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Published in: Journal of Neurology 12/2019

01-12-2019 | Amyotrophic Lateral Sclerosis | Original Communication

Elevated serum creatine kinase in the early stage of sporadic amyotrophic lateral sclerosis

Authors: Daisuke Ito, Atsushi Hashizume, Yasuhiro Hijikata, Shinichiro Yamada, Yohei Iguchi, Madoka Iida, Yoshiyuki Kishimoto, Hideyuki Moriyoshi, Akihiro Hirakawa, Masahisa Katsuno

Published in: Journal of Neurology | Issue 12/2019

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Abstract

Objective

To assess the changes of muscle-related biomarkers at the early stage of amyotrophic lateral sclerosis, and to confirm these findings in an experimental animal model.

Methods

Thirty-nine subjects with sporadic amyotrophic lateral sclerosis and 20 healthy controls were enrolled and longitudinally evaluated. We evaluated serum creatine kinase and creatinine levels and appendicular lean soft-tissue mass using dual X-ray absorptiometry. The levels of biomarkers at early ALS stages were estimated using linear mixed models with unstructured correlation and random intercepts. We also analyzed the longitudinal changes of serum creatine kinase and creatinine, together with the mRNA levels of acetylcholine receptor subunit γ (Chrng) and muscle-associated receptor tyrosine kinase, markers of denervation, in the gastrocnemius muscle of superoxide dismutase 1 (SOD1)G93A transgenic mice, an animal model of amyotrophic lateral sclerosis.

Results

The estimated levels of creatine kinase were higher in subjects with amyotrophic lateral sclerosis at the early stage than in healthy controls, although the estimated appendicular lean soft-tissue mass and creatinine levels were equivalent between both groups, suggesting that the elevation of creatine kinase precedes both muscular atrophy and subjective motor symptoms in sporadic amyotrophic lateral sclerosis. In SOD1G93A mice, the serum levels of creatine kinase were elevated at 9 weeks of age (peri-onset) when Chrng started to be up-regulated, and were then down-regulated at 15 weeks of age, consistent with the clinical data from patients with sporadic amyotrophic lateral sclerosis.

