Real world utilization of the myositis autoantibody panel.

Epidemiology Idiopathic inflammatory myopathy Myositis Myositis antibody panel Test utilization

Journal

Clinical rheumatology
ISSN: 1434-9949
Titre abrégé: Clin Rheumatol
Pays: Germany
ID NLM: 8211469

Informations de publication

Date de publication:
Aug 2021
Historique:
received: 16 11 2020
accepted: 16 02 2021
revised: 31 01 2021
pubmed: 26 2 2021
medline: 22 7 2021
entrez: 25 2 2021
Statut: ppublish

Résumé

Myositis autoantibody panel results can offer diagnostic and prognostic information in patients with concern for idiopathic inflammatory myopathy (IIM). However, there has been widespread utilization of myositis autoantibody testing clinically, often in situations where concern for an IIM is unclear. We sought to determine ordering practices and factors predicting positive results on ordered myositis antibody panels. We included all patients in the Duke University Health System who had a "myositis antibody panel" ordered from October 2014 through December 2016. Retrospective chart review was performed evaluating antibody positivity, provider specialty, ordering location, demographics, medical history, review of systems (ROS), physical examination (PE), and laboratory values. Fisher's exact and t test tests and backward multivariable regression analysis were performed for statistical analysis. There were 642 unique tests obtained with 114 positive autoantibodies (17.7%) over the 26-month period. Myositis-specific autoantibodies (MSAs) were the most common and anti-Mi-2 was the most frequent (40% of MSAs). Pulmonology providers ordered the majority of tests (383; 59.6%). Adult Rheumatology had the highest antibody positivity rate (34.3%, p=0.0001) among specialties with at least 10 panels ordered. In backward multivariable regression analysis, factors independently associated with a positive myositis antibody panel were chronic corticosteroid use (OR: 2.10, 95% CI: 1.30-3.38) and sclerodermoid skin changes (OR: 6.89; 95% CI: 2.02-23.47). The positivity rate of myositis antibody panel testing in this real-world clinical setting was 18%. Anti-Mi-2 antibody was the most frequent autoantibody present. Specific factors associated with positive results can be utilized to identify patients at higher risk for IIM. • Only eighteen percent of all myositis antibody panel tests ordered returned positive. • Anti-Mi-2 antibody was the most frequent autoantibody in our cohort. • Specific factors associated with positive results can help identify patients at higher risk for IIM, particularly for non-rheumatologists.

Identifiants

pubmed: 33629202
doi: 10.1007/s10067-021-05658-y
pii: 10.1007/s10067-021-05658-y
doi:

Substances chimiques

Autoantibodies 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3195-3205

Informations de copyright

© 2021. International League of Associations for Rheumatology (ILAR).

