Skip to main content
Top
Published in: Pediatric Drugs 6/2009

01-12-2009 | Review Article

Juvenile Dermatomyositis

Advances in Pathogenesis, Evaluation, and Treatment

Author: Dr Adam M. Huber

Published in: Pediatric Drugs | Issue 6/2009

Login to get access

Abstract

Juvenile dermatomyositis (JDM) is a rare, presumably autoimmune illness that causes proximal muscle weakness and a variety of typical cutaneous features. The study of this illness has been hampered by its rarity but, in recent years, important developments have increased our understanding of JDM. Genetic factors are likely important in the pathogenesis of JDM. These include several Human Leukocyte Antigen alleles, in particular those associated with the 8.1 ancestral haplotype and the tumor necrosis factor-α gene 308 polymorphism. Microchimerism, activation of plasmacytoid dendritic cells, and upregulation of type-1 interferon inducible genes also appear to play an important role in the pathogenesis of JDM.
The study of JDM has also been limited by a lack of validated assessment tools. Recent work has validated the Childhood Myositis Assessment Scale and the Childhood Health Assessment Questionnaire as measures of muscle strength and function, and the Cutaneous Assessment Tool as a measure of skin disease activity and damage. Development of core sets of tools that should be used in all JDM studies has also been an important step. The use of magnetic resonance imaging and novel laboratory assessments (such as type-1 interferon inducible gene products, peripheral blood B cell and natural killer cell numbers, and myositis-associated and myositis-specific autoantibodies) are also playing an increasing role in the diagnosis and assessment of JDM.
Current treatment is with corticosteroids, frequently in combination with other medications such as methotrexate or intravenous gammaglobulin. Newer therapies, such as anti-tumor necrosis factor agents and rituximab are currently being evaluated; it is not clear what role these medications will have in the future.
Literature
1.
go back to reference Mendez EP, Lipton R, Ramsey-Goldman R, et al. US incidence of juvenile dermatomyositis, 1995–1998: results from the National Institute of Arthritis and Musculoskeletal and Skin Diseases Registry. Arthritis Rheum 2003; 49(3): 300–5PubMedCrossRef Mendez EP, Lipton R, Ramsey-Goldman R, et al. US incidence of juvenile dermatomyositis, 1995–1998: results from the National Institute of Arthritis and Musculoskeletal and Skin Diseases Registry. Arthritis Rheum 2003; 49(3): 300–5PubMedCrossRef
2.
go back to reference Feldman BM, Rider LG, Reed AM, et al. Juvenile dermatomyositis and other idiopathic inflammatory myopathies of childhood. Lancet 2008; 371: 2201–12PubMedCrossRef Feldman BM, Rider LG, Reed AM, et al. Juvenile dermatomyositis and other idiopathic inflammatory myopathies of childhood. Lancet 2008; 371: 2201–12PubMedCrossRef
3.
go back to reference Pachman LM. Juvenile dermatomyositis: pathophysiology and disease expression. Pediatr Clin North Am 1995; 42(5): 1071–98PubMed Pachman LM. Juvenile dermatomyositis: pathophysiology and disease expression. Pediatr Clin North Am 1995; 42(5): 1071–98PubMed
4.
go back to reference Wedderburn L, McHugh N, Chinoy H, et al. HLA class II haplotype and autoantibody associations in children with juvenile dermatomyositis and juvenile dermatomyositis-scleroderma overlap. Rheumatology 2007; 46:1786–9PubMedCrossRef Wedderburn L, McHugh N, Chinoy H, et al. HLA class II haplotype and autoantibody associations in children with juvenile dermatomyositis and juvenile dermatomyositis-scleroderma overlap. Rheumatology 2007; 46:1786–9PubMedCrossRef
5.
go back to reference Candore G, Lio D, Colanna Romano G, et al. Pathogenesis of autoimmune diseases associated with 8.1 ancestral haplotype: effect of multiple gene interactions. Autoimmun Rev 2002; 1(1–2): 29–35PubMedCrossRef Candore G, Lio D, Colanna Romano G, et al. Pathogenesis of autoimmune diseases associated with 8.1 ancestral haplotype: effect of multiple gene interactions. Autoimmun Rev 2002; 1(1–2): 29–35PubMedCrossRef
6.
go back to reference Mamyrova G, O’Hanlon T, Monroe J, et al. Immunogenetic risk and protective factors for juvenile dermatomyositis in Caucasians. Arthritis Rheum 2006; 54(12): 3979–87PubMedCrossRef Mamyrova G, O’Hanlon T, Monroe J, et al. Immunogenetic risk and protective factors for juvenile dermatomyositis in Caucasians. Arthritis Rheum 2006; 54(12): 3979–87PubMedCrossRef
7.
go back to reference O’Hanlon T, Rider LG, Mamyrova G, et al. HLA polymorphisms in African Americans with idiopathic inflammatory myopathy. Arthritis Rheum 2006; 54(11): 3670–81PubMedCrossRef O’Hanlon T, Rider LG, Mamyrova G, et al. HLA polymorphisms in African Americans with idiopathic inflammatory myopathy. Arthritis Rheum 2006; 54(11): 3670–81PubMedCrossRef
8.
go back to reference Tomono N, Mori M, Nakajima S, et al. HLA-DRBl*15021 is the predominant allele in Japanese patients with juvenile dermatomyositis. J Rheumatol 2004; 31(9): 1847–50PubMed Tomono N, Mori M, Nakajima S, et al. HLA-DRBl*15021 is the predominant allele in Japanese patients with juvenile dermatomyositis. J Rheumatol 2004; 31(9): 1847–50PubMed
9.
