1 |
Selva-O'Callaghan A, Pinal-Fernandez I, Trallero-Araguás E, et al. Classification and management of adult inflammatory myopathies [J].Lancet Neurol, 2018, 17(9): 816-828.
|
2 |
Aussy A, Boyer O, Cordel N. Dermatomyositis and immune-mediated necrotizing myopathies: a window on autoimmunity and cancer [J]. Front Immunol, 2017, 8: 992.
|
3 |
Zampieri S, Valente M, Adami N, et al. Polymyositis, dermatomyositis and malignancy: a further intriguing link [J]. Autoimmun Rev, 2010,9(6):449-453.
|
4 |
Marie I. Morbidity and mortality in adult polymyositis and dermatomyositis [J]. Curr Rheumatol Rep, 2012, 14(3): 275-285.
|
5 |
Gono T, Kuwana M. Inflammatory myopathies: choosing the right biomarkers to predict ILD in myositis [J]. Nat Rev Rheumatol, 2016, 12(9): 504-506.
|
6 |
Damoiseaux J, Vulsteke JB, Tseng CW, et al. Autoantibodies in idiopathic inflammatory myopathies: clinical associations and laboratory evaluation by monoand multispecific immunoassays [J]. Autoimmun Rev, 2019, 18(3): 293-305.
|
7 |
Kuwana M. Circulating anti-nuclear antibodies in systemic sclerosis: utility in diagnosis and disease subsetting [J]. J Nippon Med Sch, 2017, 84(2): 56-63.
|
8 |
Ohtsuka T. The relation between nailfold bleeding and capillary microscopic abnormality in patients with connective tissue diseases [J]. Int J Dermatol, 1998, 37(1): 23-26.
|
9 |
Narang NS, Casciola-Rosen L, Li S, et al. Cutaneous ulceration in dermatomyositis: association with anti-melanoma differentiation-associated gene 5 antibodies and interstitial lung disease [J]. Arthritis Care Res (Hoboken), 2015, 67(5): 667-672.
|
10 |
Didona D, Juratli HA, Scarsella L. Amyopathic and anti-TIF1 gamma-positive dermatomyositis: analysis of a monocentric cohort and proposal to update diagnostic criteria [J]. Eur J Dermatol, 2020, 30(3): 279-288.
|
11 |
Nakashima R, Hosono Y, Mimori T. Clinical significance and new detection system of autoantibodies in myositis with interstitial lung disease [J]. Lupus, 2016, 25(8): 925-933.
|
12 |
Hamaguchi Y, Fujimoto M, Matsushita T, et al. Common and distinct clinical features in adult patients with anti-aminoacyl-tRNA synthetase antibodies: heterogeneity within the syndrome [J]. PLoS One, 2013, 8(4): e60442.
|
13 |
Hozumi H, Enomoto N, Kono M, et al. Prognostic significance of anti-aminoacyl-tRNA synthetase antibodies in polymyositis/dermatomyositis-associated interstitial lung disease: a retrospective case control study [J]. PLoS One, 2015, 10(3): e0120313.
|
14 |
Nishio M, Endo Y, Kosaka K. Anti-aminoacyl-tRNA synthetases antibody positive overlap syndrome of systemic sclerosis and dermatomyositis associated with rapidly progressive interstitial lung disease [J]. J Dermatol, 2021, 48(2): e110-e111.
|
15 |
Rider LG, Nistala K. The juvenile idiopathic inflammatory myopathies: pathogenesis, clinical and autoantibody phenotypes, and outcomes [J]. J Intern Med, 2016, 280(1): 24-38.
|
16 |
Iwata N, Nakaseko H, Kohagura T, et al. Clinical subsets of juvenile dermatomyositis classified by myositis-specific autoantibodies: experience at a single center in Japan [J]. Mod Rheumatol, 2019, 29(5): 802-807.
|
17 |
Chen Z, Hu W, Wang Y, et al. Distinct profiles of myositis-specific autoantibodies in Chinese and Japanese patients with polymyositis/dermatomyositis [J]. Clin Rheumatol, 2015, 34(9): 1627-1631.
|
18 |
Benveniste O, Stenzel W, Allenbach Y. Advances in serological diagnostics of inflammatory myopathies [J]. Curr Opin Neurol, 2016, 29(5): 662-673.
|
19 |
González-Moreno J, Raya-Cruz M, Losada-Lopez I, et al. Rapidly progressive interstitial lung disease due to anti-MDA5 antibodies without skin involvement: a case report and literature review [J]. Rheumatol Int, 2018, 38(7): 1293-1296.
|
20 |
Aoyama J, Hayashi H, Yajima C, et al. Anti-MDA5 antibody-positive rapidly progressive interstitial pneumonia without cutaneous manifestations [J]. Respir Med Case Rep, 2019, 26: 193-196.
