Myoglobinuria and COX deficiency in a patient taking cerivastatin and gemfibrozil

被引:10
作者
Arenas, J
Fernández-Moreno, MA
Molina, JA
Fernández, V
del Hoyo, P
Campos, Y
Calvo, P
Martín, MA
García, A
Moreno, T
Martínez-Salio, A
Börnstein, B
Bermejo, F
Cabello, A
Garesse, R
机构
[1] Univ Madrid, Hosp 12 Octubre, Ctr Invest, Madrid 28041, Spain
[2] Univ Madrid, Hosp 12 Octubre, Serv Neurol, Madrid 28041, Spain
[3] Univ Madrid, Hosp 12 Octubre, Serv Anat Patol, Madrid 28041, Spain
[4] UAM, CSIC, Inst Invest Biomed Alberto Sols, Madrid, Spain
关键词
D O I
10.1212/01.WNL.0000042050.85041.FB
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The authors describe a patient who presented with myoglobinuria after starting cerivastatin-gemfibrozil therapy. Muscle histochemistry revealed ragged-red fibers and cytochrome c oxidase negative (COX) fibers, and biochemistry showed a defect of COX activity. Immunoblot analysis showed a 60% reduction of COX I and COX II polypeptides. Cerivastatin myotoxicity might be related to a depletion of essential metabolites needed to anchor COX subunit I to mitochondrial membrane.
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页码:124 / 126
页数:3
相关论文
共 9 条
[1]  
DiMauro S, 2000, BRAIN PATHOL, V10, P431
[2]   HMG CoA reductase inhibitor-induced myotoxicity: Pravastatin and lovastatin inhibit the geranylgeranylation of low-molecular-weight proteins in neonatal rat muscle cell culture [J].
Flint, OP ;
Masters, BA ;
Gregg, RE ;
Durham, SK .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1997, 145 (01) :99-110
[3]   LATE-ONSET MITOCHONDRIAL MYOPATHY [J].
JOHNSTON, W ;
KARPATI, G ;
CARPENTER, S ;
ARNOLD, D ;
SHOUBRIDGE, EA .
ANNALS OF NEUROLOGY, 1995, 37 (01) :16-23
[4]   Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA [J].
Karadimas, CL ;
Greenstein, P ;
Sue, CM ;
Joseph, JT ;
Tanji, K ;
Haller, RG ;
Taivassalo, T ;
Davidson, MM ;
Shanske, S ;
Bonilla, E ;
DiMauro, S .
NEUROLOGY, 2000, 55 (05) :644-649
[5]   A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria [J].
Keightley, JA ;
Hoffbuhr, KC ;
Burton, MD ;
Salas, VM ;
Johnston, WSW ;
Penn, AMW ;
Buist, NRM ;
Kennaway, NG .
NATURE GENETICS, 1996, 12 (04) :410-416
[6]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[7]   Familial cerebellar ataxia with muscle coenzyme Q10 deficiency [J].
Musumeci, O ;
Naini, A ;
Slonim, AE ;
Skavin, N ;
Hadjigeorgiou, GL ;
Krawiecki, N ;
Weissman, BM ;
Tsao, CY ;
Mendell, JR ;
Shanske, S ;
De Vivo, DC ;
Hirano, M ;
DiMauro, S .
NEUROLOGY, 2001, 56 (07) :849-855
[8]   Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome [J].
Rieder, MJ ;
Taylor, SL ;
Tobe, VO ;
Nickerson, DA .
NUCLEIC ACIDS RESEARCH, 1998, 26 (04) :967-973
[9]   The whole structure of the 13-subunit oxidized cytochrome c oxidase at 2.8 angstrom [J].
Tsukihara, T ;
Aoyama, H ;
Yamashita, E ;
Tomizaki, T ;
Yamaguchi, H ;
ShinzawaItoh, K ;
Nakashima, R ;
Yaono, R ;
Yoshikawa, S .
SCIENCE, 1996, 272 (5265) :1136-1144