go back to reference Pachman LM, Liotta-Davis M, Hong D, et al. TNFa-308A allele in juvenile dermatomyositis-association with increased TNF-alpha production, disease duration, and pathologic calcifications. Arthritis Rheum 2000; 43: 2368–77PubMedCrossRef Pachman LM, Liotta-Davis M, Hong D, et al. TNFa-308A allele in juvenile dermatomyositis-association with increased TNF-alpha production, disease duration, and pathologic calcifications. Arthritis Rheum 2000; 43: 2368–77PubMedCrossRef
10.
go back to reference Pachman LM, Fedczyna T, Lutz J, et al. Juvenile dermatomyositis: the association of the TNFa-308 allele and disease chronicity. Curr Opin Rheumatol 2001; 5: 379–86 Pachman LM, Fedczyna T, Lutz J, et al. Juvenile dermatomyositis: the association of the TNFa-308 allele and disease chronicity. Curr Opin Rheumatol 2001; 5: 379–86
11.
go back to reference Pachman LM, Lingen M, Caliendo J, et al. Muscle biopsy findings in 38 untreated children with juvenile dermatomyositis (JDM): capillary occlusion is associated with the TNF-alpha allele [abstract]. Arthritis Rheum 1999; 42 Suppl.: S403 Pachman LM, Lingen M, Caliendo J, et al. Muscle biopsy findings in 38 untreated children with juvenile dermatomyositis (JDM): capillary occlusion is associated with the TNF-alpha allele [abstract]. Arthritis Rheum 1999; 42 Suppl.: S403
12.
go back to reference Lutz J, Huwiler K, Fedczyna T, et al. Increased plasma thrombospondin-1 (TSP-1) levels are associated with the TNF alpha-308A allele in children with juvenile dermatomyositis. Clin Immunol 2002; 103: 260–3PubMedCrossRef Lutz J, Huwiler K, Fedczyna T, et al. Increased plasma thrombospondin-1 (TSP-1) levels are associated with the TNF alpha-308A allele in children with juvenile dermatomyositis. Clin Immunol 2002; 103: 260–3PubMedCrossRef
13.
go back to reference Chinoy H, Salway F, John S, et al. Tumour necrosis factor-alpha single nucleotide polymorphisms are not independent of HLA class I in UK Caucasians with adult onset idiopathic inflammatory myopathies. Rheumatology 2007; 46:1411–6PubMedCrossRef Chinoy H, Salway F, John S, et al. Tumour necrosis factor-alpha single nucleotide polymorphisms are not independent of HLA class I in UK Caucasians with adult onset idiopathic inflammatory myopathies. Rheumatology 2007; 46:1411–6PubMedCrossRef
14.
go back to reference Hassan A, Nikitina-Zake L, Sanjeevi C, et al. Association of the proinflammatory haplotype (MICA5.1/TNF2/TNFa2/DRB1*03) with polymyositis and dermatomyositis. Arthritis Rheum 2004; 50(3): 1013–5PubMedCrossRef Hassan A, Nikitina-Zake L, Sanjeevi C, et al. Association of the proinflammatory haplotype (MICA5.1/TNF2/TNFa2/DRB1*03) with polymyositis and dermatomyositis. Arthritis Rheum 2004; 50(3): 1013–5PubMedCrossRef
15.
go back to reference Reed AM. Microchimerism in children with rheumatic disease: what does it mean? Curr Rheumatol Rep 2003; 5: 458–62PubMedCrossRef Reed AM. Microchimerism in children with rheumatic disease: what does it mean? Curr Rheumatol Rep 2003; 5: 458–62PubMedCrossRef
16.
go back to reference Reed AM, Shock L, Picornell Y. Chimerism in JDM [abstract]. Arthritis Rheum 1999; 41 Suppl.: S362 Reed AM, Shock L, Picornell Y. Chimerism in JDM [abstract]. Arthritis Rheum 1999; 41 Suppl.: S362
17.
go back to reference Artlett C, Miller FW, Rider LG. Persistent maternally derived peripheral microchimerism is associated with the juvenile idiopathic inflammatory myopathies. Rheumatology 2001; 40(11): 1279–84PubMedCrossRef Artlett C, Miller FW, Rider LG. Persistent maternally derived peripheral microchimerism is associated with the juvenile idiopathic inflammatory myopathies. Rheumatology 2001; 40(11): 1279–84PubMedCrossRef
18.
go back to reference Artlett C, Ramos R, Jiminez S, et al. Chimeric cells of maternal origin in juvenile idiopathic inflammatory myopathies. Childhood Myositis Heterogeneity Collaborative Group. Lancet 2000; 356(9248): 2155–6PubMedCrossRef Artlett C, Ramos R, Jiminez S, et al. Chimeric cells of maternal origin in juvenile idiopathic inflammatory myopathies. Childhood Myositis Heterogeneity Collaborative Group. Lancet 2000; 356(9248): 2155–6PubMedCrossRef
19.
go back to reference McNallan K, Reed AM. Immunophenotyping of chimeric cells in juvenile dermatomyositis [abstract]. Arthritis Rheum 2003; 48(9 Suppl.): S104 McNallan K, Reed AM. Immunophenotyping of chimeric cells in juvenile dermatomyositis [abstract]. Arthritis Rheum 2003; 48(9 Suppl.): S104
20.
go back to reference Reed AM, Picornell Y, Harwood A, et al. Chimerism in children with juvenile dermatomyositis. Lancet 2000; 356: 2156–7PubMedCrossRef Reed AM, Picornell Y, Harwood A, et al. Chimerism in children with juvenile dermatomyositis. Lancet 2000; 356: 2156–7PubMedCrossRef
21.
go back to reference Reed AM, McNallan K, Wettstein P, et al. Does HLA-dependant chimerism underlie the pathogenesis of juvenile dermatomyositis? J Immunol 2004; 172: 5041–6PubMed Reed AM, McNallan K, Wettstein P, et al. Does HLA-dependant chimerism underlie the pathogenesis of juvenile dermatomyositis? J Immunol 2004; 172: 5041–6PubMed
22.
go back to reference Bakay M, Wang Z, Melcon G, et al. Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration. Brain 2006; 129: 996–1013PubMedCrossRef Bakay M, Wang Z, Melcon G, et al. Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration. Brain 2006; 129: 996–1013PubMedCrossRef
23.
