Skip to main content

Advertisement

Log in

Cerebrospinal Fluid Neurone-Specific Enolase in Mitochondrial Encephalomyopathies

  • Published:
Metabolic Brain Disease Aims and scope Submit manuscript

Abstract

Whether cerebrospinal fluid (CSF) neurone-specific enolase (NSE) contributes to the diagnosis of mitochondrial encephalomyopathies (MEMs) is unknown. Aim of the present study was thus to assess the validity of CSF-NSE in the diagnosis of MEM. CSF-NSE was determined in 24 controls, aged 28–88 years; and 23 MEM patients, aged 47–81 years. In controls, CSF-NSE was independent of sex (p = 0.849) and age (p = 0.346). Twenty-one MEM patients had clinical CNS involvement and two CNS abnormalities on imaging investigations exclusively. CSF cells were increased in 7, CSF protein in 17, CSF glucose in 1, and CSF lactate in 2 MEM patients. The upper reference limit of CSF-NSE was 14.66 ng/mL. CSF-NSE was elevated in 6 (26%) MEM patients. CSF-NSE was increased in a single MEM patient with subclinical CNS involvement. This study shows that CSF-NSE is elevated in only one quarter of the MEM patients. Determination of CSF-NSE appears to be of minor importance for the assessment of clinical or subclinical CNS involvement in MEM.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Aksamit, A.J., Jr., Preissner, C.M., and Homburger, H.A. (2001). Quantitation of 14-3-3 and neuron-specific enolase proteins in CSF in Creutzfeldt-Jakob disease. Neurology 57:728–730.

    PubMed  Google Scholar 

  • Beaudry, P., Cohen, P., Brandel, J.P., Delasnerie-Laupretre, N., Richard, S., Launay, J.M., and Laplanche, J.L. (1999). 14-3-3 Protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. Dement. Geriatr. Cogn. Disord. 10:40–46.

    Article  CAS  PubMed  Google Scholar 

  • Beems, T., Simons, K.S., Van Geel, W.J., De Reus, H.P., Vos, P.E., and Verbeek, M.M. (2003). Serum- and CSF-concentrations of brain specific proteins in hydrocephalus. Acta Neurochir. (Wien) 145:37–43.

    Article  CAS  Google Scholar 

  • Brockmann, K., Bjornstad, A., Dechent, P., Korenke, C.G., Smeitink, J., Trijbels, J.M., Athanassopoulos, S., Villagran, R., Skjeldal, O.H., Wilichowski, E., Frahm, J., and Hanefeld, F. (2002). Succinate in dystrophic white matter: A proton magnetic resonance spectroscopy finding characteristic for complex II deficiency. Ann. Neurol. 52:38–46.

    Article  CAS  PubMed  Google Scholar 

  • Finsterer, J. (2004). Mitochondriopathies. Eur. J. Neurol. 11:163–186.

    Article  CAS  PubMed  Google Scholar 

  • Finsterer, J. (2001). Cerebrospinal-fluid lactate in adult mitochondriopathy with and without encephalopathy. Acta Med. Aust. 28:152–55.

    Article  CAS  Google Scholar 

  • Finsterer, J. (2001). Visually evoked potentials in respiratory chain disorders. Acta Neurol. Scand. 104:31–35.

    Article  CAS  PubMed  Google Scholar 

  • Leonard, J.V., and Schapira, A.H.V. (2000). Mitochondrial respiratory chain disorders I: Mitochondrial DNA defects. Lancet 355:299–304.

    Article  CAS  PubMed  Google Scholar 

  • Martinez-Fernandez, E., Gil-Peralta, A., Garcia-Lozano, R., Chinchon, I., Aguilera, I., Fernandez-Lopez, O., Arenas, J., Campos, Y., and Bautista, J. (2001). Mitochondrial disease and stroke. Stroke 32:2507–2510.

