Skip to main content
Erschienen in: Journal of Neurology 5/2017

22.02.2017 | Original Communication

Correlation of insulin resistance and motor function in spinal and bulbar muscular atrophy

verfasst von: Hideaki Nakatsuji, Amane Araki, Atsushi Hashizume, Yasuhiro Hijikata, Shinichiro Yamada, Tomonori Inagaki, Keisuke Suzuki, Haruhiko Banno, Noriaki Suga, Yohei Okada, Manabu Ohyama, Tohru Nakagawa, Ken Kishida, Tohru Funahashi, Iichiro Shimomura, Hideyuki Okano, Masahisa Katsuno, Gen Sobue

Erschienen in: Journal of Neurology | Ausgabe 5/2017

Einloggen, um Zugang zu erhalten

Abstract

This study aimed to evaluate various metabolic parameters in patients with spinal and bulbar muscular atrophy (SBMA), to investigate the association between those indices and disease severity, and to explore the underlying molecular pathogenesis. We compared the degree of obesity, metabolic parameters, and blood pressure in 55 genetically confirmed SBMA patients against those in 483 age- and sex-matched healthy control. In SBMA patients, we investigated the correlation between these factors and motor functional indices. SBMA patients had lower body mass index, blood glucose, and Hemoglobin A1c, but higher blood pressure, homeostasis model assessment of insulin resistance (HOMA-IR, a marker of insulin resistance), total cholesterol, and adiponectin levels than the control subjects. There were no differences in visceral fat areas, high-density lipoprotein-cholesterol (HDL-C), or triglyceride levels in two groups. Revised amyotrophic lateral sclerosis functional rating scale (ALSFRS-R) correlated positively with HDL-C, but negatively with HOMA-IR. Through stepwise multiple regression analysis, we identified HOMA-IR as a significant metabolic determinant of ALSFRS-R. In biochemical analysis, we found that decreased expressions of insulin receptors, insulin receptor substrate-1 and insulin receptor-β, in autopsied muscles and fibroblasts of SBMA patients. This study demonstrates that SBMA patients have insulin resistance, which is associated with the disease severity. The expressions of insulin receptors are attenuated in the skeletal muscle of SBMA, providing a possible pathomechanism of metabolic alterations. These findings suggested that insulin resistance is a metabolic index reflecting disease severity and pathogenesis as well as a potential therapeutic target for SBMA.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
1.
Zurück zum Zitat Katsuno M, Tanaka F, Adachi H et al (2012) Pathogenesis and therapy of spinal and bulbar muscular atrophy (SBMA). Prog Neurobiol 99:246–256CrossRefPubMed Katsuno M, Tanaka F, Adachi H et al (2012) Pathogenesis and therapy of spinal and bulbar muscular atrophy (SBMA). Prog Neurobiol 99:246–256CrossRefPubMed
2.
Zurück zum Zitat Giorgetti E, Lieberman AP (2016) Polyglutamine androgen receptor-mediated neuromuscular disease. Cell Mol Life Sci 73(21):3991–3999CrossRefPubMed Giorgetti E, Lieberman AP (2016) Polyglutamine androgen receptor-mediated neuromuscular disease. Cell Mol Life Sci 73(21):3991–3999CrossRefPubMed
3.
Zurück zum Zitat La Spada AR, Wilson EM, Lubahn DB et al (1991) Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature 352:77–79CrossRefPubMed La Spada AR, Wilson EM, Lubahn DB et al (1991) Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature 352:77–79CrossRefPubMed
4.
Zurück zum Zitat 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 35:843–854CrossRefPubMed 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 35:843–854CrossRefPubMed
5.
Zurück zum Zitat Adachi H, Katsuno M, Minamiyama M et al (2005) Widespread nuclear and cytoplasmic accumulation of mutant androgen receptor in SBMA patients. Brain 128:659–670CrossRefPubMed Adachi H, Katsuno M, Minamiyama M et al (2005) Widespread nuclear and cytoplasmic accumulation of mutant androgen receptor in SBMA patients. Brain 128:659–670CrossRefPubMed
6.
Zurück zum Zitat Sorarù G, D’Ascenzo C, Polo A et al (2008) Spinal and bulbar muscular atrophy: skeletal muscle pathology in male patients and heterozygous females. J Neurol Sci 264:100–105CrossRefPubMed Sorarù G, D’Ascenzo C, Polo A et al (2008) Spinal and bulbar muscular atrophy: skeletal muscle pathology in male patients and heterozygous females. J Neurol Sci 264:100–105CrossRefPubMed
7.