go back to reference Tezak Z, Hoffman E, Lutz J, et al. Gene expression profiling in DQA1*0501+ children with untreated dermatomyositis: a novel model of pathogenesis. J Immunol 2002; 168(8): 4154–63PubMed Tezak Z, Hoffman E, Lutz J, et al. Gene expression profiling in DQA1*0501+ children with untreated dermatomyositis: a novel model of pathogenesis. J Immunol 2002; 168(8): 4154–63PubMed
24.
go back to reference Greenberg S, Pinkus J, Pinkus G, et al. Interferon-alpha/beta-mediated innate immune mechanisms in dermatomyositis. Ann Neurol 2005; 57(5): 664–78PubMedCrossRef Greenberg S, Pinkus J, Pinkus G, et al. Interferon-alpha/beta-mediated innate immune mechanisms in dermatomyositis. Ann Neurol 2005; 57(5): 664–78PubMedCrossRef
25.
go back to reference Fall N, Bove K, Stringer K, et al. Association between lack of angiogenic response in muscle tissue and high expression of angiostatic ELR-negative CXC chemokines in patients with juvenile dermatomyositis. Arthritis Rheum 2005; 52(10): 3175–80PubMedCrossRef Fall N, Bove K, Stringer K, et al. Association between lack of angiogenic response in muscle tissue and high expression of angiostatic ELR-negative CXC chemokines in patients with juvenile dermatomyositis. Arthritis Rheum 2005; 52(10): 3175–80PubMedCrossRef
26.
go back to reference Christen-Zaech S, Seshadri R, Sundberg J, et al. Persistent association of nailfold capillaroscopy changes and skin involvement over thirty-six months with duration of untreated disease in patients with juvenile dermatomyositis. Arthritis Rheum 2008; 58(2): 571–6PubMedCrossRef Christen-Zaech S, Seshadri R, Sundberg J, et al. Persistent association of nailfold capillaroscopy changes and skin involvement over thirty-six months with duration of untreated disease in patients with juvenile dermatomyositis. Arthritis Rheum 2008; 58(2): 571–6PubMedCrossRef
27.
go back to reference Griffin TA, Reed AM. Pathogenesis of myositis in children. Curr Opin Rheumatol 2007; 19: 489–91CrossRef Griffin TA, Reed AM. Pathogenesis of myositis in children. Curr Opin Rheumatol 2007; 19: 489–91CrossRef
28.
go back to reference O’Connor K, Abbott K, Sabin B, et al. MxA gene expression in juvenile dermatomyositis peripheral blood mononuclear cells: association with muscle involvement. Clin Immunol 2006; 120: 319–25PubMedCrossRef O’Connor K, Abbott K, Sabin B, et al. MxA gene expression in juvenile dermatomyositis peripheral blood mononuclear cells: association with muscle involvement. Clin Immunol 2006; 120: 319–25PubMedCrossRef
29.
go back to reference Baechler E, Bauer J, Slattery C, et al. An interferon signature in the peripheral blood of dermatomyositis patients is associated with disease activity. Mol Med 2007; 13(1–2): 59–68PubMed Baechler E, Bauer J, Slattery C, et al. An interferon signature in the peripheral blood of dermatomyositis patients is associated with disease activity. Mol Med 2007; 13(1–2): 59–68PubMed
30.
go back to reference Chinoy H, Salway F, John S, et al. Interferon-gamma and interleukin-4 gene polymorphisms in Caucasian idiopathic inflammatory myopathy patients in the UK. Ann Rheum Dis 2007; 66: 970–3PubMedCrossRef Chinoy H, Salway F, John S, et al. Interferon-gamma and interleukin-4 gene polymorphisms in Caucasian idiopathic inflammatory myopathy patients in the UK. Ann Rheum Dis 2007; 66: 970–3PubMedCrossRef
31.
go back to reference Page G, Chevrel G, Moissec P. Anatomic localization of immature and mature dendritic cell subsets in dermatomyositis and polymyositis: interaction with chemokines and Th1 cytokine-producing cells. Arthritis Rheum 2004; 50: 199–208PubMedCrossRef Page G, Chevrel G, Moissec P. Anatomic localization of immature and mature dendritic cell subsets in dermatomyositis and polymyositis: interaction with chemokines and Th1 cytokine-producing cells. Arthritis Rheum 2004; 50: 199–208PubMedCrossRef
32.
go back to reference Nagaraju K, Rider LG, Fan C, et al. Endothelial cell activation and neovascularization are prominent in dermatomyositis. J Autoimmune Dis 2006; 20(3): 2CrossRef Nagaraju K, Rider LG, Fan C, et al. Endothelial cell activation and neovascularization are prominent in dermatomyositis. J Autoimmune Dis 2006; 20(3): 2CrossRef
33.
go back to reference Lopez de Padilla C, Vallejo A, McNallan K, et al. Plasmacytoid dendritic cells in inflamed muscle of patients with juvenile dermatomyositis. Arthritis Rheum 2007; 56(5): 1658–68PubMedCrossRef Lopez de Padilla C, Vallejo A, McNallan K, et al. Plasmacytoid dendritic cells in inflamed muscle of patients with juvenile dermatomyositis. Arthritis Rheum 2007; 56(5): 1658–68PubMedCrossRef
34.
go back to reference Pachman LM. Juvenile dermatomyositis: immunogenetics, pathophysiology, and disease expression. Rheum Dis Clin North Am 2002; 28: 579–602PubMedCrossRef Pachman LM. Juvenile dermatomyositis: immunogenetics, pathophysiology, and disease expression. Rheum Dis Clin North Am 2002; 28: 579–602PubMedCrossRef
35.
go back to reference Mamyrova G, Rider LG. Parvovirus B19 and onset of juvenile dermatomyositis. JAMA 2005; 294(17): 2170–1PubMedCrossRef Mamyrova G, Rider LG. Parvovirus B19 and onset of juvenile dermatomyositis. JAMA 2005; 294(17): 2170–1PubMedCrossRef
36.
