease, normal forced vital capacity, and normal electromyographic examination. Relative concentrations of choline (Cho), creatine (Cr), myo-inositol (Myo), and N-acetylaspartate (NAA) were determined.

Results: NAA/Cr and NAA/Myo ratios are reduced in both SOD1+ subjects (39.7%, p = 0.001 and 18.0%, p = 0.02) and patients with ALS (41.2%, p < 0.001 and 24.0%, p = 0.01) compared to controls. Myo/Cr is reduced (10.3%, p = 0.02) in SOD1+ subjects compared to controls, but no difference was found between patients with ALS and controls. By contrast, NAA/Cho is reduced in patients with ALS (24.0%, p = 0.002), but not in presymptomatic SOD1+ subjects compared to controls.

Conclusions: Changes in neurometabolite ratios in the cervical spinal cord are evident in presymptomatic SOD1+ individuals in advance of symptoms and clinical or electromyographic signs of disease. These changes reflect a reduction in NAA/Cr and NAA/Myo. Neurometabolic changes in this population resemble changes observed in patients with clinically apparent ALS. This suggests that neurometabolic changes occur early in the course of the disease process.

GLOSSARY

%ALS=
amyotrophic lateral sclerosis;
ALSFRS-R=
revised ALS functional rating scale;
Cho=
choline;
Cr=
creatine;
FVC=
forced vital capacity;
MRS=
magnetic resonance spectroscopy;
Myo=
myo-inositol;
NAA=
N-acetylaspartate;
Pre-fALS=
Pre-familial ALS;
SOD1=
superoxide dismutase

Footnotes

  • Study funding: Supported by the Muscular Dystrophy Association (grants 4365 and 172123), the ALS Association (grants 1491 and 1712), the Swedish Brain Research Foundation, the Hållsten's Brain Research Foundation, the Swedish Science Council, and the Swedish Association for the Neurologically Disabled.

  • Received March 5, 2011.
  • Accepted June 14, 2011.
  • Copyright © 2011 by AAN Enterprises, Inc.
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