THU0625 Igg4-related disease manifestations differ between asian and non-asian subjects. (12th June 2018)

• Record Type: Journal Article
• Authors: Wallace, Z.S.; Okazaki, K.; Perugino, C.; Umehara, H.; Saeki, T.; Kawano, M.; Zen, Y.; Naden, R.; Stone, J.H.
• Is Part Of: Annals of the rheumatic diseases. Volume 77(2018)Supplement 2
• Page Start: 509
• Page End: 509
• Publication Date: 2018-06-12
• Subjects: Rheumatism -- Periodicals; 616.723005
• DOI: 10.1136/annrheumdis-2018-eular.5245
• Languages: English
• ISSNs: 0003-4967

Abstract

Abstract : Background: Background: IgG4-related disease (IgG4-RD) is a multi-system immune-mediated condition that can affect nearly any organ. No study has evaluated differences in disease manifestations according to race. We evaluated this in a large cohort of IgG4-RD subjects submitted by an international group of investigators. Objectives: Objectives: To evaluate racial differences in manifestations of IgG4-RD. Methods: Methods: To validate the ACR/EULAR IgG4-RD Classification Criteria, 76 investigators from North America, South America, Europe, and Asia submitted cases they considered to be IgG4-RD in either the preliminary phase or the validation phase. For each case, investigators included details related to diagnostic certainty, age at disease onset and diagnosis, race, organ involvement, biopsy findings, and laboratory results. Based on reported race, we dichotomized subjects into either Asian or non-Asian categories; subjects of South Asian (n=14) descent (e.g., India, Pakistan), all of whom resided in North America or Europe were grouped with non-Asian subjects. We compared the distribution of disease features according to race using t-tests, Wilcoxon tests, and Chi square tests, where appropriate, as well as in multivariable-adjusted models. Results: Results: In the validation phase, there were 493 cases of IgG4-RD submitted by 23 investigators who practice in Asia and 29 investigators who practice in North America or Europe. There was no significant difference in the distribution of specialists (e.g., rheumatology, gastroenterology) between Asian and non-Asian investigators (p=0.3). The majority of IgG4-RD subjects, both Asian (n=208) and non-Asian (n=285), were male (61% and 69%, respectively). Asian subjects were significantly older both at symptom onset and diagnosis (61.2±13.2 years and 62.6±12.8 years, respectively) compared to non- Asian subjects (55.1±14.9 years and 57.2±14.4 years, respectively, p<0.0001 for both comparisons). There was a significantly shorter diagnostic delay among Asian subjects compared to non-Asian subjects (1.4±2.7 years vs 2.2±3.7 years, p=0.01). Head/neck involvement was more common in Asians (52% vs 27%, p<0.0001) whereas hepatobiliary involvement was more common in non-Asians (52% vs. 42%, p=0.04). Asian subjects had a significantly higher median serum IgG4 concentration (666 mg/dL, IQR 320.5–1230 vs 240.5, IQR 100–505, p<0.0001) and were more likely to have a serum IgG4 concentration greater than five times the upper limit of normal (48% vs 20%, p<0.0001). In multivariable-adjusted models, differences in age and serum IgG4 concentration according to race remained strongly significant (p<0.001 for both comparisons). Conclusions: Conclusions: Asian and non-Asian subjects differed regarding the age of disease onset and diagnosis, the distribution of organ involvement, and baseline serum IgG4 concentrations. There was a significantly shorter diagnostic delay among Asian subjects compared to non-Asian subjects. The etiology(ies) of these observed differences in the respective presentation of IgG4-RD in Asian and non-Asian subjects requires further investigation, but could include differences in diagnostic approach, environmental factors, and genetic predisposition. Disclosure of Interest: None declared