go back to reference Pachman LM, Hayford J, Hochberg M, et al. New-onset juvenile dermatomyositis: comparisons with a healthy cohort and children the juvenile rheumatoid arthritis. Arthritis Rheum 1997; 40(8): 1526–33PubMedCrossRef Pachman LM, Hayford J, Hochberg M, et al. New-onset juvenile dermatomyositis: comparisons with a healthy cohort and children the juvenile rheumatoid arthritis. Arthritis Rheum 1997; 40(8): 1526–33PubMedCrossRef
37.
go back to reference Pachman LM, Lipton R, Ramsey-Goldman R, et al. History of infection before the onset of juvenile dermatomyositis: results from the National Institute of Arthritis and Musculoskeletal and Skin Diseases Research Registry. Arthritis Rheum 2005; 53(2): 166–72PubMedCrossRef Pachman LM, Lipton R, Ramsey-Goldman R, et al. History of infection before the onset of juvenile dermatomyositis: results from the National Institute of Arthritis and Musculoskeletal and Skin Diseases Research Registry. Arthritis Rheum 2005; 53(2): 166–72PubMedCrossRef
38.
go back to reference Vegosen L, Weinberg C, O’Hanlon T, et al. Seasonal birth patterns in myositis subgroups suggest an etiologic role for early environmental exposures. Arthritis Rheum 2007; 56(8): 2719–28PubMedCrossRef Vegosen L, Weinberg C, O’Hanlon T, et al. Seasonal birth patterns in myositis subgroups suggest an etiologic role for early environmental exposures. Arthritis Rheum 2007; 56(8): 2719–28PubMedCrossRef
39.
go back to reference Massa M, Costouros N, Mazzoli F, et al. Self epitopes shared between human skeletal myosin and Streptococcus pyogenes M5 protein are targets of immune responses in active juvenile dermatomyositis. Arthritis Rheum 2002; 46(11): 3015–25PubMedCrossRef Massa M, Costouros N, Mazzoli F, et al. Self epitopes shared between human skeletal myosin and Streptococcus pyogenes M5 protein are targets of immune responses in active juvenile dermatomyositis. Arthritis Rheum 2002; 46(11): 3015–25PubMedCrossRef
40.
go back to reference Elst E, Klein M, de Jager W, et al. Hsp60 in inflamed muscle tissue is the target of regulatory autoreactive T cells in patients with juvenile dermatomyositis. Arthritis Rheum 2008; 58(2): 547–55PubMedCrossRef Elst E, Klein M, de Jager W, et al. Hsp60 in inflamed muscle tissue is the target of regulatory autoreactive T cells in patients with juvenile dermatomyositis. Arthritis Rheum 2008; 58(2): 547–55PubMedCrossRef
41.
go back to reference Medical Research Council. War memorandum no. 7. Aids to the investigation of peripheral nerve injuries. London: H.M. Stationery Office, 1942 Medical Research Council. War memorandum no. 7. Aids to the investigation of peripheral nerve injuries. London: H.M. Stationery Office, 1942
42.
go back to reference Jain M, Smith M, Cintas H, et al. Intra-rater and inter-rater reliability of the 10-point manual muscle test (MMT) of strength in children with juvenile idiopathic inflammatory myopathies (JIIM). Phys Occup Ther Pediatr 2006; 26(3): 5–17PubMedCrossRef Jain M, Smith M, Cintas H, et al. Intra-rater and inter-rater reliability of the 10-point manual muscle test (MMT) of strength in children with juvenile idiopathic inflammatory myopathies (JIIM). Phys Occup Ther Pediatr 2006; 26(3): 5–17PubMedCrossRef
43.
go back to reference Lovell DJ, Lindsley CB, Rennebohm RM, et al. Development of disease activity and damage indices for the juvenile idiopathic inflammatory myopathies: II. The Childhood Myositis Assessment Scale (CMAS): a quantitative tool for the evaluation of muscle function. Arthritis Rheum 1999; 42(10): 2213–9PubMedCrossRef Lovell DJ, Lindsley CB, Rennebohm RM, et al. Development of disease activity and damage indices for the juvenile idiopathic inflammatory myopathies: II. The Childhood Myositis Assessment Scale (CMAS): a quantitative tool for the evaluation of muscle function. Arthritis Rheum 1999; 42(10): 2213–9PubMedCrossRef
44.
go back to reference Huber AM, Feldman BM, Rennebohm RM, et al. Validation and clinical significance of the Childhood Myositis Assessment Scale (CMAS) for assessment of muscle function in the juvenile idiopathic inflammatory myopathies. Arthritis Rheum 2004; 50(5): 1595–603PubMedCrossRef Huber AM, Feldman BM, Rennebohm RM, et al. Validation and clinical significance of the Childhood Myositis Assessment Scale (CMAS) for assessment of muscle function in the juvenile idiopathic inflammatory myopathies. Arthritis Rheum 2004; 50(5): 1595–603PubMedCrossRef
45.
go back to reference Singh G, Athreya BH, Fries JF, et al. Measurement of health status in children with juvenile rheumatoid arthritis. Arthritis Rheum 1994; 37(12): 1761–9PubMedCrossRef Singh G, Athreya BH, Fries JF, et al. Measurement of health status in children with juvenile rheumatoid arthritis. Arthritis Rheum 1994; 37(12): 1761–9PubMedCrossRef
46.
go back to reference Feldman BM, Ayling-Campos A, Luy L, et al. Measuring disability in juvenile dermatomyositis. Validity of the Childhood Health Assessment Questionnaire. J Rheumatol 1995; 22(2): 326–31PubMed Feldman BM, Ayling-Campos A, Luy L, et al. Measuring disability in juvenile dermatomyositis. Validity of the Childhood Health Assessment Questionnaire. J Rheumatol 1995; 22(2): 326–31PubMed
47.
go back to reference Huber AM, Hicks JE, Lachenbruch PA, et al. Validation of the Childhood Health Assessment Questionnaire in the juvenile idiopathic inflammatory myopathies. J Rheumatol 2001; 28(5): 1106–11PubMed Huber AM, Hicks JE, Lachenbruch PA, et al. Validation of the Childhood Health Assessment Questionnaire in the juvenile idiopathic inflammatory myopathies. J Rheumatol 2001; 28(5): 1106–11PubMed
