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  1. Johanna Sigaux1,2,
  2. Catherine Cavalin3,4,5,
  3. Odile Macchi4,6,
  4. Salima Challal2,
  5. Sarah El Rharras2,
  6. Mylene Petit2,
  7. Marie-Christophe Boissier1,2,
  8. Paul-Andre Rosental4,6,7,
  9. Luca Semerano1,2
  1. 1INSERM UMR 1125, Université Paris 13, 93000 Bobigny, France, Bobigny, France
  2. 2Assistance Publique-Hôpitaux de Paris, Hôpital Avicenne Service de Rhumatologie, 93000 Bobigny, France, Bobigny, France
  3. 3IRISSO – UMR CNRS-INRA 7170-1427 Université Paris-Dauphine, Paris, France
  4. 4SILICOSIS project, ERC Advanced Grant, Centre for European Studies, Sciences Po, Paris, France, Paris, France
  5. 5Laboratory for Interdisciplinary Evaluation of Public Policies (LIEPP, Sciences Po, Paris), Paris, France
  6. 6Centre for Historical Research, CNRS-EHESS, Paris, Paris, France
  7. 7National Institute for Demographic Studies (INED), Paris, France


Background Occupational exposure to silica dust is associated with increased risk of developing ACPA positive Rheumatoid arthritis (RA). Little is known about non-occupational exposure, as there are no available tools to assess it in clinical practice.

The Dust Exposure Life-Course Questionnaire (DELCQ), developed within the SILICOSIS project, a European Research Council Advanced Grant, provides clinical research with a tool derived from social sciences. The DELCQ allows to quantify both occupational and non-occupational (e.g. body care; hobbies such as DIY, woodworking, stone cutting, etc..) exposure to silica and some other inorganic particles during the whole lifetime.

In the DELCQ, the identification of sources of exposure is grounded on an extensive list of products and activities summed up by the International Agency on Research on Cancer and on a wide overview of the literature addressing silica exposure and silica-related (or suspected-to-be-related) diseases.

Objectives To explore occupational and non-occupational silica exposure in a series of consecutive RA patients and the association of quantified silica dust exposure with major disease features (ACPA positivity) or outcomes (erosive disease).

Methods The DELCQ was administered to 97 consecutive RA patients (77F, 20M, mean age 59.1+/- 13.3 yrs.,75 ACPA positives, 66 with erosive disease) attending the rheumatology department of Avicenne Hospital (Bobigny, FRANCE). The DELCQ scores of patients were compared to those of 388 controls, matched for sex, age and smoking status, from a 2739-subject national cohort, representative of the general French population (ELIPSSilice). Within RA subjects, the association of the scores with ACPA positivity and with erosive disease was assessed after adjustment for tobacco use.

Results RA patients had higher median scores of occupational (10 [0, 17] vs. 0 [0, 4]) exposure vs. controls (p<0.0001). Median occupational exposure was higher in both men and women compared to controls matched by age, sex and tobacco use (23.5 [18, 34.5] vs. 2.5 [0, 12] for men and 7 [3, 14] vs. 0 [0, 5] for women, p<0.0001 for both). Non-occupational median exposure was significantly higher only in women with RA (15 [9, 21] vs. 12 [5, 21], p< 0.05). Male vs. female RA patients had higher median occupational scores of exposure (p<0.001), while non-occupational exposure was not significantly different. After adjusting for smoking (smokers>5 pack/y vs. nonsmokers or smokers <5 pack/y), neither professional of non-professional scores were associated with erosive disease, despite a strong negative interaction with tobacco use.

Conclusion Women with RA have higher professional and nonprofessional lifetime exposure to silica dust compared to age, and sex-matched subjects from the French general population. In this series, constituted mainly of non-smoking women, exposure to silica may be a relevant environmental factor for the development of RA. Higher occupational exposure in RA is confirmed in men with RA. Neither occupational nor non-occupational exposure was associated with ACPA positivity or erosive disease, likely due to the high prevalence these features in the patient series.

Disclosure of Interests Johanna Sigaux Speakers bureau: celgene, Catherine Cavalin: None declared, Odile Macchi: None declared, Salima Challal: None declared, Sarah El Rharras: None declared, Mylene Petit: None declared, marie-Christophe Boissier Grant/research support from: Pfizer MSD, Speakers bureau: Pfizer Lilly Biogen, Paul-Andre Rosental: None declared, Luca Semerano Grant/research support from: pfizer, Speakers bureau: pfizer, roche, msd, bms

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