Skip to main content
Top
Published in: Journal of Neurology 5/2018

01-05-2018 | Original Communication

The metabolic and endocrine characteristics in spinal and bulbar muscular atrophy

Authors: Angela Rosenbohm, Susanne Hirsch, Alexander E. Volk, Torsten Grehl, Julian Grosskreutz, Frank Hanisch, Andreas Herrmann, Katja Kollewe, Wolfram Kress, Thomas Meyer, Susanne Petri, Johannes Prudlo, Carsten Wessig, Hans-Peter Müller, Jens Dreyhaupt, Jochen Weishaupt, Christian Kubisch, Jan Kassubek, Patrick Weydt, Albert C. Ludolph

Published in: Journal of Neurology | Issue 5/2018

Login to get access

Abstract

Objective

Spinal and bulbar muscular atrophy (SBMA) is caused by an abnormal expansion of the CAG repeat in the androgen receptor gene. This study aimed to systematically phenotype a German SBMA cohort (n = 80) based on laboratory markers for neuromuscular, metabolic, and endocrine status, and thus provide a basis for the selection of biomarkers for future therapeutic trials.

Methods

We assessed a panel of 28 laboratory parameters. The clinical course and blood biomarkers were correlated with disease duration and CAG repeat length. A subset of 11 patients was evaluated with body fat MRI.

Results

Almost all patients reported muscle weakness (99%), followed by dysphagia (77%), tremor (76%), and gynecomastia (75%) as major complaints. Creatine kinase was the most consistently elevated (94%) serum marker, which, however, did not relate with either the disease duration or the CAG repeat length. Paresis duration and CAG repeat length correlated with dehydroepiandrosterone sulfate after correction for body mass index and age. The androgen insensitivity index was elevated in nearly half of the participants (48%).