Interpretation

Creatine kinase elevation precedes muscular atrophy and reflects muscle denervation at the early stage.
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Literature
1.
go back to reference Rowland L, Shneider N (2001) Amyotrophic lateral sclerosis. N Engl J Med 344:1688–1700PubMed Rowland L, Shneider N (2001) Amyotrophic lateral sclerosis. N Engl J Med 344:1688–1700PubMed
3.
go back to reference Renton AE, Chiò A, Traynor BJ (2014) State of play in amyotrophic lateral sclerosis genetics. Nat Neurosci 17:17–23PubMed Renton AE, Chiò A, Traynor BJ (2014) State of play in amyotrophic lateral sclerosis genetics. Nat Neurosci 17:17–23PubMed
4.
go back to reference Nakamura R, Sone J, Atsuta N et al (2016) Next-generation sequencing of 28 ALS-related genes in a Japanese ALS cohort. Neurobiol Aging 39:219.e1–219.e8 Nakamura R, Sone J, Atsuta N et al (2016) Next-generation sequencing of 28 ALS-related genes in a Japanese ALS cohort. Neurobiol Aging 39:219.e1–219.e8
6.
go back to reference Bensimon G, Lacomblez L, Meininger V (1994) A controlled trial of riluzole in amyotrophic lateral sclerosis. N Engl J Med 330:585–591PubMed Bensimon G, Lacomblez L, Meininger V (1994) A controlled trial of riluzole in amyotrophic lateral sclerosis. N Engl J Med 330:585–591PubMed
7.
go back to reference Abe K, Itoyama Y, Sobue G et al (2014) Confirmatory double-blind, parallel-group, placebo-controlled study of efficacy and safety of edaravone (MCI-186) in amyotrophic lateral sclerosis patients. Amyotroph Lateral Scler Front Degener 15:610–617 Abe K, Itoyama Y, Sobue G et al (2014) Confirmatory double-blind, parallel-group, placebo-controlled study of efficacy and safety of edaravone (MCI-186) in amyotrophic lateral sclerosis patients. Amyotroph Lateral Scler Front Degener 15:610–617
8.
go back to reference Villemagne VL, Burnham S, Bourgeat P et al (2013) Amyloid β deposition, neurodegeneration, and cognitive decline in sporadic Alzheimer’s disease: a prospective cohort study. Lancet Neurol 12:357–367PubMed Villemagne VL, Burnham S, Bourgeat P et al (2013) Amyloid β deposition, neurodegeneration, and cognitive decline in sporadic Alzheimer’s disease: a prospective cohort study. Lancet Neurol 12:357–367PubMed
9.
go back to reference Cooper CA, Chahine LM (2016) Biomarkers in prodromal parkinson disease: a qualitative review. J Int Neuropsychol Soc 22:956–967PubMed Cooper CA, Chahine LM (2016) Biomarkers in prodromal parkinson disease: a qualitative review. J Int Neuropsychol Soc 22:956–967PubMed
10.
go back to reference Vos SJB, Xiong C, Visser PJ et al (2013) Preclinical Alzheimer’s disease and its outcome: a longitudinal cohort study. Lancet Neurol 12:957–965PubMedPubMedCentral Vos SJB, Xiong C, Visser PJ et al (2013) Preclinical Alzheimer’s disease and its outcome: a longitudinal cohort study. Lancet Neurol 12:957–965PubMedPubMedCentral
11.
go back to reference Katsuno M, Tanaka F, Sobue G (2012) Perspectives on molecular targeted therapies and clinical trials for neurodegenerative diseases. J Neurol Neurosurg Psychiatry 83:329–335PubMed Katsuno M, Tanaka F, Sobue G (2012) Perspectives on molecular targeted therapies and clinical trials for neurodegenerative diseases. J Neurol Neurosurg Psychiatry 83:329–335PubMed
13.
go back to reference Solomon A, Mangialasche F, Richard E et al (2014) Advances in the prevention of Alzheimer’s disease and dementia. J Intern Med 275:229–250PubMedPubMedCentral Solomon A, Mangialasche F, Richard E et al (2014) Advances in the prevention of Alzheimer’s disease and dementia. J Intern Med 275:229–250PubMedPubMedCentral
14.
go back to reference Schapira AHV, Olanow CW, Greenamyre JT, Bezard E (2014) Slowing of neurodegeneration in Parkinson’s disease and Huntington’s disease: Future therapeutic perspectives. Lancet 384:545–555PubMed Schapira AHV, Olanow CW, Greenamyre JT, Bezard E (2014) Slowing of neurodegeneration in Parkinson’s disease and Huntington’s disease: Future therapeutic perspectives. Lancet 384:545–555PubMed
15.
go back to reference Lehmer C, Oeckl P, Weishaupt JH et al (2017) Poly-GP in cerebrospinal fluid links C9orf72 -associated dipeptide repeat expression to the asymptomatic phase of ALS/FTD. EMBO Mol Med 9:859–868PubMedPubMedCentral Lehmer C, Oeckl P, Weishaupt JH et al (2017) Poly-GP in cerebrospinal fluid links C9orf72 -associated dipeptide repeat expression to the asymptomatic phase of ALS/FTD. EMBO Mol Med 9:859–868PubMedPubMedCentral