Zurück zum Zitat Dejager S, Bry-Gauillard H, Bruckert E et al (2002) A comprehensive endocrine description of Kennedy’s disease revealing androgen insensitivity linked to CAG repeat length. J Clin Endocrinol Metab 87:3893–3901PubMed Dejager S, Bry-Gauillard H, Bruckert E et al (2002) A comprehensive endocrine description of Kennedy’s disease revealing androgen insensitivity linked to CAG repeat length. J Clin Endocrinol Metab 87:3893–3901PubMed
9.
Zurück zum Zitat Hashizume A, Katsuno M, Banno H et al (2012) Longitudinal changes of outcome measures in spinal and bulbar muscular atrophy. Brain 135:2838–2848CrossRefPubMed Hashizume A, Katsuno M, Banno H et al (2012) Longitudinal changes of outcome measures in spinal and bulbar muscular atrophy. Brain 135:2838–2848CrossRefPubMed
10.
Zurück zum Zitat Vagelatos NT, Eslick GD (2013) Type 2 diabetes as a risk factor for Alzheimer’s disease: the confounders, interactions, and neuropathology associated with this relationship. Epidemiol Rev 35:152–160CrossRefPubMed Vagelatos NT, Eslick GD (2013) Type 2 diabetes as a risk factor for Alzheimer’s disease: the confounders, interactions, and neuropathology associated with this relationship. Epidemiol Rev 35:152–160CrossRefPubMed
12.
Zurück zum Zitat Dupuis L, Corcia P, Fergani A et al (2008) Dyslipidemia is a protective factor in amyotrophic lateral sclerosis. Neurology 70:1004–1009CrossRefPubMed Dupuis L, Corcia P, Fergani A et al (2008) Dyslipidemia is a protective factor in amyotrophic lateral sclerosis. Neurology 70:1004–1009CrossRefPubMed
13.
Zurück zum Zitat Kioumourtzoglou MA, Rotem RS, Seals RM et al (2015) Diabetes mellitus, obesity, and diagnosis of amyotrophic lateral sclerosis: a population-based study. JAMA Neurol 72:905–911CrossRefPubMedPubMedCentral Kioumourtzoglou MA, Rotem RS, Seals RM et al (2015) Diabetes mellitus, obesity, and diagnosis of amyotrophic lateral sclerosis: a population-based study. JAMA Neurol 72:905–911CrossRefPubMedPubMedCentral
14.
Zurück zum Zitat Shimojo D, Onodera K, Doi-Torii Y et al (2015) Rapid, efficient, and simple motor neuron differentiation from human pluripotent stem cells. Mol Brain 8:79CrossRefPubMedPubMedCentral Shimojo D, Onodera K, Doi-Torii Y et al (2015) Rapid, efficient, and simple motor neuron differentiation from human pluripotent stem cells. Mol Brain 8:79CrossRefPubMedPubMedCentral
15.
Zurück zum Zitat Hijikata H, Katsuno M, Suzuki K et al (2016) Impaired muscle uptake of creatine in spinal and bulbar muscular atrophy. Ann Clin Transl Neurol 3:537–546CrossRefPubMedPubMedCentral Hijikata H, Katsuno M, Suzuki K et al (2016) Impaired muscle uptake of creatine in spinal and bulbar muscular atrophy. Ann Clin Transl Neurol 3:537–546CrossRefPubMedPubMedCentral
16.
Zurück zum Zitat Nakatsuji H, Kishida K, Kitamura T et al (2010) Dysregulation of glucose, insulin, triglyceride, blood pressure, and oxidative stress after an oral glucose tolerance test in men with abdominal obesity. Metabolism 59:520–526CrossRefPubMed Nakatsuji H, Kishida K, Kitamura T et al (2010) Dysregulation of glucose, insulin, triglyceride, blood pressure, and oxidative stress after an oral glucose tolerance test in men with abdominal obesity. Metabolism 59:520–526CrossRefPubMed
17.
Zurück zum Zitat Matthews DR, Hosker JP, Rudenski AS et al (1985) Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia 28:412–419CrossRefPubMed Matthews DR, Hosker JP, Rudenski AS et al (1985) Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia 28:412–419CrossRefPubMed
18.
Zurück zum Zitat Querin G, Bertolin C, Da Re E et al (2016) Non-neural phenotype of spinal and bulbar muscular atrophy: results from a large cohort of Italian patients. J Neurol Neurosurg Psychiatry 87:810–816CrossRefPubMed Querin G, Bertolin C, Da Re E et al (2016) Non-neural phenotype of spinal and bulbar muscular atrophy: results from a large cohort of Italian patients. J Neurol Neurosurg Psychiatry 87:810–816CrossRefPubMed
19.
Zurück zum Zitat Iida M, Katsuno M, Nakatsuji H et al (2015) Pioglitazone suppresses neuronal and muscular degeneration caused by polyglutamine-expanded androgen receptors. Hum Mol Genet 24:314–329CrossRefPubMed Iida M, Katsuno M, Nakatsuji H et al (2015) Pioglitazone suppresses neuronal and muscular degeneration caused by polyglutamine-expanded androgen receptors. Hum Mol Genet 24:314–329CrossRefPubMed
20.
