Literature DB >> 1834009

Phosphorus magnetic resonance spectroscopy (31P MRS) in neuromuscular disorders.

Z Argov1, W J Bank.   

Abstract

Phosphorus magnetic resonance spectroscopy monitors muscle energy metabolism by recording the ratio of phosphocreatine to inorganic phosphate at rest, during exercise, and during recovery from exercise. In mitochondrial diseases, abnormalities may appear during some or all these phases. Low phosphocreatine-inorganic phosphate ratios at rest are not disease-specific, but can be increased by drug therapy in several myopathies. Phosphorus magnetic resonance spectroscopy can also record intracellular pH and thus identify disorders of glycogen metabolism in which the production of lactic acid is blocked during ischemic exercise. The measurements of accumulated sugar phosphate intermediates further delineate glycolytic muscle defects. Myophosphorylase deficiency responds to intravenous glucose administration with improved exercise bioenergetics, but no such response is seen in phosphofructokinase deficiency. The muscular dystrophies show no specific bioenergetic abnormality; however, elevation of phospholipids metabolites and phosphodiesters was detected in some cases. While phosphorus magnetic resonance spectroscopy remains primarily a research tool in metabolic myopathies, it will be clinically useful in identifying new therapies and monitoring their effects in a variety of neuromuscular disorders.

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Year:  1991        PMID: 1834009     DOI: 10.1002/ana.410300116

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  16 in total

Review 1.  Mitochondria.

Authors:  P F Chinnery; E A Schon
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-09       Impact factor: 10.154

Review 2.  Metabolic Myoglobinuria.

Authors:  Emanuele Barca; Valentina Emmanuele; Salvatore Billi DiMauro
Journal:  Curr Neurol Neurosci Rep       Date:  2015-10       Impact factor: 5.081

3.  Delayed calf muscle phosphocreatine recovery after exercise identifies peripheral arterial disease.

Authors:  David C Isbell; Stuart S Berr; Alicia Y Toledano; Frederick H Epstein; Craig H Meyer; Walter J Rogers; Nancy L Harthun; Klaus D Hagspiel; Arthur Weltman; Christopher M Kramer
Journal:  J Am Coll Cardiol       Date:  2006-05-15       Impact factor: 24.094

4.  31P-MRS of skeletal muscle is not a sensitive diagnostic test for mitochondrial myopathy.

Authors:  Tina Dysgaard Jeppesen; Bjørn Quistorff; Flemming Wibrand; John Vissing
Journal:  J Neurol       Date:  2007-02-04       Impact factor: 4.849

Review 5.  The role of magnetic resonance spectroscopy in the investigation of lactic acidosis and inborn errors of energy metabolism.

Authors:  D G Gadian; J V Leonard
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

6.  Influence of cytosolic pH on in vivo assessment of human muscle mitochondrial respiration by phosphorus magnetic resonance spectroscopy.

Authors:  R Lodi; G J Kemp; S Iotti; G K Radda; B Barbiroli
Journal:  MAGMA       Date:  1997-06       Impact factor: 2.310

7.  Non-invasive quantitative 31P MRS assay of mitochondrial function in skeletal muscle in situ.

Authors:  J A Jeneson; R W Wiseman; M J Kushmerick
Journal:  Mol Cell Biochem       Date:  1997-09       Impact factor: 3.396

8.  In vivo assessment of human skeletal muscle mitochondria respiration in health and disease.

Authors:  B Barbiroli; S Iotti; R Lodi
Journal:  Mol Cell Biochem       Date:  1997-09       Impact factor: 3.396

9.  Deficit of in vivo mitochondrial ATP production in patients with Friedreich ataxia.

Authors:  R Lodi; J M Cooper; J L Bradley; D Manners; P Styles; D J Taylor; A H Schapira
Journal:  Proc Natl Acad Sci U S A       Date:  1999-09-28       Impact factor: 11.205

10.  Peripheral arterial disease assessment: wall, perfusion, and spectroscopy.

Authors:  Christopher M Kramer
Journal:  Top Magn Reson Imaging       Date:  2007-10
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