16.
go back to reference Freischmidt A, Müller K, Zondler L et al (2014) Serum microRNAs in patients with genetic amyotrophic lateral sclerosis and pre-manifest mutation carriers. Brain 137:2938–2950PubMed Freischmidt A, Müller K, Zondler L et al (2014) Serum microRNAs in patients with genetic amyotrophic lateral sclerosis and pre-manifest mutation carriers. Brain 137:2938–2950PubMed
17.
go back to reference Vucic S, Nicholson GA, Kiernan MC (2008) Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosis. Brain 131:1540–1550PubMed Vucic S, Nicholson GA, Kiernan MC (2008) Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosis. Brain 131:1540–1550PubMed
18.
go back to reference Aggarwal A, Nicholson G (2002) Detection of preclinical motor neurone loss in SOD1 mutation carriers using motor unit number estimation. J Neurol Neurosurg Psychiatry 73:199–201PubMedPubMedCentral Aggarwal A, Nicholson G (2002) Detection of preclinical motor neurone loss in SOD1 mutation carriers using motor unit number estimation. J Neurol Neurosurg Psychiatry 73:199–201PubMedPubMedCentral
19.
go back to reference Gallo V, Wark PA, Jenab M et al (2013) Prediagnostic body fat and risk of death from amyotrophic lateral sclerosis: the EPIC cohort. Neurology 80:829–838PubMedPubMedCentral Gallo V, Wark PA, Jenab M et al (2013) Prediagnostic body fat and risk of death from amyotrophic lateral sclerosis: the EPIC cohort. Neurology 80:829–838PubMedPubMedCentral
20.
go back to reference Mariosa D, Hammar N, Malmström H et al (2017) Blood biomarkers of carbohydrate, lipid, and apolipoprotein metabolisms and risk of amyotrophic lateral sclerosis: a more than 20-year follow-up of the Swedish AMORIS cohort. Ann Neurol 81:718–728PubMed Mariosa D, Hammar N, Malmström H et al (2017) Blood biomarkers of carbohydrate, lipid, and apolipoprotein metabolisms and risk of amyotrophic lateral sclerosis: a more than 20-year follow-up of the Swedish AMORIS cohort. Ann Neurol 81:718–728PubMed
21.
go back to reference Ohashi Y, Tashiro K, Itoyama Y et al (2001) Study of functional rating scale for amyotrophic lateral sclerosis: revised ALSFRS(ALSFRS-R) Japanese version. No To Shinkei 53:346–355PubMed Ohashi Y, Tashiro K, Itoyama Y et al (2001) Study of functional rating scale for amyotrophic lateral sclerosis: revised ALSFRS(ALSFRS-R) Japanese version. No To Shinkei 53:346–355PubMed
22.
go back to reference Hashizume A, Katsuno M, Suzuki K et al (2015) A functional scale for spinal and bulbar muscular atrophy: cross-sectional and longitudinal study. Neuromuscul Disord 25:554–562PubMedPubMedCentral Hashizume A, Katsuno M, Suzuki K et al (2015) A functional scale for spinal and bulbar muscular atrophy: cross-sectional and longitudinal study. Neuromuscul Disord 25:554–562PubMedPubMedCentral
23.
go back to reference Haarbo J, Gotfredsen A, Hassager C, Christiansen C (1991) Validation of body composition by dual energy X-ray absorptiometry (DEXA). Clin Physiol 11:331–341PubMed Haarbo J, Gotfredsen A, Hassager C, Christiansen C (1991) Validation of body composition by dual energy X-ray absorptiometry (DEXA). Clin Physiol 11:331–341PubMed
24.
go back to reference Hijikata Y, Katsuno M, Suzuki K et al (2016) Impaired muscle uptake of creatine in spinal and bulbar muscular atrophy. Ann Clin Transl Neurol 3:537–546PubMedPubMedCentral Hijikata Y, Katsuno M, Suzuki K et al (2016) Impaired muscle uptake of creatine in spinal and bulbar muscular atrophy. Ann Clin Transl Neurol 3:537–546PubMedPubMedCentral
25.
go back to reference Gurney ME, Pu H, Chiu AY et al (1994) Motor neuron degeneration in mice that express a human Cu, Zn superoxide dismutase mutation. Science 264:1772–1775PubMed Gurney ME, Pu H, Chiu AY et al (1994) Motor neuron degeneration in mice that express a human Cu, Zn superoxide dismutase mutation. Science 264:1772–1775PubMed
27.
go back to reference Rocchi A, Milioto C, Parodi S et al (2016) Glycolytic-to-oxidative fiber-type switch and mTOR signaling activation are early-onset features of SBMA muscle modified by high-fat diet. Acta Neuropathol 132:127–144PubMedPubMedCentral Rocchi A, Milioto C, Parodi S et al (2016) Glycolytic-to-oxidative fiber-type switch and mTOR signaling activation are early-onset features of SBMA muscle modified by high-fat diet. Acta Neuropathol 132:127–144PubMedPubMedCentral
