Comparison of weakness progression in inclusion body myositis during treatment with methotrexate or placebo

We investigated whether 5 to 20mg per week oral methotrexate could slow down disease progression in 44 patients with inclusion body myositis in a randomized double‐blind placebo‐controlled study over 48 weeks. Mean change of quantitative muscle strength testing sum scores was the primary study outcome measure. Quantitative muscle strength testing sum scores declined in both treatment groups, −0.2% for methotrexate and −3.4% for placebo (95% confidence interval = −2.5% to +9.1% for difference). There were also no differences in manual muscle testing sum scores, activity scale scores and patients' own assessments after 48 weeks of treatment. Serum creatine kinase activity decreased significantly in the methotrexate group. We conclude that oral methotrexate did not slow down progression of muscle weakness but decreased serum creatine kinase activity.

[1]  M. Goedert,et al.  Tau proteins with FTDP‐17 mutations have a reduced ability to promote microtubule assembly , 1998, FEBS letters.

[2]  Carol P. Geer,et al.  Interstitial fluid flow along white matter tracts: A potentially important mechanism for the dissemination of primary brain tumors , 1997, Journal of Neuro-Oncology.

[3]  R. Rau,et al.  Long-term treatment of destructive rheumatoid arthritis with methotrexate. , 1997, The Journal of rheumatology.

[4]  P. Wall,et al.  Textbook of pain , 1989 .

[5]  Robert Turner,et al.  Diffusion and perfusion magnetic resonance imaging in brain tumors , 1993, Topics in magnetic resonance imaging : TMRI.

[6]  P A Bandettini,et al.  Relationship between Finger Movement Rate and Functional Magnetic Resonance Signal Change in Human Primary Motor Cortex , 1996, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[7]  N. Kennaway,et al.  Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene. , 2000, American journal of human genetics.

[8]  Karl J. Friston,et al.  Multisubject fMRI Studies and Conjunction Analyses , 1999, NeuroImage.

[9]  M. Han,et al.  Brain abscess and necrotic or cystic brain tumor: discrimination with signal intensity on diffusion-weighted MR imaging. , 1998, AJR. American journal of roentgenology.

[10]  J. Vallat,et al.  Endoneurial proliferation of perineurial cells in leprosy , 2004, Acta Neuropathologica.

[11]  W. Kamphorst,et al.  Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22. , 2001, Brain : a journal of neurology.

[12]  R. Weller,et al.  THE BLOOD‐NERVE BARRIER AND RECONSTITUTION OF THE PERINEURIUM FOLLOWING NERVE GRAFTING , 1979, Neuropathology and applied neurobiology.

[13]  W. Engel,et al.  Abnormal accumulation of prion protein mRNA in muscle fibers of patients with sporadic inclusion-body myositis and hereditary inclusion-body myopathy. , 1994, The American journal of pathology.

[14]  W. Shabana,et al.  Use of diffusion-weighted MR imaging in differential diagnosis between intracerebral necrotic tumors and cerebral abscesses. , 1999, AJNR. American journal of neuroradiology.

[15]  S. Spector,et al.  A controlled study of intravenous immunoglobulin combined with prednisone in the treatment of IBM , 2001, Neurology.

[16]  J. Grafman,et al.  Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation , 2000, Annals of neurology.

[17]  M. Goedert,et al.  Pick’s disease: hyperphosphorylated tau protein segregates to the somatoaxonal compartment , 1996, Acta Neuropathologica.

[18]  Karl J. Friston,et al.  Psychophysiological and Modulatory Interactions in Neuroimaging , 1997, NeuroImage.

[19]  D. Dickson Pick's Disease: A Modern Approach , 1998, Brain pathology.

[20]  M. Bronskill,et al.  Anisotropy of NMR properties of tissues , 1994, Magnetic resonance in medicine.

[21]  F. Wolfe,et al.  Methotrexate in rheumatoid arthritis. A five-year prospective multicenter study. , 1994, Arthritis and rheumatism.

[22]  C. Beaulieu,et al.  Determinants of anisotropic water diffusion in nerves , 1994, Magnetic resonance in medicine.

[23]  M. Schuelke,et al.  Epilepsia partialis continua associated with a homoplasmic mitochondrial tRNASer(UCN) mutation , 1998, Annals of neurology.

