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Citation
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HERO ID
2588426
Reference Type
Journal Article
Title
Cancer-associated myositis and anti-p155 autoantibody in a series of 85 patients with idiopathic inflammatory myopathy
Author(s)
Trallero-Araguás, E; Labrador-Horrillo, M; Selva-O'Callaghan, A; Martínez, MA; Martínez-Gómez, X; Palou, E; Rodriguez-Sanchez, JL; Vilardell-Tarrés, M
Year
2010
Is Peer Reviewed?
1
Journal
Medicine
ISSN:
0025-7974
EISSN:
1536-5964
Volume
89
Issue
1
Page Numbers
47-52
Language
English
PMID
20075704
DOI
10.1097/MD.0b013e3181ca14ff
Web of Science Id
WOS:000273719500005
Abstract
A new autoantibody against a 155-kDa protein has been described in patients with myositis. We conducted a study to determine the occurrence and types of cancer occurring in a cohort of patients with polymyositis (PM) or dermatomyositis (DM) and analyzed the value of this autoantibody as a serologic marker of cancer-associated myositis (CAM). Serum samples from all patients were examined by protein immunoprecipitation assays with HeLa cells to determine the presence of a 155-kDa protein band. HLA-DRB1 and DQA1 typing was performed by polymerase chain reaction-reverse sequence specific oligonucleotide. Statistical analyses were carried out with the Mann Whitney U and Fisher exact tests. Associations were determined using odds ratios (ORs) with 95% confidence intervals (CI). Eighty-five patients with myositis (20 PM and 65 DM) were included. CAM was detected in 16 patients (19%), 14 with DM. The shawl sign rash was significantly more frequent in patients with CAM than in those without (p < 0.01). Adenocarcinoma was the most frequent type of cancer (87.5%). Anti-p155 autoantibody was found in 1 of the 20 (5%) patients with PM and in 15 of the 65 (23%) patients with DM. A relationship between anti-p155 and CAM was found in DM patients (OR, 23; 95% CI, 5.23-101.2). The HLA-DQA1*0102 allele was not found in any of the anti-p155-positive patients. The prevalence of CAM in our cohort was 19%. Autoantibody against p155 was highly related to CAM and could be a reliable marker of cancer in patients with DM.
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