48.
go back to reference Huber AM, Dugan EM, Lachenbruch PA, et al. The Cutaneous Assessment Tool (CAT): development and reliability in juvenile idiopathic inflammatory myopathy. Rheumatology 2007; 46(10): 1606–11PubMedCrossRef Huber AM, Dugan EM, Lachenbruch PA, et al. The Cutaneous Assessment Tool (CAT): development and reliability in juvenile idiopathic inflammatory myopathy. Rheumatology 2007; 46(10): 1606–11PubMedCrossRef
49.
go back to reference Huber AM, Dugan EM, Lachenbruch PA, et al. Preliminary validation and clinical meaning of the cutaneous assessment tool (CAT) in juvenile dermatomyositis. Arthritis Rheum 2008; 59(2): 214–21PubMedCrossRef Huber AM, Dugan EM, Lachenbruch PA, et al. Preliminary validation and clinical meaning of the cutaneous assessment tool (CAT) in juvenile dermatomyositis. Arthritis Rheum 2008; 59(2): 214–21PubMedCrossRef
50.
go back to reference Huber AM, Lachenbruch PA, Dugan EM, et al. Alternative scoring of the Cutaneous Assessment Tool (CAT) in juvenile dermatomyositis: results using an abbreviated format. Arthritis Rheum 2008; 59(3): 352–6PubMedCrossRef Huber AM, Lachenbruch PA, Dugan EM, et al. Alternative scoring of the Cutaneous Assessment Tool (CAT) in juvenile dermatomyositis: results using an abbreviated format. Arthritis Rheum 2008; 59(3): 352–6PubMedCrossRef
51.
go back to reference Carroll CL, Lang W, Snively B, et al. Development and validation of the Dermatomyositis Skin Severity Index. Br J Dermatol 2008; 158(2): 345–50PubMedCrossRef Carroll CL, Lang W, Snively B, et al. Development and validation of the Dermatomyositis Skin Severity Index. Br J Dermatol 2008; 158(2): 345–50PubMedCrossRef
52.
go back to reference Klein R, Bangert C, Costner M, et al. Comparison of the reliability and validity of outcome instruments for cutaneous dermatomyositis. Br J Dermatol 2008 Sep; 159(4): 887–94PubMedCrossRef Klein R, Bangert C, Costner M, et al. Comparison of the reliability and validity of outcome instruments for cutaneous dermatomyositis. Br J Dermatol 2008 Sep; 159(4): 887–94PubMedCrossRef
53.
go back to reference Maricq H, Blume R, LeRoy E. Wide-field study of nailfold capillary bed in disorders of connective tissue. In: 6th European Conference on Microcirculation; 1970 Jun 22–26; Aalborg. Basel: Karger, 1971: 116–22 Maricq H, Blume R, LeRoy E. Wide-field study of nailfold capillary bed in disorders of connective tissue. In: 6th European Conference on Microcirculation; 1970 Jun 22–26; Aalborg. Basel: Karger, 1971: 116–22
54.
go back to reference Smith R, Sundberg J, Shamiyah E, et al. Skin involvement in juvenile dermatomyositis is associated with loss of end row nailfold capillary loops. J Rheumatol 2004; 31(8): 1644–9PubMed Smith R, Sundberg J, Shamiyah E, et al. Skin involvement in juvenile dermatomyositis is associated with loss of end row nailfold capillary loops. J Rheumatol 2004; 31(8): 1644–9PubMed
55.
go back to reference Nascif A, Terreri M, Len C, et al. Inflammatory myopathies in childhood: correlation between nailfold capillaroscopy findings and clinical and laboratory data. J Pediatr (Rio J) 2006; 82(1): 40–5CrossRef Nascif A, Terreri M, Len C, et al. Inflammatory myopathies in childhood: correlation between nailfold capillaroscopy findings and clinical and laboratory data. J Pediatr (Rio J) 2006; 82(1): 40–5CrossRef
56.
go back to reference Punaro L, Stichweh D, Powell M, et al. Aspiration: hidden risk for patients with juvenile dermatomyositis [abstract]. Clin Exp Rheumatol 2004; 22 Suppl.: S104 Punaro L, Stichweh D, Powell M, et al. Aspiration: hidden risk for patients with juvenile dermatomyositis [abstract]. Clin Exp Rheumatol 2004; 22 Suppl.: S104
57.
go back to reference McCann L, Garay S, Ryan M, et al. Oropharyngeal dysphagia in juvenile dermatomyositis (JDM): an evaluation of videofluoroscopy swallow study (VFSS) changes in relation to clinical symptoms and objective muscle scores. Rheumatology 2007; 46: 1363–6PubMedCrossRef McCann L, Garay S, Ryan M, et al. Oropharyngeal dysphagia in juvenile dermatomyositis (JDM): an evaluation of videofluoroscopy swallow study (VFSS) changes in relation to clinical symptoms and objective muscle scores. Rheumatology 2007; 46: 1363–6PubMedCrossRef
58.
go back to reference Rider LG, Feldman BM, Perez MD, et al. Development of validated disease activity and damage indices for the juvenile idiopathic inflammatory myopathies I: physician, parent and patient global assessments. Arthritis Rheum 1997; 40(11): 1976–83PubMedCrossRef Rider LG, Feldman BM, Perez MD, et al. Development of validated disease activity and damage indices for the juvenile idiopathic inflammatory myopathies I: physician, parent and patient global assessments. Arthritis Rheum 1997; 40(11): 1976–83PubMedCrossRef
59.
go back to reference Bode RK, Klein-Gitelman MS, Miller ML, et al. Disease activity score for children with juvenile dermatomyositis: reliability and validity evidence. Arthritis Care Res 2003; 49(1): 7–15CrossRef Bode RK, Klein-Gitelman MS, Miller ML, et al. Disease activity score for children with juvenile dermatomyositis: reliability and validity evidence. Arthritis Care Res 2003; 49(1): 7–15CrossRef
60.
