Occupational quantitative exposure to crystalline silica, solvents and pesticides and risk of clinical forms of systemic sclerosis

Author:

Galli Gaël12,De Pous-Gerardin Camille3,Hanguehard Remi4,Berthy Florine4,Le Moal Cyril5,Lourde Come6,Barnetche Thomas2,Skopinski Sophie2,Contin-Bordes Cecile12,Delva Fleur4,Carles Camille34,Truchetet Marie-Elise12

Affiliation:

1. University of Bordeaux, CNRS, ImmunoConcEpT, UMR 5164 , Bordeaux, Nouvelle-Aquitaine, France

2. CHU de Bordeaux, FHU ACRONIM, Centre National de référence Des Maladies Autoimmunes et Systémiques Rares Est/Sud-Ouest (RESO) , Bordeaux, Nouvelle-Aquitaine, France

3. CHU de Bordeaux, Service Santé Travail Environnement , Bordeaux, Nouvelle-Aquitaine, France

4. University of Bordeaux, INSERM, UMR 1219, Equipe EPICENE , Bordeaux, Nouvelle-Aquitaine, France

5. Centre Hospitalier des Pays de Morlaix, Service de Médecine Interne , Morlaix, Bretagne, France

6. 14èbme Centre Médical des Armées, 97ème Antenne Médicale , Olivet, Centre Val de Loire, France

Abstract

Abstract Objectives To estimate the association between SSc clinical phenotypes and quantitative occupational exposure to crystalline silica, chlorinated solvents, trichloroethylene and pesticides using job-exposure matrices. Methods In the VISS-EXPOSITION transversal study, data on declarative occupational exposure to crystalline silica, solvents and pesticides were retrieved. In parallel, the lifetime occupational history was evaluated using a questionnaire and cursus laboris for SSc patients followed at Bordeaux University Hospital (France). Using job-exposure matrices, we assessed patients’ occupational exposure in relation to relevant clinical phenotypic forms of the disease. Results Toxic exposure to crystalline silica and pesticides is underestimated by patients. Non-biased job-exposure matrices retrieved more exposed patients than the declarative assessment (10.1% of patients by job-exposure matrices vs 6.3% by declaration for crystalline silica and 25.9% vs 12.2% for pesticides). Patients overestimate their solvent exposure (7.9% for chlorinated solvents and 4.8% for trichlorethylene assessed by job-exposure matrices and 24.4% declarative exposure to solvents at large). Clinical form evaluation revealed a non-significant trend toward an increased risk of crystalline silica occupational exposure in the pulmonary fibrotic group of SSc patients [odds ratio (OR) 3.12 (95% CI 0.80, 12.15)]. We also observed a non-significant trend toward an elevated OR ([2.89 (95% CI 0.93, 8.95)] for chlorinated solvent occupational exposure and the vascular phenotype of SSc. Of note, pesticide occupational exposure evaluation represents one of the largest to date in SSc patients. Conclusion This study emphasizes that many exposed SSc patients are unaware of their occupational exposure. Job-exposure matrices allow better exposure screening for SSc secondary prevention and occupational exposure compensation. Clinical trial registration clinicaltrials.gov (https://www.clinicaltrials.gov), NCT03543956

Funder

Association des Sclérodermiques de France Young Researcher Program

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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