Zurück zum Zitat Yu IC, Lin HY, Sparks JD et al (2014) Androgen receptor roles in insulin resistance and obesity in males: the linkage of androgen-deprivation therapy to metabolic syndrome. Diabetes 63:3180–3188CrossRefPubMedPubMedCentral Yu IC, Lin HY, Sparks JD et al (2014) Androgen receptor roles in insulin resistance and obesity in males: the linkage of androgen-deprivation therapy to metabolic syndrome. Diabetes 63:3180–3188CrossRefPubMedPubMedCentral
21.
Zurück zum Zitat Maeda N, Shimomura I, Kishida K et al (2002) Diet-induced insulin resistance in mice lacking adiponectin/ACRP30. Nat Med 8:731–737CrossRefPubMed Maeda N, Shimomura I, Kishida K et al (2002) Diet-induced insulin resistance in mice lacking adiponectin/ACRP30. Nat Med 8:731–737CrossRefPubMed
22.
Zurück zum Zitat Cortes CJ, Ling SC, 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 82:295–307CrossRefPubMedPubMedCentral Cortes CJ, Ling SC, 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 82:295–307CrossRefPubMedPubMedCentral
23.
Zurück zum Zitat 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 63:316–328CrossRefPubMedPubMedCentral 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 63:316–328CrossRefPubMedPubMedCentral
24.
Zurück zum Zitat Srikanthan P, Hevener AL, Karlamangla AS (2010) Sarcopenia exacerbates obesity-associated insulin resistance and dysglycemia: findings from the National Health and Nutrition Examination Survey III. PLoS One 5:e10805CrossRefPubMedPubMedCentral Srikanthan P, Hevener AL, Karlamangla AS (2010) Sarcopenia exacerbates obesity-associated insulin resistance and dysglycemia: findings from the National Health and Nutrition Examination Survey III. PLoS One 5:e10805CrossRefPubMedPubMedCentral
25.
Zurück zum Zitat Wijngaarden MA, van der Zon GC, van Dijk KW et al (2013) Effects of prolonged fasting on AMPK signaling, gene expression, and mitochondrial respiratory chain content in skeletal muscle from lean and obese individuals. Am J Physiol Endocrinol Metab 304:E1012–E1021CrossRefPubMed Wijngaarden MA, van der Zon GC, van Dijk KW et al (2013) Effects of prolonged fasting on AMPK signaling, gene expression, and mitochondrial respiratory chain content in skeletal muscle from lean and obese individuals. Am J Physiol Endocrinol Metab 304:E1012–E1021CrossRefPubMed
26.
Zurück zum Zitat Swan JW, Anker SD, Walton C et al (1997) Insulin resistance in chronic heart failure: relation to severity and etiology of heart failure. J Am Coll Cardiol 30:527–532CrossRefPubMed Swan JW, Anker SD, Walton C et al (1997) Insulin resistance in chronic heart failure: relation to severity and etiology of heart failure. J Am Coll Cardiol 30:527–532CrossRefPubMed
28.
Zurück zum Zitat Nishizawa H, Shimomura I, Kishida K et al (2002) Androgens decrease plasma adiponectin, an insulin-sensitizing adipocyte-derived protein. Diabetes 51:2734–2741CrossRefPubMed Nishizawa H, Shimomura I, Kishida K et al (2002) Androgens decrease plasma adiponectin, an insulin-sensitizing adipocyte-derived protein. Diabetes 51:2734–2741CrossRefPubMed
29.
Zurück zum Zitat Craft S, Watson GS (2004) Insulin and neurodegenerative disease: shared and specific mechanisms. Lancet Neurol 3:169–178CrossRefPubMed Craft S, Watson GS (2004) Insulin and neurodegenerative disease: shared and specific mechanisms. Lancet Neurol 3:169–178CrossRefPubMed
30.
Zurück zum Zitat Santiago JA, Potashkin JA (2013) Shared dysregulated pathways lead to Parkinson’s disease and diabetes. Trends Mol Med 19:176–186CrossRefPubMed Santiago JA, Potashkin JA (2013) Shared dysregulated pathways lead to Parkinson’s disease and diabetes. Trends Mol Med 19:176–186CrossRefPubMed
31.
Zurück zum Zitat Lalić NM, Marić J, Svetel M et al (2008) Glucose homeostasis in Huntington disease: abnormalities in insulin sensitivity and early-phase insulin secretion. Arch Neurol 65:476–480CrossRefPubMed Lalić NM, Marić J, Svetel M et al (2008) Glucose homeostasis in Huntington disease: abnormalities in insulin sensitivity and early-phase insulin secretion. Arch Neurol 65:476–480CrossRefPubMed
32.
Zurück zum Zitat Lalić NM, Dragasević N, Stefanova E et al (2010) Impaired insulin sensitivity and secretion in normoglycemic patients with spinocerebellar ataxia type 1. Mov Disord 25:1976–1980CrossRefPubMed Lalić NM, Dragasević N, Stefanova E et al (2010) Impaired insulin sensitivity and secretion in normoglycemic patients with spinocerebellar ataxia type 1. Mov Disord 25:1976–1980CrossRefPubMed
33.