|
21 |
Sakamoto N, Ishimoto H, Nakashima S, et al. Clinical features of anti-MDA5 antibody-positive rapidly progressive interstitial lung disease without signs of dermatomyositis [J]. Intern Med, 2019, 58(6): 837-841.
|
22 |
Hozumi H, Fujisawa T, Nakashima R, et al. Comprehensive assessment of myositis-specific autoantibodies in polymyositis/dermatomyositis-associated interstitial lung disease [J]. Respir Med, 2016, 121: 91-99.
|
23 |
Sato S, Murakami A, Kuwajima A, et al. Clinical utility of an enzyme-linked immunosorbent assay for detecting anti-melanoma differentiation-associated gene 5 autoantibodies [J]. PLoS One, 2016, 11(4): e0154285.
|
24 |
Luo L, Huang WH, Ren FF. Pharyngeal ulceration and perforation: a rare manifestation in anti-MDA5 dermatomyositis [J]. Rheumatology (Oxford), 2021, 60(4): e132-e133.
|
25 |
Kanaoka M, Yamaguchi K, Watanabe T. Clinically amyopathic dermatomyositis with anti-transcriptional intermediary factor 1-γ autoantibody positivity [J]. Rheumatology (Oxford), 2020, 59(10): e68-e69.
|
26 |
Fiorentino DF, Kuo K, Chung L, et al. Distinctive cutaneous and systemic features associated with antitranscriptional intermediary factor-1γ antibodies in adults with dermatomyositis [J]. J Am Acad Dermatol, 2015, 72(3): 449-455.
|
27 |
DeWane ME, Waldman R, Lu J. Dermatomyositis: clinical features and pathogenesis [J]. J Am Acad Dermatol, 2020, 82(2): 267-281.
|
28 |
Chung MP, Richardson C, Kirakossian D. Calcinosis biomarkers in adult and juvenile dermatomyositis [J]. Autoimmun Rev, 2020, 19(6): 102533.
|
29 |
Vooght JD, Vulsteke JB, Haes PD. Anti-TIF1-γ autoantibodies: warning lights of a tumour autoantigen [J]. Rheumatology(Oxford), 2020, 59(3): 469-477.
|
30 |
Ikeda N, Yamaguchi Y, Kanaoka M. Clinical significance of serum levels of anti-transcriptional intermediary factor 1-γ antibody in patients with dermatomyositis [J]. J Dermatol, 2020, 47(5): 490-496.
|
31 |
Sung Y, Jung S, Kim H, et al. Temporal relationship between idiopathic inflammatory myopathies and malignancies and its mortality: a nationwide population-based study [J]. Clin Rheumatol, 2020, 39(11): 3409-3416.
|
32 |
Fujimoto M, Hamaguchi Y, Kaji K, et al. Myositis-specific anti-155/140 autoantibodies target transcription intermediary factor 1 family proteins [J]. Arthritis Rheum, 2012, 64(2): 513-522.
|
33 |
Shimizu K, Kobayashi T, Kano M. Anti-transcriptional intermediary factor 1-γ antibody as a biomarker in patients with dermatomyositis [J]. J Dermatol, 2020, 47(1): 64-68.
|
34 |
Yang H, Peng Q, Yin L, et al. Identification of multiple cancer-associated myositis-specific autoantibodies in idiopathic inflammatory myopathies: a large longitudinal cohort study [J]. Arthritis Res Ther, 2017, 19(1): 259.
|
35 |
Okiyama N, Yamaguchi Y, Kodera M. et al. Distinct histopathologic patterns of finger eruptions in dermatomyositis based on myositis-specific autoantibody profiles [J]. JAMA Dermatol, 2019, 155(9): 1080-1082.
|
36 |
Ono N, Kai K, Maruyama A, et al. The relationship between type 1 IFN and vasculopathy in anti-MDA5 antibody-positive dermatomyositis patients [J]. Rheumatology(Oxford), 2019, 58(5): 786-791.
|
37 |
DeWane ME, Waldman R, Lu J. Dermatomyositis: clinical features and pathogenesis [J]. J Am Acad Dermatol, 2020, 82(2): 267-281.
|
38 |
Wolstencroft PW, Fiorentino DF. Dermatomyositis clinical and pathological phenotypes associated with myositis-specific autoantibodies [J]. Curr Rheumatol Rep, 2018, 20(5): 28.
|
39 |
Monseau G, Landon-Cardinal O, Stenzel W. Systematic retrospective study of 64 patients with anti-Mi2 dermatomyositis: A classic skin rash with a necrotizing myositis and high risk of malignancy [J].J Am Acad Dermatol, 2020, 83(6): 1759-1763.