[24]  F. Mahoney,et al.  FUNCTIONAL EVALUATION: THE BARTHEL INDEX. , 2018, Maryland state medical journal.

[25]  Toshinori Hirai,et al.  Usefulness of diffusion‐weighted MRI with echo‐planar technique in the evaluation of cellularity in gliomas , 1999, Journal of magnetic resonance imaging : JMRI.

[26]  E. Mayatepek,et al.  The clinical manifestation of the kwashiorkor syndrome is related to increased lipid peroxidation. , 1998, The Journal of pediatrics.

[27]  M. Toepfer,et al.  High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled study , 2000, Journal of Neurology.

[28]  M. Schuelke,et al.  Treatment of ataxia in isolated vitamin E deficiency caused by alpha-tocopherol transfer protein deficiency. , 1999, The Journal of pediatrics.

[29]  G. Tate,et al.  A novel mutation of desert hedgehog in a patient with 46,XY partial gonadal dysgenesis accompanied by minifascicular neuropathy. , 2000, American journal of human genetics.

[30]  H. Mitsumoto,et al.  Perineurioma as the cause of localized hypertrophic neuropathy , 1980, Muscle & nerve.

[31]  A. Sinclair,et al.  Genetic evidence equating SRY and the testis-determining factor , 1990, Nature.

[32]  R. Wanders,et al.  Cerebellar hypoplasia in respiratory chain dysfunction. , 1996, Neuropediatrics.

[33]  S. Dimauro,et al.  Mutations in mtDNA: Are We Scraping the Bottom of the Barrel? , 2000, Brain pathology.

[34]  W. Jurecka,et al.  Regeneration of a transected peripheral nerve , 1975, Acta Neuropathologica.

[35]  Mahoney Fi,et al.  FUNCTIONAL EVALUATION: THE BARTHEL INDEX. , 1965 .

[36]  B. Day,et al.  Interhemispheric inhibition of the human motor cortex. , 1992, The Journal of physiology.

[37]  G. Geffen,et al.  Interhemispheric control of manual motor activity , 1994, Behavioural Brain Research.

[38]  E. Mayatepek,et al.  Leukotrienes: Biosynthesis, Metabolism, and Pathophysiologic Significance , 1995, Pediatric Research.

[39]  Shin J. Oh,et al.  Rimmed vacuoles of inclusion body myositis and oculopharyngeal muscular dystrophy contain amyloid precursor protein and lysosomal markers , 1993, Brain Research.

[40]  C. Moraes,et al.  An out‐of‐frame cytochrome b gene deletion from a patient with parkinsonism is associated with impaired complex III assembly and an increase in free radical production , 2000, Annals of neurology.

[41]  R D Tien,et al.  MR imaging of high-grade cerebral gliomas: value of diffusion-weighted echoplanar pulse sequences. , 1994, AJR. American journal of roentgenology.

[42]  R. J. Harris,et al.  Septo-optic dysplasia with growth hormone deficiency (De Morsier syndrome). , 1972, Archives of disease in childhood.

[43]  F. Breedveld,et al.  Epidemiology of inclusion body myositis in the Netherlands: A nationwide study , 2000, Neurology.

[44]  Jen-Chuen Hsieh,et al.  Central representation of chronic ongoing neuropathic pain studied by positron emission tomography , 1995, PAIN®.

[45]  E. Mandelkow,et al.  Phosphorylation that detaches tau protein from microtubules (Ser262, Ser214) also protects it against aggregation into Alzheimer paired helical filaments. , 1999, Biochemistry.

[46]  Sinisa Pajevic,et al.  Color schemes to represent the orientation of anisotropic tissues from diffusion tensor data: Application to white matter fiber tract mapping in the human brain , 1999, Magnetic resonance in medicine.

[47]  P. Hof,et al.  Specific Pathological Tau Protein Variants Characterize Pick's Disease , 1996, Journal of neuropathology and experimental neurology.

[48]  J. M. Taylor,et al.  Diffusion magnetic resonance imaging: an early surrogate marker of therapeutic efficacy in brain tumors. , 2000, Journal of the National Cancer Institute.

[49]  Ronald C. Petersen,et al.  Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 , 1998, Nature.

[50]  T. L. Davis,et al.  Morphometry of in vivo human white matter association pathways with diffusion‐weighted magnetic resonance imaging , 1997, Annals of neurology.