28.
go back to reference Yau W-YW, Tudorascu DL, McDade EM et al (2015) Longitudinal assessment of neuroimaging and clinical markers in autosomal dominant Alzheimer’s disease: a prospective cohort study. Lancet Neurol 14:804–813PubMedPubMedCentral Yau W-YW, Tudorascu DL, McDade EM et al (2015) Longitudinal assessment of neuroimaging and clinical markers in autosomal dominant Alzheimer’s disease: a prospective cohort study. Lancet Neurol 14:804–813PubMedPubMedCentral
29.
go back to reference Chan YH (2003) Biostatistics 104: correlation analysis. Singap Med J 44:614–619 Chan YH (2003) Biostatistics 104: correlation analysis. Singap Med J 44:614–619
30.
go back to reference Wyss M, Kaddurah-Daouk R (2000) Creatine and creatinine metabolism. Physiol Rev 80:1107–1213PubMed Wyss M, Kaddurah-Daouk R (2000) Creatine and creatinine metabolism. Physiol Rev 80:1107–1213PubMed
31.
go back to reference Panitch HS, Franklin GM (1972) Elevation of serum creatine phosphokinase in amyotrophic lateral sclerosis. Neurology 22:964–966PubMed Panitch HS, Franklin GM (1972) Elevation of serum creatine phosphokinase in amyotrophic lateral sclerosis. Neurology 22:964–966PubMed
32.
go back to reference Harrington TM, Cohen MD, Bartleson JD, Ginsburg WW (1983) Elevation of creatine kinase in amyotrophic lateral sclerosis. Potential confusion with pols. Potential confusion with polmyositis. Arthritis Rheum 26:201–205PubMed Harrington TM, Cohen MD, Bartleson JD, Ginsburg WW (1983) Elevation of creatine kinase in amyotrophic lateral sclerosis. Potential confusion with pols. Potential confusion with polmyositis. Arthritis Rheum 26:201–205PubMed
33.
go back to reference Gibson SB, Kasarskis EJ, Hu N et al (2015) Relationship of creatine kinase to body composition, disease state, and longevity in ALS. Amyotroph Lateral Scler Front Degener 16:473–477 Gibson SB, Kasarskis EJ, Hu N et al (2015) Relationship of creatine kinase to body composition, disease state, and longevity in ALS. Amyotroph Lateral Scler Front Degener 16:473–477
34.
go back to reference Felice KJ, North WA (1998) Creatine kinase values in amyotrophic lateral sclerosis. J Neurol Sci 160:3–5 Felice KJ, North WA (1998) Creatine kinase values in amyotrophic lateral sclerosis. J Neurol Sci 160:3–5
35.
go back to reference Iłzecka J, Stelmasiak Z (2003) Creatine kinase activity in amyotrophic lateral sclerosis patients. Neurol Sci 24:286–287PubMed Iłzecka J, Stelmasiak Z (2003) Creatine kinase activity in amyotrophic lateral sclerosis patients. Neurol Sci 24:286–287PubMed
36.
go back to reference Rafiq MK, Lee E, Bradburn M et al (2016) Creatine kinase enzyme level correlates positively with serum creatinine and lean body mass, and is a prognostic factor for survival in amyotrophic lateral sclerosis. Eur J Neurol 23:1071–1078PubMed Rafiq MK, Lee E, Bradburn M et al (2016) Creatine kinase enzyme level correlates positively with serum creatinine and lean body mass, and is a prognostic factor for survival in amyotrophic lateral sclerosis. Eur J Neurol 23:1071–1078PubMed
37.
go back to reference Tai H, Cui L, Guan Y et al (2017) Correlation of creatine kinase levels with clinical features and survival in amyotrophic lateral sclerosis. Front Neurol 8:1–5 Tai H, Cui L, Guan Y et al (2017) Correlation of creatine kinase levels with clinical features and survival in amyotrophic lateral sclerosis. Front Neurol 8:1–5
38.
go back to reference Tai H, Cui L, Liu M et al (2018) Creatine kinase level and its relationship with quantitative electromyographic characteristics in amyotrophic lateral sclerosis. Clin Neurophysiol 129:926–930PubMed Tai H, Cui L, Liu M et al (2018) Creatine kinase level and its relationship with quantitative electromyographic characteristics in amyotrophic lateral sclerosis. Clin Neurophysiol 129:926–930PubMed
39.
go back to reference Satoh J, Okada K, Kishi T et al (2000) Cramping pain and prolonged elevation of serum creatine kinase levels in a patient with Guillain-Barré syndrome following Campylobacter jejuni enteritis. Eur J Neurol 7:107–109PubMed Satoh J, Okada K, Kishi T et al (2000) Cramping pain and prolonged elevation of serum creatine kinase levels in a patient with Guillain-Barré syndrome following Campylobacter jejuni enteritis. Eur J Neurol 7:107–109PubMed