|
40 |
Albayda J, Pinal-Fernandez I, Huang W, et al. Dermatomyositis patients with anti-nuclear matrix protein-2 autoantibodies have more edema, more severe muscle disease, and increased malignancy risk [J]. Arthritis Care Res (Hoboken), 2017, 69(11): 1771-1776.
|
41 |
Rogers A, Chung L, Li S, et al. The cutaneous and systemic findings associated with nuclear matrix protein-2 antibodies in adult dermatomyositis patients [J]. Arthritis Care Res (Hoboken), 2017, 69(12): 1909-1914.
|
42 |
Liu Y, Zheng Y, Gang Q. Perimysial microarteriopathy in dermatomyositis with anti-nuclear matrix protein-2 antibodies [J]. Eur J Neurol, 2020, 27(3): 514-521.
|
43 |
Pachman LM, Khojah AM. Advances in juvenile dermatomyositis: myositis specific antibodies aid in understanding disease heterogeneity [J]. J Pediatr, 2018, 195: 16-27.
|
44 |
Ge Y, Lu X, Shu X, et al. Clinical characteristics of anti-SAE antibodies in Chinese patients with dermatomyositis in comparison with different patient cohorts [J]. Sci Rep, 2017, 7(1): 188.
|
45 |
Gono T, Tanino Y, Nishikawa A, et al. Two cases with autoantibodies to small ubiquitin-like modifier activating enzyme: a potential unique subset of dermatomyositis-associated interstitial lung disease [J]. Int J Rheum Dis, 2019, 22(8): 1582-1586.
|
46 |
Kishi T, Rider LG, Pak K, et al. Association of anti-3-hydroxy-3-methylglutaryl-coenzyme a reductase autoantibodies with DRB1*07:01 and severe myositis in juvenile myositis patients [J]. Arthritis Care Res (Hoboken), 2017, 69(7): 1088-1094.
|
47 |
Watanabe Y, Uruha A, Suzuki S, et al. Clinical features and prognosis in anti-SRP and anti-HMGCR necrotising myopathy [J]. J Neurol Neurosurg Psychiatry, 2016, 87(10): 1038-1044.
|
48 |
Allenbach Y, Keraen J, Bouvier AM, et al. High risk of cancer in autoimmune necrotizing myopathies: usefulness of myositis specific antibody [J]. Brain, 2016, 139(Pt 8): 2131-2135.
|
49 |
De Lorenzo R, Pinal-Fernandez I, Huang W, et al. Muscular and extramuscular clinical features of patients with anti-PM/Scl autoantibodies [J]. Neurology, 2018, 90(23): e2068-e2076.
|
50 |
Spielmann L, Nespola B, Séverac F, et al. Anti-Ku syndrome with elevated CK and anti-Ku syndrome with anti-dsDNA are two distinct entities with different outcomes [J]. Ann Rheum Dis, 2019, 78(8): 1101-1106.
|
51 |
Kaji K, Fertig N, Medsger TA, et al. Autoantibodies to RuvBL1 and RuvBL2: a novel systemic sclerosis-related antibody associated with diffuse cutaneous and skeletal muscle involvement [J]. Arthritis Care Res (Hoboken), 2014, 66(4): 575-584.
|
52 |
Wang J, Guo G, Chen G, et al. Meta-analysis of the association of dermatomyositis and polymyositis with cancer [J]. Br J Dermatol, 2013, 169(4): 838-847.
|
53 |
Sato S, Masui K, Nishina N, et al. Initial predictors of poor survival in myositis-associated interstitial lung disease: a multicentre cohort of 497 patients [J]. Rheumatology (Oxford), 2018, 57(7): 1212-1221.
|
54 |
Tsuji H, Nakashima R, Hosono Y, et al. A multicenter prospective study of the efficacy and safety of combined immunosuppressive therapy with high-dose glucocorticoid, tacrolimus, and cyclophosphamide in interstitial lung diseases accompanied by anti-melanoma differentiation-associated gene 5-positive dermatomyositis [J]. Arthritis Rheumatol, 2020, 72(3): 488-498.
|
55 |
Chen Z, Wang X, Ye S. Tofacitinib in amyopathic dermatomyositis-associated interstitial lung disease [J].N Engl J Med, 2019, 381(3): 291-293.
|
56 |
Andersson H, Sem M, Lund MB, et al. Long-term experience with rituximab in anti-synthetase syndrome-related interstitial lung disease [J]. Rheumatology (Oxford), 2015, 54(8): 1420-1428.
|
57 |
Kawasumi H, Gono T, Kawaguchi Y, et al. Recent treatment of interstitial lung disease with idiopathic inflammatory myopathies [J]. Clin Med Insights Circ Respir Pulm Med, 2015, 9(Suppl 1): 9-17.
|