Clinical phenotypes of IgG4-related disease: an analysis of two international cross-sectional cohorts
説明
<jats:sec><jats:title>Objective</jats:title><jats:p>IgG4-related disease (IgG4-RD) is a heterogeneous, multiorgan condition of unclear aetiology that can cause organ failure. Difficulty recognising IgG4-RD contributes to diagnostic delays. We sought to identify key IgG4-RD phenotypes.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>We used two cross-sectional studies assembled by an international, multispecialty network of IgG4-RD specialists who submitted 765 cases to derive and replicate phenotypic groups. Phenotype groups of disease manifestations and key covariate distributions across the identified groups were measured using latent class analysis.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>In the derivation cohort (n=493), we identified four groups with distinct manifestations: Group 1 (31%), Pancreato-Hepato-Biliary disease; Group 2 (24%), Retroperitoneal Fibrosis and/or Aortitis; Group 3 (24%), Head and Neck-Limited disease and Group 4 (22%), classic Mikulicz syndrome with systemic involvement. We replicated the identification of four phenotype groups in the replication cohort. Compared with cases in Groups 1, 2 and 4, respectively, cases in Group 3 were more likely to be female (OR 11.60 (95% CI 5.39 to 24.98), 10.35 (95% CI 4.63 to 23.15) and 9.24 (95% CI 3.53 to 24.20)) and Asian (OR 6.68 (95% CI 2.82 to 15.79), 7.43 (95% CI 2.97 to 18.56) and 6.27 (95% CI 2.27 to 17.29)). Cases in Group 4 had a higher median serum IgG4 concentration (1170 mg/dL) compared with groups 1–3 (316, 178 and 445 mg/dL, respectively, p<0.001).</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>We identified four distinctive IgG4-RD phenotypes according to organ involvement. Being Asian or female may predispose individuals to head and neck-limited disease. These phenotypes serve as a framework for identifying IgG4-RD and studying its aetiology and optimal treatment.</jats:p></jats:sec>
収録刊行物
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- Annals of the Rheumatic Diseases
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Annals of the Rheumatic Diseases 78 (3), 406-412, 2019-01-05
BMJ
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詳細情報 詳細情報について
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- CRID
- 1360848660969368192
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- ISSN
- 14682060
- 00034967
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- データソース種別
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- Crossref
- KAKEN