High metabolic level in patients with familial amyotrophic lateral sclerosis

Amyotrophic Lateral Sclerosis

Volumn 10, Issue 2, 2009, Pages 113-117

  Funalot, Benoit ^a,b   Desport, Jean Claude ^a,b   Sturtz, Franck ^a,b   Camu, William ^b   Couratier, Philippe ^a,b  

^a LIMOGES UNIVERSITY HOSPITAL   (France)

^b MONTPELLIER UNIVERSITY HOSPITAL   (France)

Author keywords

Amyotrophic lateral sclerosis; Familial; Genetics; Hypermetabolism; Indirect calorimetry

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE;

ADULT; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; CALORIMETRY; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE CLASSIFICATION; ENERGY EXPENDITURE; FAMILIAL DISEASE; FEMALE; GENE MUTATION; HUMAN; HYPERMETABOLISM; MALE; NUTRITIONAL ASSESSMENT; PRIORITY JOURNAL;

AGED; AMYOTROPHIC LATERAL SCLEROSIS; CALORIMETRY, INDIRECT; ENERGY INTAKE; ENERGY METABOLISM; FAMILY HEALTH; FEMALE; GENES, DOMINANT; HUMANS; MALE; MIDDLE AGED; NUTRITION ASSESSMENT; PEDIGREE; SUPEROXIDE DISMUTASE;

EID: 62549123753     PISSN: 17482968     EISSN: 1471180X     Source Type: Journal    
DOI: 10.1080/17482960802295192     Document Type: Article

References (23)

1. Kunst, CB. (2004) Complex genetics of amyotrophic lateral sclerosis. Am J Hum Genet., 75, pp. 933-947.
2. Gros-Louis, F., Gaspar, C. and Rouleau, G. (2006) Genetics of familial and sporadic amyotrophic lateral sclerosis. Biochim Biophys Acta., 1762, pp. 956-972.
3. Kasarskis, EJ, Berryman, S., Vanderleest, JG, Schneider, AR and McClain, CJ. (1996) Nutritional status of patients with amyotrophic lateral sclerosis: Relation to the proximity of death. Am J Clin Nutr., 63, pp. 130-137.
4. Desport, JC, Preux, PM, Magy, L., Boirie, Y., Vallat, JM Beaufrere, B. et al. (2001) Factors correlated with hypermetabolism in patients with amyotrophic lateral sclerosis. Am J Clin Nutr., 74, pp. 328-334.
5. Desport, JC, Torny, F., Lacoste, M., Preux, PM and Couratier, P. (2005) Hypermetabolism in ALS: Correlations with clinical and paraclinical parameters. Neurodegenerative Dis., 2, pp. 202-207.
6. Dupuis, L., Oudart, H., René, F., Gonzalez de Aguilar, JL and Loeffler, JP. (2004) Evidence for defective energy homeostasis in amyotrophic lateral sclerosis: Benefit of a high-energy diet in a transgenic mouse model. Proc Natl Acad Sci USA., 101, pp. 11159-11164.
7. Jafari-Schluep, HF, Khoris, J., Mayeux-Portas, V., Hand, C., Rouleau, G. and Camu, W. (2004) Groupe Francais d'Etude des Maladies du Motoneurone. Les anomalies du gène superoxyde dismutase 1 dans la sclérose latérale amyotrophique familiale: corrélations phénotype/génotype et implications pratiques. Expérience française et revue de la littérature. Rev Neurol (Paris), 160, pp. 44-50.
8. Brooks, BR, Miller, RG, Swash, M. and Munsat, TL (2000) World Federation of Neurology Research Group on Motor Neuron Diseases. El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord., 1, pp. 293-299.
9. Medical Resarch Council (1943) War memorandum, 2, pp. 11-46. His Majesty's Stationery Office, London
10. The ALS CNTF treatment study (ACTS) phase I-II Study Group (1996) The Amyotrophic Lateral Sclerosis Functional Rating Scale. Assessment of activities of daily living in patients with amyotrophic lateral sclerosis. Arch Neurol, 53, pp. 141-147.
11. Ferrannini, E. (1988) The theoretical bases of indirect calorimetry: A review. Metabolism., 37, pp. 287-301.
12. Harris, JA and Benedict, FG. (1919) A biometric study of basal metabolism in man, Carnegie Institute of Washington, Washington, DC
13. Desport, JC, Preux, PM, Bouteloup-Demange, C., Clavelou, P., Beaufrère, B. Bonnet, C. et al. (2003) Validation of bioelectrical impedance analysis in patients with amyotrophic lateral sclerosis. Am J Clin Nutr., 77, pp. 1179-1185.
14. Dupuis, L., di Scala, F, René, F., de Tapia, M., Oudart, H. Pradat, PF et al. (2003) Up-regulation of mitochondrial uncoupling protein 3 reveals an early muscular metabolic defect in amyotrophic lateral sclerosis. FASEB J., 17, pp. 2091-2093.
15. Criscuolo, F., Mozo, J., Hurtaud, C., Nübel, T. and Bouillaud, F. (2006) UCP2, UCP3, avUCP, what do they do when proton transport is not stimulated? Possible relevance to pyruvate and glutamine metabolism. Biochim Biophys Acta., 1757, pp. 1284-1291.
16. Manfredi, G. and Xu, Z. (2005) Mitochondrial dysfunction and its role in motor neuron degeneration in ALS. Mitochondrion., 5, pp. 77-87.
17. Afifi, AK, Aleu, FP, Goodgold, J. and MacKay, B. (1966) Ultrastructure of atrophic muscle in amyotrophic lateral sclerosis. Neurology., 16, pp. 475-481.
18. Hirano, A., Donnenfeld, H., Sasaki, S. and Nakano, I. (1984) Fine structural observations of neurofilamentous changes in amyotrophic lateral sclerosis. J Neuropathol Exp Neurol., 43, pp. 461-470.
19. Sasaki, S. and Iwata, M. (1996) Impairment of fast axonal transport in the proximal axons of anterior horn neurons in amyotrophic lateral sclerosis. Neurology., 47, pp. 535-540.
20. Wiedemann, FR, Winkler, K., Kuznetsov, AV, Bartels, C., Vielhaber, S. Feistner, H. et al. (1998) Impairment of mitochondrial function in skeletal muscle of patients with amyotrophic lateral sclerosis. J Neurol Sci., 156, pp. 65-72.
21. Vielhaber, S., Kunz, D., Winkler, K., Wiedemann, FR, Kirches, E. and Feistner, H. (2000) Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis. Brain., 123, pp. 1339-1348.
22. Desport, JC, Preux, PM, Truong, TC, Vallat, JM, Sautereau, D. and Couratier, P. (1999) Nutritional status is a prognostic factor for survival in ALS patients. Neurology., 53, pp. 1059-1063.
23. Heffernan, C., Jenkinson, C., Holmes, T., Feder, G., Kupfer, R. Leigh, PN et al. (2004) Nutritional management in MND/ALS patients: An evidence based review. Amyotroph Lateral Scler Other Motor Neuron Disord., 5, pp. 72-83.