Références

Dimachkie MM, Barohn RJ, Amato AA (2014) Idiopathic inflammatory myopathies. Neurol Clin 32(3):595–628 vii
pubmed: 25037081 pmcid: 4104537 doi: 10.1016/j.ncl.2014.04.007
Ghirardello A, Borella E, Beggio M, Franceschini F, Fredi M, Doria A (2014) Myositis autoantibodies and clinical phenotypes. Auto Immunol Highlights 5(3):69–75
doi: 10.1007/s13317-014-0060-4
Gunawardena H (2017) The clinical features of myositis-associated autoantibodies: a review. Clin Rev Allergy Immunol 52(1):45–57
pubmed: 26453338 doi: 10.1007/s12016-015-8513-8
Pinal-Fernandez I, Casciola-Rosen LA, Christopher-Stine L, Corse AM, Mammen AL (2015) The Prevalence of individual histopathologic features varies according to autoantibody status in muscle biopsies from patients with dermatomyositis. J Rheumatol 42(8):1448–1454
pubmed: 26443871 pmcid: 6544046 doi: 10.3899/jrheum.141443
Betteridge Z, McHugh N (2016) Myositis-specific autoantibodies: an important tool to support diagnosis of myositis. J Intern Med 280(1):8–23
pubmed: 26602539 doi: 10.1111/joim.12451
Fujimoto M, Watanabe R, Ishitsuka Y, Okiyama N (2016) Recent advances in dermatomyositis-specific autoantibodies. Curr Opin Rheumatol 28(6):636–644
pubmed: 27533321 doi: 10.1097/BOR.0000000000000329
Hoshino K, Muro Y, Sugiura K, Tomita Y, Nakashima R, Mimori T (2010) Anti-MDA5 and anti-TIF1-gamma antibodies have clinical significance for patients with dermatomyositis. Rheumatology (Oxford) 49(9):1726–1733
doi: 10.1093/rheumatology/keq153
Li L, Wang Q, Yang F, Wu C, Chen S, Wen X, Liu C, Li Y (2017) Anti-MDA5 antibody as a potential diagnostic and prognostic biomarker in patients with dermatomyositis. Oncotarget. 8(16):26552–26564
pubmed: 28460448 pmcid: 5432278 doi: 10.18632/oncotarget.15716
Tokunaga K, Hagino N (2017) Dermatomyositis with rapidly progressive interstitial lung disease treated with rituximab: a report of 3 cases in Japan. Intern Med 56(11):1399–1403
pubmed: 28566605 pmcid: 5498206 doi: 10.2169/internalmedicine.56.7956
Satoh M, Tanaka S, Ceribelli A, Calise SJ, Chan EK (2017) A comprehensive overview on myositis-specific antibodies: new and old biomarkers in idiopathic inflammatory myopathy. Clin Rev Allergy Immunol 52(1):1–19
pubmed: 26424665 pmcid: 5828023 doi: 10.1007/s12016-015-8510-y
van Dooren SH, van Venrooij WJ, Pruijn GJ (2011) Myositis-specific autoantibodies: detection and clinical associations. Auto Immunol Highlights 2(1):5–20
doi: 10.1007/s13317-011-0018-8
Yang H, Peng Q, Yin L, Li S, Shi J, Zhang Y, Lu X, Shu X, Zhang S, Wang G (2017) Identification of multiple cancer-associated myositis-specific autoantibodies in idiopathic inflammatory myopathies: a large longitudinal cohort study. Arthritis Res Ther 19(1):259
pubmed: 29178913 pmcid: 5702134 doi: 10.1186/s13075-017-1469-8
Hozumi H, Enomoto N, Kono M, Fujisawa T, Inui N, Nakamura Y, Sumikawa H, Johkoh T, Nakashima R, Imura Y, Mimori T, Suda T (2015) Prognostic significance of anti-aminoacyl-tRNA synthetase antibodies in polymyositis/dermatomyositis-associated interstitial lung disease: a retrospective case control study. PLoS One 10(3):e0120313
pubmed: 25789468 pmcid: 4366175 doi: 10.1371/journal.pone.0120313
Cavazzana I, Fredi M, Ceribelli A, Mordenti C, Ferrari F, Carabellese N, Tincani A, Satoh M, Franceschini F (2016) Testing for myositis specific autoantibodies: comparison between line blot and immunoprecipitation assays in 57 myositis sera. J Immunol Methods 433:1–5
pubmed: 26906088 doi: 10.1016/j.jim.2016.02.017
Leclair V, Lundberg IE (2018) New myositis classification criteria-what we have learned since Bohan and Peter. Curr Rheumatol Rep 20(4):18
pubmed: 29550929 pmcid: 5857275 doi: 10.1007/s11926-018-0726-4
Lundberg IE, Tjarnlund A, Bottai M, Werth VP, Pilkington C, Visser M et al (2017) 2017 European League Against Rheumatism/American College of Rheumatology classification criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups. Ann Rheum Dis 76(12):1955–1964
pubmed: 29079590 doi: 10.1136/annrheumdis-2017-211468
