Literature DB >> 21778100

New frontiers in neuroimaging applications to inborn errors of metabolism.

Morgan J Prust1, Andrea L Gropman, Natalie Hauser.   

Abstract

Most inborn errors of metabolism (IEMs) are associated with potential for injury to the developing central nervous system resulting in chronic encephalopathy, though the etiopathophysiology of neurological injury have not been fully established in many disorders. Shared mechanisms can be envisioned such as oxidative injury due to over-activation of N-Methyl-d-Aspartate (NMDA) receptors with subsequent glutamatergic damage, but other causes such as energy depletion or inflammation are possible. Neuroimaging has emerged as a powerful clinical and research tool for studying the brain in a noninvasive manner. Several platforms exist to study neural networks underlying cognitive processes, white matter/myelin microstructure, and cerebral metabolism in vivo. The scope and limitations of these methods will be discussed in the context of valuable information they provide in the study and management of selected inborn errors of metabolism. This review is not meant to be an exhaustive coverage of diagnostic findings on MRI in multiple IEMs, but rather to illustrate how neuroimaging modalities beyond T1 and T2 images, can add depth to an understanding of the underlying brain changes evoked by the selected IEMs. Emphasis will be placed on techniques that are available in the clinical setting. Though technically complex, many of these modalities have moved - or soon will - to the clinical arena. Copyright Â
© 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21778100      PMCID: PMC3758691          DOI: 10.1016/j.ymgme.2011.06.020

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  79 in total

Review 1.  An approach to MRI of metabolic disorders in children.

Authors:  A J Barkovich
Journal:  J Neuroradiol       Date:  2007-05       Impact factor: 3.447

2.  Diffuse central neuronal involvement in Fabry disease: a proton MRS imaging study.

Authors:  G Tedeschi; S Bonavita; T K Banerjee; A Virta; R Schiffmann
Journal:  Neurology       Date:  1999-05-12       Impact factor: 9.910

Review 3.  Multi-slice proton MR spectroscopy and diffusion-weighted imaging in methylmalonic acidemia: report of two cases and review of the literature.

Authors:  B C Trinh; E R Melhem; P B Barker
Journal:  AJNR Am J Neuroradiol       Date:  2001-05       Impact factor: 3.825

4.  1H MRS identifies symptomatic and asymptomatic subjects with partial ornithine transcarbamylase deficiency.

Authors:  A L Gropman; S T Fricke; R R Seltzer; A Hailu; A Adeyemo; A Sawyer; J van Meter; W D Gaillard; R McCarter; M Tuchman; M Batshaw
Journal:  Mol Genet Metab       Date:  2008-07-26       Impact factor: 4.797

5.  Phenylketonuria: white-matter changes assessed by 3.0-T magnetic resonance (MR) imaging, MR spectroscopy and MR diffusion.

Authors:  T Scarabino; T Popolizio; M Tosetti; D Montanaro; G M Giannatempo; R Terlizzi; S Pollice; A Maiorana; N Maggialetti; A Carriero; V Leuzzi; U Salvolini
Journal:  Radiol Med       Date:  2009-03-10       Impact factor: 3.469

6.  Type I glutaric aciduria, part 2: a model of acute striatal necrosis.

Authors:  Kevin A Strauss; D Holmes Morton
Journal:  Am J Med Genet C Semin Med Genet       Date:  2003-08-15       Impact factor: 3.908

7.  Neurological deterioration in young adults with phenylketonuria.

Authors:  A J Thompson; I Smith; D Brenton; B D Youl; G Rylance; D C Davidson; B Kendall; A J Lees
Journal:  Lancet       Date:  1990-09-08       Impact factor: 79.321

Review 8.  Pathogenesis of CNS involvement in disorders of amino and organic acid metabolism.

Authors:  S Kölker; S W Sauer; G F Hoffmann; I Müller; M A Morath; J G Okun
Journal:  J Inherit Metab Dis       Date:  2008-04-04       Impact factor: 4.982

9.  Proton magnetic resonance spectroscopy reflects metabolic decompensation in maple syrup urine disease.

Authors:  W Heindel; H Kugel; U Wendel; B Roth; G Benz-Bohm
Journal:  Pediatr Radiol       Date:  1995

10.  The pathogenesis of the white matter abnormalities in phenylketonuria. A multimodal 3.0 tesla MRI and magnetic resonance spectroscopy (1H MRS) study.

Authors:  V Leuzzi; M Tosetti; D Montanaro; C Carducci; C Artiola; C Carducci; I Antonozzi; M Burroni; F Carnevale; F Chiarotti; T Popolizio; G M Giannatempo; V D'Alesio; T Scarabino
Journal:  J Inherit Metab Dis       Date:  2007-01-23       Impact factor: 4.750

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  3 in total

1.  Increased susceptibility of brain acetylcholinesterase activity to methylmalonate in young rats with renal failure.

Authors:  André C Affonso; Daniele G Machado; Fernanda Malgarin; Daiane B Fraga; Fernando Ghedim; Alexandra Zugno; Emílio L Streck; Patrícia F Schuck; Gustavo C Ferreira
Journal:  Metab Brain Dis       Date:  2013-03-09       Impact factor: 3.584

2.  Radio-imaging for detecting congenitally defective metabolic pathways: A review.

Authors:  Sushil Kachewar; Devidas Kulkarni; Smita Sankaye
Journal:  Australas Med J       Date:  2011-09-30

3.  Atypical imaging findings in the setting of methylmalonic acidemia in an infant.

Authors:  Warren Chang; Neilesh Gupta; Dawn Duane; Patrick Barnes; Kristen Yeom
Journal:  Radiol Case Rep       Date:  2015-12-07
  3 in total

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