    CAS  PubMed  Google Scholar 

  • Musumeci, O., Naini, A., Slonim, A.E., Skavin, N., Hadjigeorgiou, G.L., Krawiecki, N., Weissman, B.M., Tsao, C.Y., Mendell, J.R., Shanske, S., De Vivo, D.C., Hirano, M., and DiMauro, S. (2001). Familial cerebellar ataxia with muscle coenzyme Q10 deficiency. Neurology 56:849–855.

    CAS  PubMed  Google Scholar 

  • Ohkoshi, N., Ishii, A., Shiraiwa, N., Shoji, S., and Yoshizawa, K. (1998). Dysfunction of the hypothalamic-pituitary system in mitochondrial encephalomyopathies. J. Med. 29:13–29.

    CAS  PubMed  Google Scholar 

  • Ohno, K., Isotani, E., and Hirakawa, K. (1997). MELAS presenting as migraine complicated by stroke: Case report. Neuroradiology 39:781–784.

    Article  CAS  PubMed  Google Scholar 

  • Osterlundh, G., Bjure, J., Lannering, B., Kjellmer, I., Uvebrant, P., and Marky, I. (1999). Regional cerebral blood flow and neuron-specific enolase in cerebrospinal fluid in children with acute lymphoblastic leukemia during induction treatment. J. Pediatr. Hematol. Oncol. 21:378–383.

    Article  CAS  PubMed  Google Scholar 

  • Pleines, U.E., Morganti-Kossmann, M.C., Rancan, M., Joller, H., Trentz, O., and Kossmann, T. (2001). S-100 beta reflects the extent of injury and outcome, whereas neuronal specific enolase is a better indicator of neuroinflammation in patients with severe traumatic brain injury. J. Neurotrauma 18:491–498.

    Article  CAS  PubMed  Google Scholar 

  • Steinhoff, B.J., Tumani, H., Otto, M., Mursch, K., Wiltfang, J., Herrendorf, G., Bittermann, H.J., Felgenhauer, K., Paulus, W., and Markakis, E. (1999). Cisternal S100 protein and neuron-specific enolase are elevated and site-specific markers in intractable temporal lobe epilepsy. Epilepsy Res. 36:75–82.

    Article  CAS  PubMed  Google Scholar 

  • Studahl, M., Rosengren, L., Gunther, G., and Hagberg, L. (2000). Difference in pathogenesis between herpes simplex virus type 1 encephalitis and tick-borne encephalitis demonstrated by means of cerebrospinal fluid markers of glial and neuronal destruction. J. Neurol. 247:636–642.

    Article  CAS  PubMed  Google Scholar 

  • Thornberg, E., Thiringer, K., Hagberg, H., and Kjellmer, I. (1995). Neuron specific enolase in asphyxiated newborns: Association with encephalopathy and cerebral function monitor trace. Arch. Dis. Child. Fetal Neonatal. Ed. 72:F39–F42.

    CAS  PubMed  Google Scholar 

  • Weinstock, A., Giglio, P., Cohen, M.E., Bakshi, R., Januario, J., and Balos, L. (2002). Diffuse magnetic resonance imaging white-matter changes in a 15-year-old boy with mitochondrial encephalomyopathy. J. Child. Neurol. 17:47–49.

    PubMed  Google Scholar 

  • Younes-Mhenni, S., Thobois, S., Streichenberger, N., Giraud, P., Mousson-de-Camaret, B., Montelescaut, M.E., Broussolle, E., and Chazot, G. (2002). Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (Melas) associated with a Fahr disease and cerebellar calcifications. Rev. Med. Int. 23:1027–1029.

    CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Josef Finsterer.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Finsterer, J., Exner, M. & Rumpold, H. Cerebrospinal Fluid Neurone-Specific Enolase in Mitochondrial Encephalomyopathies. Metab Brain Dis 20, 81–86 (2005). https://doi.org/10.1007/s11011-005-2479-9

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11011-005-2479-9

Keywords

Navigation