go back to reference Ruperto N, Ravelli A, Pistorio A, et al. The provisional Pediatric Rheumatology International Trials Organization/American College of Rheumatology/European League Against Rheumatism disease activity core set for the evaluation of response to therapy in juvenile dermatomyositis: a prospective validation study. Arthritis Rheum 2008; 59(1): 4–13PubMedCrossRef Ruperto N, Ravelli A, Pistorio A, et al. The provisional Pediatric Rheumatology International Trials Organization/American College of Rheumatology/European League Against Rheumatism disease activity core set for the evaluation of response to therapy in juvenile dermatomyositis: a prospective validation study. Arthritis Rheum 2008; 59(1): 4–13PubMedCrossRef
61.
go back to reference Miller FM, Rider LG, Chung Y, et al. Proposed preliminary core set measures for disease outcome assessment in adult and juvenile idiopathic inflammatory myopathy. Rheumatology 2001; 40: 1262–73PubMedCrossRef Miller FM, Rider LG, Chung Y, et al. Proposed preliminary core set measures for disease outcome assessment in adult and juvenile idiopathic inflammatory myopathy. Rheumatology 2001; 40: 1262–73PubMedCrossRef
62.
go back to reference Ruperto N, Ravelli A, Murray K, et al. Preliminary core sets of measures for disease activity and damage assessment in juvenile systemic lupus erythematosus and juvenile dermatomyositis. Rheumatology 2003; 42(12): 1452–9PubMedCrossRef Ruperto N, Ravelli A, Murray K, et al. Preliminary core sets of measures for disease activity and damage assessment in juvenile systemic lupus erythematosus and juvenile dermatomyositis. Rheumatology 2003; 42(12): 1452–9PubMedCrossRef
63.
go back to reference Rider LG, Giannini EH, Brunner HI, et al. International consensus on preliminary definitions of improvement in adult and juvenile myositis. Arthritis Rheum 2004; 50(7): 2281–90PubMedCrossRef Rider LG, Giannini EH, Brunner HI, et al. International consensus on preliminary definitions of improvement in adult and juvenile myositis. Arthritis Rheum 2004; 50(7): 2281–90PubMedCrossRef
64.
go back to reference Maillard S, Jones R, Owens C, et al. Quantitative assessment of MRI T2 relaxation time in thigh muscles in juvenile dermatomyositis. Rheumatology 2004; 43: 603–8PubMedCrossRef Maillard S, Jones R, Owens C, et al. Quantitative assessment of MRI T2 relaxation time in thigh muscles in juvenile dermatomyositis. Rheumatology 2004; 43: 603–8PubMedCrossRef
65.
go back to reference Kimball AB, Summers RM, Turner M, et al. Magnetic resonance imaging detection of occult skin and subcutaneous abnormalities in juvenile dermatomyositis: implications for diagnosis and therapy. Arthritis Rheum 2000; 43(8): 1866–73PubMedCrossRef Kimball AB, Summers RM, Turner M, et al. Magnetic resonance imaging detection of occult skin and subcutaneous abnormalities in juvenile dermatomyositis: implications for diagnosis and therapy. Arthritis Rheum 2000; 43(8): 1866–73PubMedCrossRef
66.
go back to reference Summers RM, Brune AM, Choyke PL, et al. Juvenile idiopathic inflammatory myopathy: exercise-induced changes in muscle at short inversion time inversion-recovery imaging. Radiology 1998; 209(1): 191–6PubMed Summers RM, Brune AM, Choyke PL, et al. Juvenile idiopathic inflammatory myopathy: exercise-induced changes in muscle at short inversion time inversion-recovery imaging. Radiology 1998; 209(1): 191–6PubMed
67.
go back to reference Brown V, Pilkington C, Feldman BM, et al. An international consensus survey on the diagnostic criteria for juvenile dermatomyositis (JDM). Rheumatology (Oxf) 2006; 45: 990–3CrossRef Brown V, Pilkington C, Feldman BM, et al. An international consensus survey on the diagnostic criteria for juvenile dermatomyositis (JDM). Rheumatology (Oxf) 2006; 45: 990–3CrossRef
68.
go back to reference De Benedetti F, De Amici M, Aramini L, et al. Correlation of serum neopterin concentrations with disease activity in juvenile dermatomyositis. Arch Dis Child 1993; 69(2): 232–5PubMedCrossRef De Benedetti F, De Amici M, Aramini L, et al. Correlation of serum neopterin concentrations with disease activity in juvenile dermatomyositis. Arch Dis Child 1993; 69(2): 232–5PubMedCrossRef
69.
go back to reference Rider LG, Schiffenbauer A, Zito M, et al. Neopterin and quinolinic acid are surrogate measures of disease activity in the juvenile idiopathic inflammatory myopathies. Clin Chem 2002; 48(10): 1681–8PubMed Rider LG, Schiffenbauer A, Zito M, et al. Neopterin and quinolinic acid are surrogate measures of disease activity in the juvenile idiopathic inflammatory myopathies. Clin Chem 2002; 48(10): 1681–8PubMed
70.
go back to reference Eisenstein D, O’Gorman M, Pachman LM. Correlations between change in disease activity and changes in peripheral blood lymphocyte subsets in patients with juvenile dermatomyositis. J Rheumatol 1997; 24(9): 1830–2PubMed Eisenstein D, O’Gorman M, Pachman LM. Correlations between change in disease activity and changes in peripheral blood lymphocyte subsets in patients with juvenile dermatomyositis. J Rheumatol 1997; 24(9): 1830–2PubMed
71.
go back to reference O’Gorman M, Bianchi L, Zaas D, et al. Decreased levels of CD54 (ICAM-1)-positive lymphocytes in the peripheral blood in untreated patients with active juvenile dermatomyositis. Clin Diagn Lab Immunol 2000; 7(4): 693–7PubMed O’Gorman M, Bianchi L, Zaas D, et al. Decreased levels of CD54 (ICAM-1)-positive lymphocytes in the peripheral blood in untreated patients with active juvenile dermatomyositis. Clin Diagn Lab Immunol 2000; 7(4): 693–7PubMed