Zurück zum Zitat Yu Z, Wang AM, Adachi H et al (2011) Macroautophagy is regulated by the UPR-mediator CHOP and accentuates the phenotype of SBMA mice. PLoS Genet 7:e1002321CrossRefPubMedPubMedCentral Yu Z, Wang AM, Adachi H et al (2011) Macroautophagy is regulated by the UPR-mediator CHOP and accentuates the phenotype of SBMA mice. PLoS Genet 7:e1002321CrossRefPubMedPubMedCentral
34.
Zurück zum Zitat Navarro G, Allard C, Xu W et al (2015) The role of androgens in metabolism, obesity, and diabetes in males and females. Obesity (Silver Spring) 23:713–719CrossRef Navarro G, Allard C, Xu W et al (2015) The role of androgens in metabolism, obesity, and diabetes in males and females. Obesity (Silver Spring) 23:713–719CrossRef
35.
Zurück zum Zitat Chang PY, Benecke H, Le Marchand-Brustel Y et al (1994) Expression of a dominant-negative mutant human insulin receptor in the muscle of transgenic mice. J Biol Chem 269:16034–16040PubMed Chang PY, Benecke H, Le Marchand-Brustel Y et al (1994) Expression of a dominant-negative mutant human insulin receptor in the muscle of transgenic mice. J Biol Chem 269:16034–16040PubMed
36.
Zurück zum Zitat Hilder TL, Tou JC, Grindeland RE et al (2003) Phosphorylation of insulin receptor substrate-1 serine 307 correlates with JNK activity in atrophic skeletal muscle. FEBS Lett 553:63–67CrossRefPubMed Hilder TL, Tou JC, Grindeland RE et al (2003) Phosphorylation of insulin receptor substrate-1 serine 307 correlates with JNK activity in atrophic skeletal muscle. FEBS Lett 553:63–67CrossRefPubMed
37.
Zurück zum Zitat Minamiyama M, Katsuno M, Adachi H et al (2012) Naratriptan mitigates CGRP1-associated motor neuron degeneration caused by an expanded polyglutamine repeat tract. Nat Med 18:1531–1538CrossRefPubMed Minamiyama M, Katsuno M, Adachi H et al (2012) Naratriptan mitigates CGRP1-associated motor neuron degeneration caused by an expanded polyglutamine repeat tract. Nat Med 18:1531–1538CrossRefPubMed
38.
Zurück zum Zitat Lee CG, Boyko EJ, Strotmeyer ES et al (2011) Association between insulin resistance and lean mass loss and fat mass gain in older men without diabetes mellitus. J Am Geriatr Soc 59:1217–1224CrossRefPubMedPubMedCentral Lee CG, Boyko EJ, Strotmeyer ES et al (2011) Association between insulin resistance and lean mass loss and fat mass gain in older men without diabetes mellitus. J Am Geriatr Soc 59:1217–1224CrossRefPubMedPubMedCentral
39.
Zurück zum Zitat Kalonia H, Kumar P, Kumar A (2010) Pioglitazone ameliorates behavioral, biochemical and cellular alterations in quinolinic acid induced neurotoxicity: possible role of peroxisome proliferator activated receptor-Upsilon (PPARUpsilon) in Huntington’s disease. Pharmacol Biochem Behav 96:115–124CrossRefPubMed Kalonia H, Kumar P, Kumar A (2010) Pioglitazone ameliorates behavioral, biochemical and cellular alterations in quinolinic acid induced neurotoxicity: possible role of peroxisome proliferator activated receptor-Upsilon (PPARUpsilon) in Huntington’s disease. Pharmacol Biochem Behav 96:115–124CrossRefPubMed
40.
Zurück zum Zitat Dehmer T, Heneka MT, Sastre M et al (2004) Protection by pioglitazone in the MPTP model of Parkinson’s disease correlates with I kappa B alpha induction and block of NF kappa B and iNOS activation. J Neurochem 88:494–501CrossRefPubMed Dehmer T, Heneka MT, Sastre M et al (2004) Protection by pioglitazone in the MPTP model of Parkinson’s disease correlates with I kappa B alpha induction and block of NF kappa B and iNOS activation. J Neurochem 88:494–501CrossRefPubMed
41.
Zurück zum Zitat Kiaei M, Kipiani K, Chen J et al (2005) Peroxisome proliferator-activated receptor-gamma agonist extends survival in transgenic mouse model of amyotrophic lateral sclerosis. Exp Neurol 191:331–336CrossRefPubMed Kiaei M, Kipiani K, Chen J et al (2005) Peroxisome proliferator-activated receptor-gamma agonist extends survival in transgenic mouse model of amyotrophic lateral sclerosis. Exp Neurol 191:331–336CrossRefPubMed
Metadaten
Titel
Correlation of insulin resistance and motor function in spinal and bulbar muscular atrophy
verfasst von
Hideaki Nakatsuji
Amane Araki
Atsushi Hashizume
Yasuhiro Hijikata
Shinichiro Yamada
Tomonori Inagaki
Keisuke Suzuki
Haruhiko Banno
Noriaki Suga
Yohei Okada
Manabu Ohyama
Tohru Nakagawa
Ken Kishida
Tohru Funahashi
Iichiro Shimomura
Hideyuki Okano
Masahisa Katsuno
Gen Sobue
Publikationsdatum
22.02.2017
Verlag
Springer Berlin Heidelberg
Erschienen in
Journal of Neurology / Ausgabe 5/2017
Print ISSN: 0340-5354
Elektronische ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-017-8405-3

