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Research paper
Quantitative MR spectroscopic imaging in metachromatic leukodystrophy: value for prognosis and treatment
  1. Diane F van Rappard1,2,
  2. Antoine Klauser3,
  3. Marjan E Steenweg1,2,
  4. Jaap Jan Boelens4,
  5. Marianna Bugiani1,2,5,
  6. Marjo S van der Knaap1,2,
  7. Nicole I Wolf1,2,
  8. Petra J W Pouwels2,6
  1. 1Department of Pediatric Neurology, Center for Childhood White Matter Disorders, VU University Medical Center, Amsterdam, The Netherlands
  2. 2Amsterdam Neuroscience, VU University Medical Center Amsterdam, Academic Medical Center, Vrije Universiteit Amsterdam and University of Amsterdam, Amsterdam, The Netherlands
  3. 3Department of Radiology and Medical Informatics, University of Geneva, Geneva, Switzerland
  4. 4Department of Pediatrics, Blood and Marrow Transplantation Program, University Medical Center Utrecht, Utrecht, The Netherlands
  5. 5Department of Pathology, Center for Childhood White Matter Disorders, VU University Medical Center, Amsterdam, The Netherlands
  6. 6Department of Radiology and Nuclear Medicine, VU University Medical Center, Amsterdam, The Netherlands
  1. Correspondence to Dr. Petra J W Pouwels, VU University Medical Center, Department of Radiology and Nuclear MedicineDe Boelelaan 1117, 1081 HV Amsterdam, The Netherlands; pjw.pouwels{at}vumc.nl

Abstract

Objective To determine whether proton magnetic resonance spectroscopic imaging is useful in predicting clinical course of patients with metachromatic leukodystrophy (MLD), an inherited white matter disorder treatable with haematopoietic cell transplantation (HCT).

Methods 21 patients with juvenile or adult MLD (12 HCT-treated) were compared with 16 controls in the same age range. Clinical outcome was determined as good, moderate or poor. Metabolites were quantified in white matter, and significance of metabolite concentrations at baseline for outcome prediction was assessed using logistic regression analysis. Evolution of metabolic changes was assessed for patients with follow-up examinations.

Results In this retrospective study, 16 patients with baseline scans were included, 5 with good, 3 with moderate and 8 with poor outcome, and 16 controls. We observed significant group differences for all metabolite concentrations in white matter (p<0.001). Compared with controls, patients had decreased N-acetylaspartate and glutamate, and increased myo-inositol and lactate, most pronounced in patients with poor outcome (post hoc, all p<0.05). Logistic regression showed complete separation of data. Creatine could distinguish poor from moderate and good outcome, the sum of glutamate and glutamine could distinguish good from moderate and poor outcome, and N-acetylaspartate could distinguish all outcome groups. For 13 patients (8 with baseline scans), one or more follow-up examinations were evaluated, revealing stabilisation or even partial normalisation of metabolites in patients with moderate and good outcome, clearly visible in the ratio of choline/N-acetylaspartate.

Conclusion In MLD, quantitative spectroscopic imaging at baseline is predictive for outcome and aids in determining eligibility for HCT.

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Footnotes

  • Contributors PJWP and NIW had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. All authors substantially contributed to conception or design of the work, or the acquisition, analysis or interpretation of data. DFvR, PJWP and NIW wrote the manuscript. All authors critically revised the manuscript for intellectual content. All authors did a final review and approved the manuscript. All authors agreed to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

  • Funding This study was financed by Metakids, a charity sponsoring research on metabolic disorders (project 2015-059).

  • Competing interests None declared.

  • Patient consent Parental/guardian consent obtained.

  • Ethics approval The Institutional Review Board of the VU University Medical Center approved the study.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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