[51]  S. Stone-Elander,et al.  Anticipatory coping of pain expressed in the human anterior cingulate cortex: a positron emission tomography study , 1999, Neuroscience Letters.

[52]  J. Hsieh,et al.  PET study on central processing of pain in trigeminal neuropathy , 1999, European journal of pain.

[53]  J. Nakae,et al.  A novel mutation localized in the 3' non-HMG box region of the SRY gene in 46,XY gonadal dysgenesis. , 1994, Human molecular genetics.

[54]  M. Guazzelli,et al.  Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits. , 1999, Journal of neuropathology and experimental neurology.

[55]  B. Katirji Diagnostic Criteria for Neuromuscular Disorders , 1994, Neurology.

[56]  G. Pfurtscheller,et al.  EEG-based discrimination between imagination of right and left hand movement. , 1997, Electroencephalography and clinical neurophysiology.

[57]  E. Vilain,et al.  Pathology of 46,XY pure gonadal dysgenesis: absence of testis differentiation associated with mutations in the testis-determining factor. , 1993, Differentiation; research in biological diversity.

[58]  J. Dambrosia,et al.  Treatment of inclusion-body myositis with IVIg , 1997, Neurology.

[59]  A. Munnich,et al.  The neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome mtDNA mutation (T8993G) triggers muscle ATPase deficiency and hypocitrullinaemia , 1999, European Journal of Pediatrics.

[60]  Y. Ono,et al.  Phosphorylation of Tau Is Regulated by PKN* , 2001, The Journal of Biological Chemistry.

[61]  J. Hodges,et al.  Tau Gene Mutation K257T Causes a Tauopathy Similar to Pick's Disease , 2000, Journal of neuropathology and experimental neurology.

[62]  A. Schnaufer,et al.  Antimycin A resistance in a mutant Leishmania tarentolae strain is correlated to a point mutation in the mitochondrial apocytochrome b gene , 2000, Current Genetics.

[63]  T. Cotter,et al.  Reactive Oxygen Species as Mediators of Photoreceptor Apoptosisin Vitro , 1999 .

[64]  P M Matthews,et al.  An fMRI study of the lateralization of motor cortex activation in acallosal patients , 2000, Neuroreport.

[65]  J G Pipe,et al.  In vivo MR determination of water diffusion coefficients and diffusion anisotropy: correlation with structural alteration in gliomas of the cerebral hemispheres. , 1995, AJNR. American journal of neuroradiology.

[66]  Peter T. Fox,et al.  Imaging human intra‐cerebral connectivity by PET during TMS , 1997, Neuroreport.

[67]  P. V. van Zijl,et al.  Three‐dimensional tracking of axonal projections in the brain by magnetic resonance imaging , 1999, Annals of neurology.

[68]  J. Ashburner,et al.  Nonlinear spatial normalization using basis functions , 1999, Human brain mapping.

[69]  M. Solaiyappan,et al.  In vivo three‐dimensional reconstruction of rat brain axonal projections by diffusion tensor imaging , 1999, Magnetic resonance in medicine.

[70]  A. Engel,et al.  Sporadic inclusion body myositis: Counts of different types of abnormal fibers , 1996, Annals of neurology.

[71]  A. Oldfors,et al.  Inclusion body myositis: clinical, morphological, physiological and laboratory findings in 18 cases , 1994, Acta Neurologica Scandinavica.

[72]  G. Schellenberg,et al.  Tau is a candidate gene for chromosome 17 frontotemporal dementia , 1998, Annals of neurology.

[73]  U. Ziemann,et al.  Hemispheric asymmetry of transcallosalinhibition in man , 2004, Experimental Brain Research.

[74]  C. Duijn,et al.  High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands. , 1999, American journal of human genetics.

[75]  N. Cairns,et al.  Tau proteins of alzheimer paired helical filaments: Abnormal phosphorylation of all six brain isoforms , 1992, Neuron.

[76]  G. Pearlson,et al.  Diffusion Tensor Imaging and Axonal Tracking in the Human Brainstem , 2001, NeuroImage.

[77]  W. Kamphorst,et al.  Tau pathology in two Dutch families with mutations in the microtubule-binding region of tau. , 1998, The American journal of pathology.

