Occupational silica exposure in an Australian systemic sclerosis cohort

Author:

Patel Shreeya1,Morrisroe Kathleen12,Proudman Susanna34,Hansen Dylan1,Sahhar Joanne56,Sim Malcolm R7,Ngian Gene-Siew56,Walker Jenny3,Strickland Gemma1,Wilson Michelle1,Ferdowsi Nava1,Major Gabor89,Roddy Janet10,Stevens Wendy1,Nikpour Mandana12,Nikpour Mandana,Proudman Susanna,Stevens Wendy,Sahhar Joanne,Cooley Helen,Croyle Lucy,Ferdowsi Nava,Hill Catherine,Host Lauren,Major Gabor,Morrisroe Kathleen,Ngian Gene-Siew,Rischmueller Maureen,Roddy Janet,Strickland Gemma,Tay Tien,Tymms Kathleen,Walker Jennifer,Youssef Peter,

Affiliation:

1. Department of Rheumatology, St Vincent’s Hospital Melbourne, Melbourne, Victoria

2. Department of Medicine, The University of Melbourne at St Vincent’s Hospital (Melbourne), Fitzroy, Victoria

3. Rheumatology Unit, Royal Adelaide Hospital

4. Discipline of Medicine, University of Adelaide, Adelaide, South Australia

5. Department of Rheumatology, Monash Health

6. Department of Medicine, Monash University

7. Centre for Occupational & Environmental Health, Monash University, Melbourne, Victoria

8. Department of Rheumatology, Bone and Joiny Institute, Royal Newcastle Centre, John Hunter Hospital, Newcastle, New South Wales

9. School of Medicine and Public Health, University of Newcastle, Callaghan, New South Wales

10. Department of Rheumatology, Fiona Stanley Hospital, Perth, Western Australia, Australia

Abstract

Abstract Objective To determine the frequency of self-reported occupational exposure to silica in SSc patients enrolled in the Australian Scleroderma Cohort Study, and to compare the disease characteristics of the silica-exposed patients with those of the non-exposed patients. Method Data collected over a 12-year period from 1670 SSc patients were analysed. We compared the demographic and clinical characteristics of those who reported occupational silica exposure with those who did not. A subgroup analysis of male patients was performed, as well as a multivariable analysis of correlates of silica exposure. Results Overall, 126 (7.5%) of the cohort reported occupational silica exposure. These individuals were more likely to be male (73 of 231, i.e. 31.6% males exposed) and to have worked in mining and construction industries. Those who reported silica exposure were younger at the onset of SSc skin involvement [odds ratio (OR) 0.9, P = 0.02], of male gender (OR 14.9, P < 0.001), have joint contractures (OR 1.8, P = 0.05) and have higher physical disability as defined by scleroderma HAQ (OR 1.4, P = 0.01). Conclusion The highest percentage of silica exposure was found in males. These patients were more likely to have the presence of certain clinical manifestations and Scl-70 antibody, which is known to confer a poor prognosis. These findings support the association between occupational silica exposure and the subsequent development of SSc. Further investigation is required to describe the range of clinical manifestations and disease course, including prognosis and treatment response, in those diagnosed with occupationally induced SSc compared with idiopathic SSc.

Funder

Australian Scleroderma Cohort Study

Scleroderma Clinical Trials Consortium

St Vincent’s Hospital Research Endowment Fund

Australian Rheumatology Association

GlaxoSmithKline, Roche, Pfizer, Bayer, CSL Biotherapies and Bristol-Myers Squibb

National Health and Medical Research Council of Australia Career Development Fellowship

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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