Weitere Artikel der Ausgabe 5/2017

Journal of Neurology 5/2017 Zur Ausgabe

Leitlinien kompakt für die Neurologie

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Niedriger diastolischer Blutdruck erhöht Risiko für schwere kardiovaskuläre Komplikationen

25.04.2024 Hypotonie Nachrichten

Wenn unter einer medikamentösen Hochdrucktherapie der diastolische Blutdruck in den Keller geht, steigt das Risiko für schwere kardiovaskuläre Ereignisse: Darauf deutet eine Sekundäranalyse der SPRINT-Studie hin.

Frühe Alzheimertherapie lohnt sich

25.04.2024 AAN-Jahrestagung 2024 Nachrichten

Ist die Tau-Last noch gering, scheint der Vorteil von Lecanemab besonders groß zu sein. Und beginnen Erkrankte verzögert mit der Behandlung, erreichen sie nicht mehr die kognitive Leistung wie bei einem früheren Start. Darauf deuten neue Analysen der Phase-3-Studie Clarity AD.

Viel Bewegung in der Parkinsonforschung

25.04.2024 Parkinson-Krankheit Nachrichten

Neue arznei- und zellbasierte Ansätze, Frühdiagnose mit Bewegungssensoren, Rückenmarkstimulation gegen Gehblockaden – in der Parkinsonforschung tut sich einiges. Auf dem Deutschen Parkinsonkongress ging es auch viel um technische Innovationen.

Demenzkranke durch Antipsychotika vielfach gefährdet

23.04.2024 Demenz Nachrichten

Wenn Demenzkranke aufgrund von Symptomen wie Agitation oder Aggressivität mit Antipsychotika behandelt werden, sind damit offenbar noch mehr Risiken verbunden als bislang angenommen.

Update Neurologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.