Familial autoimmunity in systemic sclerosis - results of a french-based case-control family study

26Citations
Citations of this article
82Readers
Mendeley users who have this article in their library.

Abstract

Objective. To assess the prevalence of autoimmune diseases in first-degree relatives of patients with systemic sclerosis (SSc), and to compare those results with control families in order to identify patterns of autoimmune diseases in relatives. Methods. A retrospective case-control postal questionnaire survey was performed in France to recruit patients with SSc belonging to an association of patients with SSc and unrelated age-matched and sex-matched controls. Each participant was asked to self-report on the existence of autoimmune diseases in their first-degree relatives. The prevalence of autoimmune diseases in the families of patients with SSc was compared with the corresponding prevalence in the families of controls. Results. A total of 121 families out of 373 (32.4%) with a member having SSc reported at least 1 autoimmune disease in 1 or more first-degree relatives. The most frequent autoimmune diseases in SSc families when adjusted for family size were autoimmune thyroid disease (AITD; 4.9%), rheumatoid arthritis (4.1%), psoriasis (3.9%), and type 1 diabetes mellitus (2.9%). Compared with control families, AITD and connective tissue diseases (SSc, systemic lupus erythematosus, or Sjögren's syndrome) were more likely to occur in families with SSc (p = 0.01 and p = 0.01, respectively), with OR of 3.20 (95% CI 1.25-8.18) and 5.20 (95% CI 1.22-21.8). In contrast, inflammatory bowel disease was less likely to occur within families with SSc (p = 0.02, OR 0.29, 95% CI 0.11-0.80). In addition, the coexistence of more than 1 autoimmune disease in the index SSc case was associated with familial aggregation of autoimmune diseases. Conclusion. Our results show that autoimmune diseases cluster within families of patients with SSc. This supports the notion that these diseases might arise on a shared genetic basis underlying several autoimmune phenotypes. The Journal of Rheumatology Copyright © 2012. All rights reserved.

References Powered by Scopus

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

2636Citations
N/AReaders
Get full text

Genetics and pathogenesis of inflammatory bowel disease

2000Citations
N/AReaders
Get full text

Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

1130Citations
N/AReaders
Get full text

Cited by Powered by Scopus

European Dermatology Forum S1-guideline on the diagnosis and treatment of sclerosing diseases of the skin, Part 1: localized scleroderma, systemic sclerosis and overlap syndromes

178Citations
N/AReaders
Get full text

How do autoimmune diseases cluster in families? A systematic review and meta-analysis

174Citations
N/AReaders
Get full text

Sjögren's syndrome at the crossroad of polyautoimmunity

82Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Koumakis, E., Dieudé, P., Avouac, J., Kahan, A., & Allanore, Y. (2012). Familial autoimmunity in systemic sclerosis - results of a french-based case-control family study. Journal of Rheumatology, 39(3), 532–538. https://doi.org/10.3899/jrheum.111104

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 28

64%

Researcher 12

27%

Professor / Associate Prof. 4

9%

Readers' Discipline

Tooltip

Medicine and Dentistry 44

81%

Nursing and Health Professions 4

7%

Immunology and Microbiology 4

7%

Economics, Econometrics and Finance 2

4%

Save time finding and organizing research with Mendeley

Sign up for free