Polymyositis and dermatomyositis laboratory findings
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sadaf Sharfaei M.D.[2]
Overview
Elevated sarcoplasmic enzymes are consistent with the diagnosis of polymyositis and dermatomyositis which include creatine phosphokinase, aldolase, transaminases, lactic dehydrogenase, and myoglobin. High white blood cell counts, low lymphocytes, and low hematocrit levels might be detected on CBC. Low albumin levels, high ESR and high IgM and IgG levels could be seen in patients with polymyositis and dermatomyositis. 20 myositis-specific autoantibodies are identified in patients with polymyositis and dermatomyositis. Anti-Jo-1 antibody is the most frequent myositis-specific autoantibodies which causes antisynthetase syndrome. Anti Mi-2 might be seen frequently in patients with dermatomyositis. Anti-SRP antibody is associated with very poor prognosis. Some of these myositis-specific autoantibodies are associated with malignancy. Anti-HMGCR antibody might be elevated in patients with statin-associated necrotizing autoimmune myopathy (SANAM).
Laboratory Findings
- Different laboratory tests may be used to diagnose polymyositis and dermatomyositis and exclude other myopathies which include:[1][2][3][4][5][6][7][8]
- Routine tests[9]
- Sarcoplasmic enzymes
- Myositis-specific autoantibodies[10][11]
Routine test
- Abnormal test results include:
- CBC
- High white blood cell counts
- Low lymphocyte counts
- Low hematocrit levels
- Low albumin levels
- High erythrocyte sedimentation rate
- High IgM and IgG levels
- CBC
Sarcoplasmic enzymes
- Sarcoplasmic enzymes consistent with the diagnosis of polymyositis and dermatomyositis include:[12]
Myositis-specific autoantibodies
Autoantibody | Antigen | Features | Frequency | |
---|---|---|---|---|
Antisynthetase | Anti-Jo-1 | Histidyl-tRNA synthetase |
|
20-25% |
Anti-PL-7 | Threonyl-tRNA synthetase |
|
5-10% | |
Anti PL-12 | Alanyl-tRNA synthetase |
|
<5% | |
Alanyl-tRNA | ||||
Anti-EJ | Glycyl-tRNA synthetase | 5-10% | ||
Anti-OJ | Isoleucyl-tRNA synthetase | <5% | ||
Anti-KS | Asparaginyl-tRNA synthetase | <5% | ||
Anti-Ha | Tyrosyl-tRNA synthetase | <1% | ||
Anti-Zo | Phenylalanyl-tRNA synthetase | <1% | ||
Others | Anti Mi-2 | Chromodomain helicase DNA binding protein 4 |
|
5-10% |
Anti-SRP | Signal recognition particle |
|
<5% | |
Anti-p155/140 | Transcriptional intermediary factor 1-gamma |
|
13-21% in IIM
23-29% in JDM | |
Anti-MJ | Nuclear matrix protein (NXP-2) |
|
23% in JDM | |
Anti-SAE | Small ubiquitin-like modifier activating enzyme |
|
5% | |
Anti-caDM-140 | Intracytoplasmic MDA5 |
|
50% (C-ADM) | |
Anti-PMS1 | DNA mismatch repair enzyme | 7.5% | ||
Anti-HMGCR | 3-hydroxy-3-methylglutaryl-coenzyme A reductase |
|
6% | |
Anti-FER | Elongation factor 1 alpha | |||
Anti-KJ | Unidentified cytoplasmic protein | |||
Anti-MAS | Unidentified cytoplasmic RNA | |||
Anti–PM-Scl |
|
25% |
References
- ↑ Adler BL, Christopher-Stine L (February 2018). "Triggers of inflammatory myopathy: insights into pathogenesis". Discov Med. 25 (136): 75–83. PMID 29579414.
- ↑ Bodoki L, Nagy-Vincze M, Griger Z, Betteridge Z, Szöllősi L, Dankó K (December 2014). "Four dermatomyositis-specific autoantibodies-anti-TIF1γ, anti-NXP2, anti-SAE and anti-MDA5-in adult and juvenile patients with idiopathic inflammatory myopathies in a Hungarian cohort". Autoimmun Rev. 13 (12): 1211–9. doi:10.1016/j.autrev.2014.08.011. PMID 25182203.
- ↑ Khan, Sabiha; Christopher-Stine, Lisa (2011). "Polymyositis, Dermatomyositis, and Autoimmune Necrotizing Myopathy: Clinical Features". Rheumatic Disease Clinics of North America. 37 (2): 143–158. doi:10.1016/j.rdc.2011.01.001. ISSN 0889-857X.
- ↑ Dobloug, Cecilie; Garen, Torhild; Bitter, Helle; Stjärne, Johan; Stenseth, Guri; Grøvle, Lars; Sem, Marthe; Gran, Jan Tore; Molberg, Øyvind (2015). "Prevalence and clinical characteristics of adult polymyositis and dermatomyositis; data from a large and unselected Norwegian cohort". Annals of the Rheumatic Diseases. 74 (8): 1551–1556. doi:10.1136/annrheumdis-2013-205127. ISSN 0003-4967.
- ↑ Chinoy, H.; Fertig, N.; Oddis, C. V; Ollier, W. E R; Cooper, R. G (2007). "The diagnostic utility of myositis autoantibody testing for predicting the risk of cancer-associated myositis". Annals of the Rheumatic Diseases. 66 (10): 1345–1349. doi:10.1136/ard.2006.068502. ISSN 0003-4967.
- ↑ Dalakas, Marinos C; Hohlfeld, Reinhard (2003). "Polymyositis and dermatomyositis". The Lancet. 362 (9388): 971–982. doi:10.1016/S0140-6736(03)14368-1. ISSN 0140-6736.
- ↑ Douglas, William W.; Tazelaar, Henry D.; Hartman, Thomas E.; Hartman, Robert P.; Decker, Paul A.; Schroeder, Darrell R.; Ryu, Jay H. (2001). "Polymyositis–Dermatomyositis-associated Interstitial Lung Disease". American Journal of Respiratory and Critical Care Medicine. 164 (7): 1182–1185. doi:10.1164/ajrccm.164.7.2103110. ISSN 1073-449X.
- ↑ Miller, Frederick W. (1993). "Myositis-Specific Autoantibodies". JAMA. 270 (15): 1846. doi:10.1001/jama.1993.03510150080034. ISSN 0098-7484.
- ↑ Volochayev, Rita (2012). "Laboratory Test Abnormalities are Common in Polymyositis and Dermatomyositis and Differ Among Clinical and Demographic Groups". The Open Rheumatology Journal. 6 (1): 54–63. doi:10.2174/1874312901206010054. ISSN 1874-3129.
- ↑ Targoff, Ira N. (2006). "Myositis specific autoantibodies". Current Rheumatology Reports. 8 (3): 196–203. doi:10.1007/s11926-996-0025-3. ISSN 1523-3774.
- ↑ Gunawardena, H.; Betteridge, Z. E.; McHugh, N. J. (2009). "Myositis-specific autoantibodies: their clinical and pathogenic significance in disease expression". Rheumatology. 48 (6): 607–612. doi:10.1093/rheumatology/kep078. ISSN 1462-0324.
- ↑ Bohan, Anthony; Peter, James B. (1975). "Polymyositis and Dermatomyositis". New England Journal of Medicine. 292 (8): 403–407. doi:10.1056/NEJM197502202920807. ISSN 0028-4793.