Literature DB >> 31881814

Reply to Lescoat et al.: Silica Exposure and Scleroderma: More Bridges and Collaboration between Disciplines Are Needed.

Marianne T Turner1,2, Sameh R Samuel3, Elizabeth J Silverstone1,2, Deborah H Yates1,2.   

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Year:  2020        PMID: 31881814      PMCID: PMC7124711          DOI: 10.1164/rccm.201912-2335LE

Source DB:  PubMed          Journal:  Am J Respir Crit Care Med        ISSN: 1073-449X            Impact factor:   21.405


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From the Authors: We thank Lescoat and colleagues for their correspondence and their interest in our work (1). We fully agree about the importance of a new awareness regarding silica hazards and their relationship with connective tissue disease (CTD) in artificial-stone workers. We certainly hope that our joint efforts in highlighting this important area result in greater collaboration among subspecialty physicians, toxicologists, and leaders in occupational medicine and public health globally. Lescoat and colleagues are right to point out the broader history of the observed association between CTD and silica exposure. We were restricted by word limits in our report from acknowledging the work of the Scottish physician B. Bramwell, who in 1914 first noted an increased prevalence of scleroderma among stonemasons in his seminal paper (2). Increased mortality from “chronic rheumatism” in coalminers was subsequently reported by Collis and Yule in the United Kingdom in 1933 (3) and by Anthony Caplan, a physician working on the Cardiff Pneumoconiosis Panel, who described pneumoconiosis in coal miners with rheumatoid arthritis in 1953 (4). L. D. Erasmus reported a high prevalence of scleroderma among South African gold miners in 1957 (5), and the association between silica exposure and CTD, especially systemic sclerosis or scleroderma, has subsequently been confirmed in many publications. Our suggestion regarding systematic screening of patients for CTD after silica exposure, both with and without pulmonary involvement, would not only aid interdisciplinary research but would also assist in the clinical diagnosis of CTD in line with the VEDOSS (Very Early Diagnosis of Systemic Sclerosis) strategy (6), as Lescoat and colleagues note. The VEDOSS strategy centers on a combination of autoimmune antibody testing, capillaroscopic findings, and clinical detection of “puffy fingers” preceding sclerodactyly. Importantly, longitudinal follow-up for 5 years or more is required. Applying this strategy with longitudinal follow-up of patients occupationally exposed to silica may enable earlier diagnosis of both silicosis and associated CTD and improve patient outcomes with earlier intervention. We would welcome the interdisciplinary clinical use of capillaroscopy and optimal surveillance strategies, and we hope that by working together we can gain a better understanding of the pathogenesis of both silicosis and CTD.
  3 in total

1.  Scleroderma in goldminers on the Witwatersrand with particular reference to pulmonary manifestations.

Authors:  L D ERASMUS
Journal:  S Afr J Lab Clin Med       Date:  1957-09

2.  Certain unusual radiological appearances in the chest of coal-miners suffering from rheumatoid arthritis.

Authors:  A CAPLAN
Journal:  Thorax       Date:  1953-03       Impact factor: 9.139

3.  Silica Exposure and Connective Tissue Disease: An Underrecognized Association in Three Australian Artificial Stone Workers.

Authors:  Marianne T Turner; Sameh R Samuel; Elizabeth J Silverstone; Deborah H Yates
Journal:  Am J Respir Crit Care Med       Date:  2020-02-01       Impact factor: 21.405

  3 in total

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