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Erythropoietin and amyotrophic lateral sclerosis: Plasma level determination.

Authors :
Carilho, Rita
de Carvalho, Mamede
Kuehl, Ute
Pinto, Susana
Pinto, Anabela
Kromminga, Arno
Costa, Júlia
Source :
Amyotrophic Lateral Sclerosis. Nov2011, Vol. 12 Issue 6, p439-443. 5p. 1 Chart, 1 Graph.
Publication Year :
2011

Abstract

In amyotrophic lateral sclerosis (ALS), respiratory muscle weakness causes ventilatory insufficiency and tissue hypoxia, which induces a number of metabolic pathways, and in particular increases erythropoietin (EPO) synthesis. EPO is a glycoprotein with neuroprotective properties that stimulates erythropoiesis. Here, EPO plasma level in a large population of ALS patients, with and without respiratory failure, was measured. Plasma EPO level of patients with ALS ( n == 98), controls with other neuromuscular diseases ( n == 58) and healthy controls ( n == 20) has been quantified by ELISA. No significant difference was found between ALS patients and the two control groups. EPO level was not different between bulbar- and spinal-onset patients and was not correlated with disease duration or functional impairment. However, in the ALS group EPO level was higher in females ( p == 0.0006) and correlated positively with age ( p == 0.006). The subgroup of ALS patients with respiratory failure had higher plasma levels of EPO compared with ALS patients with preserved respiratory function ( p == 0.016), but short-term non-invasive ventilation did not change EPO level. In conclusion, EPO levels were found to be significantly higher in ALS patients with respiratory impairment representing preservation of this homeostatic mechanism. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17482968
Volume :
12
Issue :
6
Database :
Academic Search Index
Journal :
Amyotrophic Lateral Sclerosis
Publication Type :
Academic Journal
Accession number :
66792331
Full Text :
https://doi.org/10.3109/17482968.2011.584881