Raghu G, Remy-Jardin M, Myers JL, Richeldi L, Ryerson CJ, Lederer DJ, Behr J, Cottin V, Danoff SK, Morell F, Flaherty KR, Wells A, Martinez FJ, Azuma A, Bice TJ, Bouros D, Brown KK, Collard HR, Duggal A, Galvin L, Inoue Y, Jenkins RG, Johkoh T, Kazerooni EA, Kitaichi M, Knight SL, Mansour G, Nicholson AG, Pipavath SNJ, Buendía-Roldán I, Selman M, Travis WD, Walsh S, Wilson KC, American Thoracic Society, European Respiratory Society, Japanese Respiratory Society, and Latin American Thoracic Society (2018) Diagnosis of idiopathic pulmonary fibrosis. An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline. Am J Respir Crit Care Med 198(5):e44–e68
pubmed: 30168753 doi: 10.1164/rccm.201807-1255ST
Bernatsky S, Joseph L, Pineau CA, Belisle P, Boivin JF, Banerjee D, Clarke AE (2009) Estimating the prevalence of polymyositis and dermatomyositis from administrative data: age, sex and regional differences. Ann Rheum Dis 68(7):1192–1196
pubmed: 18713785 doi: 10.1136/ard.2008.093161
U.S. Census Bureau (2018). American Community Survey 1-year estimates. Retrieved from Census Reporter Profile page for Raleigh-Durham-Chapel Hill, NC CSA. http://censusreporter.org/profiles/33000US450-raleigh-durham-chapel-hill-nc-csa/ [Internet]
Ghirardello A, Zampieri S, Iaccarino L, Tarricone E, Bendo R, Gambari PF et al (2005) Anti-Mi-2 antibodies. Autoimmunity. 38(1):79–83
pubmed: 15966133 doi: 10.1080/08916930400022681
Fidler L, Doubelt I, Kandel S, Fisher JH, Mittoo S, Shapera S (2019) Screening for myositis antibodies in idiopathic interstitial lung disease. Lung. 197(3):277–284
pubmed: 30838434 doi: 10.1007/s00408-019-00212-9
Stevenson BR, Thompson GA, Watson MC, Bundell CS, Klinken EM, John M, Lake FR, McLean-Tooke AP (2019) Autoantibodies in interstitial lung diseases. Pathology. 51(5):518–523
pubmed: 31230817 doi: 10.1016/j.pathol.2019.03.007
Prasad JD, Mahar A, Bleasel J, Ellis SJ, Chambers DC, Lake F, Hopkins PMA, Corte TJ, Allan H, Glaspole IN (2017) The interstitial lung disease multidisciplinary meeting: a position statement from the Thoracic Society of Australia and New Zealand and the Lung Foundation Australia. Respirology. 22(7):1459–1472
pubmed: 28891101 doi: 10.1111/resp.13163
Wolstencroft PW, Fiorentino DF (2018) Dermatomyositis clinical and pathological phenotypes associated with myositis-specific autoantibodies. Curr Rheumatol Rep 20(5):28
pubmed: 29637414 doi: 10.1007/s11926-018-0733-5
Song JS, Hwang J, Cha HS, Jeong BH, Suh GY, Chung MP, Kang ES (2015) Significance of myositis autoantibody in patients with idiopathic interstitial lung disease. Yonsei Med J 56(3):676–683
pubmed: 25837172 pmcid: 4397436 doi: 10.3349/ymj.2015.56.3.676
Fischer A, Antoniou KM, Brown KK, Cadranel J, Corte TJ, du Bois RM, Lee JS, Leslie KO, Lynch DA, Matteson EL, Mosca M, Noth I, Richeldi L, Strek ME, Swigris JJ, Wells AU, West SG, Collard HR, Cottin V (2015) An official European Respiratory Society/American Thoracic Society research statement: interstitial pneumonia with autoimmune features. Eur Respir J 46(4):976–987
pubmed: 26160873 doi: 10.1183/13993003.00150-2015
Wilfong EM, Lentz RJ, Guttentag A, Tolle JJ, Johnson JE, Kropski JA, Kendall PL, Blackwell TS, Crofford LJ (2018) Interstitial pneumonia with autoimmune features: an emerging challenge at the intersection of rheumatology and pulmonology. Arthritis Rheum 70(12):1901–1913
doi: 10.1002/art.40679
Scire CA, Gonzalez-Gay MA, Selva-O'Callaghan A, Cavagna L (2017) Clinical spectrum time course of interstitial pneumonia with autoimmune features in patients positive for antisynthetase antibodies. Respir Med 132:265–266
pubmed: 28385573 doi: 10.1016/j.rmed.2017.03.028

Auteurs

Mithu Maheswaranathan (M)

Fellow in the Division of Rheumatology & Immunology, Department of Medicine, Duke University Hospital, DUMC 2918, Durham, NC, 27710, USA. mithunan.maheswaranathan@duke.edu.

Andrew Johannemann (A)

Division of Rheumatology and Immunology, Duke University Health, Durham, NC, USA.

Jason J Weiner (JJ)

Division of Rheumatology and Endocrinology, Naval Medical Readiness and Training Center, San Diego, CA, USA.

Ryan Jessee (R)

Division of Rheumatology and Immunology, Duke University Health, Durham, NC, USA.

Amanda M Eudy (AM)

Division of Rheumatology and Immunology, Department of Medicine, Duke University School of Medicine, Durham, NC, USA.

Lisa Criscione-Schreiber (L)

Division of Rheumatology and Immunology, Department of Medicine, Duke University School of Medicine, Durham, NC, USA.

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