Cross-sectional and longitudinal analysis of an oxidative stress biomarker for spinal and bulbar muscular atrophy

被引:12
作者
Mano, Tomoo [1 ]
Katsuno, Masahisa [1 ]
Banno, Haruhiko [1 ,2 ]
Suzuki, Keisuke [1 ]
Suga, Noriaki [1 ]
Hashizume, Atsushi [1 ]
Tanaka, Fumiaki [1 ]
Sobue, Gen [1 ]
机构
[1] Nagoya Univ, Dept Neurol, Grad Sch Med, Showa Ku, Nagoya, Aichi 4668550, Japan
[2] Nagoya Univ, Inst Adv Res, Nagoya, Aichi 4668550, Japan
基金
日本科学技术振兴机构;
关键词
androgen receptor; biomarker; motor neuron; oxidative stress; spinal and bulbar muscular atrophy; 6-MINUTE WALK TEST; BULBOSPINAL NEURONOPATHY; DISEASE PATHOGENESIS; PARKINSONS-DISEASE; FRIEDREICHS-ATAXIA; KENNEDY-DISEASE; DNA-DAMAGE; CAG REPEAT; NEURODEGENERATION; PERSPECTIVES;
D O I
10.1002/mus.23413
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Spinal and bulbar muscular atrophy (SBMA) is an adult-onset motor neuron disease caused by a CAG repeat expansion in the androgen receptor gene. The aim of this study was to verify whether urinary 8-hydroxydeoxyguanosine (8-OHdG), an oxidative stress marker, is a biomarker for SBMA. Methods: We measured the levels of urinary 8-OHdG in 33 genetically confirmed SBMA patients and 32 age-matched controls over a 24-month period at 6-month intervals. Results: Urinary 8-OHdG levels in SBMA patients were significantly elevated compared with those of controls and correlated well with motor function scores. During the follow-up period, urinary 8-OHdG levels increased and correlated with motor function at each time-point. In addition, urinary 8-OHdG levels at baseline were correlated with changes in the 6-minute walk test during 24 months. Conclusions: Urinary 8-OHdG is a biomarker for SBMA, reflecting the severity and possibly predicting the deterioration of motor function. Muscle Nerve, 2012
引用
收藏
页码:692 / 697
页数:6
相关论文
共 44 条
[1]   Oxidative DNA damage in the parkinsonian brain: An apparent selective increase in 8-hydroxyguanine levels in substantia nigra [J].
Alam, ZI ;
Jenner, A ;
Daniel, SE ;
Lees, AJ ;
Cairns, N ;
Marsden, CD ;
Jenner, P ;
Halliwell, B .
JOURNAL OF NEUROCHEMISTRY, 1997, 69 (03) :1196-1203
[2]   Rethinking genotype and phenotype correlations in polyglutamine expansion disorders [J].
Andrew, SE ;
Goldberg, YP ;
Hayden, MR .
HUMAN MOLECULAR GENETICS, 1997, 6 (12) :2005-2010
[3]   Natural history of spinal and bulbar muscular atrophy (SBMA): a study of 223 Japanese patients [J].
Atsuta, Naoki ;
Watanabe, Hirohisa ;
Ito, Mizuki ;
Banno, Haruhiko ;
Suzuki, Keisuke ;
Katsuno, Masahisa ;
Tanaka, Fumiaki ;
Tamakoshi, Akiko ;
Sobue, Gen .
BRAIN, 2006, 129 :1446-1455
[4]   Mutant androgen receptor accumulation in spinal and bulbar muscular atrophy scrotal skin: A pathogenic marker [J].
Banno, H ;
Adachi, H ;
Katsuno, M ;
Suzuki, K ;
Atsuta, N ;
Watanabe, H ;
Tanaka, F ;
Doyu, M ;
Sobue, G .
ANNALS OF NEUROLOGY, 2006, 59 (03) :520-526
[5]   Neurological Effects of Recombinant Human Erythropoietin in Friedreich's Ataxia: A Clinical Pilot Trial [J].
Boesch, Sylvia ;
Sturm, Brigitte ;
Hering, Sascha ;
Scheiber-Mojdehkar, Barbara ;
Steinkellner, Hannes ;
Goldenberg, Hans ;
Poewe, Werner .
MOVEMENT DISORDERS, 2008, 23 (13) :1940-1944
[6]   Mitochondria and Huntington's Disease Pathogenesis Insight from Genetic and Chemical Models [J].
Browne, Susan E. .
MITOCHONDRIA AND OXIDATIVE STRESS IN NEURODEGENERATIVE DISORDERS, 2008, 1147 :358-382
[7]   Increased isoprostane and prostaglandin are prominent in neurons in Alzheimer disease [J].
Casadesus, Gemma ;
Smith, Mark A. ;
Basu, Samar ;
Hua, Jing ;
Capobianco, Dae E. ;
Siedlak, Sandra L. ;
Zhu, Xiongwei ;
Perry, George .
MOLECULAR NEURODEGENERATION, 2007, 2 (1)
[8]   ATS statement: Guidelines for the six-minute walk test [J].
Crapo, RO ;
Casaburi, R ;
Coates, AL ;
Enright, PL ;
MacIntyre, NR ;
McKay, RT ;
Johnson, D ;
Wanger, JS ;
Zeballos, RJ ;
Bittner, V ;
Mottram, C .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 166 (01) :111-117
[9]   Transcriptional repression of PGC-α by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration [J].
Cui, Libin ;
Jeong, Hyunkyung ;
Borovecki, Fran ;
Parkhurst, Christopher N. ;
Tanese, Naoko ;
Krainc, Dimitri .
CELL, 2006, 127 (01) :59-69
[10]   A comprehensive endocrine description of Kennedy's disease revealing androgen insensitivity linked to CAG repeat length [J].
Dejager, S ;
Bry-Gauillard, H ;
Bruckert, E ;
Eymard, B ;
Salachas, F ;
Leguern, E ;
Tardieu, S ;
Chadarevian, R ;
Giral, P ;
Turpin, G .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (08) :3893-3901