Arthritis in idiopathic inflammatory myopathy: clinical features and autoantibody associations
Jazyk angličtina Země Kanada Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
18474
Arthritis Research UK - United Kingdom
18474
Versus Arthritis - United Kingdom
PubMed
24786927
DOI
10.3899/jrheum.131223
PII: jrheum.131223
Knihovny.cz E-zdroje
- Klíčová slova
- ARTHRITIS, AUTOANTIBODIES, IDIOPATHIC INFLAMMATORY MYOPATHIES,
- MeSH
- alely MeSH
- artritida epidemiologie genetika imunologie MeSH
- autoprotilátky * MeSH
- dospělí MeSH
- genotyp MeSH
- HLA-DQ beta řetězec genetika MeSH
- HLA-DRB1 řetězec genetika MeSH
- komorbidita MeSH
- lidé středního věku MeSH
- lidé MeSH
- myozitida epidemiologie genetika imunologie MeSH
- prevalence MeSH
- průřezové studie MeSH
- senioři MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- autoprotilátky * MeSH
- HLA-DQ beta řetězec MeSH
- HLA-DQB1 antigen MeSH Prohlížeč
- HLA-DRB1 řetězec MeSH
OBJECTIVE: To determine the prevalence, distribution, and clinical manifestations of arthritis in a cohort of patients with idiopathic inflammatory myopathies (IIM). Associations with autoantibody status and HLA genetic background were also explored. METHODS: Consecutive patients with IIM treated in a single center were included in this cross-sectional study (n = 106). History of arthritis, 68-joint and 66-joint tender and swollen joint index, clinical features of IIM, and autoantibody profiles were obtained by clinical examination, personal interview, and review of patient records. High-resolution genotyping in HLA-DRB1 and HLA-DQB1 loci was performed in 71 and 73 patients, respectively. RESULTS: A combination of patients' medical history and cross-sectional physical examination revealed that arthritis at any time during the disease course had occurred in 56 patients (53%). It was present at the beginning of the disease in 39 patients (37%) including 23 cases (22%) with arthritis preceding the onset of muscle weakness. On physical examination, 29% of patients had at least 1 swollen joint. The most frequently affected areas were wrists, and metacarpophalangeal and proximal interphalangeal joints. Twenty-seven out of the 29 anti-Jo1-positive patients had arthritis at any time during the course of their illness; this prevalence was significantly higher compared to patients without the anti-Jo1 autoantibody (p < 0.0001). No association of arthritis with individual HLA alleles was found. CONCLUSION: Our data suggest that arthritis is a common feature of myositis. It is frequently present at the onset of disease and it may even precede muscular manifestations of IIM. The most common presentation is a symmetrical, nonerosive polyarthritis affecting particularly the wrists, shoulders, and small joints of the hands. We have confirmed a strong association of arthritis with the presence of the anti-Jo1 antibody.
Citace poskytuje Crossref.org
Idiopathic inflammatory myopathies
Arthritis in Idiopathic Inflammatory Myopathies