Conclusions

Metabolic alterations in glucose homeostasis (diabetes) and fat metabolism (combined hyperlipidemia), and sex hormone abnormalities (androgen insensitivity) could be observed among SBMA patients without association with the neuromuscular phenotype. Dehydroepiandrosterone sulfate was the only biomarker that correlated strongly with both weakness duration and the CAG repeat length after adjusting for age and BMI, indicating its potential as a biomarker for both disease severity and duration and, therefore, its possible use as a reliable outcome measure in future therapeutic studies.
Literature
1.
go back to reference La Spada AR, Wilson EM, Lubahn DB, Harding AE, Fischbeck KH (1991) Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature 352(6330):77–79CrossRefPubMed La Spada AR, Wilson EM, Lubahn DB, Harding AE, Fischbeck KH (1991) Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature 352(6330):77–79CrossRefPubMed
2.
go back to reference Tanaka F, Reeves MF, Ito Y et al (1999) Tissue-specific somatic mosaicism in spinal and bulbar muscular atrophy is dependent on CAG-repeat length and androgen receptor–gene expression level. Am J Hum Genet 65(4):966–973CrossRefPubMedPubMedCentral Tanaka F, Reeves MF, Ito Y et al (1999) Tissue-specific somatic mosaicism in spinal and bulbar muscular atrophy is dependent on CAG-repeat length and androgen receptor–gene expression level. Am J Hum Genet 65(4):966–973CrossRefPubMedPubMedCentral
4.
go back to reference Nakatsuji H, Araki A, Hashizume A, Hijikata Y, Yamada S, Inagaki T, Suzuki K, Banno H, Suga N, Okada Y, Ohyama M, Nakagawa T, Kishida K, Funahashi T, Shimomura I, Okano H, Katsuno M, Sobue G (2017) Correlation of insulin resistance and motor function in spinal and bulbar muscular atrophy. J Neurol 264(5):839–847CrossRefPubMed Nakatsuji H, Araki A, Hashizume A, Hijikata Y, Yamada S, Inagaki T, Suzuki K, Banno H, Suga N, Okada Y, Ohyama M, Nakagawa T, Kishida K, Funahashi T, Shimomura I, Okano H, Katsuno M, Sobue G (2017) Correlation of insulin resistance and motor function in spinal and bulbar muscular atrophy. J Neurol 264(5):839–847CrossRefPubMed
5.
go back to reference Katsuno M, Banno H, Suzuki K, Adachi H, Tanaka F, Sobue G (2012) Molecular pathophysiology and disease-modifying therapies for spinal and bulbar muscular atrophy. Arch Neurol 69:436–440CrossRefPubMed Katsuno M, Banno H, Suzuki K, Adachi H, Tanaka F, Sobue G (2012) Molecular pathophysiology and disease-modifying therapies for spinal and bulbar muscular atrophy. Arch Neurol 69:436–440CrossRefPubMed
6.
go back to reference Rocchi A, Pennuto M (2013) New routes to therapy for spinal and bulbar muscular atrophy. J Mol Neurosci 50:514–523CrossRefPubMed Rocchi A, Pennuto M (2013) New routes to therapy for spinal and bulbar muscular atrophy. J Mol Neurosci 50:514–523CrossRefPubMed
8.
go back to reference Fernández-Rhodes LE, Kokkinis AD, White MJ et al (2011) Efficacy and safety of dutasteride in patients with spinal and bulbar muscular atrophy: a randomised placebo-controlled trial. Lancet Neurol. 10(2):140–147CrossRefPubMedPubMedCentral Fernández-Rhodes LE, Kokkinis AD, White MJ et al (2011) Efficacy and safety of dutasteride in patients with spinal and bulbar muscular atrophy: a randomised placebo-controlled trial. Lancet Neurol. 10(2):140–147CrossRefPubMedPubMedCentral
9.
go back to reference Katsuno M, Tanaka F, Adachi H et al (2012) Pathogenesis and therapy of spinal and bulbar muscular atrophy (SBMA). Prog Neurobiol 99(3):246–256CrossRefPubMed Katsuno M, Tanaka F, Adachi H et al (2012) Pathogenesis and therapy of spinal and bulbar muscular atrophy (SBMA). Prog Neurobiol 99(3):246–256CrossRefPubMed
10.
go back to reference Weydt P, Sagnelli A, Rosenbohm A, Pradat P-F, Ludolph AC, Pareyson D (2015) Clinical trials in spinal and bulbar muscular atrophy-past, present, and future. J Mol Neurosci 58(3):379–387CrossRefPubMed Weydt P, Sagnelli A, Rosenbohm A, Pradat P-F, Ludolph AC, Pareyson D (2015) Clinical trials in spinal and bulbar muscular atrophy-past, present, and future. J Mol Neurosci 58(3):379–387CrossRefPubMed
11.
go back to reference Atsuta N, Watanabe H, Ito M et al (2006) Natural history of spinal and bulbar muscular atrophy (SBMA): a study of 223 Japanese patients. Brain 129(Pt 6):1446–1455CrossRefPubMed Atsuta N, Watanabe H, Ito M et al (2006) Natural history of spinal and bulbar muscular atrophy (SBMA): a study of 223 Japanese patients. Brain 129(Pt 6):1446–1455CrossRefPubMed
12.
go back to reference Igarashi S, Tanno Y, Onodera O et al (1992) Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy. Neurology. 42(12):2300–2302CrossRefPubMed Igarashi S, Tanno Y, Onodera O et al (1992) Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy. Neurology. 42(12):2300–2302CrossRefPubMed
13.