72.
go back to reference Mizuno K, Yachie A, Nagaoki S, et al. Oligoclonal expansion of circulating and tissue-infiltrating CD8+ T cells with killer/effector phenotypes in juvenile dermatomyositis syndrome. Clin Exp Immunol 2004; 137: 187–94PubMedCrossRef Mizuno K, Yachie A, Nagaoki S, et al. Oligoclonal expansion of circulating and tissue-infiltrating CD8+ T cells with killer/effector phenotypes in juvenile dermatomyositis syndrome. Clin Exp Immunol 2004; 137: 187–94PubMedCrossRef
74.
go back to reference Mimori T, Imura Y, Nakashima R, et al. Autoantibodies in idiopathic inflammatory myopathy: an update on clinical and pathophysiological significance. Curr Opin Rheumatol 2007; 19: 523–9PubMedCrossRef Mimori T, Imura Y, Nakashima R, et al. Autoantibodies in idiopathic inflammatory myopathy: an update on clinical and pathophysiological significance. Curr Opin Rheumatol 2007; 19: 523–9PubMedCrossRef
75.
go back to reference Targoff I, Mamyrova G, Trieu E, et al. A novel autoantibody to a 155-kd protein is associated with dermatomyositis. Arthritis Rheum 2006; 54(11): 3682–9PubMedCrossRef Targoff I, Mamyrova G, Trieu E, et al. A novel autoantibody to a 155-kd protein is associated with dermatomyositis. Arthritis Rheum 2006; 54(11): 3682–9PubMedCrossRef
76.
go back to reference Feldman BM, Reichlin M, Laxer RM, et al. Clinical significance of specific autoantibodies in juvenile dermatomyositis. J Rheumatol 1996; 23(10): 1794–7PubMed Feldman BM, Reichlin M, Laxer RM, et al. Clinical significance of specific autoantibodies in juvenile dermatomyositis. J Rheumatol 1996; 23(10): 1794–7PubMed
77.
go back to reference Rider LG, Miller FW, Targoff I, et al. A broadened spectrum of juvenile myositis: myositis-specific autoantibodies in children. Arthritis Rheum 1994; 37(10): 1534–8PubMedCrossRef Rider LG, Miller FW, Targoff I, et al. A broadened spectrum of juvenile myositis: myositis-specific autoantibodies in children. Arthritis Rheum 1994; 37(10): 1534–8PubMedCrossRef
78.
go back to reference Gunawardena H, Wedderburn L, North J, et al. Clinical associations of autoantibodies to a p155/140 kDa doublet protein in juvenile dermatomyositis. Rheumatology 2008; 47(3): 324–8PubMedCrossRef Gunawardena H, Wedderburn L, North J, et al. Clinical associations of autoantibodies to a p155/140 kDa doublet protein in juvenile dermatomyositis. Rheumatology 2008; 47(3): 324–8PubMedCrossRef
79.
go back to reference Li C, Hemlata V, Holton J, et al. MHC Class I overexpression on muscles in early juvenile dermatomyositis. J Rheumatol 2004; 31(3): 605–9PubMed Li C, Hemlata V, Holton J, et al. MHC Class I overexpression on muscles in early juvenile dermatomyositis. J Rheumatol 2004; 31(3): 605–9PubMed
80.
go back to reference McCann L, Li C, Varsani H, et al. Failure to over express MHC Class I on muscle biopsy in a case of amyopathic juvenile dermatomyositis. Clin Exp Rheumatol 2007; 25(1): 96–8PubMed McCann L, Li C, Varsani H, et al. Failure to over express MHC Class I on muscle biopsy in a case of amyopathic juvenile dermatomyositis. Clin Exp Rheumatol 2007; 25(1): 96–8PubMed
81.
go back to reference Miles L, Bove K, Lovell DJ, et al. Predictability of the clinical course of juvenile dermatomyositis based on initial muscle biopsy: a retrospective study of 72 patients. Arthritis Rheum 2007; 57(7): 1183–91PubMedCrossRef Miles L, Bove K, Lovell DJ, et al. Predictability of the clinical course of juvenile dermatomyositis based on initial muscle biopsy: a retrospective study of 72 patients. Arthritis Rheum 2007; 57(7): 1183–91PubMedCrossRef
82.
go back to reference Wedderburn L, Varsani H, Li C, et al. International consensus on a proposed score system for muscle biopsy evaluation in patients with juvenile dermatomyositis: a tool for potential use in clinical trials. Arthritis Rheum 2007; 57(7): 1192–201PubMedCrossRef Wedderburn L, Varsani H, Li C, et al. International consensus on a proposed score system for muscle biopsy evaluation in patients with juvenile dermatomyositis: a tool for potential use in clinical trials. Arthritis Rheum 2007; 57(7): 1192–201PubMedCrossRef
83.
go back to reference Miller ML, Smith R, Abbott K, et al. Use of etanecept in chronic juvenile dermatomyositis (JDM) [abstract]. Arthritis Rheum 2002; 46 Suppl.: S306 Miller ML, Smith R, Abbott K, et al. Use of etanecept in chronic juvenile dermatomyositis (JDM) [abstract]. Arthritis Rheum 2002; 46 Suppl.: S306
84.
go back to reference Miller ML, Mendez EP, Klein-Gitelman MS, et al. Experience with etanercept in chronic juvenile dermatomyositis (JDM): preliminary results [abstract]. Arthritis Rheum 2000; 43 Suppl.: S380CrossRef Miller ML, Mendez EP, Klein-Gitelman MS, et al. Experience with etanercept in chronic juvenile dermatomyositis (JDM): preliminary results [abstract]. Arthritis Rheum 2000; 43 Suppl.: S380CrossRef
85.
go back to reference Stringer E, Feldman BM. Advances in the treatment of juvenile dermatomyositis. Curr Opin Rheumatol 2006; 18: 503–6PubMedCrossRef Stringer E, Feldman BM. Advances in the treatment of juvenile dermatomyositis. Curr Opin Rheumatol 2006; 18: 503–6PubMedCrossRef