40.
go back to reference Linkhart TA, Wilson BW (1975) Appearance of acetylcholinesterase and creatine kinase in plasma of normal chickens after denervation. J Neurol Sci 26:193–201PubMed Linkhart TA, Wilson BW (1975) Appearance of acetylcholinesterase and creatine kinase in plasma of normal chickens after denervation. J Neurol Sci 26:193–201PubMed
41.
go back to reference Pun S, Santos AF, Saxena S et al (2006) Selective vulnerability and pruning of phasic motoneuron axons in motoneuron disease alleviated by CNTF. Nat Neurosci 9:408–419PubMed Pun S, Santos AF, Saxena S et al (2006) Selective vulnerability and pruning of phasic motoneuron axons in motoneuron disease alleviated by CNTF. Nat Neurosci 9:408–419PubMed
43.
go back to reference Eisen A, Kiernan M, Mitsumoto H, Swash M (2014) Amyotrophic lateral sclerosis: a long preclinical period? J Neurol Neurosurg Psychiatry 85:1232–1238PubMed Eisen A, Kiernan M, Mitsumoto H, Swash M (2014) Amyotrophic lateral sclerosis: a long preclinical period? J Neurol Neurosurg Psychiatry 85:1232–1238PubMed
44.
go back to reference Williams AH, Valdez G, Moresi V et al (2009) MicroRNA-206 delays ALS progression and promotes regeneration of neuromuscular synapses in mice. Science 326:1549–1554PubMedPubMedCentral Williams AH, Valdez G, Moresi V et al (2009) MicroRNA-206 delays ALS progression and promotes regeneration of neuromuscular synapses in mice. Science 326:1549–1554PubMedPubMedCentral
45.
go back to reference Bruneteau G, Simonet T, Bauché S et al (2013) Muscle histone deacetylase 4 upregulation in amyotrophic lateral sclerosis: Potential role in reinnervation ability and disease progression. Brain 136:2359–2368PubMed Bruneteau G, Simonet T, Bauché S et al (2013) Muscle histone deacetylase 4 upregulation in amyotrophic lateral sclerosis: Potential role in reinnervation ability and disease progression. Brain 136:2359–2368PubMed
46.
go back to reference Andrés V, Cussó R, Carreras J (1990) Effect of denervation on the distribution and developmental transition of phosphoglycerate mutase and creatine phosphokinase isozymes in rat muscles of different fiber-type composition. Differentiation 43:98–103PubMed Andrés V, Cussó R, Carreras J (1990) Effect of denervation on the distribution and developmental transition of phosphoglycerate mutase and creatine phosphokinase isozymes in rat muscles of different fiber-type composition. Differentiation 43:98–103PubMed
47.
go back to reference Dupuis L, Corcia P, Fergani A et al (2008) Dyslipidemia is a protective factor in amyotrophic lateral sclerosis. Neurology 70:1004–1009PubMed Dupuis L, Corcia P, Fergani A et al (2008) Dyslipidemia is a protective factor in amyotrophic lateral sclerosis. Neurology 70:1004–1009PubMed
48.
go back to reference Ikeda K, Hirayama T, Takazawa T et al (2012) Relationships between disease progression and serum levels of lipid, urate, creatinine and ferritin in Japanese patients with amyotrophic lateral sclerosis: a cross-sectional study. Intern Med 51:1501–1508PubMed Ikeda K, Hirayama T, Takazawa T et al (2012) Relationships between disease progression and serum levels of lipid, urate, creatinine and ferritin in Japanese patients with amyotrophic lateral sclerosis: a cross-sectional study. Intern Med 51:1501–1508PubMed
49.
go back to reference Ogaki K, Li Y, Atsuta N et al (2012) Analysis of C9orf72 repeat expansion in 563 Japanese patients with amyotrophic lateral sclerosis. Neurobiol Aging 33:11–16 Ogaki K, Li Y, Atsuta N et al (2012) Analysis of C9orf72 repeat expansion in 563 Japanese patients with amyotrophic lateral sclerosis. Neurobiol Aging 33:11–16
Metadata
Title
Elevated serum creatine kinase in the early stage of sporadic amyotrophic lateral sclerosis
Authors
Daisuke Ito
Atsushi Hashizume
Yasuhiro Hijikata
Shinichiro Yamada
Yohei Iguchi
Madoka Iida
Yoshiyuki Kishimoto
Hideyuki Moriyoshi
Akihiro Hirakawa
Masahisa Katsuno
Publication date
01-12-2019
Publisher
Springer Berlin Heidelberg
Published in
Journal of Neurology / Issue 12/2019
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-019-09507-6

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