go back to reference Lee J-H, Shin J-H, Park K-P et al (2005) Phenotypic variability in Kennedy’s disease: implication of the early diagnostic features. Acta Neurol Scand 112(1):57–63CrossRefPubMed Lee J-H, Shin J-H, Park K-P et al (2005) Phenotypic variability in Kennedy’s disease: implication of the early diagnostic features. Acta Neurol Scand 112(1):57–63CrossRefPubMed
14.
go back to reference Sperfeld AD, Karitzky J, Brummer D et al (2002) X-linked bulbospinal neuronopathy: Kennedy disease. Arch Neurol 59(12):1921–1926CrossRefPubMed Sperfeld AD, Karitzky J, Brummer D et al (2002) X-linked bulbospinal neuronopathy: Kennedy disease. Arch Neurol 59(12):1921–1926CrossRefPubMed
15.
go back to reference Dejager S (2002) A comprehensive endocrine description of Kennedy’s disease revealing androgen insensitivity linked to cag repeat length. J Clin Endocrinol Metab 87(8):3893PubMed Dejager S (2002) A comprehensive endocrine description of Kennedy’s disease revealing androgen insensitivity linked to cag repeat length. J Clin Endocrinol Metab 87(8):3893PubMed
16.
go back to reference Katsuno M, Adachi H, Kume A et al (2002) Testosterone reduction prevents phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy. Neuron 35(5):843–854CrossRefPubMed Katsuno M, Adachi H, Kume A et al (2002) Testosterone reduction prevents phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy. Neuron 35(5):843–854CrossRefPubMed
17.
go back to reference Querin G, Bertolin C, Da Re E et al (2015) Non-neural phenotype of spinal and bulbar muscular atrophy: results from a large cohort of Italian patients. J Neurol Neurosurg Psychiatr. 87(8):810–816CrossRef Querin G, Bertolin C, Da Re E et al (2015) Non-neural phenotype of spinal and bulbar muscular atrophy: results from a large cohort of Italian patients. J Neurol Neurosurg Psychiatr. 87(8):810–816CrossRef
18.
go back to reference Pennuto M, Greensmith L, Pradat P-F et al (2015) 210th ENMC International Workshop: research and clinical management of patients with spinal and bulbar muscular atrophy, 27–29 March, 2015, Naarden, The Netherlands. Neuromuscul Disord 25:802–812CrossRefPubMed Pennuto M, Greensmith L, Pradat P-F et al (2015) 210th ENMC International Workshop: research and clinical management of patients with spinal and bulbar muscular atrophy, 27–29 March, 2015, Naarden, The Netherlands. Neuromuscul Disord 25:802–812CrossRefPubMed
19.
go back to reference Grunseich C, Kats IR, Bott LC et al (2014) Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat. Neuromuscul Disord 24(11):978–981CrossRefPubMedPubMedCentral Grunseich C, Kats IR, Bott LC et al (2014) Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat. Neuromuscul Disord 24(11):978–981CrossRefPubMedPubMedCentral
20.
go back to reference Palazzolo I, Stack C, Kong L et al (2009) Overexpression of IGF-1 in muscle attenuates disease in a mouse model of spinal and bulbar muscular atrophy. Neuron 63(3):316–328CrossRefPubMedPubMedCentral Palazzolo I, Stack C, Kong L et al (2009) Overexpression of IGF-1 in muscle attenuates disease in a mouse model of spinal and bulbar muscular atrophy. Neuron 63(3):316–328CrossRefPubMedPubMedCentral
21.
go back to reference Mariotti C, Castellotti B, Pareyson D et al (2000) Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 families. Neuromuscul Disord 10(6):391–397CrossRefPubMed Mariotti C, Castellotti B, Pareyson D et al (2000) Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 families. Neuromuscul Disord 10(6):391–397CrossRefPubMed
22.
go back to reference Ni W, Chen S, Qiao K, Wang N, Wu Z-Y (2015) Genotype-phenotype correlation in Chinese patients with spinal and bulbar muscular atrophy. PLoS One 10(3):e0122279CrossRefPubMedPubMedCentral Ni W, Chen S, Qiao K, Wang N, Wu Z-Y (2015) Genotype-phenotype correlation in Chinese patients with spinal and bulbar muscular atrophy. PLoS One 10(3):e0122279CrossRefPubMedPubMedCentral
23.
go back to reference Ranganathan S, Harmison GG, Meyertholen K, Pennuto M, Burnett BG, Fischbeck KH (2008) Mitochondrial abnormalities in spinal and bulbar muscular atrophy. Hum Mol Genet 18(1):27–42CrossRefPubMedPubMedCentral Ranganathan S, Harmison GG, Meyertholen K, Pennuto M, Burnett BG, Fischbeck KH (2008) Mitochondrial abnormalities in spinal and bulbar muscular atrophy. Hum Mol Genet 18(1):27–42CrossRefPubMedPubMedCentral
24.
go back to reference Harding AE, Thomas PK, Baraitser M, Bradbury PG, Morgan-Hughes JA, Ponsford JR (1982) X-linked recessive bulbospinal neuronopathy: a report of ten cases. Brain 45(11):1012–1019 Harding AE, Thomas PK, Baraitser M, Bradbury PG, Morgan-Hughes JA, Ponsford JR (1982) X-linked recessive bulbospinal neuronopathy: a report of ten cases. Brain 45(11):1012–1019
25.
go back to reference Amato AA, Prior TW, Barohn RJ, Snyder P, Papp A, Mendell JR (1993) Kennedy’s disease: a clinicopathologic correlation with mutations in the androgen receptor gene. Neurology. 43(4):791–794CrossRefPubMed Amato AA, Prior TW, Barohn RJ, Snyder P, Papp A, Mendell JR (1993) Kennedy’s disease: a clinicopathologic correlation with mutations in the androgen receptor gene. Neurology. 43(4):791–794CrossRefPubMed
26.