86.
go back to reference Riley P, McCann L, Maillard S, et al. Effectiveness of infliximab in the treatment of refractory juvenile dermatomyositis with calcinosis. Rheumatology 2008; 47(6): 877–80PubMedCrossRef Riley P, McCann L, Maillard S, et al. Effectiveness of infliximab in the treatment of refractory juvenile dermatomyositis with calcinosis. Rheumatology 2008; 47(6): 877–80PubMedCrossRef
87.
go back to reference Levine T. A pilot study of rituximab therapy for refractory dermatomyositis [abstract]. Arthritis Rheum 2002; 46 Suppl.: S488 Levine T. A pilot study of rituximab therapy for refractory dermatomyositis [abstract]. Arthritis Rheum 2002; 46 Suppl.: S488
88.
go back to reference Endo L, Theos A, Atkinson T. Use of rituximab in refractory juvenile dermatomyositis [abstract]. Arthritis Rheum 2005; 52 Suppl.: S288 Endo L, Theos A, Atkinson T. Use of rituximab in refractory juvenile dermatomyositis [abstract]. Arthritis Rheum 2005; 52 Suppl.: S288
89.
go back to reference Cooper M, Willingham D, Brown D, et al. Rituximab for the treatment of juvenile dermatomyositis: a report of 4 pediatric cases. Arthritis Rheum 2007; 56(9): 3107–11PubMedCrossRef Cooper M, Willingham D, Brown D, et al. Rituximab for the treatment of juvenile dermatomyositis: a report of 4 pediatric cases. Arthritis Rheum 2007; 56(9): 3107–11PubMedCrossRef
90.
go back to reference Dinh H, McCormack C, Hall S, et al. Rituximab for the treatment of the skin manifestations of dermatomyositis: a report of 3 cases. J Am Acad Dermatol 2007; 56(1): 148–53PubMedCrossRef Dinh H, McCormack C, Hall S, et al. Rituximab for the treatment of the skin manifestations of dermatomyositis: a report of 3 cases. J Am Acad Dermatol 2007; 56(1): 148–53PubMedCrossRef
91.
go back to reference Fisler RE, Liang MG, Fuhlbrigge RC, et al. Aggressive management of juvenile dermatomyositis results in improved outcome and decreased incidence of calcinosis. J Am Acad Dermatol 2002; 47: 505–11PubMedCrossRef Fisler RE, Liang MG, Fuhlbrigge RC, et al. Aggressive management of juvenile dermatomyositis results in improved outcome and decreased incidence of calcinosis. J Am Acad Dermatol 2002; 47: 505–11PubMedCrossRef
92.
go back to reference Ramanan A, Campbell-Webster N, Ota S, et al. The effectiveness of treating juvenile dermatomyositis with methotrexate and aggressively tapered corticosteroids. Arthritis Rheum 2005; 52(11): 3570–8PubMedCrossRef Ramanan A, Campbell-Webster N, Ota S, et al. The effectiveness of treating juvenile dermatomyositis with methotrexate and aggressively tapered corticosteroids. Arthritis Rheum 2005; 52(11): 3570–8PubMedCrossRef
93.
go back to reference Riley P, Maillard S, Wedderburn L, et al. Intravenous cyclophosphamide pulse therapy in juvenile dermatomyositis: a review of efficacy and safety. Rheumatology 2004; 43: 491–6PubMedCrossRef Riley P, Maillard S, Wedderburn L, et al. Intravenous cyclophosphamide pulse therapy in juvenile dermatomyositis: a review of efficacy and safety. Rheumatology 2004; 43: 491–6PubMedCrossRef
94.
go back to reference Yamada A, Ohshima Y, Omata N, et al. Steroid-sparing effect of tacrolimus in a patient with juvenile dermatomyositis presenting with poor bioavailability of cyclosporine A. Eur J Pediatr 2004; 163(9): 561–2PubMedCrossRef Yamada A, Ohshima Y, Omata N, et al. Steroid-sparing effect of tacrolimus in a patient with juvenile dermatomyositis presenting with poor bioavailability of cyclosporine A. Eur J Pediatr 2004; 163(9): 561–2PubMedCrossRef
95.
go back to reference Martin Nalda A, Modesto Caballero C, Arnal Guimeral C, et al. Efficacy of tacrolimus (FK-506) in the treatment of recalcitrant juvenile dermatomyositis: study of 6 cases [in Spanish]. Med Clin (Barc) 2006; 127(18): 697–701CrossRef Martin Nalda A, Modesto Caballero C, Arnal Guimeral C, et al. Efficacy of tacrolimus (FK-506) in the treatment of recalcitrant juvenile dermatomyositis: study of 6 cases [in Spanish]. Med Clin (Barc) 2006; 127(18): 697–701CrossRef
96.
go back to reference Garcia-Doval I, Cruces M. Topical tacrolimus in cutaneous lesions of dermatomyositis: lack of effect in side-by-side comparison in five patients. Dermatology 2004; 209(3): 247–8PubMedCrossRef Garcia-Doval I, Cruces M. Topical tacrolimus in cutaneous lesions of dermatomyositis: lack of effect in side-by-side comparison in five patients. Dermatology 2004; 209(3): 247–8PubMedCrossRef
97.
go back to reference Hollar C, Jorizzo JL. Topical tacrolimus 0.1% ointment for refractory skin disease in dermatomyositis: a pilot study. J Dermatol Treat 2004; 15(1): 35–9CrossRef Hollar C, Jorizzo JL. Topical tacrolimus 0.1% ointment for refractory skin disease in dermatomyositis: a pilot study. J Dermatol Treat 2004; 15(1): 35–9CrossRef
Metadata
Title
Juvenile Dermatomyositis
Advances in Pathogenesis, Evaluation, and Treatment
Author
Dr Adam M. Huber
Publication date
01-12-2009
Publisher
Springer International Publishing
Published in
Pediatric Drugs / Issue 6/2009
Print ISSN: 1174-5878
Electronic ISSN: 1179-2019
DOI
https://doi.org/10.2165/11310550-000000000-00000

Other articles of this Issue 6/2009

Pediatric Drugs 6/2009 Go to the issue

Acknowledgments

Acknowledgment

Adis Drug Evaluation

Topical Pimecrolimus

Original Research Article

Pediatric Safety of Tizanidine