[78]  P. Basser,et al.  Estimation of the effective self-diffusion tensor from the NMR spin echo. , 1994, Journal of magnetic resonance. Series B.

[79]  S. Röricht,et al.  Topography of fibers in the human corpus callosum mediating interhemispheric inhibition between the motor cortices , 1998, Annals of neurology.

[80]  I. D. de Coo,et al.  A 4–base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome , 1999, Annals of neurology.

[81]  P. Matthews,et al.  Functional MRI cerebral activation and deactivation during finger movement , 2000, Neurology.

[82]  J. Muscat,et al.  Treatment of recurrent high grade astrocytoma; results of a systematic review of 1,415 patients. , 1998, Anticancer research.

[83]  P H Plotz,et al.  The Treatment of Inclusion Body Myositis: A Retrospective Review and a Randomized, Prospective Trial of Immunosuppressive , 1993, Medicine.

[84]  J Deisenhofer,et al.  Crystal structure of the cytochrome bc1 complex from bovine heart mitochondria. , 1997, Science.

[85]  H. T. ter Laak,et al.  Lethal infantile mitochondrial disease with isolated complex I deficiency in fibroblasts but with combined complex I and IV deficiencies in muscle , 1996, Neurology.

[86]  A Klug,et al.  Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[87]  P. Basser,et al.  Toward a quantitative assessment of diffusion anisotropy , 1996, Magnetic resonance in medicine.

[88]  W. Engel,et al.  Sporadic inclusion-body myositis and its similarities to Alzheimer disease brain. Recent approaches to diagnosis and pathogenesis, and relation to aging. , 1998, Scandinavian journal of rheumatology.

[89]  J. Martinez-Barbera,et al.  Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse , 1998, Nature Genetics.

[90]  W J Litchy,et al.  Inclusion body myositis. Observations in 40 patients. , 1989, Brain : a journal of neurology.

[91]  F. Gabreëls,et al.  Clinical heterogeneity in respiratory chain complex III deficiency in childhood , 1997, Journal of the Neurological Sciences.

[92]  Emery Diagnostic Criteria for Neuromuscular Disorders , 1997 .

[93]  E. Mandelkow,et al.  Structure of tau protein and assembly into paired helical filaments. , 2000, Biochimica et biophysica acta.

[94]  A. Munnich,et al.  Superoxide-induced massive apoptosis in cultured skin fibroblasts harboring the neurogenic ataxia retinitis pigmentosa (NARP) mutation in the ATPase-6 gene of the mitochondrial DNA. , 2001, Human molecular genetics.

[95]  U. Ziemann,et al.  Hemispheric asymmetry of transcallosal inhibition in man. , 1995, Experimental brain research.

[96]  R. Crowther,et al.  Pick's disease associated with the novel Tau gene mutation K369I , 2001, Annals of neurology.

[97]  T. Cotter,et al.  Reactive oxygen species as mediators of photoreceptor apoptosis in vitro. , 1999, Experimental cell research.

[98]  K. Arimura,et al.  Polyneuropathy with minifascicle formation in a patient with 46XY mixed gonadal dysgenesis , 1999, Acta Neuropathologica.

[99]  A. Munnich,et al.  A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure , 2001, Nature Genetics.

[100]  P. Matthews,et al.  Cerebral dysgenesis and lactic acidemia: an MRI/MRS phenotype associated with pyruvate dehydrogenase deficiency. , 1994, Pediatric neurology.

[101]  L. Lemieux,et al.  Diffusion tensor imaging demonstrates deviation of fibres in normal appearing white matter adjacent to a brain tumour , 2000, Journal of neurology, neurosurgery, and psychiatry.

[102]  D. Wade,et al.  The Rivermead Mobility Index: a further development of the Rivermead Motor Assessment. , 1991, International disability studies.

[103]  J. Hardy,et al.  Pick's disease is associated with mutations in the tau gene , 2000, Annals of neurology.

[104]  M. Davison,et al.  Identification of 3‐ and 4‐repeat tau isoforms within the PHF in Alzheimer's disease. , 1991, The EMBO journal.

[105]  P. McDonough,et al.  The presence of the testicular determining sequence, SRY, in 46,XY females with gonadal dysgenesis (Swyer syndrome). , 1991, American journal of obstetrics and gynecology.