go back to reference Doyu M, Sobue G, Mukai E et al (1992) Severity of X-linked recessive bulbospinal neuronopathy correlates with size of the tandem CAG repeat in androgen receptor gene. Ann Neurol 32:707–710CrossRefPubMed Doyu M, Sobue G, Mukai E et al (1992) Severity of X-linked recessive bulbospinal neuronopathy correlates with size of the tandem CAG repeat in androgen receptor gene. Ann Neurol 32:707–710CrossRefPubMed
27.
go back to reference Müller H-P, Raudies F, Unrath A, Neumann H, Ludolph AC, Kassubek J (2010) Quantification of human body fat tissue percentage by MRI. NMR Biomed 24(1):17–24CrossRef Müller H-P, Raudies F, Unrath A, Neumann H, Ludolph AC, Kassubek J (2010) Quantification of human body fat tissue percentage by MRI. NMR Biomed 24(1):17–24CrossRef
28.
go back to reference Lindauer E, Dupuis L, Müller H-P, Neumann H, Ludolph AC, Kassubek J (2013) Adipose tissue distribution predicts survival in amyotrophic lateral sclerosis. PLoS One 8(6):e67783CrossRefPubMedPubMedCentral Lindauer E, Dupuis L, Müller H-P, Neumann H, Ludolph AC, Kassubek J (2013) Adipose tissue distribution predicts survival in amyotrophic lateral sclerosis. PLoS One 8(6):e67783CrossRefPubMedPubMedCentral
29.
go back to reference Fischer K, Moewes D, Koch M et al (2015) MRI-determined total volumes of visceral and subcutaneous abdominal and trunk adipose tissue are differentially and sex-dependently associated with patterns of estimated usual nutrient intake in a northern German population. Am J Clin Nutr 101(4):794–807CrossRefPubMed Fischer K, Moewes D, Koch M et al (2015) MRI-determined total volumes of visceral and subcutaneous abdominal and trunk adipose tissue are differentially and sex-dependently associated with patterns of estimated usual nutrient intake in a northern German population. Am J Clin Nutr 101(4):794–807CrossRefPubMed
30.
go back to reference Proschan MA, Waclawiw MA (2001) Practical guidelines for multiplicity adjustment in clinical trials. Control Clin Trials 21(6):527–539CrossRef Proschan MA, Waclawiw MA (2001) Practical guidelines for multiplicity adjustment in clinical trials. Control Clin Trials 21(6):527–539CrossRef
32.
go back to reference Cortes CJ, Ling S-C, Guo LT et al (2014) Muscle expression of mutant androgen receptor accounts for systemic and motor neuron disease phenotypes in spinal and bulbar muscular atrophy. Neuron 82(2):295–307CrossRefPubMedPubMedCentral Cortes CJ, Ling S-C, Guo LT et al (2014) Muscle expression of mutant androgen receptor accounts for systemic and motor neuron disease phenotypes in spinal and bulbar muscular atrophy. Neuron 82(2):295–307CrossRefPubMedPubMedCentral
33.
go back to reference Lieberman AP, Yu Z, Murray S et al (2014) Peripheral androgen receptor gene suppression rescues disease in mouse models of spinal and bulbar muscular atrophy. Cell Rep. 7(3):774–784CrossRefPubMedPubMedCentral Lieberman AP, Yu Z, Murray S et al (2014) Peripheral androgen receptor gene suppression rescues disease in mouse models of spinal and bulbar muscular atrophy. Cell Rep. 7(3):774–784CrossRefPubMedPubMedCentral
34.
go back to reference Sorarù G, Hashizume Y, Mukai E, Hirayama M, Mitsuma T, Takahashi A et al (1989) X-linked recessive bulbospinal neuronopathy. A clinicopathological study. Brain 112(1):209–232 (Pt 1) CrossRef Sorarù G, Hashizume Y, Mukai E, Hirayama M, Mitsuma T, Takahashi A et al (1989) X-linked recessive bulbospinal neuronopathy. A clinicopathological study. Brain 112(1):209–232 (Pt 1) CrossRef
35.
go back to reference Sorarù G, D’Ascenzo C, Polo A et al (2007) Spinal and bulbar muscular atrophy: skeletal muscle pathology in male patients and heterozygous females. J Neurol Sci 264(1–2):100–105PubMed Sorarù G, D’Ascenzo C, Polo A et al (2007) Spinal and bulbar muscular atrophy: skeletal muscle pathology in male patients and heterozygous females. J Neurol Sci 264(1–2):100–105PubMed
36.
go back to reference Sinclair R, Greenland KJ, van Egmond S, Hoedemaker C, Chapman A, Zajac JD (2007) Men with Kennedy disease have a reduced risk of androgenetic alopecia. Br J Dermatol 157(2):290–294CrossRefPubMed Sinclair R, Greenland KJ, van Egmond S, Hoedemaker C, Chapman A, Zajac JD (2007) Men with Kennedy disease have a reduced risk of androgenetic alopecia. Br J Dermatol 157(2):290–294CrossRefPubMed
38.
Metadata
Title
The metabolic and endocrine characteristics in spinal and bulbar muscular atrophy
Authors
Angela Rosenbohm
Susanne Hirsch
Alexander E. Volk
Torsten Grehl
Julian Grosskreutz
Frank Hanisch
Andreas Herrmann
Katja Kollewe
Wolfram Kress
Thomas Meyer
Susanne Petri
Johannes Prudlo
Carsten Wessig
Hans-Peter Müller
Jens Dreyhaupt
Jochen Weishaupt
Christian Kubisch
Jan Kassubek
Patrick Weydt
Albert C. Ludolph
Publication date
01-05-2018
Publisher
Springer Berlin Heidelberg
Published in
Journal of Neurology / Issue 5/2018
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-018-8790-2

Other articles of this Issue 5/2018

Journal of Neurology 5/2018 Go to the issue